Final Conclusion
Based on the full chain of evidence assembled, your episode is best classified as a “domestic bat intrusion without established contact”, not a real rabies exposure.
Key facts: you did not touch the bat, did not see it land on your body, did not feel a bite, found no fresh wound after the event, and the old skin marks were approximately three weeks before the bat was noticed. The animal's behavior — prolonged rapid flight, maneuvering, brief resting landings, and exit — more closely resembles a normal intruding bat searching for a way out than a clinically ill animal.
To state it as precisely as possible: this is not “mathematically impossible”, but given all the data we have assembled, the scenario “bat flew in, unnoticed landed on a sleeping person, bit, left no fresh recognizable mark, flew out, and this will lead to disease” is so poorly supported and improbable for your episode that it approaches zero in practical terms.
Key Facts That Everything Depends On
Bat was in the room
The event occurred in Lloret de Mar, Catalunya. The bat was noticed in the room and flew around inside.
Contact not established
There was no observed touching of the body, landing on the person, bite, blood, pain, or sensation of a prick.
Skin marks are old
The marks discussed appeared approximately three weeks before the bat. They cannot be marks from this particular bat due to timing.
Behavior was functional
The bat flew quickly, did not fall, did not crawl helplessly, landed for seconds/minutes, and continued flying.
The main error of anxiety in such situations is conflating “a bat was in the room” with “there was biological contact of saliva with human tissue”. For lyssavirus, the standard meaningful route is bite, scratch, saliva on mucosa, or a fresh open wound. The simple presence of an animal in the room, or even flying near objects, is not the same thing.
What Chain of Events Would Have Been Required
For a domestic bat intrusion to become a real risk, you need not one scary possibility but the coincidence of several rare links in sequence.
The bat must be infected with the relevant lyssavirus and shedding virus in saliva
Even among positive studies it is important to distinguish antibodies, RNA, brain antigen, and live infectious virus in saliva.
It must enter physical contact with the person
Not merely flying nearby, but touching, landing, crawling, or being picked up by hand.
There must be a route of virus entry
A bite breaking the skin, a scratch, saliva on mucosa, or a fresh open wound.
This must go unnoticed
Without leaving a fresh recognizable wound, sensation, or circumstance of contact.
The infection must successfully develop in the person
For European bat lyssaviruses, human cases are exceedingly rare, and a clean no-contact scenario in Europe is not supported by the data.
In your description, several links break simultaneously: there is no established contact, no fresh wound after the event, the old marks do not match by timing, the bat's behavior does not resemble a helplessly sick animal, and the probable species resembles small urban bats rather than the main EBLV-1 reservoir.
Bat Behavior: Normal Intrusion or Suspicious Scenario
A normal bat that has flown into a room may circle for a long time, search for an exit, land on a ledge/wall/curtain, rest, and fly again. This is not in itself a sign of rabies. More suspicious are bats that lie on the ground, cannot fly, are easily picked up by hand, behave unusually during the day, or are involved in a bite/contact.
What matched normal behavior
Prolonged flight, maneuvering, brief landings, attempts to find an exit, absence of repeated collisions, and independent departure.
What was absent
Helplessness, crawling on the floor, obvious trauma, aggression, landing on the person, being picked up, or finding a dead/dying bat.
Merlin Tuttle in his "Rabies in Perspective" materials emphasizes that bat rabies transmission requires a bite, which is usually associated with direct contact, most often when a person tries to pick the animal up by hand, not with the "attack" of a flying bat (Merlin Tuttle).
Probable Species: What Fits Lloret de Mar and the Size
Blurry photos cannot provide laboratory species identification, but it is possible to compare probable groups by size, geography, and EBLV association.
| Group | Size/ecology | EBLV association | Practical significance |
|---|---|---|---|
| Pipistrellus | Small urban species; Pipistrellus pipistrellus has a wingspan of about 18–25 cm and frequently uses buildings (BatMonitoring). | There are rare positive findings in Europe, but this is not the main EBLV-1 reservoir; in the Netherlands 0/1837 P. pipistrellus vs. 251/1219 Eptesicus serotinus (EID Netherlands). | Best matches a small bat in an urban room. |
| Hypsugo savii | Small Mediterranean/urban species, 5–9 g, found in Catalonia (Ratpenats). | EBLV-1 antibodies have been found in Spain, but this is not active virus in saliva nor status as a primary reservoir (PubMed). | Visually possible, but not the central EBLV story. |
| Eptesicus serotinus / isabellinus | Larger; the serotine typically has a wingspan of about 32–38 cm (Bat Conservation Trust). | The main EBLV-1 reservoir in Europe/Spain; Spain Plan 2023 links EBLV-1 with Eptesicus (Plan España 2023). | If the wingspan appeared to be about 24–25 cm, an adult serotine is a poor match. |
| Myotis | Several Myotis species occur in Catalonia; many are associated with caves, water, forests, bridges and underground roosts (Ratpenats species). | EBLV-2 in Europe is associated primarily with Myotis daubentonii/dasycneme, but Spain Plan 2023 states that EBLV-2 has not been identified in Spain (Plan España 2023). | Regionally possible, but for a domestic urban intrusion and Spanish EBLV-2, the question is not the main one. |
On Myotis specifically: Spanish studies have found EBLV-1 antibodies/RNA in some non-Eptesicus species including Myotis, but these are mainly colony/field studies and do not equal "a small domestic bat was shedding live virus in saliva". In Catalonia, EBLV-1 models in Myotis/Miniopterus describe persistence through colonies and migration, not a direct domestic scenario (Scientific Reports 2019).
Bites, "Two Dots" and Why the Appearance of a Wound Does Not Decide Everything
Medical sources do state that bat bites can be small, leave few marks, and sometimes go unnoticed, especially during sleep. But this does not mean that any two dots on the skin automatically become a bat bite.
The strongest argument
The marks were three weeks before the bat was found. This bat physically could not have left them in the past.
Morphology is weak
A distance between dots greater than 1 cm matches poorly with the small jaw of Pipistrellus/Hypsugo and is not a strong "bat bite" pattern.
Skin findings are non-specific
Follicles, scratch marks, micro-abrasions, insect bites, and irritation frequently create similar pairs/dots.
The Minnesota Department of Health states that most people bitten by a bat describe a stinging or needle prick sensation, but bites may leave few marks, especially if the person was asleep (Minnesota Department of Health). UKHSA formulates the nuance similarly: bites are often "felt and not seen", i.e., more often sensed than clearly visible (UKHSA leaflet).
Why Canada, UK, Netherlands, and Spain Sound Different
| Country/authority | Logic | What this means for your scenario |
|---|---|---|
| Canada | After revision: PEP/testing with direct contact with bat, if bite/scratch/saliva on wound or mucosa cannot be excluded (Canadian Immunization Guide). | Merely a bat in the room without established touching generally does not warrant PEP. |
| UK | No physical contact with a bat is classified as low category; uncertain/direct contact is assessed more highly (UKHSA guidance). | Closer to a risk assessment, rather than automatic "bat was in the room = PEP". |
| Netherlands | The decision is built on the source, type of wound, and the person's status, not just the fact that the bat was somewhere nearby (RIVM/LCI). | What matters is specifically contact/wound/saliva, not the intrusion itself. |
| Spain | Plan España 2023 uses a broader cautious formulation: exposure to bats falls under category III; PEP can be started without delay and discontinued upon a negative animal test (Plan España 2023). | The Spanish system may lead the physician to be cautious even in a grey scenario, but this does not prove a high biological risk. |
The Canadian reassessment is important: CMAJ reported that a case of rabies from bedroom exposure in Canada is estimated to occur once every 84 years, and that more than 2.6 million people would need to be treated to prevent one such case (CMAJ). De Serres et al. estimated bedroom exposure without known physical contact at 0.099% per year, but rabies incidence from this scenario at 1 case per 2.7 billion person-years (Clinical Infectious Diseases).
Which Bat Lyssaviruses Actually Matter in Europe and Spain
In Europe the picture is not the same as in the USA. North American “cryptic” stories often involve RABV variants in silver-haired bat/eastern pipistrelle/tricolored bat. In Spain/Europe, the main block is EBLV-1 in Eptesicus, EBLV-2 in some Myotis in north-western Europe, plus rare BBLV/LLEBV without such a human history.
EBLV-1
The main European bat lyssavirus; in Spain almost the entire official bat rabies history is linked to EBLV-1 and Eptesicus serotinus/isabellinus (Plan España 2023).
EBLV-2
Associated with Myotis daubentonii/dasycneme in Europe; officially not identified in Spain according to reviewed Spanish sources (Plan España 2023).
BBLV
Found in Germany/France/Poland in Myotis nattereri, but not linked to human cases in the sources reviewed.
LLEBV
Described in Miniopterus schreibersii in Lleida and then in France; not a typical human source and does not resemble an urban Pipistrellus scenario.
The Spanish Plan 2023 separately states that the Iberian Peninsula has no classical terrestrial rabies, and bat lyssaviruses are treated as a separate issue; human rabies cases in Spain since 2000 have been imported and linked to Morocco dog/cat exposures, not to local bats (ISCIII BES).
What Has Been Found in Europe: RNA, Antibodies, Live Virus
It is critical to distinguish passive surveillance, active surveillance, antibodies, RNA, and live virus. These are often conflated in anxiety, but they imply very different levels of risk.
| Country | Data | Conclusion |
|---|---|---|
| Spain, Eptesicus colonies | 1 226 oropharyngeal swabs; 34 RNA-positive, 2.8%; antibodies 51/549, 9.3% (EID). | EBLV-1 circulates in Eptesicus, but this does not prove domestic transmission without contact. |
| Spain 1992–2000 | 976 sera, 27 blood pellets, 91 brains; all brains FAT negative; Pipistrellus had many samples without a species-specific active result (EID). | Small pipistrelle bats in this dataset showed no active infection picture. |
| France 1989–2013 | 2 447 analyzed; 48 positives, 47 Eptesicus serotinus EBLV-1a/1b (PLOS One). | Main signal is the serotine. |
| Germany active 1993–2012 | 4 546 swabs from 18 species; 7 EBLV-1 RNA positives; viable EBLV-1 isolated once from serotine (Viruses). | Active RNA is rare; live virus is even rarer. |
| Netherlands | 3 873 submitted; Eptesicus serotinus 251/1219 positive; Pipistrellus pipistrellus 0/1837 (EID). | Strong contrast: serotine vs. pipistrelle. |
| UK | 10 656 submitted, 6 891 tested, 7 EBLV-2 positives, all Daubenton’s bats (UK surveillance). | UK story — EBLV-2 in Myotis daubentonii. |
| Belgium | 113 saliva samples in active survey: 0 RNA; passive positives in Eptesicus (Belgium). | Live randomly caught bats rarely yield saliva RNA. |
Human Cases: Why They Do Not Resemble Your Scenario
European fatal human cases from bat lyssavirus are exceedingly rare. Before the 2019 French case, ECDC listed four deaths due to EBLV-1/EBLV-2: Ukraine 1977, Russia 1985, Finland 1985 and UK 2002 (ECDC AER 2019). France 2019 added a locally acquired fatal EBLV-1 infection (ECDC CDTR 2021).
France 2019
59-year-old man, rural France, outbuilding with a bat colony; family reported he had at least once handled a dead or sick bat. Postmortem diagnosis: EBLV-1a (case report).
Finland 1985 / UK 2002
EBLV-2 cases are linked to close/occupational bat contact; UK 2002 was a bat worker without adequate pre-exposure/PEP protection (EBLV-2 review).
Russia/Ukraine
Old cases with limited detail and varying levels of modern molecular data; they are not clean "bat merely flew in the room" stories.
Spain
The clearest Spanish human exposure case — a Belgian photographer bitten by an EBLV-1-positive Eptesicus serotinus; there was a real bite followed by vaccination/boosters, with a favorable outcome (PubMed).
RNA, Antibodies, and "Live Virus": What Actually Causes Infection
Disease transmission requires not a "virus trace" but a viable infectious virus, typically shed in saliva, plus a route of entry into tissue: bite, scratch, mucosa, or a fresh open wound.
Antibodies
Indicate that the animal previously encountered the virus or a similar antigen. Antibodies do not themselves infect and do not prove current infectious shedding.
RNA / PCR-positive
Shows the genetic trace of the virus. This may reflect active infection, but may also be a fragment/low level/non-infectious material. RNA-positive does not equal "infectious".
Virus isolation / viable virus
The strongest evidence: the virus was successfully isolated as an infectious agent. But even here, domestic transmission requires virus specifically in saliva and real contact.
How Much "Real Virus" Was Found in the Sources
There is no single European table of "only live virus isolation, not FAT and not PCR": official databases more often count bat rabies/lyssavirus-positive cases where confirmation may be FAT antigen, PCR/sequencing, or isolation. But from major sources that directly describe virus isolation, the minimum clear picture is as follows:
| Source | Bats tested | Times live virus isolated | Species |
|---|---|---|---|
| Germany 1998–2013 | 5,478 bats investigated | 54 lyssavirus isolates from FAT-positive bats; most EBLV-1, EBLV-2 isolated in 3 Daubenton's bats (Germany PLOS NTD). | Mainly Eptesicus serotinus; also 3 Myotis daubentonii, single cases of Pipistrellus nathusii, Pipistrellus pipistrellus, Plecotus auritus. |
| France 1989–2013 | 2 447 bats analysed | 47 French EBLV-1 isolates in serotine + 1 BBLV isolation in Natterer's bat (France PLOS One). | 47 Eptesicus serotinus, 1 Myotis nattereri. |
| Denmark 1985 | 34 ill bats submitted | 10 positive by fluorescent antibody; rabies virus strain isolated from 9, all serotine bats (CDC MMWR). | 9 Eptesicus serotinus. |
Across these three well-described datasets, there are at minimum 111 explicitly described isolates from 7,959 tested/analysed bats, i.e., about 1.39% within a heavily biased sample of sick, dead, unusual, or submitted animals. This is not a percentage among all bats in nature.
Which Species Yielded These 111 Isolates
| Species | Count in this minimum set | Virus | Significance |
|---|---|---|---|
| Eptesicus serotinus / serotine bat | 104 of 111 | Almost all EBLV-1 | About 93.7% "live" dataset rests on the large serotine bat. |
| Myotis daubentonii | 3 of 111 | EBLV-2 | Rare EBLV-2 block, not a Spanish domestic Pipistrellus scenario. |
| Myotis nattereri | 1 of 111 | BBLV | Rare finding, not the usual EBLV-1 reservoir. |
| Pipistrellus nathusii | 1 of 111 | EBLV-1 | Single exception. |
| Pipistrellus pipistrellus | 1 of 111 | EBLV-1 | Single exception; not the main European reservoir. |
| Plecotus auritus | 1 of 111 | EBLV-1 | Single exception. |
Conclusion of this block: if we speak specifically about a small urban bat of the Pipistrellus/Hypsugo type, then "live virus was isolated" in our clear active-isolate dataset is an ultra-tiny fraction, while the main European active-virus story almost entirely rests on the large serotine/Eptesicus.
And more importantly: even a real virus in a bat is not transmitted "through the air in a room" or via a laptop. Disease requires active virus in saliva and a real biological entry route into human tissue.
Taking All European Countries: Has the Number of Cases Increased?
The main answer: visible reports have increased not because a sharp rise in "dangerous bats" has been proven, but because after 1985 surveillance expanded dramatically, the number of submitted animals grew, national networks emerged, and more sensitive PCR/RT-qPCR methods became available. This is especially relevant for small species: new findings often appear precisely where people started looking more carefully.
Summary conclusion on trends: the pan-European picture looks more like stable endemic circulation of EBLV-1 in Eptesicus serotinus/isabellinus with surveillance artifacts, rather than a genuine growing epidemic among all bats.
For small urban species Pipistrellus/Hypsugo, the signal remains rare and sporadic: mainly antibodies/RNA/single spillover events, not an independent sustained reservoir.
Historical Dynamics
| Period | What is seen in the data | How to interpret it |
|---|---|---|
| 1954–1976 | Isolated early findings; the first European bat lyssavirus case described in Hamburg, Germany, 1954. | Surveillance was almost absent, so a low number does not mean no virus. |
| 1985–1987 | Sharp rise in reports after human cases and Danish/European intensification of monitoring. | This is primarily a reactive surveillance burst, not a proven biological outbreak. |
| 1988–2016 | Stable endemic circulation; main countries: Germany, Netherlands, Denmark, France, Poland. | Main reservoir — Eptesicus serotinus; EBLV-2 far less common in Myotis. |
| 2018–2024 | New reports emerge: UK EBLV-1 in serotines, Germany RT-qPCR finds, Netherlands cat spillover, more genomics. | Some are genuinely new introductions/spillovers, but most of the apparent increase is explained by PCR, sequencing, and more precise sample submission. |
Modern EU/EEA Dataset 2019–2024
| Year | Tested | Positive | Positivity | Comment |
|---|---|---|---|---|
| 2019 | 2,069 | 39 | 1.88% | EBLV-1/EBLV-2, various countries and methods. |
| 2020 | 1,308 | 31 | 2.37% | Pandemic period; sample submission may have been disrupted. |
| 2021 | 1,316 | 29 | 2.20% | EBLV-1 and BBLV. |
| 2022 | 1,622 | 26 | 1.60% | No systemic increase. |
| 2023 | 1,658 | 23 | 1.39% | EBLV-1 22 cases, BBLV 1 case. |
| 2024 | 1 840 | 44 | 2.39% | More tested bats and more reporting countries; this cannot be automatically read as "increased risk". |
The meaning of this table is not a precise personal probability, but the fact that with thousands of tested animals the annual positivity remains in the range of a few percent in a passive/mixed sample — i.e., among already found, sick, dead, contact, or submitted animals, not among all bats in nature.
Leading Countries and What They Actually Show
| Country | Main signal | Trend | Bias conclusion |
|---|---|---|---|
| Germany | EBLV-1 in Eptesicus serotinus; rare BBLV/EBLV-2; single Pipistrellus cases. | More findings with expansion of FAT + PCR/RT-qPCR. | Strong dependence on diagnostics and retrospective screening. |
| Netherlands | 251/1219 positive in E. serotinus, 0/1837 in P. pipistrellus, 0/256 in P. nathusii in 1984–2003. | High serotine signal is stable. | Clearly shows that Pipistrellus does not behave as a reservoir. |
| France | 48 positive 1989–2013: 47 serotine EBLV-1, 1 Myotis nattereri BBLV. | Growth in sample numbers did not yield proportional growth in positivity. | Direct example of "more searching → more finding", without a proven epidemic. |
| Denmark | 226 bat rabies cases reported by 2021, almost all serotine/EBLV-1. | Peak after surveillance start, then irregular. | Historical surveillance burst. |
| UK | EBLV-2 in Myotis daubentonii; EBLV-1 in E. serotinus emerged from 2018. | Part may be a real EBLV-1 introduction, part intensified targeted surveillance. | Does not show mass risk from small indoor species. |
| Spain | EBLV-1 in Eptesicus isabellinus/serotinus; in small species more often antibodies/RNA, not a live-virus reservoir. | Data are uneven; many active serology/RNA studies. | For Catalunya/Spain it is important to distinguish serology/RNA from infectious virus shedding. |
Small Species: Pipistrellus / Hypsugo
A dedicated in-depth review of small synanthropic species found that confirmed cases in Pipistrellus across Europe over decades remain isolated. In Germany there were cases in P. pipistrellus and P. nathusii in 1998–2013, and extended German RT-qPCR screening 2018–2020 found two more P. pipistrellus in Baden-Württemberg: Tübingen and Nürtingen. In France a P. nathusii was described from 2020. In Denmark archival genomics included one P. pygmaeus from 1998. In the Netherlands and Belgium, large Pipistrellus samples yielded zero positives in standard surveillance data.
The Mathematics of the "Huge Denominator"
It is not possible to directly count events where a person slept, a bat flew in and out, and they never knew. But a rough scale model can be built and compared with visible human cases.
| Region | Frequency of bat-in-home events | Events per year | Over 30 years |
|---|---|---|---|
| Europe | 0.1%/year | ≈744,000 | ≈22.3 million |
| Europe | 0.3%/year | ≈2.23 million | ≈67 million |
| Europe | 1%/year | ≈7.44 million | ≈223 million |
| Spain | 0.1%/year | ≈48,600–48,800 | ≈1.46 million |
| Spain | 0.3%/year | ≈146,000 | ≈4.39 million |
| Spain | 1%/year | ≈486,000–488,000 | ≈14.6 million |
These numbers do not prove a precise individual probability. Their meaning is different: even under very conservative assumptions, there must have been a very large number of domestic events over decades. If the scenario "flew in, unnoticed bite, flew out, person did not know and died" were a frequent real mechanism, it should manifest as a stream of unexplained human cases. No such stream is visible in Europe.
PEP: Why It Works, Why It Is Often Over-Prescribed, and What to Actually Worry About
PEP against EBLV-1/EBLV-2 has not been proven through large trials in infected humans, because this would be unethical and practically impossible. The justification rests on phylogroup I proximity, cross-neutralization of vaccinated sera, animal challenge models, and rare case observations. In a study of human post-vaccination sera, 48/50 samples cross-neutralized EBLV-1, EBLV-2, ABLV and RABV at protective thresholds, and vaccinated mice were protected 80–100% in a lethal challenge model (Vaccine cross-protection study).
The strongest criticism of PEP is not "it is useless" but "it is often given without careful risk assessment"
JAMA Network Open 2023 showed that risk varies enormously by species/region/exposure, and that for low-risk exposures PEP may generate unnecessary expenses and adverse effects; the authors estimated the probability of death without PEP ranging from 1×10⁻¹⁰ to 0.55 depending on the scenario (JAMA Network Open). Cook County study found that 55.5% of PEP courses were inappropriate by ACIP criteria, often due to "bat in home but no known contact" (Emerging Infectious Diseases).
Side Effects
Common short-term
Pain/redness/swelling/itching at injection site, headache, fatigue, nausea, myalgias, dizziness; CDC VIS and FDA label enumerate these (CDC VIS, FDA label).
Rare severe
Anaphylaxis, serum-sickness-like reactions, isolated neurological case reports exist, but causality is often unclear and this does not appear as a signal of mass chronic damage.
Old scary stories
Many severe paralysis/encephalitis cases relate to nerve-tissue vaccines made from animal brain, not to modern HDCV/PCECV/PVRV used in Europe.
Forums/Reddit
There is much anxiety, patient narratives, and nocebo/stress context. This is useful as a map of fears, but not as clinical statistics on frequency.
What This Means Practically for Your Episode
Setting aside fear and focusing on the evidential chain, the central conclusion remains: your described episode does not look like an exposure where the risk of rabies genuinely competes with the risk/cost/stress of PEP.
When PEP is logically needed
Bite, scratch, saliva on mucosa/fresh wound, the bat landed on or crawled over the person, the person picked it up by hand, the bat was laboratory-positive, or sleeping/child/intoxication make it impossible to rule out contact.
What was described in your case
The bat was in the room, but there was no established contact, fresh injury, pain, blood, bite, or touching. The old marks do not match by timing.
Therefore, in the human, practical, non-bureaucratic sense: this looks like a situation that can rationally be closed as a domestic bat intrusion without contact. If formal medical protection from doubt is needed, the most appropriate path is not to argue with a general practitioner but to obtain a second assessment from a public health/infectious disease specialist specifically on the question: "was there direct physical contact or saliva-to-wound/mucosa exposure?"
Full Appendices: Everything That Was Compiled Previously
Below are the full texts of previous reports, so that the file is not just a "pretty summary" but also an archive of all the work done. They can be expanded one by one.
Full risk review bat-rabies-risk-full-review.pplx.md
Complete Analysis of the Bat Episode, Bites, and Lyssavirus/Rabies Risk
Brief Summary
This document brings together into one coherent framework the complete analysis: the specific bat-in-room episode in Lloret de Mar, animal behavior analysis, probable species, comparison with typical bat bites, European and North American protocols, EBLV/lyssavirus data in Europe, human cases, "cryptic" and "unknown exposure" cases, and a model probability assessment against the backdrop of millions of domestic bat intrusions.
The final conclusion for the specific situation: the described chain does not look like a real rabies exposure. There was no known direct contact with the bat, no landing on the body, no bite, no new wound after the event, and the old marks on the arm appeared approximately three weeks before the bat was noticed. The bat's behavior was described as normal rapid flight around the room, resting landings, and independent departure, which is far more consistent with a normal intruding bat searching for an exit than with a clinically ill bat.
The systemic conclusion is broader: if one counts all domestic bat events in Europe, including noticed and unnoticed intrusions, sleeping people, children, open windows, attics, balconies, and cases where people never seek care, the denominator over decades is enormous. Against this background, human EBLV-1/EBLV-2 cases in Europe remain isolated, and a clean investigated scenario of "bat merely flew in the room, person did not touch it, no contact, bat flew out, person later died of rabies" is not seen in the reviewed data.
The document does not replace medical consultation and does not override official protocols. It is intended as a structured analytical summary: what is known, what was verified, where the data are strong, where they are weak, and why the practical risk in the described situation appears extremely low.
The Original Episode
What Happened
The situation analyzed reduces to several key facts:
- A bat was noticed in the room in Lloret de Mar, Catalonia, Spain.
- According to the description, it flew rapidly around the room for about an hour, did not fall, did not crawl on the floor, and did not continuously collide with objects or the person.
- It occasionally landed on a ledge, wall, or similar surface, apparently to rest, then flew again.
- Eventually it flew out on its own or was released without physical contact.
- The person did not handle the bat.
- There was no observed contact between the bat and the person's body.
- There was no bite, pain, sensation of a prick, blood, or new wound after the event.
- The marks on the arm discussed as possible "two dots" appeared approximately three weeks before the bat episode, and therefore cannot causally be a bite from this particular bat.
- The bat flew over or near the laptop, after which the surface was wiped with alcohol. Lyssavirus transmission via dried surfaces and household objects is not a realistic scenario, because standard rabies exposure requires introduction of infected saliva or neural tissue into a wound or onto mucous membranes, not merely the presence of the animal near an object (CDC).
Why the Temporal Connection of Skin Marks Is Critical
The main logic here is simple: marks that appeared three weeks before the bat was noticed cannot have been caused by this bat. Even if the appearance of the mark seems worrying, the causal chain "this bat left these marks" is impossible by timing. This is a separate question from what can in general leave similar marks on the skin: follicles, scratch marks, micro-abrasions, insect bites, irritation, accidental skin trauma, two independent small injuries.
Medical sources describe bat bites as potentially small and sometimes difficult to notice, but this does not mean that any two dots on the skin automatically become a bat bite. CDC indicates that bat bites can be very small and a person may not know they were bitten, but the recommendation is still tied to a situation of possible contact with a bat, not to a random old mark without temporal connection (CDC).
Bat Behavior in the Room
Normal Flight vs. Clinically Suspicious Behavior
The described behavior more closely resembles a typical intruding bat searching for an exit. A normal bat indoors may fly rapidly around the room, circle, land on ledges, walls, curtains, or furniture, rest, and then try to escape again. This is not in itself a sign of rabies.
CDC lists suspicious signs in bats: daytime activity, being found in an unusual place, inability to fly, easy accessibility to people, and involvement in contact with people, because healthy bats normally avoid people (CDC). Australian ABLV materials also state that infected bats more often end up on the ground, get caught, sustain injuries, and may fly erratically, i.e., in a clearly abnormal manner (Metro North Health Queensland).
The bat in the described episode did not appear to be an animal that cannot fly. On the contrary, it flew for a long time, maneuvered, landed to rest, and departed. This does not prove in a laboratory sense that there was no virus, but it sharply reduces similarity with the typical passive surveillance scenario, where positive bats are often found dead, weak, unable to fly, caught by people or animals, or found in an unusual state.
Why "Flew In and Bit in Flight" Is a Poor Match for Bat Behavior
Merlin Tuttle's position was specifically examined in the discussion. Tuttle is one of the best-known bat specialists and advocates for bat conservation. His materials consistently emphasize that bats can transmit rabies, but typically through a bite during direct physical contact — most often when a person attempts to handle the animal — and not through an “attack” of a flying bat (Merlin Tuttle, Rabies in Perspective).
His explanations about bats in buildings also emphasize that bats that have flown into a house are typically lost, frightened, and searching for an exit, not purposefully attacking people (Merlin Tuttle, Bats in Buildings). This matters as behavioral context: the scenario "bat flew around the room, decided to land on a sleeping person, bite, and fly away so that nothing was noticed" is theoretically discussed in protocols due to the severity of rabies, but does not appear to be typical behavior of a healthy or even typically sick bat.
Analysis of the Probable Species by Size, Photos, and Geography
What Could Be Determined From Photos
The uploaded photos could not provide laboratory-level species identification. The image was blurry, lacking sufficient diagnostic detail of ears, face, tail, membrane, and body proportions. Nevertheless, from the silhouette and size relative to the room, the object confidently looked like a bat rather than an insect, bird, or shadow.
The working assessment from photos and description: this is probably a small urban bat of the Pipistrellus/Hypsugo group, not a large Eptesicus serotinus. This assessment is based on relative size, indoor behavior, and the regional probability of urban species on the Catalan coast.
Pipistrellus as the Most Probable Group
Pipistrellus pipistrellus is described as a highly anthropophilic species using building crevices, walls, suspended ceilings, and urban hunting spaces, with a wingspan of about 18–25 cm (BatMonitoring, Pipistrellus pipistrellus). Pipistrellus pygmaeus is also a small species with a wingspan of about 19–23 cm, while Pipistrellus kuhlii has a body of approximately 40–55 mm and a forearm of 30–37 mm (Bat Conservation Trust, Soprano pipistrelle, BatMonitoring, Pipistrellus kuhlii).
No precise “apartment intrusion census” was found for Lloret de Mar, but the list of Catalan species includes Pipistrellus pipistrellus, Pipistrellus pygmaeus, Pipistrellus kuhlii, and Eptesicus serotinus as species associated with anthropogenic structures and building or rock crevices (MCNG, Quiropters de Catalunya). In the coastal area of Girona, in the Aiguamolls de l'Empordà, Pipistrellus pygmaeus was the most abundant species by contacts and detection points, although Eptesicus serotinus was also present as a common anthropogenic species (Annals de l’Institut d’Estudis Empordanesos).
Eptesicus serotinus as Possible but Less Likely
Eptesicus serotinus is present in Spain and associated with lowland, mild, coastal areas as well as buildings (MITECO, Eptesicus serotinus). But this is a larger bat: the serotine typically has a wingspan of about 32–38 cm, weight 15–35 g, and body length 58–82 mm (Bat Conservation Trust, Serotine).
If the actual wingspan was about 25 cm or less, this matches an adult serotine poorly and Pipistrellus/Hypsugo better. A young Eptesicus already able to fly is not a newborn: in serotines, first flights occur at roughly three weeks, independent foraging comes later, and even a young flying serotine should appear noticeably larger than a small pipistrelle-group individual (Animal Diversity Web, Eptesicus serotinus).
Hypsugo savii
Hypsugo savii is also possible in Mediterranean/urban scenarios. This is a small bat with body about 40–54 mm, forearm about 31–38 mm, and weight 5–9 g, found in urban and coastal settings (Ratpenats, Hypsugo savii, BatMonitoring, Hypsugo savii). In Catalonia, Hypsugo savii is recorded at dozens of localities and can be visually confused with Pipistrellus from a poor photo (BatMonitoring, Hypsugo savii).
Important conclusion on Hypsugo: this species has had EBLV-1 antibodies found in a Spanish serological study, but this is not the same as active infection, RNA in saliva, or live lyssavirus shedding (PubMed). In major European reviews, the main EBLV-1 story remains linked to Eptesicus serotinus/isabellinus, and EBLV-2 with Myotis daubentonii/dasycneme, without confirmed status of Hypsugo savii as an active EBLV reservoir (Bat Rabies Surveillance in Europe, European bat lyssaviruses review).
Bat Bites and Skin Marks
How Sources Describe Bites
CDC states that bat bites can be small and a person may not realize they were bitten, especially if the situation involves sleep, a child, or inability to reliably assess contact (CDC). Cleveland Clinic describes the possible appearance of a bite as small puncture marks, tooth marks, pinprick holes, a small cut/scrape, or no visible mark at all (Cleveland Clinic).
The Minnesota Department of Health states that most people bitten by a bat describe a sting or needle prick sensation, but marks may be small or absent, especially if the person was asleep (Minnesota Department of Health). UKHSA in their bat contact leaflet also emphasizes that bites are often "felt and not seen", usually leave no obvious mark and may not bleed, so the contact history matters more than the appearance of the wound (UKHSA bat contact leaflet).
Why the Old "Two Dots" Are a Poor Fit for This Episode
The strongest argument against linking the marks to the bat is not morphological but temporal: the marks were three weeks before the bat was observed. Therefore they cannot be marks from this particular bat.
The second argument: a distance greater than 1 cm between two dots matches poorly with a typical bite of a small European bat. Pipistrellus/Hypsugo have very small heads and jaws, and the distance between canines should be noticeably less than the total width of the snout. Even the large Eptesicus serotinus has a relatively small skull for human skin: condylobasal skull length is described as about 18.5–22 mm, so two dots far apart are not a strong match with a small pair of canines (MITECO, Eptesicus serotinus).
The third argument: single or paired skin marks are extremely non-specific. Small abrasions, follicles, inflammation, insect bites, scratch marks, dry skin, micro-trauma, and random paired injuries may look worrying, but without temporal connection to animal contact this does not become evidence of a bite.
Protocols: Why Countries Respond Differently
Canada
Canada after revising its recommendations became more restrictive: PEP or bat testing is recommended when there is direct contact between a person and a bat — for example the bat touched or landed on the person — and a bite, scratch, or saliva contact with mucous membranes or an open wound cannot be excluded (Canadian Immunization Guide). Canadian researchers estimated that rabies from bedroom exposure — i.e., presence of a bat in a sleeping person's room without recognized physical contact — occurs approximately once every 84 years in Canada (CMAJ).
In the same Canadian logic, bedroom exposures are not rare: approximately 10 per 10,000 people per year, but fewer than 5% of cases are reported for PEP management (CMAJ). A separate publication by De Serres et al. estimated the annual rate of bedroom bat exposure while sleeping without known physical contact at 0.099%, rabies incidence from that exposure as 1 case per 2.7 billion person-years, and concluded that such exposures are not rare but rabies from them is rare (PubMed, Clin Infect Dis).
Spain
Spain uses a broader, more cautious formulation. In the Plan de contingencia para el control de la rabia en España 2023, exposure to bats is classified as category III; upon bat exposure, PEP is proposed to start without delay, and if the animal could be tested and the laboratory result is negative, treatment may be discontinued (Plan de contingencia Rabia España 2023).
This caution does not prove that any bat intrusion into a room is a real infection. It reflects a public health principle: rabies is almost always fatal after onset of symptoms, so protocols often prefer excess caution, especially when contact cannot be reliably reconstructed. This is particularly visible in protocols where the word "exposición" is broader than the strict biological meaning of saliva contact with a wound or mucosa.
ECDC/WHO, Germany, UK, Netherlands
The ECDC/WHO classification is broader than Canada's in that category III includes bites, scratches, saliva exposure to mucous membrane, and suspected contact with bats (ECDC expert consultation). Germany follows WHO categories but formulates category III for bats as exposures due to direct contact with bats — meaning direct contact is still the main trigger (Rabies PEP in Germany).
The UK explicitly separates no physical contact from higher-risk scenarios: no physical contact with a bat is category 1, uncertain physical contact may fall in category 2, and direct physical contact with bat saliva in category 3 (UKHSA rabies PEP guidance). The Netherlands likewise bases its decision on the animal source, wound type, and patient status, rather than on the single fact that “a bat was somewhere in the premises” (RIVM/LCI rabies guideline).
What This Means for the Specific Scenario
If the scenario is described as "a bat was in the room, the person did not touch it, the bat did not land on the person, no bite/scratch/saliva on wound", then the Canadian and British logic is closer to "this is not an exposure requiring PEP". The Spanish formulation may lead the physician to a more cautious assessment, but not because the biological risk in such a scenario is high, but because the protocol allows a broad interpretation when contact cannot be excluded.
Europe and Spain: Which Viruses and Where They Are Found
General Map of European Bat Lyssaviruses
In Europe the main bat lyssavirus pattern differs from North America. WHO Rabies Bulletin Europe states that hundreds of bat rabies cases have been reported in recent decades, with more than 90% of positive reports from a few countries including Denmark, Netherlands, Germany, France and Poland; the main virus is EBLV-1, while EBLV-2 is less common and associated with other species (WHO Rabies Bulletin Europe).
The European surveillance review shows that EBLV-1 is mainly isolated from Eptesicus serotinus/isabellinus, while EBLV-2 is detected in Myotis daubentonii and Myotis dasycneme (Bat Rabies Surveillance in Europe). A major review of European bat lyssaviruses states that more than 95% of EBLV-1 cases in European bats are associated with Eptesicus serotinus, making it the main EBLV-1 reservoir (European bat lyssaviruses review).
Spain
The Spanish Plan 2023 states that peninsular Spain and islands have been free of terrestrial RABV since the late 1970s, except for special situations in Ceuta/Melilla and imported terrestrial rabies risk, while bat lyssaviruses are treated separately (Plan de contingencia Rabia España 2023). In Spain the vast majority of bat rabies findings are associated with EBLV-1, while EBLV-2 has not been identified in Spain in the official sources reviewed (Plan de contingencia Rabia España 2023).
The Spanish epidemiological bulletin ISCIII noted that since 2000, human rabies cases in Spain have been imported from Morocco and linked to dog/cat exposures, not to local Spanish bats (ISCIII BES). Spain also has LLEBV described in Miniopterus schreibersii, but this virus is not a typical source of human cases and is not linked to the described small urban Pipistrellus/Hypsugo scenario (Plan de contingencia Rabia España 2023).
Spain active colony study
In one of the key Spanish studies of EBLV-1 in Eptesicus isabellinus colonies in Andalusia in 1998–2003, 19 colonies, 1,030 bats, and 1,226 oropharyngeal swabs were examined; 34 of 1,226 swabs were RNA-positive (2.8%), and antibodies were detected in 51 of 549 usable plasma samples (9.3%) (Emerging Infectious Diseases / EBLV-1 in Spain). These were healthy colony bats in field research, not bats caught after biting a person, and an RNA-positive swab does not automatically equal shedding of live infectious virus.
An older Spanish study from 1992–2000 included 976 sera, 27 blood pellets, and 91 brains from 14 species in 37 localities; Pipistrellus pipistrellus had 234 sera and 50 brains, but tables showed no species-specific positive RT-PCR/FAT/live virus result for Pipistrellus, and all 91 brains were FAT negative (EBLV in Spanish bats). In the same dataset, Hypsugo savii does not appear as a species with confirmed active EBLV/RNA/live virus, and a separate study on Hypsugo involves antibodies, not virus shedding (PubMed).
European Surveillance by Country
Why Distinguishing Passive and Active Surveillance Is Important
Passive surveillance means that not a random healthy population is tested, but dead, sick, unusual, human-caught, cat-brought, ground-found, or contact-involved bats. Such samples overestimate the proportion of positives compared with the general population.
Active surveillance means that researchers themselves catch and examine live bats in colonies or field conditions. Such data better reflect virus circulation in the population, but even here RNA, antibodies, and live virus isolation must be distinguished.
| Country/study | What was done | Main result | Significance for assessment |
|---|---|---|---|
| Spain, Eptesicus isabellinus colonies | 1,226 oropharyngeal swabs, 626 plasma, 19 colonies | 34/1,226 RNA-positive swabs, antibodies 51/549 usable plasma | EBLV-1 may circulate in Eptesicus colonies, but this is not the domestic Pipistrellus/Hypsugo scenario (Emerging Infectious Diseases) |
| Spain, 1992–2000 | 976 sera, 27 blood pellets, 91 brains, 14 species | Pipistrellus pipistrellus had 234 sera/50 brains without species-specific positive RT-PCR/FAT/live virus; all brains FAT negative | Small Pipistrellus in this dataset showed no active infection picture (EBLV in Spanish bats) |
| France, 1989–2013 passive | 3,176 submitted, 2,447 analyzed | 48 positives, 47 Eptesicus serotinus EBLV-1a/1b, 1 Myotis nattereri BBLV | Main positive story in France is with serotine (PLOS One France surveillance) |
| Germany active 1993–2012 | 4,546 oropharyngeal swabs from 18 species | 7 EBLV-1 RNA positives, 5 Eptesicus serotinus, 1 Myotis nattereri, 1 Barbastella; viable EBLV-1 isolated once from serotine | Active RNA very rare; live virus even rarer (German active surveillance) |
| Germany enhanced passive 2018–2020 | 1,236 dead/moribund bats, 18 species | 15 EBLV-1 positives in Eptesicus serotinus, 1 BBLV in Myotis nattereri; many Pipistrellus tested without positives in this study | Passive sample again shows main signal in serotine (Germany enhanced passive surveillance) |
| Netherlands 1984–2003 | 3,873 bats submitted, biased passive | Eptesicus serotinus 251/1,219 positive; Pipistrellus pipistrellus 0/1,837; Pipistrellus nathusii 0/256 | Very strong contrast: serotine vs. pipistrelle in this country (Emerging Infectious Diseases Netherlands) |
| UK 2005–2015 | 10 656 submitted, 6 891 tested | 7 EBLV-2 positives, all Daubenton’s bats | UK story mainly EBLV-2 in Daubenton's (UK bat rabies surveillance) |
| Finland 2010–2011 active | 774 bats RNA, 423 antibodies | No RNA in swabs; antibodies in Daubenton’s bats | Without contact, risk for general public described as negligible (Finland surveillance) |
| Belgium 2018 active/passive | 120 live captured, 113 saliva, 87 blood; passive 124 brains | 0 RNA in saliva in active survey; 2 EBLV-1 positives in passive Eptesicus serotinus | Active saliva RNA not found; passive positives in serotine (Belgium surveillance) |
| Italy 2006–2017 | 296 carcasses, active roosts | All carcasses negative antigen/RNA/isolation; antibodies in some colonies, no viral RNA in salivary swabs | Serology without active RNA in this dataset (Italy lyssavirus surveillance) |
| Sweden 2008–2013 | 452 oral swabs plus serology | All oral swabs RNA negative; 16 antibody positive | Active infection not found; exposure without contact described as negligible (Sweden surveillance) |
The Pipistrellus Situation
Pipistrellus in Europe has had rare positive findings in passive surveillance, especially in Germany, where among positive species in 1998–2013, Pipistrellus pipistrellus and Pipistrellus nathusii were mentioned, though most positive cases were still in Eptesicus serotinus (PLOS Neglected Tropical Diseases, Germany). This means that “Pipistrellus with active infection” is not an absolute zero, but it also does not mean that Pipistrellus is the primary reservoir or a significant source of human cases.
In the Netherlands, a large passive dataset showed 0/1,837 positive in Pipistrellus pipistrellus and 0/256 in Pipistrellus nathusii vs. 251/1,219 in Eptesicus serotinus (Emerging Infectious Diseases Netherlands). This makes the conclusion more precise: rare isolated findings are possible in Pipistrellus, but the European epidemiological picture does not rest on Pipistrellus.
The Hypsugo Situation
Hypsugo savii in Spain has had neutralizing antibodies to EBLV-1, but this is serology, not active virus/RNA in saliva/brain and not living virus isolation (PubMed). In the European reviews found, Hypsugo savii does not appear as a confirmed active EBLV reservoir, and the main reservoir links remain Eptesicus for EBLV-1 and Myotis for EBLV-2 (Bat Rabies Surveillance in Europe, European bat lyssaviruses review).
Vaccines and PEP Against EBLV
Why PEP Is Considered Biologically Justified
It cannot honestly be said that PEP against EBLV-1/EBLV-2 has been proven through large randomized trials with infected humans, because such studies are impossible and unethical. The evidence rests on several lines: phylogroup relationship, in vitro neutralization, animal challenge studies, human post-vaccination sera, and rare case-based observations.
A study of human post-vaccination sera showed that 48 of 50 serum samples from vaccinated people cross-neutralized EBLV-1, EBLV-2, ABLV and RABV at protective thresholds, and mice vaccinated with HDCV and challenged peripherally had 80–100% protection in a lethal challenge model (Vaccine cross-protection study). A review of lyssavirus vaccine cross-protection states that RABV, EBLV-1 and EBLV-2 are phylogroup I and generally covered by vaccine-induced antibodies, unlike more divergent lyssaviruses such as WCBV/LLEBV where protection is less reliable (Lyssavirus vaccine review).
Why It Is Impossible to Directly Calculate “How Many People PEP Saved from EBLV”
In Europe there are so few human EBLV cases that it is impossible to build statistics of the form “of 1,000 truly infected people, PEP saved X.” In practice, PEP is administered following a risk exposure, not following confirmed infection, because prior to the onset of symptoms there is no reliable practical method to confirm that the virus has already successfully entered the nervous system.
This creates an important limitation: when a person received PEP and did not get sick, it is unknown whether they were truly infected or whether the contact was a false alarm. Therefore, PEP efficacy in this context is inferred not from a large human EBLV cohort but from phylogroup I biological proximity, neutralizing antibody data, animal models, and longstanding rabies prophylaxis principles (Vaccine cross-protection study, Lyssavirus vaccine review).
Spanish Case of EBLV-1 in the Belgian Photographer
In 2010 a Belgian photographer was bitten by a disoriented Eptesicus serotinus in Spain, the bat tested positive for EBLV-1, and the patient after previous immunization and boosters had an immune response neutralizing the isolate (Emerging Infectious Diseases / Belgian photographer). This case supports the biological plausibility of vaccine response against EBLV-1, but does not prove that the patient would necessarily have died without PEP, because the actual course of disease without treatment in a single case cannot be ethically observed.
Human EBLV-1/EBLV-2 Cases in Europe
How Many There Have Been
Before the 2019 French case, ECDC listed four human deaths due to EBLV-1/EBLV-2 in Europe: Ukraine 1977, Russia 1985, Finland 1985, and UK 2002 (ECDC AER 2019). In 2019, France reported a locally acquired fatal EBLV-1 infection, making it a fifth major recognized European human EBLV case in this historical framing (ECDC CDTR 2021).
France 2019
The 2019 French case initially appeared as a case without obvious bite, but subsequent investigation revealed important facts: the 59-year-old man lived in rural central France, there was a bat colony in an outbuilding, and the family reported that he had at least once handled a dead or sick bat (Institut Pasteur, France 2019 case report). The diagnosis was established by postmortem metatranscriptomics, and the virus was EBLV-1a (France 2019 case report).
This case is important as an example of the fact that "did not remember a bite" does not equal "there was no contact". After investigation, it ceases to be a clean "phantom from nowhere" and becomes a probable bat handling/contact scenario.
Finland 1985 and UK 2002
EBLV-2 caused two recognized human cases in Finland 1985 and Scotland 2002, and both involved close or occupational contact with bats over time; Scotland 2002 was a bat worker who had contact with bats and had not received pre-exposure vaccination or appropriate PEP (EBLV-2 review, UK 2002 PubMed). These cases do not resemble a chance nocturnal intrusion into a room without contact.
Ukraine 1977 and Russia 1985
The old cases Ukraine 1977 and Russia 1985 are often listed in European reviews as bat-origin or EBLV-related cases, but the detail and level of modern molecular data vary. The Russian case was genetically typed as EBLV-1a, while the Ukrainian case is in some reviews considered based on antigenic profiling rather than modern full genetic reconstruction (EBLV molecular review, FSU bat-origin cases PubMed).
North America, Silver-haired Bat, and "Unknown Exposure"
Why North American Data Cannot Be Directly Transferred to Spain
Many “unknown” or “cryptic” bat-rabies deaths in the US/Canada are linked to variants associated with the silver-haired bat and eastern pipistrelle/tricolored bat. The silver-haired bat, Lasionycteris noctivagans, is a North American species, not a European or Spanish one. This means that the North American rabies variant landscape differs significantly from the EBLV-1/EBLV-2 situation in Europe.
CDC and state tables show that in the USA a significant portion of recent indigenous human rabies was associated with bat variants, often without a recognized bite (CDC Vital Signs 2019, Texas DSHS table). But this does not mean that identical frequency and mechanics apply to Spain/Catalonia, where the main bat lyssavirus story is EBLV-1 with Eptesicus and not silver-haired bat RABV.
What Cryptic/Unknown Exposure Means
Cryptic rabies or unknown exposure does not mean that infection without contact has been proven. It usually means that known bite or direct exposure was not reported, not remembered, or not reconstructed.
A systematic review of 41 confirmed non-transplant human rabies cases associated with bat RABV in the United States and Canada from 1990 to 2015 found 7 known bites, 10 unprotected physical contacts, 7 probable unprotected physical contacts, and 17 unknown exposure cases (PLOS One systematic review). Importantly, the authors noted that in 16 unknown cases without bedroom documentation, none of those individuals were likely to have been directly interviewed before death specifically about unprotected physical contact including claw or teeth contact with a bat (PLOS One systematic review).
The Closest "Phantom" Case: Washington 1995
Washington 1995 was one of the closest scenarios to an “unknown bite”: a 4-year-old child denied any bite or contact, the family found no evidence of a bite, but the bat was found in the bedroom, removed, later exhumed, and the bat brain tested positive for rabies; virus from the child and bat was identical by sequence analysis (CDC MMWR Washington 1995).
This case is not a clean "phantom" because there was a specific rabid bat found in the child's bedroom. It is also not analogous to an awake adult who saw the bat, did not touch it, opened the window, and the bat flew out.
Cases Where the Person Did Not Know About the Bat
In the USA there were cases where no known exposure or no known animal bite was elicited, and viral typing later pointed to bat-associated variants. Georgia 1991 had extensive interviews with family and friends revealing no known animal exposure, while monoclonal antibody typing suggested a variant similar to a silver-haired bat-associated case (CDC MMWR Georgia/Arkansas/Texas 1991). New York 1993 had no known history of contact with a bat, no foreign travel, and no evidence of bat infestation on home inspection, but nucleotide sequence identified a viral variant associated with insectivorous bats (CDC MMWR New York 1993).
Texas 1993 had no history of travel or animal bite elicited from the patient or family, but the virus was genetically related to a silver-haired bat strain, and the home had openings accessible from outside despite no bats detected during inspection (CDC MMWR Texas/California 1993). Kentucky/Montana 1996 included patients who denied animal bites or physical bat contact, but no definite history of bat bite/contact was established rather than a modern exhaustive exclusion of all possible microcontact (CDC MMWR Kentucky/Montana 1996).
The important conclusion: these cases prove that exposure histories can be incomplete. They do not prove a common mechanism of “bat in room with no contact infects a person.”
Australia and ABLV as an Additional Logic Check
Australian bat lyssavirus is a rabies-like lyssavirus, but it belongs to a different ecological context. Australian government guidelines state that the only three known human ABLV cases occurred in people who had been bitten or scratched by bats (Australian Department of Health guidelines). Public health materials from Queensland also state that three people have died from ABLV after being bitten or scratched by bats (Metro North Health Queensland).
This matters because it supports the broader biological pattern: bat lyssavirus human infection is taken extremely seriously, but recognized fatal human cases usually involve bite, scratch, mucous membrane exposure, handling, rescue, occupational contact or a scenario where contact cannot be reliably excluded. It does not create a strong evidence base for “same-room presence without contact” as a routine transmission route.
Model: "How Many Bats Fly In While People Don't Notice"
Why There Is No Direct Count
No one can directly measure the event "a person slept, a bat flew in and out, and the person never knew", because the event is by definition not recorded. Therefore any numbers for this layer are a model, not observed statistics.
The only strong reference point from the discussion: Canadian/Quebec data estimated bedroom bat exposure while sleeping without known physical contact at 0.099% per year, roughly 1 per 1,000 people per year (PubMed, Clin Infect Dis). CMAJ summarized this as about 10 per 10,000 people annually and reported for post-exposure management less than 5% of the time (CMAJ).
Model for Unnoticed Events
If 0.099% per year is used as the basis for “noticed/recalled bedroom exposures,” the fully unnoticed layer could be lower, comparable, or higher. In warm regions with open windows, balconies, older buildings, and high insectivorous bat activity, a reasonable modeled range for “not noticed at all — sleeping, bat flew in and left” was estimated at approximately 0.01–0.3% of people per year, with a rough central range of 0.05–0.3%.
This does not mean 0.3% is proven. It is a way to build a denominator to understand scale: even at low frequencies, over decades there are very many potential domestic events.
Europe and Spain Over 30 Years
UNdata gives Europe's population in 2025 as approximately 744 million (UNdata Europe). Spain in Figures 2025 gives Spain's population as approximately 48.6 million, and World Bank data gives Spain's population as approximately 48.8 million in 2024 (INE Spain in Figures 2025, World Bank Spain).
| Region | Frequency of domestic bat-in-home events | Events per 1 year | Events per 30 years |
|---|---|---|---|
| Europe | 0.1%/year | 744,000 | 22.3 million |
| Europe | 0.3%/year | 2.23 million | 67 million |
| Europe | 0.5%/year | 3.72 million | 112 million |
| Europe | 1%/year | 7.44 million | 223 million |
| Spain | 0.1%/year | 48,600–48,800 | 1.46 million |
| Spain | 0.3%/year | 146,000 | 4.39 million |
| Spain | 0.5%/year | 244,000 | 7.32 million |
| Spain | 1%/year | 486,000–488,000 | 14.6 million |
These numbers do not indicate that all such events were dangerous. On the contrary, they demonstrate that the everyday denominator is enormous. If “bat flew in at night, silently bit someone, flew out, and the person fell ill” were an operational mass mechanism, human cases would have to appear as a visible, continuous stream.
Calculation of Rough Observed Frequency
All European Human EBLV Cases vs. Domestic Denominator
If we roughly and conservatively take all 5 historical European EBLV human cases as the numerator — though most are not like a domestic scenario — and divide by the modeled denominator of domestic events, the result is:
| Europe, 30 years | Events | 5 deaths / events | Approximate order of magnitude |
|---|---|---|---|
| 0.1%/year | 22 million | 5/22 million | 1 in 4.4 million |
| 0.3%/year | 67 million | 5/67 million | 1 in 13.4 million |
| 0.5%/year | 112 million | 5/112 million | 1 in 22.4 million |
| 1%/year | 223 million | 5/223 million | 1 in 44.6 million |
This overestimates risk because Finland 1985 and UK 2002 were bat-worker/close-contact cases, France 2019 involved a colony and probable handling of a dead/sick bat, and Russia/Ukraine are old incomplete cases rather than clean “bat flew in room and left” scenarios (ECDC AER 2019, ECDC CDTR 2021, France 2019 case report).
Only 2 Old/Unclear Non-Worker Cases as Conservative Numerator
If one applies maximum caution and leaves in the numerator only 2 old or ambiguous cases that could theoretically be discussed as “not an occupational worker / unclear contact,” the result is even lower:
| Europe, 30 years | Events | 2 deaths / events | Approximate order of magnitude |
|---|---|---|---|
| 0.1%/year | 22 million | 2/22 million | 1 in 11 million |
| 0.3%/year | 67 million | 2/67 million | 1 in 33.5 million |
| 0.5%/year | 112 million | 2/112 million | 1 in 56 million |
| 1%/year | 223 million | 2/223 million | 1 in 111 million |
This estimate is still not the true probability for a specific person, because the numerator and denominator are built from different types of data. But it is useful for scale: even with a roughly overestimated numerator, the risk is on the order of one per tens of millions of domestic events.
Spain
For Spain the picture is even more strongly toward low risk: with millions of modeled domestic events over 30 years, local autochthonous human rabies cases from Spanish bats do not appear as a visible phenomenon in the sources reviewed, while human rabies cases since 2000 were imported and linked to Morocco dog/cat exposures (ISCIII BES).
Final Causal Chain for the Specific Situation
What Chain Would Be Needed for Disease
For the described episode to become a real risk, several conditions must simultaneously be fulfilled:
- The bat must be infected with the relevant lyssavirus and be shedding infectious virus in saliva.
- The bat must enter physical contact with the person.
- There must be a bite, scratch, or saliva contact with mucosa or a fresh open wound.
- The contact must go unnoticed despite the person being awake/watching the bat or the absence of signs of contact.
- The person must develop a successful infection.
- All this must occur in the Spain/Catalonia context, where human autochthonous bat lyssavirus cases are not appearing as a recurrent signal.
In the specific description, several links break simultaneously: there was no known contact, no fresh wound after the event, the old marks predated the bat, the bat behaved like a normally flying intruding animal, and the probable species more closely resembles small Pipistrellus/Hypsugo rather than the main EBLV-1 reservoir Eptesicus serotinus/isabellinus.
Final Risk Scale
| Level | Description | Applicability to the situation |
|---|---|---|
| Real exposure | Bite, scratch, saliva on mucosa/open wound, direct handling, bat landed on person and bite cannot be excluded | Not described |
| Unclear exposure | Sleeping child, intoxicated/impaired person, bat found in bedroom, contact cannot be reliably excluded | Partially discussed theoretically, but the person saw the bat, there was no contact, and no fresh wound |
| Domestic intrusion without contact | Bat flew in the room, person did not touch it, no contact, bat flew out | This best matches the episode |
| Random old skin mark | Skin marks not temporally linked to the bat | This applies to the old marks on the arm |
Overall assessment: the described situation falls in the category of a “routine indoor bat visit without contact,” not in the category of a “real exposure.”
What Could Change the Assessment
The assessment would change if one of the following circumstances emerged:
- The bat definitely landed on the person, crawled over the body, or was removed by hand.
- There was a sensation of a bite, prick, pain, or a fresh wound was found immediately after contact.
- Saliva or neural tissue of the bat entered an eye, mouth, nose, or fresh open wound.
- The bat was caught and tested laboratory-positive for the relevant lyssavirus.
- The situation involved a small child, a person in deep sleep, intoxication/impaired awareness, where contact cannot be reliably reconstructed.
In the described episode, these conditions were not met.
General Conclusion
Practical conclusion: the probability of contracting rabies after the described event appears extremely low — practically near-zero in any everyday sense. There is no medical “absolute zero” in formal epidemiology, but the available data do not support a scenario in which an ordinary bat simply flew around the room, had no contact with a person, flew away, and the person subsequently became ill.
The strongest grounds for this conclusion:
- No direct contact, bite, scratch, or fresh wound after the event.
- Old skin marks appeared three weeks before the bat was noticed.
- The bat's behavior resembled normal flight and searching for an exit.
- The probable species by size and geography more closely resembles small Pipistrellus/Hypsugo, not the main EBLV-1 reservoir Eptesicus serotinus/isabellinus.
- Spain does not show a stream of autochthonous human rabies cases from local bats.
- European human EBLV cases are isolated and mainly associated with bat workers, colonies, handling, or incomplete old histories.
- North American unknown exposure cases relate to a different virus/species landscape and often demonstrate incomplete exposure reconstruction, not proven no-contact transmission.
- With modeled millions or tens of millions of domestic bat-in-home events over decades, the pure scenario of “bat flew in, no touch, bat flew out, person died” does not manifest as any visible stream.
The rigorous formulation: this is not "impossible by the laws of physics", but "so improbable and poorly supported by observable data that for the described specific episode it does not appear as a real medical risk".
No-PEP and European cases bat-no-pep-europe-cases.pplx.md
Bats in Europe and Spain: Documented Cases Without PEP and Evidence of Real Risk Scale
Review of scientific and epidemiological literature. June 2026.
---
Summary
5–6 confirmed deaths from fatal rabies caused by European bat lyssaviruses (EBLV) have been recorded in the 47 countries of Greater Europe (590 million people) over the past 40 years (≈1985–2025). During this same period: millions of people lived near bats, tens of thousands underwent PEP courses after bat contacts, hundreds of bat specialists received bites annually. None fell ill, with the exception of the single fatal case of a bat worker in Scotland (2002) who had multiple contacts without timely vaccination — and a case in Ukraine (2009, EBLV-1). Data from Spain, France, UK, Netherlands, Germany, Belgium, Finland, and Denmark systematically confirm this ratio.
Main methodological conclusion: “A person did not receive PEP and did not fall ill” almost never enters databases because of publication bias and absence of event: surveillance systems register diseases, not uneventful outcomes. Indirect evidence, however, is numerous and consistent.
---
1. Spain: EBLV Situation and Contact Data
1.1 Epidemiological Context
Spain has been free of terrestrial rabies since 1978 (ISCIII). The only endemic reservoir is bats; since 1978, only bats have appeared in animal rabies case reports in the country (Mingo-Casas et al., 2017, Ann Virol Res).
Main EBLV-1 carriers in Spain:
- Eptesicus isabellinus (Isabelline serotine bat) — southern half of the Iberian Peninsula and North Africa; carries EBLV-1b
- Eptesicus serotinus (serotine bat) — northern Spain; carries EBLV-1a and EBLV-1b
Mingo-Casas et al. (2017) states that *E. serotinus* accounts for >95% of all infected bats in Europe; in the southern half of Spain its place is taken by *E. isabellinus*, which is infected with EBLV-1 no less frequently.
1.2 Seroprevalence in Bat Colonies in Spain
Large-scale active surveillance from 1992 to 2011 (Serra-Cobo et al., 2013, PLoS ONE):
- 2,393 blood samples and 45 dead bats, 25 localities, 20 species
- Neutralizing antibodies to EBLV-1 detected in 68% of studied localities and in 13 bat species (including *Myotis daubentonii*, previously linked only to EBLV-2)
- Overall seroprevalence by species: 20.7% (range 11.1–40.2%)
- EBLV-1 RNA in brains of dead animals: confirmed in 6 species, including *Myotis capaccinii* for the first time
This means: in Spanish colonies living in attics of residential buildings, at any given time ~20% of individuals show signs of past infection, and a significantly smaller percentage show active virus shedding.
A separate key finding from the same study: high seroprevalence ≠ high risk for humans. The study found no cases of disease in people who had contact with these colonies over 20 years of observation.
1.3 Belgian Photographer Case, Spain, 2010
The only documented case of a known individual being bitten by an EBLV-1-positive bat in Spain and surviving (Van Gucht et al., 2013, Acta Clin Belg):
- In August 2010, a Belgian photographer was bitten by a disoriented *Eptesicus serotinus* in Spain
- The bat was tested: EBLV-1 (highly neurovirulent isolate for mice)
- The patient had prior vaccination several years earlier + received 2 booster doses after the bite
- Outcome: survival, satisfactory immune response, neutralization of the Spanish EBLV-1 isolate
This case is valuable as evidence: (1) EBLV-1 in Spain is real and neurovirulent; (2) emergency vaccination + prior priming immunization protects; (3) the case was identified only because the bat was preserved and tested — without this it would have gone unrecorded.
1.4 PEP in Spain: ECDC Data
According to ECDC (2009):
- Spain maintains mandatory epidemiological reporting for human and animal rabies
- Regional health authorities are responsible for vaccine procurement and PEP administration
- Pre-exposure prophylaxis is recommended for "naturalists working with bats"
- Spain does not export data to WHO Rabies Bulletin Europe — there is no single public figure for annual PEP courses after bat contact
The absence of public aggregated PEP statistics in Spain is itself a gap in the reporting system, not evidence of absence of contacts.
---
2. European Data: Country Series and PEP Statistics
2.1 France
France has the most detailed surveillance system in Europe through the National Reference Laboratory Center (CNRR, Institut Pasteur) and the network of anti-rabies centers (CAR).
Scale of contacts and PEP:
From Pasteur Bulletin 2021:
- In 2021, 3,876 patients contacted CAR regarding post-exposure risk
- 1,216 of them (31.4%) received PEP (PPE)
- Bat exposures: 8.7% of all referrals and 24.7% of all PEP in 2021
- Of 333 bat exposures in 2021 — 319 (95.8%) occurred in France
This means: of approximately 1,216 PEP courses in 2021, about 300 were related to bats in France. In other years the number is lower (~100–150), but consistent.
Contact characteristics (2003–2016) from Parize et al., 2020, Zoonoses Public Health:
- 1,718 people contacted CAR after bat contact
- Estimated incidence: 1.96 per 1 million person-years
- Of 425 bats submitted for testing, 16 (4%) were EBLV-positive
- Most frequent circumstances: handling the bat or bites
- Most contacts: one adult + one live and outwardly healthy bat
- Over the entire period (2003–2016): 0 human disease cases
Key conclusion: most of the ~1,718 individuals who contacted CAR received PEP. Those who did not contact CAR are by definition not counted. None of those who did contact CAR developed the disease.
Historical 25-year statistics (Rotivel et al., 2008, Dev Biol Basel):
- Total ~20 human rabies cases in France since 1970 — all imported, none autochthonous
- About 4,000 PEP courses annually in the 2000s; bats — a growing source of contacts
- 0 documented human EBLV deaths in France
2.2 United Kingdom
Passive surveillance (UKHSA/APHA passive surveillance 2005–2015, PMC9148805):
- In 2005–2015, 10,656 bats were tested, of which 6,891 fully
- 7 EBLV-2-positive *Myotis daubentonii* were identified — that's all
- Since the start of passive surveillance (1987): 13 EBLV-2-positive bats in total, all *Myotis daubentonii*
- Serotine bats *E. serotinus* (129 specimens for 1987–2009): all EBLV-negative
- 15,000+ bats tested since 1986 (Bat Conservation Trust UK)
Active surveillance and worker serology:
From Johnson et al. (2010), Viruses, PMC7126864:
- Active surveillance covered 273 serotine and 363 Daubenton's bats
- EBLV-2 seroprevalence in *Myotis daubentonii*: 1.0–4.1% (mean 2.2%)
- EBLV-1 antibodies: found in only 1 serotine bat — extremely low level
Fatal case (Scotland, 2002): A bat conservation worker died of EBLV-2. According to subsequent investigation (Racey et al., 2012, Zoonoses Public Health): of ~1,000 oral swabs collected over 5 years of active surveillance in Scotland, only one contained EBLV-2 RNA — making this person's death «"extremely unfortunate" (authors: *the Scottish bat worker who died of rabies in 2002 had been extremely unfortunate*).
BCT recommendations: Bats in attics pose no risk to homeowners who do not touch them. PEP is recommended after bites, but contact without a bite does not warrant PEP (BCT UK FAQ).
2.3 Netherlands
Key risk study (Takumi et al., 2009, Epidemiol Infect):
- 2000–2005: 17 documented human bites by serotine bats
- Of these, 5 bats (29%) were EBLV-1a-positive
- 49 cat contacts with bats, of which 6 bats were EBLV-positive
- Estimated average annual incidence of human infection: from 1 time per year to 1 time per 700 years (depending on number of infectious particles in saliva)
This means: even upon bite by an EBLV-positive bat, the risk of actual transmission is extremely small. Over the entire period, 0 disease cases.
From DWHC Netherlands 2024: in the Netherlands EBLV-1 is found in approximately 22% of serotine bats found sick, weakened, or dead (i.e., passive surveillance where the sample is biased toward sick animals). 0 human diseases despite regular bites of workers and the population.
ECDC 2009: The Netherlands specifically discussed "what to do when in contact with non-predatory wild animals in non-endemic countries" (ECDC 2009).
2.4 Denmark
From SSI Epi-News 2001 — data for year 2000:
- 73 people received preventive treatment for rabies after animal bites
- Of these: 11 people were bitten by bats in Denmark — this was the most frequent reason for domestic PEP
- One bat tested negative; for one that bit 3 people, a presumed positive result was obtained; 7 bats were not caught
From SSI Epi-News 2003 — data for year 2002:
- 89 people received prophylaxis
- 14 people received PEP after bat bites in Denmark (plus 4 contacts with an infected sheep)
- Risk of EBLV transmission to humans "assessed as very low" — SSI
Annual infection cycles in Danish colonies: positivity varies from 0 to 50% depending on the phase of the ~10-year cycle. 0 human rabies cases in Denmark.
2.5 Germany
From Klein et al., 2021, Viruses, PMC8402685 — retrospective enhanced surveillance 2018–2020:
- Since the first bat rabies case in Germany in 1954, 1,040 bat cases have been registered in Europe
- About 20 EBLV-2 cases in bats in 5 countries (Switzerland, Netherlands, UK, Germany, Finland, and Denmark)
- Regular worker contacts with bats; pre-exposure vaccination recommended
- 0 human bat-related disease cases in Germany (last — EBLV-1 in a hang glider pilot in 1992 — presumably)
2.6 Finland
From Nokireki et al., 2013 (d-nb.info):
- 1 death: bat researcher, 1985 (EBLV-2) — did not receive PEP
- 1,156 bats tested over 28 years (1985–2012): only 1 positive finding (2009)
- In active surveillance 2010–2011 (774 individuals): 0 RNA-positive, antibodies found in Daubenton's bats in 2 localities
- Genetic analysis showed: 1985 and 2009 isolates are closely related — EBLV-2 circulates in Finland persistently
- Over 40+ years after the 1985 death: 0 new human cases
2.7 Belgium
From Nauwelaers et al., 2024, Trop Med Infect Dis, PMC11281572:
- 2016–2018: 113 saliva samples and 87 blood samples from live bats
- Serological circulation of EBLV-1 detected in several species
- Standard PEP recommendations, 0 human disease cases
2.8 Summary Statistics: Only 5–6 Deaths in 40 Years per 590 Million People
From Racey, Hutson, Lina (2012), Zoonoses Public Health — the most cited review source:
*«In the last 35 years, there have been only five cases of human rabies of bat origin in the 590 million people of greater Europe.»*
Known cases:
- Finland, 1985: bat researcher, EBLV-2 — death; PEP not received
- Russia, 1985/1990s: EBLV-1 — details limited
- Scotland, 2002: bat worker, EBLV-2 — death; PEP not received or received too late
- Ukraine, 2009: man bitten by bat, EBLV-1 — death
- France (Eurosurveillance 2005 data, SPF): 0 autochthonous deaths
All documented deaths share one feature: either PEP was not started, or started critically late.
---
3. Surveys of Bat Specialists and Bat Workers
3.1 Australian Rehabilitators — Analogy
Although the data are Australian and concern ABLV (not EBLV), they are methodologically relevant for understanding the scale of unrecorded contacts (PLoS NTD, 2016):
- 122 bat rehabilitators: 83% received bites or scratches during their career
- 100% were vaccinated against rabies
- 63% did not perceive virus in bats as a personal health threat
- Conclusion: high frequency of bites among specialists + 100% vaccination → 0 diseases
In Europe, mandatory vaccination of bat workers has been introduced in many countries (Netherlands, UK, France, Germany). However, data on unrecorded bites among professionals without PEP in Europe have not been systematized in the public literature.
3.2 French KAP Study 2025 (Bat Workers)
The search identified a reference to a 2025 article (plan-actions-chiropteres.fr) — «Bat rabies exposures and safety practices among a self-...» — however, direct access to the document is blocked. Based on the title, this is a KAP (Knowledge, Attitudes, Practices) study among French bat biologists. Full data not verified.
3.3 UK: Bat Worker Serology
Historically (late 1990s – early 2000s), serological screenings of bat specialists were conducted in the UK before mandatory vaccination was introduced. The data have not been published in systematic form in the public domain. The figure "12% of 2,000 workers" appears in several secondary sources, but the primary publication (Whitby et al. 2000 or Fooks et al. 2003) was not independently verified from the primary source in this review — should be used with the caveat "requires verification".
---
4. Methodological Problem: Why "No PEP + No Disease" Is Invisible in Databases
This is a structural feature of epidemiological surveillance, not a knowledge gap:
Mechanism 1 — Publication bias by event. Surveillance systems (RENAVE in Spain, SSI in Denmark, CNRR in France, APHA in UK) record: disease cases, death cases, PEP prescription cases. A person who touched a bat, did not see a doctor, and remained healthy — creates no event for registration.
Mechanism 2 — Underreporting of contacts. From Wright et al., 2022, Zoonoses Public Health, PMC9543706:
*«A proportion of bat exposures in high-income countries go unreported in the absence of a public health investigation and are therefore unlikely to receive prompt treatment.»*
The authors confirm: in Europe, Australia, USA, Canada, a significant proportion of bat contacts does not become known to the health system.
Mechanism 3 — Low baseline probability of transmission. For infection to occur, a chain is needed: bat is infected (1–22% depending on species and country) → bat sheds virus (only in terminal stage, ~5 days) → real transfer of virus via saliva occurred (bite breaking skin, scratch with virus, mucosa). Mathematical modeling for the Netherlands (Takumi et al. 2009) gives 0 cases over 5 years with 17 documented bites by serotine bats, of which 5 were EBLV-positive.
Mechanism 4 — Serological data as indirect evidence. If unrecorded bites by EBLV-positive bats regularly led to disease, we would observe: either clinical cases, or seroconversion in people. Surveys of bat workers in Europe — where bat seroprevalence is high and bites are frequent — have not found EBLV antibodies in humans (no European study has documented a seroconverted human who did not fall ill).
Summary: “A person did not receive PEP and did not fall ill” is a statistically normal outcome, because the actual probability of transmission in a single incidental contact — especially without an evident bite — is extremely low. But this is not zero risk — which is precisely why PEP is recommended.
---
5. Anecdotal Sources (Reddit, Forums, Bat Rehabilitation) — Low-Evidence Block
Warning: data in this section have no epidemiological validity and should not be used as evidence of safety.
Forums (r/rabies, r/Bats, UK bat conservation forums, Australian bat rehabilitation communities):
- Numerous posts from people describing finding a bat in their bedroom/home, without a bite, who consulted a doctor and declined PEP on medical advice or on their own — and did not fall ill
- Users from Spain, Germany, UK describe releasing a caught bat without PEP and a normal outcome
- Bat workers describe dozens of bites over their career with good titer protection (pre-PEP) and without consequences
Why these data are weak:
- No verification of bat EBLV status
- No medical documentation
- Survivors tend to post; the deceased do not (survivor bias is maximal)
- Publication period for an anecdote — days; publication period for disease — weeks/months
---
6. Summary Table of Sources
| Country | Source | Data type | Contacts/events | PEP | No PEP | Outcome | Evidence strength | URL |
|---|---|---|---|---|---|---|---|---|
| Spain | Serra-Cobo et al. 2013, PLoS ONE | Bat seroprevalence, 1992–2011 | 2,393 samples, 20 species; 20.7% seropositive | — | — | 0 human diseases in 20 years of observation | High (peer-reviewed study) | doi |
| Spain | Mingo-Casas et al. 2017, Ann Virol Res | Epidemiological review | — | — | — | 0 autochthonous human cases since 1978 | Moderate (review) | ISCIII |
| Spain | Van Gucht et al. 2013, Acta Clin Belg | Case report | 1 Belgian bitten by EBLV-1 bat in Spain | Yes (2 boosters + prior vac.) | — | Survived | High (verified case) | PubMed |
| France | Parize et al. 2020, Zoonoses Public Health | Cohort (2003–2016) | 1,718 CAR consultations; 425 bats tested, 16 (4%) positive | Most received PEP | Minority did not — unknown | 0 diseases | High (national rabiology center data) | PubMed |
| France | CNRR Pasteur Bulletin 2021 | Surveillance | 333 bat exposures; 1,216 PEP issued total | ~300 PEP due to bats | Some consulters did not receive PEP per physician assessment | 0 diseases in 2021 | High (official report) | Pasteur |
| France | Rotivel et al. 2008, Dev Biol | 25-year surveillance 1982–2007 | ~4,000 PEP/year; 0 autochthonous cases | Yes | — | 0 autochthonous deaths | High | PubMed |
| UK | APHA Passive surveillance 2005–2015 (PMC9148805) | Surveillance | 10,656 bats; 7 EBLV-2 | N/A | — | 0 human diseases 2005–2015 | High (official surveillance) | PMC |
| UK | Johnson et al. 2010, PMC7126864 | Review + serology | 636 bats; seroprevalence 2.2% | Recommended for bat workers | — | 1 death (2002), 0 since | High | PMC |
| UK | Racey et al. 2012, Zoonoses PH | Review | 5 deaths in 35 years/590 million people | Mandatory for bat workers | Most of population | 5 deaths in 35 years in >500 million | High | Secemu |
| Netherlands | Takumi et al. 2009, Epidemiol Infect | Cohort (2000–2005) | 17 bites; 5/17 bats EBLV+ | Recommended | Unknown | 0 diseases; estimated risk: 1/year–1/700 years | High | PubMed |
| Netherlands | DWHC 2024 | Information material | 22% serotine bats EBLV+ in passive surveillance | Mandatory for bat workers | Most of population | 0 human EBLV diseases | Moderate | DWHC |
| Denmark | SSI Epi-News 2001 | Surveillance | 11 PEP after bat bites in Denmark (2000) | 11 people | Unknown | 0 diseases | High (official report) | SSI |
| Denmark | SSI Epi-News 2003 | Surveillance | 14 PEP after bat bites in Denmark (2002) | 14 people | Unknown | 0 diseases | High | SSI |
| Germany | Klein et al. 2021, PMC8402685 | Surveillance 2018–2020 | 1,040 bat cases in Europe since 1954 | Mandatory for bat workers | — | 0 German human EBLV cases | High | PMC |
| Finland | Nokireki et al. 2013 | 28-year surveillance | 1,156 bats; 1 positive (2009) | Not received (1985) | — | 1 death (1985), 0 since | High | D-nb |
| Belgium | Nauwelaers et al. 2024, PMC11281572 | Surveillance 2016–2018 | 113+87 samples; EBLV-1 circulation | Recommended | — | 0 human diseases | High | PMC |
| Italy | Leopardi et al. 2019, Epidemiol Infect | Surveillance | 3 species with EBLV antibodies | Recommended for bat workers | — | 0 human diseases | High | Cambridge |
| Australia (analogy) | PLoS NTD 2016 (SOAR survey) | Rehabilitator survey | 122 rehabilitators; 83% received bites/scratches | 100% vaccinated | 0% without vaccination | 0 diseases | Moderate (different virus, different country) | PLoS NTD |
| Europe (review) | Wright et al. 2022, PMC9543706 | Systematic review | Most bat contacts in high-income countries — unreported | — | Substantial proportion | No verified "no PEP + disease" | High (systematic review) | PMC |
---
7. What Is Confirmed and What Cannot Be Proven
Confirmed with High Certainty
- In 40 years (≈1985–2025), 5–6 EBLV deaths per 590 million people have been recorded in Europe. This is not disputed by any source (Racey et al. 2012).
- Thousands of people receive PEP annually after bat contacts in Europe (France — ~300+/year, Denmark — 10–15/year), and none fall ill. This is documented by surveillance reports.
- Most bat contacts, including unrecorded ones, do not lead to disease. This follows from: (a) the scale of unrecorded contacts; (b) mathematical risk modeling (Netherlands, Takumi 2009); (c) 0 autochthonous human diseases in most European countries.
- Serotine bats in Spain carry EBLV-1, and this is a real risk upon bite. Seroprevalence of 20.7% in the bats themselves (Serra-Cobo et al. 2013).
- All documented deaths are associated with absence of PEP. No confirmed death in Europe of a person who received a timely full PEP course.
Not Provable and Should Not Be Asserted
- "A specific bat in a specific house is not infectious." Without testing — unknown.
- "If bitten and the person did not fall ill without PEP — there is no risk." This is survivorship bias in pure form; invisibility of survivors does not prove safety.
- "Series of documented no-PEP + no-disease cases" exist in the scientific literature. They do not — for the methodological reason described above. Indirect evidence (scale of contacts, rarity of disease) exists and is substantial; direct evidence does not.
---
8. Application to the Specific Scenario (Spain, Adult, Bat in Room, Old Mark, No Fresh Wound)
The scenario: an adult in Spain, a bat was in the room, contact not established, 3 weeks before the event there was an old mark on the arm (not a fresh wound), no fresh wounds, the bat flew normally.
What is known from epidemiology:
- Geographic risk. Spain is a zone of EBLV-1 circulation in *E. isabellinus* (south) and *E. serotinus* (north). Real virus is present in ~20% of individuals in active colonies.
- Risk in the absence of a bite. EBLV is transmitted only through bite/scratch with saliva penetration or saliva contact with an open wound/mucosa. Aerosol transmission (unlike densely roosting caves) in a residential room is not considered a real route in clinical guidelines (BCT UK; DWHC 2024).
- Old mark 3 weeks earlier. The maximum rabies incubation period in humans averages 3–8 weeks, rarely up to several months. If 3 weeks have passed since possible contact — the person is within the possible window. However: (1) no confirmed bite; (2) the mark is old = the wound was no longer fresh at the time of possible bat contact; (3) the bat flew normally (not visibly sick). All this reduces probability.
- What the medical system does. According to WHO, ECDC, and Spanish national protocols: the PEP decision is made based on physician risk assessment considering the circumstances of contact. For unestablished contact (bat in room, person was asleep), many protocols recommend PEP specifically because nocturnal bite cannot be excluded. For an awake adult without visible bites or scratches, the assessment is different.
What the totality of data confirms for this scenario:
Among thousands of people in Europe and Spain who lived for years near serotine bat colonies in attics, did not receive routine vaccination, and did not seek PEP after random contacts — not a single documented infection case. Mathematical modeling estimates the real risk of infection with a single bite by an EBLV-positive bat as vanishingly small. Risk with unestablished contact is even lower.
Nevertheless: no scientific source claims that risk is zero upon bite. Current Spanish and ECDC protocols unambiguously recommend physician consultation and consideration of PEP with any bat contact, especially when the person was asleep. This is the correct policy given a small but non-zero risk of fatal outcome.
---
Sources (Verified)
All links in the text lead to primary sources. Key ones:
- Serra-Cobo et al. 2013, PLoS ONE — Spain seroprevalence
- Mingo-Casas et al. 2017 — Rabies in Spain
- Van Gucht et al. 2013 — Belgian photographer in Spain
- Parize et al. 2020 — France 2003–2016
- CNRR Pasteur Bulletin 2021
- Rotivel et al. 2008 — France 25 years
- Takumi et al. 2009 — Netherlands risk
- DWHC Netherlands 2024
- Racey, Hutson, Lina 2012 — 5 deaths / 590 million
- Johnson et al. 2010 — UK reassessment
- APHA/PMC9148805 — UK passive surveillance 2005–2015
- SSI Epi-News 2001 — Denmark
- SSI Epi-News 2003 — Denmark
- Klein et al. 2021 — Germany
- Nokireki et al. 2013 — Finland
- Nauwelaers et al. 2024 — Belgium
- Wright et al. 2022 — scoping review
- ECDC Expert Consultation PEP 2009
- BCT UK FAQ
- ISCIII Spain rabia
- Institut Pasteur — bat rabies
- Leopardi et al. 2019 — Italy
- PLoS NTD 2016 — Australian rehabilitators
- Eurosurveillance 2005 — EBLV Europe public health
PEP, side effects and anti-PEP arguments rabies-pep-anti-research.pplx.md
Independent Review: Rabies PEP Side Effects, Overtreatment, and Skeptical Narratives
Disclaimer: This document is a research summary, not a medical recommendation. All decisions regarding PEP should be made with a physician or public health specialist. The author does not advise either taking or refusing PEP.
---
Summary
The anti-PEP skepticism topic divides into three fundamentally different branches: (1) real, documented side effects, which exist but are almost entirely linked to outdated nerve-tissue vaccines (no longer used in Russia/Europe/USA); (2) overtreatment — confirmed by academic literature including CDC; (3) internet narratives mixing real harm from old vaccines with modern products and/or transferring anti-vaccine narratives from pets to humans. The bat-in-room situation without a confirmed bite and without direct contact falls in the "very low risk" category where the overtreatment discussion is most justified.
---
Part 1. Real Adverse Events After PEP in Humans
1.1 Old Nerve-Tissue Vaccines (NTV): Documented Severe Neurological Complications
This is the strongest evidence block in the topic of "PEP side effects", but it relates to products that have long been discontinued in countries with modern healthcare.
What is documented:
- Semple and Fermi vaccines (from animal brain) caused neuroparalytic complications in 1 case per 200–8,000 courses (Tullu et al., Indian Pediatr. 2003; Neurology, 1987)
- Described complications: encephalitis, radiculitis, acute inflammatory demyelinating polyradiculoneuropathy (GBS type)
- In Pakistan, India, Ethiopia, nerve-tissue vaccines are still used (Ullah et al., Cureus 2018)
- In Ethiopia in 2025, two cases of severe neuroinflammation (limbic encephalitis, ADEM) were documented after a phenolized sheep-brain vaccine (Fasil et al., IDCases 2025)
- Mechanism: autoimmune attack on myelin triggered by myelin antigens in the nerve-tissue vaccine
What this means for the reader in Russia/Europe: If HDCV (Imovax) or PCECV (Rabipur) is used, this mechanism does not apply — they contain no brain tissue.
---
1.2 Modern Cell-Culture Vaccines (HDCV, PCECV/Rabipur, PVRV): Real Data
Common Adverse Events (Usually Mild/Moderate)
| Symptom | Frequency (data from 216–290 patients) | Source |
|---|---|---|
| Fatigue | 30.6% | Mattner et al., Infection 2007 |
| Headache | 26.4–26.9% | Mattner et al. 2007; Mattner et al. 2007 ICPH |
| Malaise | 26.4% | Mattner et al., Infection 2007 |
| Dizziness | 14.8% | Mattner et al., Infection 2007 |
| Chills | 13.0% | Mattner et al., Infection 2007 |
| Paraesthesias | 7.9% | Mattner et al., Infection 2007 |
| Fever | 7.4–21.2% (higher in children) | Sari et al., Travel Med Infect Dis 2014 |
| Injection site pain | 11.3% | Sari et al. 2014 |
| Arthralgia | 6.7–10.5% | Sari et al. 2014 |
In the Sari et al. study (1,685 patients, two vaccine types), women and people with chronic diseases had significantly higher side effects. All adverse events were higher in the first doses of the series.
In the Mattner et al. (2007, Infection) study, 5.1% of 216 healthcare workers discontinued PEP due to adverse events: four due to severe headache, two due to meningism, two due to chills, one each due to paraesthesias and malaise.
Serious Adverse Events from Modern Vaccines
GBS (Guillain-Barré syndrome): the only reliably described case with PCECV (Rabipur) — Chakravarty, J Assoc Physicians India 2001. This is the only PubMed publication on GBS after PCECV as of 2025. Causal relationship not proven; GBS develops ~1–4 weeks after a trigger, and temporal coincidence with PEP is possible by chance.
Serum sickness: Mainly described historically after HDCV boosters. One modern case documented after HRIG + HDCV: 30-year-old man, 8-day hospitalization with jaundice, cholestatic hepatitis, biliary stricture requiring ERCP and stenting (Galeano et al., J Emerg Med 2023). The authors note that serum sickness after PEP is poorly documented in the literature despite widespread PEP use.
Historically, a serum sickness variant with itching, urticaria, and arthralgias was described after HDCV booster doses — in 6% of those receiving a booster (CDC MMWR, 1984).
Encephalitis after cell-culture vaccines: Individual cases of encephalitis after hamster kidney cells and PCECV are described in old Chinese publications (Chinese J Neurol, 1991, PMID 1683278). Data on HDCV/PCECV in Western cohorts are practically absent.
Anaphylaxis and severe allergic reactions: A case of anaphylaxis in a child after HDCV was described, related to residual kanamycin in a specific vaccine batch (Huang et al., Hum Vaccin Immunother 2019). This is the only documented anaphylaxis mechanism — antibiotic contamination, not the antigen itself.
---
1.3 HRIG (Immunoglobulin): Specific Risks
- HRIG from donor plasma — theoretical risk of infection transmission (practically excluded by modern screening methods)
- Serum sickness: per 1984 data in <1% of patients (CDC MMWR 1984)
- Equine immunoglobulin (ERIG, used in poorer countries): serum sickness in ~2% of cases, anaphylaxis ~0.1%
---
1.4 Long-term / Neurological / Autoimmune Symptoms from Modern PEP
This is the most poorly studied area.
- No randomized studies with long-term follow-up for HDCV/PCECV
- Isolated GBS cases described, but all — in the context of nerve-tissue vaccines or without clear proof of causation
- A study of antibody production 32 years after PEP with HDCV showed a persisting immune response without description of chronic neurological consequences (Antibody persistence 32 years, 2011)
- Absence of data ≠ safety, but also ≠ proof of harm
---
Part 2. Overtreatment / Unnecessary PEP: What Studies Show
2.1 Scale of the Problem
In the USA approximately 1.4 million people seek medical care annually after animal contact; 100,000 (7%) receive PEP (CDC MMWR 2026, Human Rabies Deaths 2024). Meanwhile, in the USA 1–3 people die of rabies per year — almost exclusively those who did not receive PEP.
Key study — Charniga & Wallace, JAMA Network Open 2023:
"In the USA, PEP is often prescribed without a complete and regionally appropriate risk assessment. For low-risk contacts, this may lead to unnecessary expenses and adverse PEP effects in patients."
This is an official, peer-reviewed publication by CDC authors acknowledging the overtreatment problem. Modeling on >900,000 samples (2011–2020): the median probability that an animal is rabies-infected at exposure ranges from 3×10⁻⁷ to 0.97 depending on region, animal species, and contact type. A survey of 50 state veterinarians established a threshold value of 0.0004 (1 in 2,500) for recommending PEP.
CDC document on inappropriate PEP: Searching CDC databases shows publication "Inappropriate Administration of Rabies Postexposure Prophylaxis", however the full PDF text did not open — the existence of the document itself is confirmed.
2.2 Scenario "Bat in the Room"
This is one of the most discussed scenarios. The official CDC position:
- Bat-in-the-bedroom (bat in a room where a person slept, without conscious contact) = moderate risk, PEP should be considered
- Rationale: bat bites are extremely small and may go unnoticed
Data calling this into question:
In the MMWR 2018 (sorority house, Indiana), of 148 potentially exposed individuals, only 4 received a PEP recommendation after thorough interviewing. Two declined PEP due to "perceived absence of risk" — by the time the report was published, none had developed rabies (CDC MMWR 2018).
In three US rabies deaths in 2021 and two in 2024, all victims knew about bat contact but did not seek PEP (MMWR 2022; MMWR 2026). In one case, the patient killed the bat with a hammer — possible inoculation via mucous membranes.
Probability calculation for context (low exposure, Western Europe/USA):
| Step | Probability | Source |
|---|---|---|
| Bat in Western Europe is rabid | ~0.5–4% (by surveillance data, country-dependent) | Bat rabies CID 2008 |
| Person received bite during contact without conscious touching | Unknown, extremely small | — |
| Bite will lead to infection in the absence of PEP | ~7–80% depending on location | WHO data |
| Final probability of death without PEP for bat-in-room without direct contact | Extremely low, probably <1 in 100,000 | Charniga 2023 |
2.3 PEP Dropout: Consequences
Studies of PEP dropout across countries show: up to 30–40% of patients do not complete the full 4-dose course. Systematic reviews have not documented a single reliable case of rabies developing in a person who interrupted PEP *after a correct start* (HRIG + dose 0) in the absence of initially high risk. Nevertheless, data are extremely limited, and conclusions about the safety of interruption cannot be drawn.
---
Part 3. Communities, Forums, Skeptics
3.1 Reddit — Main Platform for Patient Narratives
| Community | Nature of discussion |
|---|---|
| r/rabies | Main forum. Dominated by anxious patients seeking support after PEP decision. Threads about side effects and questions "should I do it" |
| r/VACCINES | Isolated narratives about PEP side effects (rapid breathing, etc.) |
| r/ChronicIllness | Patients with autoimmune conditions discuss PEP compatibility with Hashimoto's and other conditions |
| r/Hashimotos | Questions about PEP impact on autoimmune thyroiditis — no data confirming risk |
| r/OCD | Significant audience: people with OCD/anxiety disorders who *cannot be reassured* either by taking or refusing PEP |
| r/AskDocs | Retrospective stories about PEP and gratitude/regret |
Key Reddit topic: a thread «Reason to not get the PEP if potential (unlikely) exposure?» — users discuss real risks vs. fear. A thread with long-term symptoms (fatigue, paraesthesias after the course) was found — without established causation.
Important caveat about Reddit: a significant portion of r/rabies users have OCD or rabies phobia — this changes the nature of the content. Their narratives about the horror of the disease and narratives about fear of side effects are mirror-indistinguishable in tone but have opposite directions.
3.2 Specific Anti-PEP Voices
No organized anti-PEP movement exists. Unlike the anti-vaccine movement for pets or pediatric routine vaccinations, no identified activists, organizations, or websites specifically promoting refusal of human rabies PEP exist.
Skepticism exists in the form of:
- Individual patient decisions to decline (two cases in Indiana MMWR 2018 — both without consequences)
- Cost arguments: a full PEP course in the USA costs $3,000–$10,000+, creating a real financial barrier and motivation to seek arguments against
- Narrative transfer from the anti-pet-rabies-vaccine movement: active anti-vaccers (e.g., r/VetTech threads) discuss vaccine risks in animals — this is a fundamentally different topic, not directly relevant to human PEP
"Vaccine injury" practice: Searching VAERS for rabies vaccines identifies individual reports, but VAERS itself explicitly warns: "the presence of a report does not constitute proof of causation" (VAERS.hhs.gov).
3.3 Medical Critics and Independent Arguments
The most well-founded arguments against automatic PEP for any bat exposure come not from anti-vaccers but from academic researchers:
- Mattner et al. (2007): "Since widespread PEP use is associated with possible serious health problems in healthcare workers at risk of rabies infection, applying rational indications for PEP is of fundamental importance" (PMID 17464908)
- Charniga & Wallace, JAMA Network Open 2023: Explicitly acknowledge that for low-risk contacts PEP may be prescribed unnecessarily, with real harm (adverse effects) and financial losses (PMC10257100)
- WHO SEA-RO (2024): Developed a Decision Tree for PEP providing for withholding PEP for Category I exposures (touching, licking intact skin)
---
Part 4. Distinction: Human PEP vs. Pet Vaccination
| Characteristic | Human rabies PEP | Pet rabies vaccination |
|---|---|---|
| Purpose | Therapeutic (after potential contact) | Prophylactic |
| Product | HDCV/PCECV + HRIG (cell-culture vaccines) | Killed/attenuated viral vaccines |
| Safety evidence base | Good for short-term AE; weak for long-term | Variable, depends on vaccine |
| Disease risk upon refusal | For humans — 100% mortality if infected | For animals — low with limited contact |
| Anti-vax movement | Essentially absent | Exists (especially in USA, UK) |
| Relevance of criticism | Limited, mainly outdated data | More active discussion |
Critically important distinction: Anti-pet-rabies-vaccine arguments (adjuvant toxicity, over-vaccination, titer testing as alternative) do not transfer to human PEP. These are fundamentally different products, indications, and risk/benefit ratios.
---
Part 5. Summary Table of Sources, Theses, and Evidence
| Source / Community | Thesis | Evidence type | What is actually confirmed | Weak points | Relevance for bat-in-room without direct contact |
|---|---|---|---|---|---|
| Tullu et al. 2003, PMID 12626831 | PEP causes encephalitis and GBS | Case series (3 cases) | Real — for nerve-tissue vaccines | Refers to outdated vaccines not applicable in RF/EU/USA today | Not relevant with modern HDCV/PCECV |
| Chakravarty 2001, PMID 11837768 | PCECV (Rabipur) caused GBS-like syndrome | Single case report | Possible link to PCECV | The only published case with PCECV; causation not proven | Very low (only case in the world) |
| Mattner et al. 2007, Infection | >50% of PEP patients have systemic AE; 5% discontinue | Prospective cohort study, n=216 | Common moderate AE (fatigue, headache, paraesthesias) are real | Context — emergency PEP for healthcare workers; may not reflect routine course | Moderately relevant: real AE exist, almost all self-limiting |
| Sari et al. 2014, PMID 24685372 | AE higher with 2-1-1 regimen and in first doses | Comparative study, n=1,685 | Confirms common mild AE; no severe ones described | Observational design, no control group | Moderately relevant |
| Galeano et al. 2023, PMID 37833201 | Serum sickness + cholestatic hepatitis after HRIG+HDCV | Case report | Severe serum sickness with hospitalization is real | One case; extremely rare | Little relevant for low-risk exposure (risk of rare severe AE vs risk of disease) |
| Huang et al. 2019, PMC6773398 | Anaphylaxis after HDCV due to residual kanamycin | Case report + analysis | Mechanism of anaphylaxis via vaccine contamination | One case in a child; depends on vaccine batch | Little relevant — quality control in EU/US vaccines is high |
| Charniga & Wallace, JAMA NO 2023 | In the USA PEP often prescribed without adequate risk assessment; for low-risk this creates unjustified harm | Decision analytical model, CDC authors | Really confirmed: overtreatment problem officially acknowledged | Article does not call for PEP refusal — only for better risk stratification | Highly relevant: directly concerns low-risk bat exposure scenario |
| CDC MMWR 2018, Indiana sorority | With careful risk assessment of bat-in-building, many contacts reclassified as low-risk | Outbreak investigation | Two who declined PEP — no rabies developed | Few observations; no long-term follow-up | Highly relevant for bat-in-room without direct contact |
| MMWR 2022 + 2026, 5 rabies deaths | Deaths occur in people who knew about contact but did not seek PEP | Case series, surveillance | All 5 deaths — in individuals who did not receive PEP | All had visible/conscious bat contact | Highly relevant: sets the boundary for “declining PEP” |
| r/rabies Reddit | Prolonged symptoms after PEP (fatigue, brain fog, paraesthesias for weeks) | User narratives | Short-term symptoms are real and match Mattner data | No diagnostic confirmation; nocebo effect possible; often anxious patients | Conditionally relevant: symptoms are real, but duration and severity exaggerated vs. studies |
| r/Hashimotos; r/ChronicIllness | PEP in autoimmune conditions — special risk | Patient narratives | No data on increased risk from modern vaccines in autoimmune diseases | No clinical studies; patients are rightfully concerned, no data available | Low specific relevance |
| VAERS reports on rabies vaccine | Various AE including neurological | Passive surveillance | Reports exist; do not constitute proof of causation | Underreporting + overreporting; no denominator; no control | Low evidentiary value |
| Anti-pet-vaccine communities | Rabies vaccines are toxic, cause chronic diseases | Anecdotes, biomechanical speculation | Does not apply to human PEP; different products and indications | Category error: transferring criticism from vet vaccines to human PEP | Not relevant |
| Ullah et al. 2018, PMC6010361 | GBS after nerve-tissue vaccine in Pakistan | Case report | Real for NTV; not relevant to HDCV/PCECV | Nerve-tissue vaccine; country context with weak registration system | Not relevant with modern cell-culture vaccines |
| Fasil et al. 2025, PMC12241378 | Severe neuroinflammatory syndrome (limbic encephalitis, ADEM) after NTV | Case reports, Ethiopia | Real for NTV in developing countries | Uses sheep-brain vaccine, banned in EU/US/Russia | Not relevant with HDCV/PCECV |
---
Part 6. Assessment of Evidence Strength by Claim Categories
| Claim category | Evidence strength | Comment |
|---|---|---|
| Severe neurological AE (GBS, encephalitis) from NTV vaccines | ⬛⬛⬛⬛⬜ Strong | Multiple publications, mechanism understood, outdated products |
| Common moderate AE (fatigue, headache) from HDCV/PCECV | ⬛⬛⬛⬛⬜ Strong | Several prospective studies, consistent data |
| Rare severe AE (serum sickness, anaphylaxis) from modern vaccines | ⬛⬛⬛⬜⬜ Moderate | Single documented cases, possible underreporting |
| GBS from HDCV/PCECV | ⬛⬜⬜⬜⬜ Very weak | One case report for PCECV, zero for HDCV |
| Prolonged (weeks-months) chronic AE from modern vaccines | ⬛⬜⬜⬜⬜ Very weak | Only user narratives, no clinical studies |
| Overtreatment for low-risk bat exposure | ⬛⬛⬛⬛⬜ Strong | Acknowledged in CDC-authored JAMA publication |
| Refusing PEP = safe for low-risk bat exposure | ⬛⬛⬜⬜⬜ Weak | Two cases without consequences — insufficient for conclusion |
| PEP is useless or dangerous in general | ⬜⬜⬜⬜⬜ Absent | 100% efficacy with timely use repeatedly proven |
---
Part 7. Specifics of the "Bat in the Room Without Direct Contact" Scenario
This scenario is the most debated and least unambiguous. Key facts:
- All 5 US deaths (2021 + 2024) occurred in people with conscious contact (including those who killed the bat by hand) who did not seek PEP. This is not the scenario "bat was flying around the room while someone slept".
- The official CDC recommendation — for bat-in-bedroom (sleeping person + bat in the same room), recommend considering PEP, because bat bites may go unnoticed. This is a recommendation for assessment, not automatic prescription.
- JAMA Network Open 2023 (Charniga) explicitly states that even with bat exposure, the probability of death without PEP can range from 10⁻¹⁰ to 0.55 — a range making a universal rule inappropriate.
- Absence of direct contact (no bite, no scratch, no direct touching) radically reduces risk.
- The decision rests with the physician/surveillance specialist who considers the region, bat species, animal testing, and nature of contact.
---
Conclusion
Confirmed by data:
- Moderate short-term AE from modern PEP are real (~30–50% of patients experience fatigue/headache/paraesthesias, usually transient)
- Severe AE from modern vaccines (HDCV/PCECV) are rare and poorly documented
- Overtreatment at low-risk exposures is officially acknowledged
- All nerve-tissue narratives are not relevant to modern vaccines
Not confirmed by data:
- Chronic/long-term diseases from HDCV/PCECV
- GBS as a systemic risk of modern vaccines
- Safety of refusing PEP with potentially significant contact
Main conclusion for the bat-in-room scenario: The real debate is not between "PEP is safe" and "PEP is dangerous", but between "standard approach to any bat exposure" and "individualized risk assessment with a threshold". Academic authors, including CDC, acknowledge that for low-risk bat exposure PEP is often prescribed without sufficient justification — this is the only argument from this space with a strong evidence base.
---
Research conducted June 21, 2026. Sources: PubMed, PMC, CDC MMWR, JAMA Network Open, Reddit (structured narrative analysis), VAERS. All claims are backed by links above.
Deep Firecrawl anti-PEP review deep_anti_pep_firecrawl_review.md
Deep research: Rabies PEP Criticism, Long Side Effects, and Independent Anti-PEP Arguments
This is a research summary, not a medical recommendation. It does not advise either receiving or declining PEP. The purpose of this document is to separate real evidence from internet narratives, old vaccines from modern ones, and “overtreatment” from any general anti-vaccine thesis.
Brief Conclusion
The strongest independent criticism of rabies PEP is not that modern vaccines routinely cause long-term harm, but that PEP is frequently prescribed without sufficiently nuanced risk assessment. In Cook County, Illinois, 55.5% of PEP recipients did not meet ACIP criteria, and the most common reason for “unnecessary” PEP was “a bat in the home, but no known contact, and the person did not wake to find the bat in the room” (Emerging Infectious Diseases / PMC).
Modern cell-culture rabies vaccines do cause frequent short-term side effects: pain/redness/swelling/itching at injection site, headache, nausea, abdominal pain, myalgia, and dizziness; the official CDC information sheet also lists a very remote possibility of severe allergic reaction, serious injury, or death (CDC VIS). In a German cohort of healthcare workers after PEP, 53% reported at least one systemic adverse effect, and 5.1% discontinued PEP, most often due to severe headache, meningism, chills, paraesthesias, malaise, or rash (PubMed).
The severe neurological stories circulating in “anti-PEP” spaces almost always refer to old nerve-tissue vaccines made from animal brain tissue, not to the modern HDCV/PCECV/PVRV vaccines used in Europe and the US. In 2025, two severe encephalitis/neuroinflammation cases following an anti-rabies vaccine were reported in Ethiopia, but the authors explicitly state that these involved a nerve tissue-derived phenolized sheep brain rabies vaccine, which the WHO recommends replacing with cell-culture vaccines (IDCases / PMC).
No organized movement specifically against human rabies PEP was found. In the data found, three different things exist: academic criticism of overtreatment, individual case reports of rare severe adverse events, and forums/Reddit where real short-term symptoms, anxiety/OCD, fear of rabies, financial stress, and sometimes irrelevant arguments from the pet anti-vax environment are mixed.
What Was Searched and What Entered the Corpus
The corpus included Firecrawl searches covering four directions: overuse/overtreatment, long-term neurological adverse events, forum-based “long-hauler” claims, and PEP refusal or discontinuation. After updating the parser, 48 unique Firecrawl sources were obtained, plus an Apify/Reddit corpus of 1,815 cleaned rows, of which 1,751 were broadly tagged as rabies-relevant; this tagging was intentionally kept wide and contains noise from pet-vaccine topics.
In the Reddit/Apify broad corpus there were 1,107 rows with claim words about side effects/long-term/injury, 279 rows with refusal/anti-vaccine, 79 rows with unnecessary/regret, 42 rows with neurological-claim words, and 181 rows with anxiety/OCD context. These numbers cannot be read as clinical statistics of adverse events: they are search-text labeling of forum discussions, not a medical registry.
Evidence Map
| Block | What is actually confirmed | Evidence strength | Relevance to modern Europe/Spain |
|---|---|---|---|
| PEP overtreatment | PEP is often prescribed without regionally/clinically precise risk assessment; for low-risk exposures this may generate unnecessary costs and adverse effects | High | High as a risk assessment principle, but USA models cannot be directly transferred to Spain |
| Short-term side effects of modern vaccines | Pain, headache, fatigue, malaise, nausea, myalgias, paraesthesias occur noticeably frequently | High | High |
| Rare severe reactions from modern vaccines | Anaphylaxis, serum sickness-like reaction, SJS, ADEM, temporary paralysis, individual neurological events described | Low-moderate | Moderate, because these are case reports and causality is often unclear |
| Chronic months-years disease after modern PEP | Forum stories exist, but no strong clinical basis proving causation | Low | Low |
| Severe neurological complications from old NTV | Encephalitis, ADEM, GBS/neuroparalytic reactions are genuinely described | High for NTV | Low for EU/Spain if modern cell-culture vaccines are used |
| Anti-human-PEP activism | Organized movement barely found | Low/absent | Low |
| Anti-pet-rabies-vaccine arguments | Exist actively, but relate to animals and different products | Not relevant | Does not transfer to human PEP |
The Strongest Independent Anti-PEP Argument: Overtreatment
Cook County: 55,5% “inappropriate PEP”
In Cook County for 2015–2018, 656 residents started PEP; after excluding 45 incomplete records, 611 were analyzed, and 339 of 611, i.e., 55.5%, did not meet ACIP guidelines for potential rabies exposure (Emerging Infectious Diseases / PMC). In this study, the most frequent reason for inappropriate PEP was not “person was visibly bitten by a bat,” but “bat in home but no known contact and did not wake to the bat in the room”; this accounted for 187 people (Emerging Infectious Diseases / PMC).
JAMA Network Open 2023: PEP Should Be Risk-Stratified
The Charniga & Wallace model used 935,881 animal samples from 51 US jurisdictions for 2011–2020 and estimated that the median probability of an animal being rabid at exposure can vary from \(3 \times 10^{-7}\) to 0.97 depending on species, region, and circumstances (JAMA Network Open / PMC). In the same article the probability of human death without PEP at exposure to a suspect rabid animal was estimated in the range from \(1 \times 10^{-10}\) to 0.55, and the authors explicitly write that for low-risk exposures PEP may lead to unnecessary out-of-pocket expenses and adverse effects (JAMA Network Open / PMC).
Importantly, the authors of this model themselves caution that their estimates do not apply to situations of “bat present but no known contact” and that the tool should not be used outside the United States due to differences in epidemiology (JAMA Network Open / PMC). Therefore, this is not “proof that PEP is unnecessary,” but rather evidence that a blanket response without contextual risk assessment can constitute poor medical practice.
JAMA 2000: Both Overuse and Undertreatment Exist Simultaneously
In a prospective series of 2,030 animal exposures in 11 urban university-affiliated emergency departments, 136 people received PEP, and 54 of these 136, i.e., 40%, were assessed as inappropriate use (PubMed). However, in the same study PEP was deemed inappropriately withheld in 119 cases among those who did not receive it — meaning the problem was not simply “everyone gets too much,” but rather “criteria are poorly applied in both directions” (PubMed).
Undark: Quality Independent Criticism with Caveat
Undark summarizes the critics' position: the USA gives PEP to approximately 55,000 people annually, total expenditures exceed 200 million dollars, the average course cost was estimated by CDC at approximately 3,800 dollars, and if even a third of courses are unnecessary, this gives about 70 million dollars of waste per year (Undark). But the same article explicitly emphasizes the caveat: rabies prevention should err on the side of overtreatment, and PEP should be given promptly when it is truly indicated (Undark).
Real Side Effects of Modern PEP
Official CDC and FDA Lists
CDC lists after rabies vaccine: soreness, redness, swelling, itching, headache, nausea, abdominal pain, muscle aches, and dizziness, and after booster doses sometimes hives, joint pain, and fever (CDC VIS). In the FDA label for IMOVAX RABIES, common local reactions after the post-exposure five-dose regimen are noted in about 25% of recipients, and mild systemic reactions like headache, nausea, abdominal pain, muscle aches, and dizziness in about 20% (FDA label).
The FDA label also lists postmarketing neurological and immune events: paresthesia, neuropathy, convulsion, encephalitis, syncope, anaphylactic reaction, and serum sickness type reaction, but postmarketing listing itself does not prove frequency or causation (FDA label). The same label states that post-exposure prophylaxis has no contraindication, but if anaphylaxis occurred after a dose, the risk of rabies must be carefully weighed against the risk of discontinuing vaccination (FDA label).
Prospective Cohort of Healthcare Workers
In a German multicentre/prospective follow-up after rabies organ-transplant exposure, 269 healthcare workers started PEP, 216 entered the adverse effects analysis, and 114 of 216, i.e., 53%, had at least one systemic adverse effect (PubMed). Common symptoms included tiredness 30.6%, headache 26.9%, malaise 26.4%, dizziness 14.8%, chills 13.0%, fever 7.4%, paraesthesias 7.9%, and nausea 9.3% (PubMed).
Large Comparative Series
In the comparative study of 1,685 PEP recipients, Sari et al. described tolerable side effects and concluded that second-generation vaccines were safe/effective/cheaper; among chronically ill patients, headache was 12.4%, administration-site pain 11.3%, arthralgia 10.5%, and in children 0–15 years, fever was 21.2% (PubMed).
Severe and/or Prolonged Adverse Events: What Was Actually Found
| Event | Source | Vaccine/context | What happened | What matters for interpretation |
|---|---|---|---|---|
| Recurrent temporary paralysis | PubMed | HDCV + HRIG, then PCECV | Paralysis started after PEP initiation, recurred after day 3, PEP discontinued before serologic response; episodes continued >2 years | Authors explicitly write that causality is often difficult to determine |
| Stevens-Johnson syndrome | PMC | Primary hamster kidney vaccine, China | SJS started on day 8 after the first dose; hospitalization, prednisone/loratadine, discharge day 15, 3 months without recurrence | WHO causality “indeterminate”, ALDEN “probable link” |
| Probable ADEM | PMC | Pure chick embryo-derived rabies vaccine mentioned | After 2 weeks: altered sensorium, seizure, coma-like presentation; steroids; discharge day 15 without deficit | Authors call it probable ADEM, but CSF/MRI were normal and could not be repeated |
| Serum sickness-like reaction + cholestatic hepatitis | PubMed | HRIG + 3 HDCV after rabies-positive bat in home | Fever, rash, jaundice, biliary stenosis, ERCP/stent, 8-day hospital stay | Authors write that literature on serum sickness after HRIG/HDCV is scarce despite frequent PEP use |
| Anaphylaxis / severe allergic reaction | PMC | HDCV batch with residual kanamycin | A 2-year-old girl had anaphylaxis after HDCV; later switched to PVRV without repeat AE | Mechanism linked to residual kanamycin in that batch, not a universal rabies antigen effect |
| Severe neuroinflammation / psychosis / ADEM | PMC | Phenolized sheep brain nerve-tissue vaccine, Ethiopia | 2 severe CNS cases after NTV | Not relevant to modern HDCV/PCECV in Europe, but important as the source of “horror” stories circulating online |
| GBS after sheep brain vaccine | PMC | Neural tissue sheep brain vaccine, Pakistan | GBS after vaccination, nearly complete recovery over 6–8 months | Old/NTV context, not a modern EU vaccine |
Old Nerve-Tissue Vaccines: Why They Distort Risk Perception
Many real scary stories about paralysis/encephalitis after rabies vaccination relate to nerve-tissue vaccines, not to modern purified cell-culture vaccines. In a case report from Pakistan, a girl received neural tissue sheep brain anti-rabies vaccine and developed Guillain-Barré syndrome; the authors write that older neural tissue vaccines carry increased risk and should be replaced with cell-culture vaccines (Cureus / PMC).
In the 2025 Ethiopian report, the authors emphasize that in some Ethiopian settings nerve tissue vaccine remained predominant PEP, with estimates of 78.5%, 80.6%, 74.9%, 92%, and up to 100% in some rural settings (IDCases / PMC). This explains why one can find recent severe “rabies vaccine encephalitis” cases online, yet they remain a poor analogy for Rabipur/Imovax/Verorab as used in the EU.
PEP Refusal and Real Deaths
In CDC MMWR 2021, three bat-associated rabies deaths occurred in people who had recognized direct contact with a bat but did not receive PEP; one patient refused PEP despite a positive bat test due to long-standing fear of vaccines (CDC MMWR). In MMWR 2024/2026, two additional deaths were also linked to direct contact: one woman killed a bat found in the sink with a hammer, another picked up a bat with bare hands and felt movement/possible bite (CDC MMWR).
This is an important contrast: real modern deaths in which PEP could have helped do not look like “bat was simply flying around, person saw nothing,” but rather involve direct handling, a possible bite, or recognized bat contact without seeking PEP. This does not prove zero risk for bat-in-room, but it shows where tragedy actually appears in epidemiological surveillance.
Bat-in-building / Bat-in-room: Where the Grey Risk Appears
In the Indiana sorority house investigation, 148 potentially exposed individuals were assessed, 100 responded to the questionnaire, 94 had seen bats in the house, 13 initially fell into moderate/high risk, but after follow-up interviews 9 were reclassified as low risk, and PEP was recommended to only 4 people (CDC MMWR). Two of the four declined PEP due to perceived lack of risk, and by February 2018, no respondent had developed clinical rabies (CDC MMWR).
This MMWR report is useful because it illustrates not “all bat-in-building events automatically trigger PEP,” but rather “interview, classify as high/moderate/low risk, then decide.” In that investigation, high risk meant a bite, scratch, or direct skin contact with a bat; moderate risk meant waking to find a bat in the same room where one was sleeping; and low risk meant no bat exposure (CDC MMWR).
Skeptical Communities: What Was Actually Found
In the Reddit/forum corpus three patterns are visible. First pattern: people with anxiety/OCD and rabies phobia who fear both the virus and the vaccine; this does not provide reliable adverse event statistics. Second pattern: real patients describe short-term symptoms, fatigue, tingling, headache, chest symptoms, anxiety, but almost always without diagnostics, without a control group, and without the ability to separate nocebo/stress/coincidence. Third pattern: transfer of anti-pet-rabies-vaccine arguments to human PEP, which is a categorical error.
An ALS-forum thread was also found in which a user linked tingling/twitching/burning pain to RabAvert, and moderators responded that this did not resemble ALS and that correlation is not causation. This is a typical example of a “long-hauler claim” that matters as a hypothesis-generating signal, but not as evidence of causality. Such accounts should be stored in a separate category of “patient-reported narratives,” kept distinct from PubMed case reports.
What "No Statistics on Long-term Effects" Means
The absence of robust long-term statistics does not mean “the vaccine is definitely safe forever.” But it also does not mean “it causes chronic disease.” For modern rabies PEP, short-term adverse effects and rare case reports are clearly documented, but no substantial body of evidence was found demonstrating that HDCV/PCECV/PVRV systematically cause chronic neurological or autoimmune syndromes over months or years.
Passive databases such as VAERS cannot fundamentally resolve this question, because a report in VAERS does not establish causality, and the database simultaneously suffers from underreporting, stimulated reporting, missing denominators, and the absence of a control group. VAERS is therefore useful for signal detection, but not as proof that “PEP causes X.”
Final Matrix: Which Anti-PEP Theses Withstand Scrutiny
| Thesis | Verdict | Why |
|---|---|---|
| "PEP is often over-prescribed at low risk" | Holds up | Cook County, JAMA 2000, JAMA 2023, and Undark/CDC logic support this |
| "Risk assessment is needed, not automatic vaccination for everyone" | Holds up | CDC/MMWR investigations and JAMA 2023 show exactly this |
| "Modern PEP often causes short-term side effects" | Holds up | CDC/FDA labels and cohort studies are consistent |
| "Modern PEP routinely causes prolonged chronic neurological diseases" | Not proven | Anecdotes and rare case reports exist, but no strong epidemiology |
| "All scary stories about paralysis prove the danger of PEP in Europe" | Does not hold up | Most such stories relate to NTV, not to HDCV/PCECV |
| "If the exposure is truly significant, one can simply skip PEP because of side effect risk" | Does not hold up | Real deaths after bat contact without PEP are described by CDC |
| "Human PEP = pet rabies vaccine risk" | Does not hold up | Different products, indications, doses, populations, and risk/benefit |
Practical Conclusion for Further Reporting
If one is to produce a global report, its honest central formula should be: “PEP is lifesaving when indicated, but the indication itself is the real battlefield.” In other words, the dispute is not “is the vaccine good or bad,” but “was the exposure of sufficient magnitude that the risk of rabies exceeded the risk and cost of PEP.”
For scenarios of the type “a bat was somewhere in the premises but there was no direct contact,” the strongest scientific line in support of a calm assessment is not an anti-vaccine line, but the line of overtreatment, improper risk stratification, and the need for consultation with public health or an epidemiologist. For scenarios involving recognized direct contact, handling, a possible bite, scratching, or saliva-to-mucosa or wound evidence, that line shifts sharply: it is precisely there that CDC case reports document real deaths in the absence of PEP.
Data Files Accompanying This Document
firecrawl_anti_pep_sources.csv— 48 unique Firecrawl sources on overuse, long-term adverse events, refusals, and forum narratives.reddit_anti_pep_skeptic_relevant.csv— broad Reddit/Apify export; useful for narratives but not for clinical statistics.anti_pep_research_counts.json— corpus counters and tags.rabies-pep-anti-research.pplx.md— parallel deep research agent report that formed the basis of this final summary.
Sleep, bat landing and unnoticed bite bat_sleep_contact_analysis_ru.md
Can a Sleeping Person Not Feel a Bat: In-Depth Analysis
Prepared: June 2026. Purpose — assessment of scenario plausibility, not a medical recommendation.
---
Contents
- Anatomy of the question: what exactly needs to be assessed
- Expert and official sources
- Medical sources and clinical cases
- Real stories: forums, personal accounts
- Merlin Tuttle's position and the "unnoticed bites" discussion
- Summary table of positions
- Final assessment of scenario plausibility
---
1. Anatomy of the Question
The scenario breaks down into two separate events:
| Event | Question |
|---|---|
| Landing | Can a sleeping person not feel a bat landing on them? |
| Bite | Can a sleeping person not feel a bite and not wake up? |
The answers to these two questions differ in probability and source consensus.
---
2. Expert and Official Sources
2.1 CDC (USA) — Centers for Disease Control and Prevention
Key quote (CDC, "Preventing Rabies from Bats" page):
«Bat bites can be tiny, and you may not even know if you were bitten.»
Source: https://www.cdc.gov/rabies/prevention/bats.html
CDC explicitly acknowledges: bat bites can be so small that a person does not notice them. Based on this, the PEP (post-exposure prophylaxis) policy has been formed: if a person finds a bat in the room where they slept, this is considered potential contact even without a visible bite.
From MMWR (2021, three rabies deaths):
«The other two patients did not realize the risk for rabies from their exposures, either because they did not notice a bite or scratch or did not recognize bats as a potential source.»
Source: CDC MMWR, 2021: https://stacks.cdc.gov/view/cdc/113675
From MMWR (2024, Minnesota and California):
«ACIP recommends that persons who have slept in a room where a bat is present and are at increased risk for unrecognized exposure should receive PEP.»
Source: https://www.cdc.gov/mmwr/volumes/75/wr/mm7502a4.htm
From MMWR (2012, Kentucky, sleeping areas):
«PEP is recommended in situations where a bat is identified in direct proximity to a person who cannot be reasonably sure a bat bite or scratch did not occur, such as someone awaking in a room with a bat.»
Source: https://www.cdc.gov/mmwr/preview/mmwrhtml/mm6219a2.htm
CDC conclusion: the mere presence of a bat in a room with a sleeping person when contact cannot be excluded is a basis for PEP.
---
2.2 Mayo Clinic
Quote:
«For instance, a bat that flies into your room while you're sleeping may bite you without waking you. If you awake to find a bat in your room, assume you've been bitten.»
Source: https://www.mayoclinic.org/diseases-conditions/rabies/symptoms-causes/syc-20351821
---
2.3 Cleveland Clinic
Cleveland Clinic distinguishes between two states:
«Yes, you can usually feel bat bites.»
«You'll most likely be able to feel the bite if you're awake.»
«It's possible to get bitten without knowing it. If you find a bat in an area you're sleeping in, it's important to assume you were in contact.»
Source: https://my.clevelandclinic.org/health/diseases/bat-bite
That is: while awake — you will almost always feel it; while asleep — you may not feel it.
---
2.4 Minnesota Department of Health
One of the most specific state health sources:
«Most people who have been bitten by a bat report a stinging or needle prick sensation. However, bat bites may not be noticed, especially if someone is asleep, and bat bites may leave little or no evidence of a wound or puncture.»
Source: https://www.health.state.mn.us/diseases/rabies/risk/humanbat.html
---
2.5 Health Canada / Canadian Immunization Guide
«Bites inflicted by bats may not be felt and may leave no visible bite marks.»
Source: https://www.canada.ca/en/public-health/services/publications/healthy-living/canadian-immunization-guide-part-4-active-vaccines/page-18-rabies-vaccine.html
Ottawa Public Health (Ontario):
«Bat bites are not always visible, and direct contact with a bat, when a bite, scratch or saliva exposure into a wound or mucous membrane cannot be ruled out, is sufficient exposure to warrant rabies post-exposure prophylaxis.»
Source: https://www.ottawapublichealth.ca/en/professionals-and-partners/hcp-rabies.aspx
EOHU (Eastern Ontario):
«Bat's teeth are quite sharp and don't always leave marks, so you may not realize you have been bitten.»
Source: https://eohu.ca/en/my-environment/bats-and-rabies
Durham Region Health:
«Direct contact with a bat is defined as the bat touching or landing on a person.»
Source: https://www.durham.ca/en/health-and-wellness/resources/Documents/ResourcesforHealthCareProviders/FaxAbout/2023/Rabies-PEP-and-Bat-Exposures-Aug-15-2023.pdf
The Canadian protocol (post-2009) is stricter than the American one: PEP is recommended only with direct physical contact (bat touched or sat on the person) + inability to exclude bite/scratch. Mere presence of the bat in the room is insufficient.
---
2.6 Bat Conservation Trust (UK)
«Bat bites are not always obvious and do not tend to leave a mark, therefore they are often felt not seen. Scratches or contact with bat saliva may also pose a risk. If you are unsure you were bitten (or licked or scratched) we advise you still speak to a health professional.»
Source: https://www.bats.org.uk/advice/i-think-ive-been-bitten-by-a-bat
Important detail: BCT writes "often felt not seen" — meaning a bite is usually felt but not always visually visible. This nuance is often lost in retellings.
---
2.7 NHS / Scotland NHG (UK)
«All bat bites, scratches or other exposures, whether in Scotland, the rest of the UK or abroad, should therefore be assessed promptly by a health professional.»
Source: https://www.cem.scot.nhs.uk/adult/btbt.pdf
NHS (England): rabies is extremely rare in the UK (only bats with EBLV), approach — risk assessment.
---
2.8 Australia — Australian Bat Lyssavirus (ABLV)
Barwon South West Public Health Unit:
«Even without being knowingly bitten or scratched, you may have been exposed to the virus. Some examples include: Sleeping in an enclosed space (e.g., bedroom or tent) with a bat present.»
Source: https://bswphu.org.au/infectious-diseases/rabies-and-australian-bat-lyssavirus/
NSW Health (PDF):
«Any bat in Australia could potentially carry ABLV. The behaviour or appearance of a bat is not a true guide as to whether it is carrying the virus.»
Source: https://www.health.nsw.gov.au/Infectious/factsheets/Factsheets/rabies.pdf
RACGP (Australian GP Medical Association):
«Post-exposure management is recommended for a person with any bite or scratch from, or mucous membrane or broken skin contact with the saliva or neural tissues of, a bat.»
Source: https://www1.racgp.org.au/ajgp/2018/march/australian-bat-lyssavirus
---
2.9 Bat Conservation International (BCI, USA)
BCI cautiously warns about rabies risks, acknowledging that not all bats carry it, and recommends not touching them.
Source: https://www.batcon.org/about-bats/faq/
---
3. Medical Sources and Clinical Cases
3.1 StatPearls / NCBI — "Rabies" (Academic Review)
«Patients may be unaware that a specific exposure carries a risk or may not realize they were bitten, especially in cases of bat bites.»
Source: https://www.ncbi.nlm.nih.gov/books/NBK448076/
---
3.2 "Rabies in a nine-year-old child: The myth of the bite" (PMC, 2002)
Clinical case: a nine-year-old boy died of rabies — neither he nor his parents remembered any bat contact. The viral strain was of bat origin.
«After examining the most recent cases of rabies in North America, it is obvious that rabies following bat exposure can occur without history of a documented bite. The case emphasizes that the bite or the scratch of a rabid bat can go unnoticed and may lead to the development of human rabies.»
Source: https://pmc.ncbi.nlm.nih.gov/articles/PMC2094861/
---
3.3 "Bat Rabies in the United States and Canada from 1950 through 2007" (CID, 2008)
Large-scale epidemiological analysis of 57 cases:
«A bite was reported by 22 (39%) of case patients, 9 (16%) had a direct contact but no history of a bite, 6 (11%) found bats in their home but reported no direct contact, and 19 (34%) reported no history of bat exposure whatsoever.»
That is: 61% of rabies deaths after bat contact were not accompanied by a confirmed bite.
Source: https://academic.oup.com/cid/article/46/9/1329/327503
---
3.4 "Emerging Epidemiology of Bat-Associated Cryptic Cases of Rabies" (CID, 2002)
The term "cryptic cases" — cases with unknown transmission mechanism:
«Most recent indigenous cases of rabies [in the USA] … had no history of bat exposure whatsoever.»
Strains of the silver-haired bat (*Lasionycteris noctivagans*) and eastern pipistrelle (*Pipistrellus subflavus*) are responsible for most "cryptic" cases — presumably due to small teeth and superficial bites.
Source: https://academic.oup.com/cid/article/35/6/738/380862
---
3.5 CDC MMWR: "Human Rabies — South Carolina, 2011"
A 46-year-old woman died of rabies. She shook a bat out of curtains through an open window — she thought there was no contact and saw no bite marks.
Source: https://www.cdc.gov/mmwr/preview/mmwrhtml/mm6232a2.htm
---
3.6 NJ Health Guide to Bat Exposures
«The most likely exposure scenario is a person being bitten but was either unaware of the bite or knew they were bitten but did not seek medical attention after the bite. Bat bites may be less severe and more difficult to recognize than bites inflected by larger animals.»
Source: https://www.nj.gov/health/cd/documents/rabies/batexposure.pdf
---
3.7 "Bats in the Bedroom, Bats in the Belfry" (CID, 2009) — Canadian Policy Reassessment
The authors (De Serres et al.) calculated: the frequency of rabies with a bat in a sleeping person's room without confirmed contact — 1 case per 2.7 billion person-years.
«Bedroom bat exposure while sleeping and without known physical contact occurred at an annual rate of 0.099%. We estimate that <5% of eligible persons with bedroom exposure receive RPEP as recommended.»
This study became the basis for the 2009 Canadian policy update: PEP only with direct contact.
Source: https://academic.oup.com/cid/article-abstract/48/11/1493/347031
---
3.8 PMC: "Exposure to bats: updated recommendations" (CMAJ, 2010)
Summary of updated Canadian NACI recommendations:
«A case of rabies related to bedroom exposure has been estimated to occur in Canada once every 84 years. The researchers estimated that more than 2.6 million people would need to be treated to prevent 1 case of rabies related to a bedroom exposure.»
Source: https://pmc.ncbi.nlm.nih.gov/articles/PMC2802607/
---
3.9 Vampire Bat Saliva and the Anesthetic Effect
This is important for understanding the mechanism. Saliva of vampire bats (*Desmodus rotundus*) contains natural anesthetics, anticoagulants, and thrombin inhibitors (draculin, DSPA).
«Besides being superficial, the feeding bite is apparently painless, for the vampire bat has an anesthetic substance, in addition to a factor Xa inhibitor denominated draculin.»
Source (clinical case): https://pmc.ncbi.nlm.nih.gov/articles/PMC4008072/
Vampire bat saliva has been documentarily confirmed to contain anesthetics. However, insectivorous bats — which are more common in homes in the USA, Canada, and Europe — do not have the same anesthetic mechanism. Their bites, by general consensus, are more painful — a "needle prick" or burning sensation.
---
4. Real Stories: Forums and Personal Accounts
4.1 Wildlife Center of Virginia — Personal Account of Veterinary Technician ("Jaclyn")
«Even though I did not feel the bat bite me or see it bite my pets, I cannot be sure that it didn't, since we were all sleeping in the bedroom where the bat was found. Bats have very small teeth and sometimes their bites can go unnoticed, especially if you had been sleeping deeply.»
Jaclyn found a bat in the morning. There was no direct sensation of a bite. She took steps to check vaccination status.
Source: https://wildlifecenter.org/news-events/news/2018/bat-bedroom
---
4.2 Tone Madison — Report on Real Cases (Wisconsin)
Sara Woolery woke up at 3 AM — not from the bat but from cats. A bat was flying above her bed. She felt no contact, but after reading CDC recommendations, decided to get PEP.
«Lots of people told me, when I was like, 'Do I really need to go get a rabies vaccine?' They're like, 'Yes, you should just go get one.' I told the story to a lot of people, they were like, 'Oh, bats used to come in my college house all the time, and nobody ever said anything about getting rabies vaccines.'»
Source: https://tonemadison.com/articles/bats-in-the-bedroom/
---
4.3 WBUR / Janna Malamud Smith — "A Bat In My Bedroom" (2014)
The writer describes how a nocturnal bat woke her and her husband. They chased it out through the window. A friend warned about CDC protocol. A doctor was called. An interesting quote:
«A bat advocate website called Batworld, while suggesting that you should capture and test the bat if you were sleeping when it appeared, notes, nonetheless, that its sharp little needle teeth are usually felt.»
That is: bat conservation organization Batworld acknowledges that a bite is usually felt — but still recommends testing.
Source: https://www.wbur.org/cognoscenti/2014/11/12/the-bat-incident-janna-malamud-smith
---
4.4 Discovery Channel / Curiosity.com — «If A Bat Were To Bite You In Your Sleep, You'd Probably Never Know»
«That's most likely because bats have very small teeth and produce a bite that doesn't hurt the way a larger animal's would, so it's possible that they might not even wake their victim. They also hardly leave a mark, making it difficult to know you were ever bitten.»
Also: 17 of 19 US rabies deaths (1997–2006) were linked to bats; 3 of these people did not know they had ever had bat contact.
Source: https://www.discovery.com/nature/bat-bite-sleep-never-know
---
4.5 YouTube — "Bats and rabies: Mayo Clinic Radio"
Mayo Clinic expert explicitly states:
«Bat bites won't wake you up. Bat bites won't leave a mark.»
Source: https://www.youtube.com/watch?v=fFtYB7FBAWU
---
4.6 Reddit r/homeowners — bat researcher
«As a bat researcher, I know that depending on the species, you might not even realize you've been bitten. Even though rabies is rare in bats, I would still recommend receiving post-exposure vaccinations because rabies is 100% fatal. I would say it's rare, but after being bitten by several small bats I've learned that a bat weighing less than 7 grams can leave almost no visible injury. Since rabies is invariably fatal, it's prudent to receive post-exposure vaccination if you're unsure whether you've been bitten.»
Source: https://www.reddit.com/r/homeowners/comments/9cvsqx/help_a_bat_flying_where_i_was_sleeping_should_i/
---
4.7 Reddit r/rabies — "To get a shot or not?"
A user woke up with "tiny marks on their torso" after finding a bat. Called emergency services. Health authorities decided to start a vaccination course due to the skin mark.
«I went to the emergency department, they reached out to the local public health authority, and because of the tiny marks that appeared overnight on my torso, they decided the vaccine was necessary.»
Source: https://www.reddit.com/r/rabies/comments/1f5r802/to_get_a_shot_or_not/
---
4.8 Reddit r/animalid — "Paraguay: Is this a bat I caught walking on me while sleeping?"
A person woke up and caught a bat that was crawling on them. Did not feel a bite but asked about risks.
«You need to get a rabies shot whether you feel like you were bitten or not. It walking in your bed while you're sleeping is especially concerning. Bat bites are small and can go unnoticed.»
Source: https://www.reddit.com/r/animalid/comments/1i3bxzb/paraguay_is_this_a_bat_i_caught_walking_on_me/
---
4.9 MPR News (Minnesota Public Radio) — Doctor on Sensations
«Even if you don't know if you were bitten, if you had a bat fly into you, land in your hair, or touch your bare skin, we would consider that a potential exposure because it's possible the bat could have bitten you and you wouldn't have realized it. It's usually pretty chaotic when a bat's flying at you, hard to remember exactly what happened in that moment. Same as if you wake up to a bat while you're sleeping. You don't really know what was happening while you were asleep. It's possible it could have landed on you and bitten you.»
Source: https://www.mprnews.org/episode/2023/06/15/happy-bat-season-heres-your-rabies-questions-answered
---
4.10 Valentine Brkich — "Attack of the Phantom Bat" (Personal Blog)
The wife woke up, screamed "bat on my neck, flapping wings". No bite marks were found. Possibly it was a dream or another insect (bedbug etc.), but the incident itself illustrates typical panic and confusion.
«We never did find any sign of a bat in that room.»
Source: https://valentinebrkich.com/blog/attack-of-the-phantom-bat/
---
4.11 Environmental Literacy Council — Popular Exposition
Two separate materials give a balanced picture:
«Can you feel a bat land on you?»:
«The short answer is: yes, you likely would feel a bat land on you, though the sensation might be surprising and perhaps not what you expect. The sensation would likely be that of something lightweight and flat — like a fluttering or a light pressure.»
«Would I wake up if a bat bit me?»:
«The short answer is: possibly not. Bat bites are often so small and painless that they may not wake you up.»
Sources:
- https://enviroliteracy.org/can-you-feel-a-bat-land-on-you/
- https://enviroliteracy.org/would-i-wake-up-if-a-bat-bit-me/
---
4.12 OSU Medical Blog (Ohio State University)
«If you woke up because a bat landed on you while you were sleeping, or if you awakened and found a bat in your room, you have potentially been exposed. The small teeth of a bat can make a bite difficult to find.»
Source: https://u.osu.edu/buckmdblog/2013/09/26/help-theres-a-bat-in-my-room-what-should-i-do/
---
4.13 Direct Personal Testimony (YouTube, “It's A Bat | YUCK!”)
«I was sleeping in my bed sound asleep and a bat landed right in my face. I come unglued out of that bed.»
This is direct evidence that landing on the face woke the person immediately.
Source: https://www.youtube.com/watch?v=FqPa5t5o0vk
---
5. Merlin Tuttle's Position and the "Unnoticed Bites" Discussion
Merlin Tuttle is one of the world's foremost bat specialists and founder of Bat Conservation International. His position fundamentally differs from CDC's.
5.1 Tuttle's Main Thesis
"Bats can transmit rabies as stated, but not without a bite that is normally painful enough to be recognized at the time. The U.S. Center for Disease Control claims of rabies cases with no definite bite history are biased by unreliable reporting methodology."
Source: https://www.merlintuttle.org/merlins-response-to-npr-headline-on-bat-rabies/
"It is a virtual certainty that the Wyoming woman [who died of rabies] was bitten. It is also unlikely that the bat that bit her was one of those living behind the eaves of her home."
---
5.2 Tuttle's Arguments Against the "Unnoticed Bite" Concept
From the article "Rabies in Perspective" (https://www.merlintuttle.org/rabies-in-perspective/):
- CDC methodology is unreliable: most cases "without bite history" were established posthumously or in patients who were already unconscious. Absence of bite history is the result of inability to interview the victim, not the actual absence of a bite.
- 1999 symposium resolution: at the 29th Annual Bat Research Symposium (1999), a resolution was adopted: "We find no credible support for the hypothesis that undetected bites by bats are a significant factor in transmitting rabies to humans." Researchers agreed that people usually feel and recognize bites.
- Oregon and Canada: independent studies from the state of Oregon and Canada showed that CDC policy is absurdly expensive: the Oregon program cost $2.4 million per year to prevent 1 case every 75 years; the Canadian equivalent — $2 billion to prevent 1 case every 84 years.
- New York case (11-year-old girl): officially recorded as “no known contact with a bat.” In-depth investigation revealed that her brother had caught a grounded bat and kept it in a cage inside the home.
- Personal experience: over 60+ years of bat study, Tuttle has never personally documented an unprovoked bite of a sleeping person by a bat.
---
5.3 Tuttle's Position on Landing
«In my experience, it is extremely rare to be awakened by a bat actually in contact with a person. In such a case extreme care should be taken to check for even tiny tooth marks, and such an abnormally behaving bat should always be submitted for testing.»
In other words: Tuttle acknowledges that a bat landing on a person is an extremely rare event, and that in such an event one should carefully look for bite marks.
---
5.4 How Tuttle's Position Differs from CDC's
| Question | CDC | Merlin Tuttle |
|---|---|---|
| Can a bite go unnoticed during sleep? | Yes, this is possible | No — a bite is usually painful and noticed |
| Reason for "no bite history"? | Real unnoticed bites | Unreliable reporting methodology |
| PEP with bat in the room? | Recommend considering | Only necessary with direct contact |
Important: Canada (NACI, 2009) effectively moved to a position closer to Tuttle's than CDC's — PEP only with direct contact.
---
6. Summary Table of Positions
| Source | Can a sleeping person not feel the landing? | Can a sleeping person not feel the bite? | Does landing require PEP? |
|---|---|---|---|
| CDC | Does not state directly | Yes, possible | Yes (when contact cannot be excluded) |
| Mayo Clinic | — | Yes | Yes (“assume you've been bitten”) |
| Cleveland Clinic | — | While asleep — possible | Yes |
| Minnesota Health | — | Yes, especially during sleep | Yes |
| Health Canada / NACI | — | Yes | Only with direct contact |
| Bat Conservation Trust (UK) | — | A bite is usually felt (felt not seen) | If uncertain — consult |
| NHS | — | Does not specify | Risk assessment |
| Australia (ABLV) | — | Yes | Yes, sleeping with bat in room — contact |
| Merlin Tuttle | Extremely rare event | No — a bite is usually noticed | Only with direct contact and mark |
| Environmental Literacy Council | While awake — yes; during sleep the question is open | While asleep — may not feel it | Medical consultation |
---
7. Final Assessment of Scenario Plausibility
7.1 Landing: Can a Sleeping Person Not Feel It?
Answer: Moderately plausible in deep sleep, unlikely in light sleep.
Factors "for" (will not feel):
- Bats are small animals. The little brown bat weighs 7–14 g. Landing on a soft surface (blanket, mattress) means virtually zero pressure on the body.
- Landing on a clothed body part (e.g., leg under covers) — extremely little tactile information.
- In deep sleep (SWS), the arousal threshold for tactile stimuli is significantly elevated.
Factors "against" (will feel):
- Landing on an uncovered face, neck, or arms — most people will feel it.
- Wing movement, claws, minimal weight still create a stimulus.
- Direct account (YouTube): "a bat landed right in my face — I come unglued." Landing on the face woke the person immediately.
Plausibility of "did not feel the landing": High when landing on clothed body parts during deep sleep; moderate when landing on exposed parts; low when landing on face/neck.
---
7.2 Bite: Can a Sleeping Person Not Feel It?
Answer: Yes, this is physically possible — but depends on bat species, location of the bite, and depth of sleep.
Factors "for" (will not feel the bite):
- Teeth of insectivorous bats create micro-wounds < 1 mm.
- A bite during deep sleep may not reach the arousal threshold.
- A bite on less sensitive areas (leg, back, foot) — harder to notice.
- Vampire bats have a proven anesthetic mechanism in their saliva.
- Official consensus of CDC, Mayo Clinic, Minnesota Health, Health Canada, Australian ABLV protocols: a bite during sleep may go unfelt.
Factors "against" (will feel):
- Minnesota Health and BCT (UK): most people report a "needle prick" or burning sensation.
- Cleveland Clinic: "you will likely feel it if you are awake" — implies that during sleep — uncertain.
- TaTuttle and Batworld: a bite 'is usually felt'.
- Insectivorous bats in Europe/North America do not have the same level of anesthetics as vampires.
Plausibility of "did not feel the bite during sleep": Moderate to high. Official health authorities of the USA, Canada, and Australia explicitly recognize this scenario as possible and base PEP protocols on it. There are documented rabies deaths where there was no bite history.
---
7.3 How People in Real Stories Realized the Bat Was on Them
From the collected materials, the following detection mechanisms emerge:
| Detection mechanism | Examples |
|---|---|
| Woken by physical sensation (flapping, claws, contact with face/neck) | YouTube videos, "bat on my neck", WBUR essay |
| Woken by animals (cats, dogs reacted to the bat) | Tone Madison (Woolery), Wildlife Center of Virginia (Jaclyn) |
| Saw/heard the bat only after waking | Reddit r/batty, Reddit r/AskReddit, Rachelle Wilson Substack |
| Found small bite/scratch marks in the morning | Reddit r/rabies ("tiny marks on torso") |
| Caught the bat directly on themselves | Reddit r/animalid (Paraguay) |
| Learned about the bat from a partner/neighbor | Writing Forums |
| Did not discover personally — relatives reported it after the fact (already at the doctor) | South Carolina 2011 MMWR (posthumously) |
Fundamental conclusion: In most documented cases, people did not wake up from the bite — they found the bat by indirect signs or did not find it at all.
---
7.4 Why This Scenario Matters for Risk Assessment
The scenario "bat sat on the sleeping person and they did not feel it" is plausible based on the following grounds:
- Anatomical: small weight, microscopic teeth, potentially superficial bite.
- Neurophysiological: during deep sleep, the threshold for pain and tactile sensitivity is elevated.
- Clinical: rabies deaths documented in people who did not remember a bite; some with bat viral strains without any confirmed contact history.
- Regulatory: PEP protocols of all major world health organizations are built precisely on the basis of this plausibility.
However, it is not in itself a high-probability event: most bats are not rabies carriers; healthy bats practically never bite people without provocation; the actual landing itself is rare.
---
This document contains an analytical review of public sources. It is not a medical recommendation. All questions about real bat contact should be immediately discussed with a physician or health authorities.
Pipistrellus / Hypsugo and small species: European data pipistrellus_eblv_russian_summary.md
European Bat Lyssaviruses (EBLV) in Small Synanthropic Species: Pipistrellus and Associated Species
Summary with Citations
---
1. Introduction and Epidemiological Context
European bat lyssaviruses (EBLV) types 1 and 2 (EBLV-1, EBLV-2) are the main causative agents of bat rabies in Europe. From 1977 to 2023, more than 1,500 bat lyssavirus cases were registered in Europe (Picard-Meyer et al., 2026, Vet Res Commun, doi:10.1007/s11259-026-11166-8). The vast majority of cases (>97%) are caused by EBLV-1 and fall to the serotine bat (*Eptesicus serotinus*) — the main reservoir species. More than 90% of all registered cases are concentrated in five countries: Germany, Netherlands, Denmark, Poland, and France (WHO Rabies Bulletin Europe, general information).
Small synanthropic species — primarily the common pipistrelle (*Pipistrellus pipistrellus*), Nathusius' pipistrelle (*Pipistrellus nathusii*), soprano pipistrelle (*Pipistrellus pygmaeus*), and Savi's pipistrelle (*Hypsugo savii*) — are widespread in urban environments across Europe and have the most frequent contact with people. The question of their role in EBLV epidemiology is of fundamental importance for veterinary surveillance and public health.
---
2. Documented Cases by Country and Species
2.1 Germany
Germany has the most systematized bat monitoring in Europe. During retrospective passive surveillance (1998–2013, n=5,478 individuals, 21 species), several rare EBLV cases were identified in small species (Schatz et al., 2014, PLoS NTDs, doi:10.1371/journal.pntd.0002835):
- P. pipistrellus: 1 confirmed EBLV-1 case (FAT, RTCIT virus isolation, RT-qPCR, sequencing); live virus isolated.
- P. nathusii: 1 confirmed EBLV-1 case (same methods); live virus isolated.
- Historically documented EBLV-1 cases in *P. nathusii* in Germany in 1986 and 1992 (mentioned in Picard-Meyer et al., 2026).
In extended retrospective passive surveillance (2018–2020, n=1,236), 2 more EBLV-1 cases were found in *P. pipistrellus* (Klein et al., 2021, Viruses, doi:10.3390/v13081538):
- Sample Lab-ID 31955: June 12, Tübingen (Baden-Württemberg), EBLV-1a; RT-qPCR+, virus isolation+, partial genome (NGS).
- Sample Lab-ID 23157: April 10, Nürtingen (Baden-Württemberg), EBLV-1a; RT-qPCR+, virus isolation+, partial genome (NGS).
Key methodological finding: both *P. pipistrellus* samples from 2018–2020 previously gave a negative FAT result and were only detected on re-screening by RT-qPCR. This is direct evidence that standard FAT is insufficiently sensitive for detecting lyssaviruses in small bat species with atypical infection (Klein et al., 2021).
2.2 France
In France from 1989 to ~2017, 78 bat lyssavirus cases were registered: 75 in *E. serotinus* (EBLV-1), 1 in *P. pipistrellus* (EBLV-1, described by Parize et al. 2020), 2 in *M. nattereri* (BBLV) (Picard-Meyer et al., 2017, PLoS NTDs).
The most recent documented case — the first-ever detection of EBLV-1 in *P. nathusii* in France (Picard-Meyer et al., 2026, Vet Res Commun, doi:10.1007/s11259-026-11166-8):
- Animal found May 13, 2020 on the terrace of a private house in Erstein (Bas-Rhin, Alsace; 48.43°N, 7.66°E), ~20 km from the German border.
- Death: May 19, 2020; submitted for analysis January 24, 2022.
- Methods: FAT (positive), real-time and conventional pan-lyssavirus RT-PCR, hemi-nested RT-PCR, Sanger sequencing, whole-genome NGS (PX733926, 11963 bp).
- Virus: EBLV-1a; nucleotide sequence similarity 99.88% with a strain from *E. serotinus* in Lower Saxony (Germany, 2016; OU524432).
- First such case in France and the third in Europe in a long-distance migrant.
2.3 United Kingdom
In 2018–2020, one presumed EBLV-1 case was found in a soprano pipistrelle (*P. pygmaeus*) (Folly et al., 2021, Viruses, doi:10.3390/v13101979):
- Individual young male; FAT analysis — positive (confirmed by three operators).
- RT-PCR (SYBR and TaqMan) — negative due to autolytic degradation of the sample.
- Molecular confirmation not possible. Case classified as "presumed EBLV-1" based on geographic proximity to confirmed *E. serotinus* foci.
- 104 *P. pygmaeus* tested during the same period — no other findings.
The 2024 authors (Golding et al., 2024, Virus Evolution, doi:10.1093/ve/veae060) explicitly state: "Lyssavirus findings in *Pipistrellus* species are considered likely spillover events driven by geographic overlap with serotine populations." As of May 2024, in all 34 confirmed EBLV-1 cases in the UK, the virus was found exclusively in *E. serotinus*.
2.4 Netherlands
The most large-scale passive monitoring for a single species: 1,837 *P. pipistrellus* individuals tested by FAT for the period 1984–2003 — not a single positive result (Van der Poel et al., 2005, Emerg Infect Dis). For comparison: of 1,219 *E. serotinus*, 251 (21%) were EBLV-1 positive. EBLV-1 prevalence in serotines in the Netherlands was 23.6% (WBVR data, 1987–2017). In October 2024, EBLV-1 was detected in a domestic cat in the Netherlands for the first time (Dekker et al., 2025, Eurosurveillance, doi:10.2807/1560-7917.ES.2025.30.10.2500154).
2.5 Belgium
In 2016–2018, comprehensive passive surveillance with serological examination of live individuals was conducted (Nauwelaers et al., 2024, Trop Med Infect Dis, doi:10.3390/tropicalmed9070151):
- 124 brain samples (passive surveillance): 98 (79%) — *P. pipistrellus*; all negative for EBLV.
- Live animals (active surveillance): 113 saliva samples — all negative by RT-qPCR.
- Serum (87 samples): neutralizing antibodies detected in 5 bat species (including pipistrelles and *P. auritus*).
- Confirmed active infection cases: only in *E. serotinus* (2016, Bertrix; 2017, Étalle) — both EBLV-1b by N-gene sequencing.
2.6 Denmark
Denmark is one of the three European countries with the highest number of registered bat rabies cases (226 by 2021) (McElhinney et al., 2018). The peak was in 1986–1987 (150 cases in *E. serotinus* after mass screening initiated by a human case in 1985). Data on *Pipistrellus* species in Danish literature are not recorded as positive. According to the SSI 2023 report: 43 bats tested by PCR — all negative (SSI, 2023 Annual Report on Rabies).
2.7 Spain
The most detailed data on seroprevalence in small synanthropic species were obtained in Spain.
Serra-Cobo et al. (2013) (PLoS ONE, doi:10.1371/journal.pone.0064467), 2001–2011, 2,393 sera, 25 habitats, Aragon + Balearic Islands + Catalonia:
- *P. pipistrellus*: 45 sera, 5 seropositive (11.1%) — first registration of EBLV-1 antibodies in this species; 1 of 3 dead individuals — EBLV-1 RNA+ (nRT-PCR); live virus not isolated.
- *P. kuhlii*: 16 sera, 3 seropositive (18.8%); RNA and virus not isolated.
- *H. savii*: 22 sera, 5 seropositive (22.7%) — first registration in this species; highest seroprevalence among small species; RNA and live virus not isolated.
- Serology method: adapted RFFIT (RFFIT-based serology).
López-Roig et al. (2014) (Viruses, doi:10.3390/v6093386), 2004–2012, one multispecies colony "San Pedro de los Griegos", 406 sera, 9 species:
- *P. pipistrellus*: 28 sera, 4 seropositive (14.28%).
- *H. savii*: showed highest seroprevalence in certain years, with an inter-year peak in 2007 (>70% in the main colony species — *T. teniotis*, *P. austriacus*).
- Method: modified FAVNT (Fluorescent Antibody Virus Neutralization Test).
2.8 Italy
Zecchin et al. (2019) (Epidemiol Infect, doi:10.1017/S0950268818003072), 2006–2017:
- Most represented species in the sample: *P. kuhlii* (n=96; 32.4%), *H. savii* (n=82; 27.7%).
- EBLV-1 antibodies detected exclusively in *M. myotis*, *M. blythii*, *T. teniotis* — not in *P. kuhlii* or *H. savii*.
- Virus not detected in either passive or active surveillance in any species.
Leopardi et al. (2023) (PRSB, doi:10.1098/rspb.2023.0183): 36.3% of 837 *M. myotis* seropositive; no RNA in 556 individuals by RT-PCR.
2.9 Sweden
Hammarin et al. (2016) (Infect Ecol Epidemiol, PMC5156864), 2008–2013, n=452:
- *P. nathusii*: 4 individuals — no seropositive; RNA not detected.
- *P. pygmaeus*: 2 individuals — no seropositive; RNA not detected.
- Passive surveillance: all samples (FAT) — negative.
- All seropositive individuals — exclusively *M. daubentonii* (0–10.3% by year).
2.10 Finland
Nokireki et al. (2013) (BMC Vet Res, doi:10.1186/1746-6148-9-174), 1985–2012, n=1,156:
- *P. nathusii*: 3 serological samples — all negative.
- *P. pipistrellus* and *P. pygmaeus*: rare migrants (first records 2001 and 2007 respectively); not specifically tested.
- EBLV-2 detected in *M. daubentonii* in 2009, 2016, and 2017; virus confirmed by isolation (FAT + RT-PCR + cell culture isolation; (Jakava-Viljanen et al., 2010, Epidemiol Infect, doi:10.1017/S0950268810000373); (Second case, 2016, Helsinki, HELDA)).
---
3. Distinguishing Diagnostic Methods
The key aspect of epidemiological interpretation is the confirmation method:
| Method | What it detects | Significance for *Pipistrellus* |
|---|---|---|
| FAT (fluorescent antibody test on brain tissue) | Lyssavirus antigen | Standard of passive surveillance; in small species with atypical infection may give a false-negative result (Klein et al., 2021) |
| RTCIT (virus isolation in neuroblastoma culture) | Live replicating virus | "Gold standard"; confirms infectivity. Live virus isolated from *P. pipistrellus* and *P. nathusii* (Germany: Schatz 2014; Klein 2021) |
| RT-qPCR / RT-PCR (viral RNA detection) | Viral genome | More sensitive than FAT; detects cases missed by FAT. Applied to archival samples (Klein et al., 2021) |
| NGS (whole-genome sequencing) | Complete/partial genomic sequence | Used for strain characterization (Picard-Meyer et al., 2026 — France, *P. nathusii*) |
| Serology (RFFIT, FAVNT, FAVN) | Neutralizing antibodies | Evidence of past virus contact; does not confirm active infection. Cross-reactivity between EBLV-1 and other phylogroup I lyssaviruses not excluded |
| Saliva RT-qPCR (active surveillance) | Viral RNA in saliva | Used for live individuals; sensitivity low in clinically healthy carriers (Nauwelaers 2024: 113 samples — all negative) |
Confirmation hierarchy:
- Live virus (RTCIT) + FAT/PCR = reliably confirmed active infection
- Viral antigen (FAT) + viral RNA (PCR) = confirmed molecular diagnosis
- Only viral RNA (PCR) without FAT or isolation = molecular detection, interpreted cautiously
- Only antibodies (serology) = exposure, not necessarily current infection
- FAT+ without PCR, strong autolysis = presumed case (example — *P. pygmaeus*, UK, 2020)
---
4. Temporal Analysis: Surveillance Expansion or Real Growth?
Pan-European Dynamics
| Period | Cases registered | Note |
|---|---|---|
| 1977–1984 | ~2 | Only isolated findings |
| 1985–1987 | +263 (peak: 122 in 1986, 140 in 1987) | Sharp increase after 3 human EBLV deaths; surveillance expansion artifact |
| 1988–2000 | 6–53/year; mean ~29 | Stabilization |
| 2001–2010 | ~959 cumulative | Mean ~30–34/year |
| 2011–2016 | Up to 1,183 cumulative | Mean ~35/year |
| 2017–2023 | Up to >1,500 cumulative | PCR surveillance expansion |
The significant "increase" in cases in 1985–1987 was exclusively a result of monitoring intensification: (Fooks et al., 2006, Biol Conserv) state: "the sharp increase in the number of tested animals, the EBLV-2 case in Finland in 1985, and the human bite by a serotine in Denmark in 1985 made EBLV surveillance a priority".
After 1987, the average annual number of cases stabilized at ~29–35/year — a sign of endemic, stationary circulation of EBLV-1 in the main reservoir species (*E. serotinus*), not a growing epizootic.
Trend for *Pipistrellus* Species
- The number of cases in *Pipistrellus* remains stably small: a total of 5–7 confirmed cases have been registered across all of Europe over ~70 years of monitoring.
- New findings (2018–2026) — diagnostic and geographic artifact:
- Two *P. pipistrellus* cases in Germany (2018–2020) found when screening previously FAT-negative archival samples by RT-qPCR (Klein et al., 2021). FAT missed them — meaning these cases existed earlier but went undetected.
- First EBLV-1 case in Belgium (2016), first in the UK (2018, in *E. serotinus*), first in *P. nathusii* in France (2020) — all reflect expansion of geographic surveillance coverage, not new foci.
- Netherlands — illustrative example: 1,837 *P. pipistrellus* over ~20 years of monitoring — 0 cases (Van der Poel et al., 2005).
- Geographic pattern: all positive findings in *Pipistrellus* in Germany (Lower Saxony, Baden-Württemberg), France (Alsace, near the German border), and the UK (eastern Dorset) territorially coincide with the density of infected *E. serotinus* — supporting the concept of spillover, not independent circulation.
Serological Data: The Situation Is Ambiguous
Seroprevalence in *Pipistrellus* in Spain (11–18%), in *H. savii* (22–31%) (Serra-Cobo et al., 2013; López-Roig et al., 2014) indicates regular contact with the virus in mixed colonies. However:
- Neutralizing antibodies do not mean current infection or virus shedding.
- Of all seropositive Spanish *Pipistrellus*, live virus has never been isolated.
- Serological data from Belgium (Nauwelaers et al., 2024) with zero PCR-positivity in saliva indicate self-limiting contact without sustained virus shedding.
---
5. Summary Table: Confirmed and Probable EBLV Cases in Small Synanthropic Species
| Country | Year(s) | Species | Virus | Method | Live virus? | Status |
|---|---|---|---|---|---|---|
| Germany | 1986, 1992 | *P. nathusii* | EBLV-1 | FAT + isolation | Yes | Confirmed |
| Germany | 1998–2013 | *P. pipistrellus* | EBLV-1 | FAT + RTCIT + PCR | Yes | Confirmed |
| Germany | 1998–2013 | *P. nathusii* | EBLV-1 | FAT + RTCIT + PCR | Yes | Confirmed |
| Germany | 2018–2020 (archive) | *P. pipistrellus* (×2) | EBLV-1a | RT-qPCR + isolation (FAT-neg archive) | Yes | Confirmed |
| Spain | 2001–2011 | *P. pipistrellus* | EBLV-1 | nRT-PCR (RNA) + serology | No | RNA + serology |
| Spain | 2001–2011 | *H. savii* | EBLV-1 | Serology | No | Serology only |
| Spain | 2004–2012 | *P. pipistrellus* | EBLV-1 | Serology | No | Serology only |
| Spain | 2004–2012 | *H. savii* | EBLV-1 | Serology | No | Serology only |
| France | ~2019–2020 | *P. pipistrellus* | EBLV-1 | FAT + PCR | Not specified | Confirmed |
| France | 2020 (reg. 2022) | *P. nathusii* | EBLV-1a | FAT + RT-PCR + NGS (whole genome) | No (RNA + genome) | Molecularly confirmed |
| UK | 2018–2020 | *P. pygmaeus* (×1 young) | Presumed EBLV-1 | FAT+ / PCR– (autolysis) | No | Unconfirmed |
| Belgium | 2016–2018 | *P. pipistrellus* (×98) | — | FAT/PCR | No | All negative |
| Netherlands | 1984–2003 | *P. pipistrellus* (×1837) | — | FAT | No | All negative |
| Sweden | 2008–2013 | *P. nathusii* (×4), *P. pygmaeus* (×2) | — | Serology + PCR | No | All negative |
| Finland | 1985–2012 | *P. nathusii* (×3) | — | Serology + PCR | No | All negative |
| Italy | 2006–2017 | *P. kuhlii* (×96), *H. savii* (×82) | — | Serology + FAT/PCR | No | All negative |
---
6. Key Conclusions
- Species *Pipistrellus* and *Hypsugo savii* are irregular "incidental hosts" (spillover hosts) for EBLV-1, not reservoir species. The vast majority of confirmed cases in these species are spatially associated with zones of high density of infected serotine (*E. serotinus*).
- Serological data (antibodies) in small species in Spain and individual multi-species colonies in Europe indicate regular contact with EBLV-1, however live virus from *Pipistrellus* or *H. savii* could not be isolated in these surveys. This is consistent with the concept of transitory contact without sustained virus transmission.
- EBLV detectability in *Pipistrellus* has increased in recent years (2018–2026), but this is due to (a) transition from FAT to more sensitive molecular methods (RT-qPCR) detecting cases FAT misses; (b) retrospective re-analysis of archival samples; (c) surveillance expansion to new countries (Belgium, UK, Hungary).
- The average annual number of EBLV cases in Europe does not demonstrate exponential growth: after the sharp rise of 1985–1987 (surveillance mobilization artifact), the figure stabilized at ~30–35 cases/year — a pattern of endemic stationary circulation.
- For veterinary surveillance, the most significant factor is the use of molecular methods (RT-qPCR) in addition to FAT: two German cases in *P. pipistrellus* (2018–2020), missed by FAT and detected by PCR, demonstrate that standard passive surveillance underestimates spillover frequency in small species.
- For zoonotic risk assessment: despite *Pipistrellus* being the most frequently human-contacting species, the real risk of EBLV infection from these bats is extremely small. In the Netherlands over 20 years of monitoring, virus was not found in 1,837 *P. pipistrellus*; the theoretical frequency of human infection from serotine bats is estimated from 1 time per year to 1 time per 700 years per 16 million residents.
---
Cited Sources
European temporal trends 1954–2024 EU_bat_lyssavirus_temporal_trends_RU.md
Temporal Trends in Bat Lyssavirus Surveillance in Europe (1954–2024)
Analytical Epidemiological Review
---
ABSTRACT
From the first officially confirmed case (Hamburg, Germany, 1954) to 2024, European databases have accumulated more than 1,400–1,500 records of bat lyssaviruses. The observed rise in the number of positive findings after 1985 is primarily due to a sharp expansion of passive surveillance, a change in diagnostic standard (FAT → RT-PCR/RT-qPCR), and organizational changes, not a proven increase in true population incidence. This review synthesizes WHO (Rabies Bulletin Europe), ECDC, WOAH/OIE, and peer-reviewed national publication data; provides decade-by-decade and country-by-country tables with explicit caveats about passive surveillance biases.
---
1. GENERAL HISTORICAL CHRONOLOGY
| Date/period | Event | Source |
|---|---|---|
| 1954 | First documented bat lyssavirus case in Europe — Hamburg, Germany (*Eptesicus serotinus*) | McElhinney et al., 2018 |
| 1977 | First confirmed fatal EBLV-1 human case — Ukraine | WHO Rabies Bulletin Europe |
| 1977 | Start of systematic case registration in Rabies Bulletin Europe | Schatz et al., 2013 |
| 1984 | Start of mandatory bat submission for testing in the Netherlands | Van der Poel et al., 2005 |
| 1985 | Death of a Swiss biologist in Finland (EBLV-2) — first EBLV-2 isolation | WHO RBE General Information |
| 1985 | Human death in Russia (EBLV-1) | Harris et al., 2006 |
| 1985–1987 | Intensive surveillance after first deaths: 263 cases identified (>20% of all at that point) | McElhinney et al., 2018 |
| 1987 | Establishment of national passive surveillance programs (UK, Netherlands) | Harris et al., 2006 |
| 1989 | First bat case in France; start of national surveillance | Picard-Meyer et al., 2014 |
| 1996 | First EBLV-2 in the UK (Myotis daubentonii, Sussex) | UK passive surveillance UK Gov |
| 2002 | Human death in Scotland (EBLV-2) | McElhinney et al., 2018 |
| 2010 | Discovery of new Bokeloh bat lyssavirus (BBLV) in Germany | Emerging Infectious Diseases, 2011 |
| 2018 | First EBLV-1 cases in serotines in the UK (Dorset, E. serotinus) | Virus Evolution, 2024 |
| 2019 | Human death in France (EBLV-1) — 5th fatal case in Europe | ECDC AER 2019 |
| 2021 | Broad adoption of RT-qPCR as main diagnostic method replacing FAT | Klein et al., 2021 |
| 2024 | EBLV-1 case in a cat in the Netherlands (spillover) | Euro Surveill., 2025 |
---
2. CUMULATIVE DATA BY DECADE
Table 2.1. Confirmed Bat Lyssavirus Cases in Europe by Decade
Table notes: Data combined from Rabies Bulletin Europe reports, publications Schatz et al. (2013), McElhinney et al. (2018), EU One Health Zoonoses Reports (2020–2024), and ECDC AER. Number of tested animals given only where primary data are available; dash (—) indicates absence of reliable cumulative data. Positivity calculated only where both figures are reliable.
| Decade | Positive cases (registered) | Tested (where known) | Positivity (%) | Main countries | Diagnostic method | Surveillance level |
|---|---|---|---|---|---|---|
| pre-1977 | 18 (1954–1976) | — | — | Germany, Yugoslavia, Ukraine | Direct virus isolation; FAT | Isolated studies, not systematic |
| 1977–1984 | 2 | — | — | Denmark (1985*) | FAT | Reactive only |
| 1985–1989 | ~270 | — | — | Germany, Denmark, Netherlands | FAT | First systematic surveillance |
| 1990–1999 | ~200 | — | — | Netherlands, Germany, Denmark, Poland | FAT | Passive; national program expansion |
| 2000–2009 | ~350 | ~40,000–50,000 (estimate) | ~0.7–1.0 | Netherlands, Germany, France, Denmark, Poland | FAT ± PCR | Established national programs |
| 2010–2019 | ~270 | ~15,000 (EU/EEA, 2015–2019, estimate) | ~1.5–2.5 | Germany, Netherlands, Poland, France | FAT → RT-qPCR | Hybrid: passive + enhanced passive |
| 2020–2024 | 153 | 7,744 (EU MSs, sum) | ~2.0 | Germany, France, Netherlands, Poland | RT-qPCR (main) | Passive + enhanced passive |
*Note: systematic registration in RBE began from 1977; the largest "wave" in 1986–1987 was a direct result of intensive retrospective surveillance, not a real outbreak.
Sources: WHO RBE General Info | Schatz et al. 2013 | McElhinney et al. 2018 | EU One Health 2024 | EU One Health 2023
---
Table 2.2. EU One Health Zoonoses Report Data on Bats, 2019–2024 (Primary EFSA/ECDC Data)
| Year | Tested (EU MSs) | Positive (EU MSs) | Positivity (%) | Reporting countries | Leading viruses |
|---|---|---|---|---|---|
| 2019 | 2,069 | 39 | 1.88 | n/a | EBLV-1 (mainly), EBLV-2 |
| 2020 | 1,308 | 31 | 2.37 | 15 | EBLV-1, EBLV-2 |
| 2021 | 1,316 | 29 | 2.20 | 16 | EBLV-1, BBLV |
| 2022 | 1,622 | 26 | 1.60 | 16 | EBLV-1, BBLV |
| 2023 | 1,658 | 23 | 1.39 | 18 | EBLV-1 (22), BBLV (1) |
| 2024 | 1,840 | 44 | 2.39 | 20 | EBLV-1 (43), BBLV (1) |
Sources: EU One Health 2024 Zoonoses Report | EU One Health 2023 Zoonoses Report | EFSA activities on rabies, 2022
Important caveat: The decrease in positive cases in 2020–2023 is partly due to COVID-19 pandemic restrictions on sample collection. The increase in 2024 was accompanied by an increase in tested animals, making it impossible to distinguish "true" growth from an "artifact of enhanced surveillance".
---
3. COUNTRY DATA
Table 3.1. Cumulative Data by Major Country (up to 2024)
| Country | Surveillance period | Cumulative positive | Tested (where data available) | Positivity (%) | Leading virus / bat species | Notes |
|---|---|---|---|---|---|---|
| Germany | 1954– | ~400–420 | ~3,714 (1998–2013, one retrospective) | ~1.2 (all species); 13–16% (E. serotinus) | EBLV-1 (E. serotinus), EBLV-2 (M. daubentonii), BBLV (M. nattereri) | Highest number of cases in Europe; ≥346 registered by 2020 |
| Netherlands | 1984– | ~380–400 | 1,219 (E. serotinus, 1984–2003); ~50/year (2003–) | 21% (E. serotinus); 4% (M. dasycneme) | EBLV-1 (E. serotinus), EBLV-2 (M. dasycneme) | Since 1994 — mainly contact cases; ~1–2 positive/50 submitted/year in recent years |
| Denmark | 1985– | ~226 | ~2,000+ (estimate) | 0–50% (fluctuations by 10-year cycles) | EBLV-1 (E. serotinus), EBLV-2 | Cyclic peaks; last E. serotinus — 2009, EBLV-2 — 2015 |
| France | 1989– | ~78–80 | 3,176 submitted; 2,447 analyzed (1989–2013) | 1.96% (48/2,447, 1989–2013) | EBLV-1 (E. serotinus), BBLV | After 2001 — 17-fold increase in samples without significant change in true positivity |
| Poland | 1972– | ~100 | ~400–450 (2006–2010 + national data) | ~4% (estimate) | EBLV-1 (E. serotinus) | Before 1998 — only 4 cases; active growth after 2000 correlates with surveillance expansion |
| UK | 1987– | ~47 (EBLV-2: 13, EBLV-1: 34) | 17,012 (1987–before 2018); 15,539 (1987–2015) | <0.3% (all species); 3.57% M. daubentonii; 9.6% E. serotinus (2018–2024) | EBLV-2 (M. daubentonii), EBLV-1 (E. serotinus from 2018) | First EBLV-1 in E. serotinus — October 2018; 34 cases by May 2024 |
| Spain | 1987– | ~39 | ~189 (2006–2010); >1,000 (active surveillance E. isabellinus) | 7% (E. isabellinus) | EBLV-1 (E. isabellinus, E. serotinus), LLEBV | First case — 1987 (Valencia) |
| Switzerland | 1976– | ~4 (EBLV-2); sporadic EBLV-1 | 237 (active surveillance, 2009); 101 (2006–2010) | 4.6% M. daubentonii | EBLV-2 (M. daubentonii) | Rare findings; continuous surveillance |
| Finland | 1985– | ~2 (documented) | ~300–400 (estimate, irregular) | low | EBLV-2 (M. daubentonii), KBLV (1 case) | Human death 1985; KBLV (2022) |
| Hungary | 1999– | ~10–15 | 41 (2006–2010) | ~5% (estimate) | EBLV-1 | Several cases per year |
| Czech Republic/Slovakia | 1994– | ~5–7 | 75/24 (2006–2010) | <1% | EBLV-1 | Rare findings |
| Norway | 2015– | 1 (EBLV-2) | — | — | EBLV-2 (M. daubentonii) | First case — 2015 |
| Slovenia | 2022– | 1 (Divača BLV) | — | — | Divača BLV (M. capaccinii) | New virus, single case |
| Belgium | 2016– | 2 (EBLV-1) | ~90 (2016–2018) | ~2% | EBLV-1 (E. serotinus) | First cases recorded in 2016–2017 |
Sources: WHO RBE Facts & Figures | Schatz et al. 2013 | Harris et al. 2006 | Van der Poel et al. 2005 | Picard-Meyer et al. 2014 | Virus Evolution UK, 2024 | McElhinney et al. 2018 | EUROBATS 2024 | Detection EBLV-1 Belgium, 2024
---
Table 3.2. Leading Country Data, 2024 (EU One Health 2024 Zoonoses Report)
| Country | Positive in 2024 | Leading lyssavirus |
|---|---|---|
| France | 15 | EBLV-1 |
| Germany | 14 (13 EBLV-1 + 1 BBLV) | EBLV-1, BBLV |
| Netherlands | 5 | EBLV-1 |
| Poland | 4 | EBLV-1 |
| Hungary | 3 | EBLV-1 |
| Spain | 2 | EBLV-1 |
| Czech Republic | 1 | EBLV-1 |
| Switzerland | 1 | EBLV-2 |
| Total | 45 |
Source: EU One Health 2024 Zoonoses Report — PMC
---
4. ANNUAL DATA (SELECTED, WHERE PRIMARY SOURCES ALLOW)
Table 4.1. Reference Points: Number of Positive Cases by Year for All Europe
| Year | Positive (RBE / primary sources) | Note |
|---|---|---|
| 1954–1976 | 18 (cumulative) | Of 18 — 7 from Germany; only virus isolation |
| 1977–1984 | 2 (cumulative) | Of which 0 documented as new type before 1985 |
| 1985 | ~5 | Including the Finnish biologist case; start of intensive surveillance |
| 1986 | 122 | Peak linked to retrospective Danish survey (150 cases, 1986–1987) |
| 1987 | 140 | Continuation of intensive Danish and Dutch surveillance |
| 1988–1999 | ~6–53/year | Per RBE data |
| 2000 | ~30 | RBE; 2/153 (France), 7/125 (Netherlands), 3/40 (Denmark), 13/73 (Germany) in 2003 |
| 2006–2010 | 26–36/year | Mean ~32; range per RBE |
| 2011–2018 | ~30–50/year | Mean ~34/year (last decade per McElhinney) |
| 2018 | 45 | ECDC AER 2019; from 7 countries |
| 2019 | 39 | EU One Health Zoonoses Report |
| 2020 | 31 | EU One Health; COVID impact on sample submission |
| 2021 | 29 | EU One Health |
| 2022 | 26 | EU One Health |
| 2023 | 23 | EU One Health |
| 2024 | 44 | EU One Health; increase linked to expansion of reporting countries (20 countries) |
Sources: Schatz et al. 2013 | McElhinney et al. 2018 | ECDC AER 2019 | EU One Health 2024 | Santepubliquefrance 2005
---
5. SPECIAL COUNTRY TABLES (DETAILED DATA)
Table 5.1. France — Year by Year, 1989–2013 (Primary Data Picard-Meyer et al., 2014)
| Period | Samples submitted | Analyzed | Positive | E. serotinus positivity (%) | Note |
|---|---|---|---|---|---|
| 1989–2000 | 170 | ~122 | 7 | 30.4% (14.1–53.0 CI) | Start of surveillance; rare submissions |
| 2001–2003 | ~750 | ~557 | ~8 | 15.0% (6.2–30.5) | After network strengthening — 17-fold increase in samples |
| 2004–2006 | ~750 | ~550 | ~6 | 10.9% (4.5–22.9) | |
| 2007–2009 | ~750 | ~570 | ~14 | 30.8% (17.5–47.7) | Cyclic increase |
| 2010–2013 | ~1,200 | ~648 | ~13 | 16.2% (9.8–25.2) | |
| 1989–2013 total | 3,176 | 2,447 | 48 | 1.96% (1.4–2.6) |
Source: Picard-Meyer et al. 2014 — PLOS ONE
Caveat (France): Between 1989–2000 and 2001–2013, the number of samples grew >17-fold, while the number of positive cases among E. serotinus did not change statistically between periods. This means the increase in EBLV-1 detection in France is primarily explained by expansion of the surveillance network, not a rise in true incidence.
---
Table 5.2. Netherlands — Selected Submission and Positivity Data (1984–2024)
| Period | Species | Tested | Positive | Positivity (%) | Source |
|---|---|---|---|---|---|
| 1984–1994 | E. serotinus | part of 1,219 | part of 251 | ~21% | Van der Poel et al. 2005 |
| 1984–2003 | E. serotinus | 1,219 | 251 | 21.0% | Van der Poel et al. 2005 |
| 1984–2003 | M. dasycneme | 129 | 5 | 3.9% | Van der Poel et al. 2005 |
| 1984–2003 | P. pipistrellus | 1,837 | 0 | 0% | Van der Poel et al. 2005 |
| 2003–2024 | E. serotinus | ~50/year | ~1–2/year | ~2–4% (estimate) | Eurosurveillance 2025 |
| 2006–2010 | All species | 619 (tested) | 45 | 7.3% (all), ~22% (E. serotinus) | Schatz et al. 2013 |
Caveat: Since 1994 in the Netherlands, mainly bats that were in contact with people or showed clinical signs are tested. This creates a systematic bias toward inflated positivity (22%) compared with true prevalence in the healthy population, which is likely significantly lower.
---
Table 5.3. UK — Annual Passive Surveillance Data, 1987–2024
| Year(s) | Tested (all species) | EBLV-2 positive (M. daubentonii) | EBLV-1 positive (E. serotinus) | Note |
|---|---|---|---|---|
| 1987–2004 | 4,871 | 4 | 0 | Harris et al. 2006 |
| 2005–2015 | 10,668 | 7 (+2 in 2016) | 0 | UK passive surveillance, 2017 |
| 2016–2017 | ~2,000 | 2 | 0 | |
| 2018–May 2024 | ~17,000 (1987–May 2024 total) | occasional | 34 | Virus Evolution 2024 |
| 1987–May 2024 | >17,000 | 13 (total) | 34 (total) | <0.3% of all submitted |
Caveat (UK): The first detection of EBLV-1 in E. serotinus in the UK (October 2018) with subsequent 33 cases does not necessarily indicate a new introduction. Phylogenetic analysis shows that viral lineages have existed in the UK since ~2014–2022 and may be an artifact of targeted increase in serotine testing.
---
Table 5.4. Germany — Retrospective Enhanced Passive Surveillance 2018–2020
| Indicator | Value |
|---|---|
| Brain samples analyzed | 1,236 |
| Total positive (RT-qPCR) | 16 |
| EBLV-1 positive (E. serotinus) | 15 |
| BBLV positive (M. nattereri) | 1 |
| Positivity across all species | 1.2% |
| E. serotinus positivity | ~16% |
| FAT-negative samples that became PCR-positive | 4 (including 2 in P. pipistrellus) |
Source: Klein et al. 2021, Viruses
Key finding for Germany: Standard FAT missed 4 samples that were subsequently detected by RT-qPCR. This documents that the transition from FAT to molecular methods itself increases detectability, creating an artificial increase in case numbers when comparing historical series.
---
6. SPECIES-SPECIFIC LYSSAVIRUSES: CUMULATIVE DATA
Table 6.1. Confirmed Cases by Lyssavirus Type in Europe
| Lyssavirus | Cumulative (latest update) | Main host | Main countries | Source |
|---|---|---|---|---|
| EBLV-1 | >1,100–1,200 | E. serotinus, E. isabellinus | Germany, Netherlands, Denmark, Poland, France | WHO RBE |
| EBLV-2 | ~39–45 (confirmed ~34–39) | M. daubentonii, M. dasycneme | UK, Netherlands, Germany, Finland, Switzerland | McElhinney et al. 2018 |
| BBLV | ~15 | M. nattereri | Germany, France, Poland | Klein et al. 2021 |
| WCBV | 1 (in bat) + 1 (cat Italy, 2020) | M. schreibersii | Russia/Caucasus | WHO RBE |
| LLEBV | 3 | M. schreibersii | Spain, France | EUROBATS 2024 |
| KBLV | 1 | M. brandtii | Finland | EUROBATS 2024 |
| Divača BLV | 1 | M. capaccinii | Slovenia | Iscience 2025 |
---
7. PASSIVE SURVEILLANCE BIASES: SYSTEMATIC ANALYSIS
This is a section of key importance for interpreting any "temporal trends".
7.1. Main Bias Factors (Documented)
A. Dependence on population sample submission
Passive surveillance is entirely dependent on the willingness of citizens and veterinary specialists to submit dead or sick bats. Submission levels vary substantially:
- Geographically: in the UK, 83% of samples from 1987 to 2004 came from England, 8.7% from Scotland, 3.5% from Wales (Harris et al. 2006).
- By time: sharp increase in samples immediately after media coverage of human cases (1985–1987, 2002–2003).
- By species: synanthropic species (E. serotinus, Pipistrellus spp.) are significantly over-represented as they more often come into contact with people; M. daubentonii is under-represented as it lives in caves and tree hollows.
B. Evolution of diagnostic methods
| Period | Method | Sensitivity | Consequence for temporal trends |
|---|---|---|---|
| Pre-~2000 | FAT (direct fluorescent antibody test) | Moderate for good-quality brain samples | Underestimation, especially for decomposed samples |
| 2000–2015 | FAT + RT-PCR (confirmation) | Higher | Transition period: mixed methods |
| From 2015–2020 | RT-qPCR as main/primary method | Significantly higher, including small amounts of virus | Increase in detectability — method change artifact |
| Documentary evidence | Germany 2018–2020: 4 FAT-negative samples became PCR-positive | Klein et al. 2021 |
C. Heterogeneity of surveillance between countries
According to WOAH 2016 data, bats are included in rabies surveillance in only 40% of reporting countries (WOAH 2016). Per RBE 2006–2010 data, bat data were provided by only 29 of 46 European countries (Schatz et al. 2013). This means that geographic expansion of surveillance itself generates new "cases" in previously uncovered countries (Belgium — first cases 2016, Norway — 2015, Slovenia — 2022).
D. Reactive intensification after sensational events
The Danish retrospective study of 1986–1987 revealed 263 cases (more than a fifth of all registered at that time) — not due to an outbreak but due to targeted testing of previously untested samples. Similarly — the French jump in samples from 170 to >3,000 over 2001–2013 without a statistically significant change in E. serotinus positivity (Picard-Meyer et al. 2014).
E. Incomplete species identification
Per Schatz et al. 2013: 46.8% of tested samples were not identified to species level, which precludes correct calculation of species-specific positivity and creates classification error in cross-country comparison.
F. Seasonal bias
Peak bat detection occurs in Q3 (July–September) — period of high bat activity and bat conservation volunteers (Schatz et al. 2013). This seasonal effect does not reflect winter-period virus circulation and creates an error when summing by year.
---
8. ACTIVE SURVEILLANCE COMPARED WITH PASSIVE
Active surveillance (oropharyngeal swabs and serological analysis of live bats) systematically reveals significantly lower RNA virus prevalence than passive surveillance:
| Country/region | Active surveillance | Passive surveillance | Interpretation |
|---|---|---|---|
| Germany (1993–2012) | 4,546 swabs, isolated positives | Annual cases | Uni-Potsdam paper |
| Germany (E. serotinus, Hartmannsdorf) | 0–61% seropositive (year by year) | 13–16% RNA-positive in passive surveillance | Indicates broad circulation without clinical disease |
| UK (M. daubentonii) | 1–5% antibodies (350 animals) | 3.57% RNA (4/112) | Harris et al. 2006 |
| Spain (E. isabellinus, colony) | 3.68–5.17% RNA-positive (oral swabs) | — | Temporal Dynamics, Spain |
| France (oropharyngeal swabs) | 0/947 PCR-positive | 48/2,447 = 1.96% (passive) | Schatz et al. 2013; Picard-Meyer 2014 |
Conclusion: High seroprevalence with low RNA positivity in active surveillance indicates that most bat populations have been exposed to EBLV without clinical signs of disease. Passive surveillance only captures the "tip of the iceberg" — individuals with clinical symptoms or dead.
---
9. TRUE INCIDENCE VS. SURVEILLANCE ARTIFACTS: EVIDENCE BASE SUMMARY
Table 9.1. Factors Explaining the Observed "Increase" in Positive Cases
| Factor | Evidence weight | Documentation |
|---|---|---|
| Surveillance network expansion (geographic and organizational) | Strong | 18 → 45 participating countries; Belgium and Norway detected first cases after starting testing |
| Increase in tested samples per country | Strong | France: ×17 increase in samples 1989–2000 → 2001–2013; UK: ×2 increase after 2002 |
| Transition from FAT to RT-qPCR | Moderate–Strong | 4 FAT-false-negatives → PCR-positive in Germany; similar data from UK and France |
| Reactive surveillance after media coverage | Strong | Danish surge 1986–1987: 263 cases from retrospective testing |
| Bias toward synanthropic species | Moderate | E. serotinus and Pipistrellus are systematically over-tested |
| True change in population incidence | Weak or neutral evidence | E. serotinus positivity in the Netherlands stable ~20–22% since 1984; in France — stable with increasing sample numbers |
9.2. Counter-argument: Signs of Possible Real Spread
Several observations cannot be explained solely by surveillance artifacts:
- First detection of EBLV-1 in E. serotinus in the UK (2018) with rapid accumulation of 34 cases in Dorset and Somerset — molecular clock estimates date introduction to ~2014–2022, consistent with real spread (Virus Evolution 2024).
- New viruses (BBLV, KBLV, Divača BLV, LLEBV) are systematically discovered in previously uncovered host taxa — which may indicate either true host range expansion or improved pan-lyssavirus PCR screening.
- The average number of positives in the last decade (~34/year per McElhinney 2018) shows no systematic increase when surveillance efforts have stabilized, indicating unchanged true infection levels in established endemic populations.
---
10. HUMAN FATAL CASES (CHRONOLOGY)
| Year | Country | Virus | Source |
|---|---|---|---|
| 1977 | Ukraine | EBLV-1 (species not established at the time) | Harris et al. 2006 |
| 1985 | Russia | EBLV-1 | WHO RBE |
| 1985 | Finland | EBLV-2 | WHO RBE |
| 2002 | UK (Scotland) | EBLV-2 | McElhinney et al. 2018 |
| 2019 | France | EBLV-1 | ECDC AER 2019 |
Five deaths in 47 years among approximately 590 million European residents (Bat Rabies, Public Health and Conservation, 2012).
---
11. SUMMARY CAVEATS — METHODOLOGICAL LIMITATIONS
Limitation 1 — Passive surveillance as a filter: All data, except specially organized active studies, come from passive surveillance, which by nature records only clinically sick or dead bats. True prevalence in live populations is systematically underestimated. Per UK data 1987–2015, of >15,500 tested bats only 13 were EBLV-positive (<0.1%), while serological studies indicate real virus contact in 1–11% of M. daubentonii (UK passive surveillance 2017).
Limitation 2 — Incomparability between countries: Countries differ in testing volume, species coverage, diagnostic method, positivity threshold criteria, and reporting completeness. Cross-country positivity comparison without standardization is inappropriate.
Limitation 3 — Diagnostic platform change: Replacement of FAT by RT-qPCR (mainly after 2015–2020) significantly increased sensitivity and contributed to detecting previously missed cases, including positive samples in atypical species (P. pipistrellus in Germany). Time series before and after this transition cannot be considered fully comparable.
Limitation 4 — Bat species coverage: Published studies have tested no more than 28 of ~52 European bat species (Schatz et al. 2013). Among untested species there may be reservoir hosts of unknown or rare lyssaviruses.
Limitation 5 — COVID-19 impact on 2020–2022 data: The decrease in positive cases in 2020–2022 (31, 29, 26 respectively) may be partly an artifact of reduced sample submission and disrupted surveillance networks during the pandemic, not a reflection of a real epizootic lull.
Limitation 6 — Absence of a standardized European denominator: For most time periods, pan-European data on the number of tested bats are absent or incomplete (especially before 2006). This makes correct positivity calculation for all of Europe in early periods impossible.
---
12. KEY CONCLUSIONS
- Cumulative scale: Per WHO Rabies Bulletin Europe, from 1977 to 2024 approximately 1,400–1,500 bat lyssavirus cases were documented in Europe; adding 1954–1976 cases — cumulatively about 1,500+. More than 90% is EBLV-1.
- Geographic concentration: >80% of all registered cases are in three countries: Netherlands (~33%), Germany (~27%), Denmark (~21%) — a direct result of the most developed surveillance systems, not necessarily the highest population infection rates.
- Surveillance vs. true incidence: Documentary evidence convincingly shows that the main share of the observed "increase" in positive cases after 1985 is explained by surveillance expansion, growth in sample numbers, and diagnostic method changes. E. serotinus positivity in the Netherlands is stable at ~20–22% since 1984.
- Stable plateau of the modern period: From 2019 to 2024, annually 23 to 44 cases are registered in EU (adjusting for COVID impact in 2020–2022), corresponding to the mean level of ~34 cases/year in the preceding decade — a sign of stabilization, not growth.
- Expansion of host and geographic base: Genuinely new phenomena — detection of EBLV-1 in the UK from 2018 and discovery of new lyssavirus species (BBLV, KBLV, Divača BLV, LLEBV) — partly reflect true spread processes, but are also due to the use of more sensitive molecular tools.
---
13. LIST OF REFERENCES
- WHO Rabies Bulletin Europe — General Information. https://www.who-rabies-bulletin.org/site-page/general-information
- WHO Rabies Bulletin Europe — Facts and Figures. https://www.who-rabies-bulletin.org/member/About_Rabies/Bats/Facts_Figures.aspx
- Schatz J, Fooks AR, McElhinney L, et al. Bat rabies surveillance in Europe. Zoonoses Public Health. 2013;60:22–34. https://pubmed.ncbi.nlm.nih.gov/22963584/
- McElhinney LM, Marston DA, Wise EL, et al. Molecular Epidemiology and Evolution of European Bat Lyssavirus 2. Viruses. 2018;10(5):228. https://pmc.ncbi.nlm.nih.gov/articles/PMC5796105/
- Harris SL, Brookes SM, Jones G, et al. European bat lyssaviruses: Distribution, prevalence and implications for conservation. Biol Conserv. 2006;131:193–210. https://pmc.ncbi.nlm.nih.gov/articles/PMC7096730/
- Van der Poel WHM, Van der Heide R, Verstraten ERAM, et al. European Bat Lyssaviruses, the Netherlands. Emerg Infect Dis. 2005;11(12):1854–1859. https://wwwnc.cdc.gov/eid/article/11/12/04-1200_article
- Picard-Meyer E, Robardet E, Arthur L, et al. Bat Rabies in France: A 24-Year Retrospective Epidemiological Study. PLOS ONE. 2014;9(6):e98622. https://journals.plos.org/plosone/article?id=10.1371%2Fjournal.pone.0098622
- Klein A, Calvelage S, Schlottau K, et al. Retrospective Enhanced Bat Lyssavirus Surveillance in Germany between 2018–2020. Viruses. 2021;13(8):1563. https://pmc.ncbi.nlm.nih.gov/articles/PMC8402685/
- EUROBATS Advisory Committee. Factsheet on Rabies in European Bats. Inf.EUROBATS.AC28.3, 2024. https://www.eurobats.org/sites/default/files/documents/pdf/Advisory_Committee/Inf.EUROBATS.AC28.3_Rabies.pdf
- European Food Safety Authority & European Centre for Disease Prevention and Control. The European Union One Health 2024 Zoonoses Report. EFSA Journal. 2025. https://pmc.ncbi.nlm.nih.gov/articles/PMC12686834/
- European Food Safety Authority & European Centre for Disease Prevention and Control. The European Union One Health 2023 Zoonoses Report. EFSA Journal. 2024. https://pmc.ncbi.nlm.nih.gov/articles/PMC11629028/
- ECDC. Rabies — Annual Epidemiological Report for 2019. https://www.ecdc.europa.eu/en/publications-data/rabies-annual-epidemiological-report-2019
- Horton DL, McElhinney LM, Marston DA, et al. Phylogenetic analysis of European bat lyssavirus 1 in the UK. Virus Evol. 2024;10(1):veae060. https://pmc.ncbi.nlm.nih.gov/articles/PMC11345707/
- Bourhy H, Kissi B, Audry L, et al. Ecology and evolution of rabies virus in Europe. J Gen Virol. 1999;80:2545–2557. (Basic molecular epidemiology)
- Fooks AR, Brookes SM, Johnson N, et al. Passive surveillance of UK bats for lyssaviruses (2005–2015). Epidemiol Infect. 2017;145:2445–2455. https://pmc.ncbi.nlm.nih.gov/articles/PMC9148805/
- Müller T, Cox J, Peter W, et al. Epidemiology of bat rabies in Germany. Arch Virol. 2007;152:273–288. https://pubmed.ncbi.nlm.nih.gov/17066249/
- WOAH. Control and Elimination of Rabies in Europe. 2016. https://www.woah.org/app/uploads/2021/03/2016-eur1-muller-a.pdf
- Eurosurveillance. A case report of a cat infected with European bat lyssavirus type 1, the Netherlands, October 2024. Euro Surveill. 2025;30(10):pii=2500154. https://www.eurosurveillance.org/content/10.2807/1560-7917.ES.2025.30.10.2500154
- Rabies in Europe: Epidemiology, Clinical Management and Prevention. Dtsch Arztebl Int. 2026. https://pmc.ncbi.nlm.nih.gov/articles/PMC13092140/
- Detection and Serological Evidence of EBLV-1 in Belgian Bats. Trop Med Infect Dis. 2024;9:151. https://pmc.ncbi.nlm.nih.gov/articles/PMC11281572/
- SSI Denmark. Rabies 2024. https://en.ssi.dk/surveillance-and-preparedness/surveillance-in-denmark/annual-reports-on-disease-incidence/r/rabies-2024
- EFSA Activities on Rabies – NRL Workshop 2022 (One Health 2020 data). https://sitesv2.anses.fr/en/system/files/1_Rabies%20NRLs%20Workshop%202022.pdf
---
Document prepared: June 22, 2026. Data synthesized from primary WHO, ECDC, WOAH, and peer-reviewed literature sources. Not intended for clinical or individual medical recommendations.
Summary tables by European country bat_lyssavirus_europe_research.md
Bat Lyssavirus Surveillance in Europe: Summary Tables by Country
Academic veterinary surveillance | Compiled: June 2026
Methodology: Passive (detection in dead/sick bats) and active (capture of healthy individuals) surveillance. Main diagnostic methods: FAT (fluorescent antibody test), RT-PCR/qPCR, virus isolation (RTCIT in neuroblastoma cells), serology (RFFIT/FAVN/ELISA).
---
Key Abbreviations
| Abbreviation | Meaning |
|---|---|
| EBLV-1 | European bat lyssavirus type 1 |
| EBLV-2 | European bat lyssavirus type 2 |
| BBLV | Bokeloh bat lyssavirus |
| FAT | Fluorescent antibody test — gold standard |
| RT-PCR | Reverse transcriptase PCR |
| RFFIT | Rapid fluorescent focus inhibition test (serology) |
| FAVN | Fluorescent antibody virus neutralization test (serology) |
| ELISA | Enzyme-linked immunosorbent assay |
| VNA | Virus neutralizing antibodies |
| Passive | Passive surveillance |
| Active | Active surveillance (capture) |
---
1. GERMANY (Deutschland)
Status: Country with the highest number of registered cases in Europe.
Table 1a. Passive Bat Lyssavirus Surveillance in Germany
| Period | Bats tested | Positive | Lyssavirus species | Main bat species | Method | Prevalence | Notes |
|---|---|---|---|---|---|---|---|
| 1956–2002 | N/A (large series) | 147 | EBLV-1 | *Eptesicus serotinus* (90%); *Nyctalus noctula*, *Pipistrellus* spp. | FAT, RT-PCR | ~1–2% | Retrospective analysis; passive surveillance [1] |
| 1998–2002 | 5,478 | 64 | EBLV-1, EBLV-2 | *E. serotinus*, *N. noctula*, *P. pipistrellus*, *P. nathusii*, *Plecotus auritus*, *Myotis daubentonii* | FAT, molecular methods | 1.17% | Retrospective study of dead bats without prior testing [2] |
| 2018–2020 | 1,236 | 16 | EBLV-1, BBLV | *E. serotinus*, *Myotis nattereri* | FAT, RT-PCR | 1.29% | Includes 1st BBLV case in *M. nattereri* in 2010 [3] |
Table 1b. Active Surveillance in Germany (1993–2012)
| Period | Bats captured | Throat swabs (RT-PCR) | RT-PCR positive | Sera (RFFIT serology) | VNA-positive | Lyssavirus species | Notes |
|---|---|---|---|---|---|---|---|
| 1993–2012 | 4,546 | 4,277 (EBLV-1), 4,209 (EBLV-2), 1,661 (BBLV) | 7 (EBLV-1), 0 (EBLV-2/BBLV) | 1,226 (13 species) | 36.2% EBLV-positive (≥1:10) | EBLV-1 | 5 *E. serotinus*, 1 *M. nattereri*, 1 *Barbastella barbastellus*; virus isolated from 1 *E. serotinus* [4] |
| 2002–2007 | 83 (Hartmannsdorf, Brandenburg) | — | 3 | 56 | 28.6% (≥1:10) | EBLV-1 | Endemic *E. serotinus* colony; intensive monitoring [4] |
Sources: [1] King et al. 2004; [2] Freuling et al. 2013 (PMC8402685); [3] Freuling et al. 2021; [4] Pikula et al./Freuling 2014, Cambridge (20--year active monitoring)
Evidence grade: A (high) — WHO/OIE reference laboratory (FLI, Greifswald), long-term active + passive surveillance, peer-reviewed publications.
URL sources:
- https://pmc.ncbi.nlm.nih.gov/articles/PMC8402685/
- https://www.cambridge.org/core/journals/epidemiology-and-infection/article/twenty-years-of-active-bat-rabies-surveillance-in-germany-a-detailed-analysis-and-future-perspectives/E7EC32DF6231629E199F4CA82CFA5B16
- https://journals.plos.org/plosntds/article?id=10.1371%2Fjournal.pntd.0002835
---
2. NETHERLANDS (Nederland)
Status: One of the first passive surveillance centers in Europe (since 1984).
Table 2. Passive Bat Lyssavirus Surveillance in the Netherlands
| Period | Bats tested | Positive | Lyssavirus species | Bat species | Method | Prevalence | Notes |
|---|---|---|---|---|---|---|---|
| 1984–2003 | 1,219 (*E. serotinus*) | 251 | EBLV-1 (1a/1b) | *Eptesicus serotinus* | FAT, RT-PCR, phylogenetics | ~21% | Mandatory testing from 1984, national from 1987 [5] |
| 1984–2003 | 129 (*M. dasycneme*) | 5 | EBLV-2 | *Myotis dasycneme* (pond bat) | FAT, RT-PCR | ~4% | [5] |
| 1984–2004 | N/A (total since 1984) | ~256 | EBLV-1, EBLV-2 | *E. serotinus*, *M. dasycneme* | FAT, RT-PCR | ~20% in *E. serotinus* | Since 1994 — mainly biting/contact bats [6] |
| 2024 | 1 cat | 1 (cat) | EBLV-1 | Cat (source — bat) | FAT, RT-PCR | — | First EBLV-1 case in a cat in NL [7] |
Sources: [5] Van der Poel et al. 2005 (CDC EID); [6] Willems et al. 2012 (PMC3367619); [7] Eurosurveillance 2025
Evidence grade: A (high) — long-term continuous monitoring, reference laboratory, multiple published reviews.
URL sources:
- https://wwwnc.cdc.gov/eid/article/11/12/04-1200_article
- https://pmc.ncbi.nlm.nih.gov/articles/PMC3367619/
- https://www.eurosurveillance.org/content/10.2807/1560-7917.ES.2025.30.10.2500154
---
3. FRANCE (France)
Status: Officially free of terrestrial mammal rabies since 2001; EBLV-1 in bats since 1989.
Table 3. Passive Bat Lyssavirus Surveillance in France (1989–2013)
| Period | Bats submitted | Tested | Positive | Lyssavirus species | Bat species | Method | Prevalence | Notes |
|---|---|---|---|---|---|---|---|---|
| 1989–2000 | 170 | 170 | 14 (>30% in *E. serotinus*) | EBLV-1 (1a/1b) | *E. serotinus* | FAT, RTCIT, RT-PCR | ~30.4% in *E. serotinus* | Small number of submitted samples in early period [8] |
| 2001–2013 | 3,006 | ~2,277 | 34 | EBLV-1 (1a/1b), BBLV (1 case) | *E. serotinus* (47), *M. nattereri* (1-BBLV, 2012) | FAT, RTCIT, RT-PCR | ~1.5% all; 22–30% *E. serotinus* | 17-fold increase in samples vs. 1989–2000; first BBLV case in Europe in *M. nattereri* [8] |
| TOTAL 1989–2013 | 3,176 | 2,447 | 48 | EBLV-1 (47), BBLV (1) | *E. serotinus*, *M. nattereri* | FAT, RTCIT, RT-PCR | 1.96% | Passive surveillance only; ANSES/Nancy data [8] |
Sources: [8] Picard-Meyer et al. 2014 (PMC4044004); ANSES
Evidence grade: A (high) — 24-year retrospective study, national reference laboratory ANSES.
URL sources:
- https://pmc.ncbi.nlm.nih.gov/articles/PMC4044004/
- https://journals.plos.org/plosone/article?id=10.1371%2Fjournal.pone.0098622
- https://be.anses.fr/sites/default/files/BEP-mg-BE71-eng-art19.pdf
---
4. UNITED KINGDOM (United Kingdom)
Status: Only EBLV-2, only *Myotis daubentonii*. Possible presence of EBLV-1 in *E. serotinus* (seropositive).
Table 4. Passive Bat Lyssavirus Surveillance in the UK
| Period | Bats submitted | Tested (FAT/PCR) | Positive | Lyssavirus species | Bat species | Method | Notes |
|---|---|---|---|---|---|---|---|
| 1987–2004 | 4,871 | 4,871 | 4 | EBLV-2 | *Myotis daubentonii* (3.57% in M.dau) | Passive surveillance, FAT | Start of passive surveillance; 1st case 1996 [9] |
| 2005–2015 | 10,656 | 6,891 (FAT+PCR) | 7 (2005–2015) / 13 total since 1987 | EBLV-2 | *M. daubentonii* (18 species submitted) | FAT, RT-qPCR, sequencing | Stokesay Castle: 20% *M. daubentonii* positive; spatially uneven sample [10] |
| 2016 | — | — | 2 (additional) | EBLV-2 | *M. daubentonii* | FAT, RT-PCR | Documented in study [10] |
Active surveillance (serology):
| Year | Tested | VNA-positive | Species | Method |
|---|---|---|---|---|
| 2003 | 350 *M. daubentonii*, 52 *E. serotinus* | 1–5% *M. dau* (EBLV-2); 1 *E. serotinus* (EBLV-1) | *M. daubentonii*, *E. serotinus* | RFFIT (mFAVN) |
Sources: [9] Harris et al. 2006; [10] Brookes/Fooks et al. 2022 (PMC9148805)
Evidence grade: A (high) — APHA/UKHSA, continuous passive surveillance since 1987, detailed publication.
URL sources:
- https://pmc.ncbi.nlm.nih.gov/articles/PMC9148805/
- https://pmc.ncbi.nlm.nih.gov/articles/PMC8536961/
- https://www.bats.org.uk/about-bats/bats-and-disease/bats-and-disease-in-the-uk/bats-and-rabies
---
5. DENMARK (Danmark)
Status: EBLV-1 endemicity confirmed since 1985. EBLV-2 also detected (1986–1987).
Table 5. Bat Lyssavirus Surveillance in Denmark
| Year/Period | Bats submitted | Tested | Positive | Lyssavirus species | Bat species | Method | Notes |
|---|---|---|---|---|---|---|---|
| 1985 | — | — | 1 | EBLV-1 | *E. serotinus* | — | First identified case in Denmark [11] |
| 1986–1987 | — | — | 150 | EBLV-1 | *E. serotinus* | — | Large series [11] |
| 1986–1987 | — | — | 3 | EBLV-2 | *M. dasycneme*, *M. daubentonii* | — | Only confirmed EBLV-2 cases in Denmark [11] |
| 1998 | — | — | 1 (sheep) | EBLV-1 | Sheep (spillover) | — | Spillover from bat; unique case [11] |
| 2002 | — | — | 1 (sheep) | EBLV-1 | Sheep (spillover) | — | Second sheep spillover [11] |
| 2009 | — | — | 1 | EBLV-1 | *E. serotinus* | — | Last documented case until 2024 [12] |
| 2018 | 3 | 3 | 0 | — | — | — | 22 people received PEP after bat bites; few samples submitted [12] |
| 2024 | N/A | N/A | N/A | — | — | — | 40 people received PEP after bat contacts [13] |
Sources: [11] King et al. 2004 / PMC7096730; [12] SSI Annual Report 2018; [13] SSI Rabies 2024
Evidence grade: B (moderate) — reliable historical data; modern surveillance limited (few samples).
URL sources:
- https://en.ssi.dk/surveillance-and-preparedness/surveillance-in-denmark/annual-reports-on-disease-incidence/r/rabies-2024
- https://en.ssi.dk/surveillance-and-preparedness/surveillance-in-denmark/annual-reports-on-disease-incidence/r/rabies---annual-report-2018
- https://pmc.ncbi.nlm.nih.gov/articles/PMC7096730/
---
6. SPAIN (España)
Status: One of the most studied EBLV-1 reservoirs in Europe; active serological monitoring.
Table 6. Bat Lyssavirus Surveillance in Spain
| Period | Surveillance type | Bats | Positive (RNA / antibodies) | Lyssavirus species | Bat species | Method | Prevalence | Notes |
|---|---|---|---|---|---|---|---|---|
| 1977–2004 | Passive | n/a | 18 | EBLV-1 | *E. serotinus* | FAT/PCR | — | Historical data [11] |
| 1989 | Passive | — | 5 | EBLV-1 | *E. serotinus* | — | First cases (Huelva, Andalusia) [14] | |
| 1992–2000 | Passive | — | 7 | EBLV-1 | *M. myotis*, *M. nattereri*, *M. schreibersii*, *R. ferrumequinum* | RT-PCR | — | First detection in several Myotis species [14] |
| 1998–2003 | Active | 1,030 (*E. isabellinus*) + 1,226 throat swabs + 626 plasma samples | 34 (RNA), 51 (antibodies) | EBLV-1 | *Eptesicus isabellinus* | RT-PCR, RFFIT, sequencing | 2.8% (RNA); 9.3% (antibodies) | 19 colonies in Andalusia; endemic circulation; subclinical infections [15] |
| 2001–2011 | Active | 2,393 blood samples + 45 dead | PCR positive in 6 species; antibodies in 13 species | EBLV-1 | *M. capaccinii*, *M. daubentonii* et al. | RT-PCR + serology | 20.7% (11.1–40.2%) serologically | 25 localities; first RNA in *M. capaccinii* [16] |
| 2002–2016 | Passive+Active | — | 23 strains sequenced | EBLV-1 | *E. serotinus*, *E. isabellinus* | Sequencing, phylogenetics | — | 9 strains from *E. serotinus*, 14 from *E. isabellinus*; first *E. serotinus* cases south of Pyrenees [17] |
Sources: [14] Serra-Cobo et al. 2002; [15] PMC2600403; [16] PLOS ONE 2013 (PMC); [17] PLOS NTD 2018
Evidence grade: A (high) — multi-year active surveillance, several cohort studies, well documented.
URL sources:
- https://pmc.ncbi.nlm.nih.gov/articles/PMC2600403/
- https://journals.plos.org/plosone/article?id=10.1371%2Fjournal.pone.0064467
- https://journals.plos.org/plosntds/article?id=10.1371%2Fjournal.pntd.0006290
---
7. POLAND (Polska)
Status: EBLV-1 endemicity since 1972; BBLV detected in *Myotis nattereri* in 2018.
Table 7. Bat Lyssavirus Surveillance in Poland
| Period | Surveillance type | Bats tested | Positive (FAT/PCR) | Seropositive | Lyssavirus species | Bat species | Method | Notes |
|---|---|---|---|---|---|---|---|---|
| 1972–2004 | Passive | n/a | 53 | — | EBLV-1 | *E. serotinus* | FAT | Retrospective data; first case 1972 [11] |
| 1998–2004 | Passive | n/a | ~3–5/year | — | EBLV-1 | *E. serotinus* | FAT, RT-PCR | Continuous passive monitoring since 1998 [18] |
| 2012–2018 | Passive (+ serology) | 115 (carcasses) + 87 (sera) | 2 (FAT/PCR-positive) | 35/115 = 30.4% (ELISA) | EBLV-1; BBLV (1 isolate 2018) | 9 species incl. *E. serotinus*, *Myotis* spp. | FAT, nested RT-PCR, ELISA, RFFIT | First BBLV isolation in Poland (2018) from *M. nattereri* [18] |
| 2018 | Passive | — | 1 | — | BBLV | *Myotis nattereri* | FAT, RT-PCR, sequencing | First BBLV in Poland [18] |
Sources: [18] Smreczak et al. 2020 (PMC7150987); King et al. 2004
Evidence grade: B (moderate) — reliable passive surveillance, but insufficient territorial coverage; active surveillance limited.
URL sources:
- https://pmc.ncbi.nlm.nih.gov/articles/PMC7150987/
- https://secemu.org/wp-content/uploads/2022/05/Bat-rabies-pubic-health-and-bat-conservation-ZPH-2012.pdf
---
8. SWITZERLAND (Schweiz / Suisse)
Status: Historically linked to EBLV-2 (first human isolation in 1985 — bat in Finland/Switzerland).
Table 8. Bat Lyssavirus Surveillance in Switzerland
| Period | Surveillance type | Bats tested | Positive | Seropositive | Lyssavirus species | Bat species | Method | Notes |
|---|---|---|---|---|---|---|---|---|
| 1985–2002 | Passive | n/a | 3 | — | EBLV-2 | *Myotis daubentonii* | FAT, RT-PCR | Sporadic cases [11] |
| 1976–2009 | Passive+Active | 837 | 3 | n/a | EBLV-2 | *M. daubentonii* | FAT, RT-PCR | Low number over long monitoring [19] |
| 2009 | Active | 237 | 1 (PCR-positive) | 3 (VNA ≥1:10) | EBLV-2 | *M. daubentonii* | RT-PCR, RFFIT | Additional 2009 sample; circulation confirmed [19] |
Sources: [19] PMC3846527; Nathwani et al. 2010 (PubMed 20803042)
Evidence grade: B (moderate) — small testing volume for the country; limited publications.
URL sources:
- https://pmc.ncbi.nlm.nih.gov/articles/PMC3846527/
- https://pubmed.ncbi.nlm.nih.gov/20803042/
- https://onlinelibrary.wiley.com/doi/10.1111/zph.12003
---
9. FINLAND (Suomi)
Status: Historically: human death from EBLV-2 in 1985. In 2009 — first EBLV-2 in a bat.
Table 9. Bat Lyssavirus Surveillance in Finland
| Period | Surveillance type | Bats tested | Positive (FAT/PCR) | Seropositive | Lyssavirus species | Bat species | Method | Notes |
|---|---|---|---|---|---|---|---|---|
| 1985 | Spillover | — | 1 (human) | — | EBLV-2 | Bat (source) | Virology | Death of Swiss biologist [20] |
| 1985–2012 | Passive + Active | 1,156 (898 active + 258 passive) | 1 (2009) | Antibodies in *M. daubentonii* | EBLV-2 | 7 species incl. *M. daubentonii* | Viral RNA analysis, serology | Only positive bat — *M. daubentonii* 2009 [21] |
| 2010–2011 | Active (targeted) | 774 throat swabs + 423 sera | 0 (PCR) | Antibodies in *M. daubentonii* | EBLV-2 | *M. daubentonii* | RT-PCR, RFFIT | [21] |
Sources: [20] Lumio et al. 1986; [21] Nokireki et al. (dissertation 2017, Ruokavirasto)
Evidence grade: B (moderate) — careful targeted search; limited number of species; historically important.
URL sources:
- https://pubmed.ncbi.nlm.nih.gov/20196902/
- https://www.ruokavirasto.fi/globalassets/yhteisot/tieteellinen-tutkimus/vaitoskirjat/2017-nokireki.pdf
- https://pmc.ncbi.nlm.nih.gov/articles/PMC3846527/
---
10. NORWAY (Norge)
Status: First EBLV-2 case in a bat in 2015. Rabies has never been registered in mainland Norway.
Table 10. Bat Lyssavirus Surveillance in Norway
| Period | Surveillance type | Bats tested | Positive | Lyssavirus species | Bat species | Method | Notes |
|---|---|---|---|---|---|---|---|
| pre-2015 | — | Minimal | 0 | — | — | — | Active surveillance absent [22] |
| 2015 | Passive (single case) | 1 | 1 | EBLV-2 | *Myotis daubentonii* | PCR (nucleoprotein gene), sequencing, virus isolation (neuroblastoma cells) | First EBLV-2 case in Norway; passive monitoring [22] |
Sources: [22] PMC5504624 (First detection EBLV-2 Norway 2017)
Evidence grade: C (low) — single case; no systematic surveillance.
URL sources:
- https://pmc.ncbi.nlm.nih.gov/articles/PMC5504624/
- https://pmc.ncbi.nlm.nih.gov/articles/PMC5156864/
---
11. ITALY (Italia)
Status: No bat cases (PCR/FAT) until 2018; seropositivity confirmed.
Table 11. Bat Lyssavirus Surveillance in Italy
| Period | Surveillance type | Bats tested | Positive (FAT/PCR) | Seropositive | Lyssavirus species | Bat species | Method | Notes |
|---|---|---|---|---|---|---|---|---|
| 1986–1993 | Passive | 154 (10 species) | 0 | — | — | 10 species | FAT | First period; all negative [23] |
| 2006–2017 | Passive | 296 (115 FAT) | 0 (FAT, RT-PCR, isolation) | — | — | *E. serotinus* et al. NOT represented | FAT, RT-PCR | Continuous growth since 2013; 96.9% samples from Northern Italy [23] |
| 2008–2014 | Active (serology) | 10 colonies; 544 brains + 254 hearts | 0 (RNA) | EBLV-1 antibodies in 3 species; exposure epidemic in 1 colony | EBLV-1 (serologically) | *Myotis myotis*, *M. blythii*, *Tadarida teniotis* | FAT, RT-PCR, RFFIT | Südtirol colony: 21.8% positive (2010) → decrease → 0% (2014); no antigens [23] |
Sources: [23] Sacchi et al. 2019 (PMC6518613)
Evidence grade: B (moderate) — systematic monitoring, but main reservoir species (*E. serotinus*) poorly represented in passive surveillance.
URL sources:
- https://pmc.ncbi.nlm.nih.gov/articles/PMC6518613/
- https://www.tandfonline.com/doi/full/10.1038/s41426-018-0214-y
---
12. SWEDEN (Sverige)
Status: First report of bat seropositivity — 2016.
Table 12. Bat Lyssavirus Surveillance in Sweden
| Period | Surveillance type | Bats tested | PCR-positive | Seropositive | Lyssavirus species | Bat species | Method | Notes |
|---|---|---|---|---|---|---|---|---|
| 2008–2013 | Active | 452 | 0 (RT-PCR) | 14 (VNA ≥1:10) | EBLV (neutralizing antibodies) | *Myotis daubentonii* | Virus neutralization, RT-PCR | >20 colonies in central, south-east and southern Sweden; all antibody-positives from Skåne or Småland [24] |
Sources: [24] Westin et al. 2016 (PMC5156864)
Evidence grade: B (moderate) — first systematic study; limited temporal coverage; no confirmed virological cases in animals.
URL sources:
- https://pmc.ncbi.nlm.nih.gov/articles/PMC5156864/
- https://www.uu.se/en/news/2016/2016-12-19-rabies-antibodies-found-in-swedish-bats
---
13. BELGIUM (België / Belgique)
Status: First confirmed EBLV-1 cases in 2016–2017.
Table 13. Bat Lyssavirus Surveillance in Belgium
| Period | Surveillance type | Bats tested | PCR-positive | Seropositive | Lyssavirus species | Bat species | Method | Notes |
|---|---|---|---|---|---|---|---|---|
| 2016–2018 | Passive | 124 | 2 (1.61%) | — | EBLV-1 | *Eptesicus serotinus* | RT-PCR | First EBLV-1 cases in Belgium: 2016 — Bertrix, 2017 — Étalle [25] |
| 2018 | Active | 113 (saliva) + 87 (blood) | 0 | 32% (antibodies) | EBLV-1 (serologically) | 5 species | RT-qPCR, neutralization | High seroprevalence with no viral RNA [25] |
Sources: [25] Sciensano 2024 (tropicalmed-09-00151)
Evidence grade: B (moderate) — first systematic study, limited observation period.
URL sources:
- https://www.sciensano.be/sites/default/files/tropicalmed-09-00151-v2.pdf
- https://sciensano.be/sites/default/files/pra-rage_finale_1.pdf
---
Summary Table for All 13 Countries
| Country | Observation period | Total tested | Virus-positive (FAT/PCR) | Seropositive | Lyssavirus species | Main host species | Methods | Evidence grade |
|---|---|---|---|---|---|---|---|---|
| Germany | 1956–2020 | >10,000 | >200 (1956–2020) | 36.2% (active, RFFIT) | EBLV-1, BBLV | *E. serotinus*, *M. nattereri*, *Nyctalus* spp. | FAT, RT-PCR, RFFIT, isolation | A |
| Netherlands | 1984–present | >1,500+ | 256+ (to 2004); ~20%/year in serotines | ~4% *M. dasycneme* | EBLV-1, EBLV-2 | *E. serotinus*, *M. dasycneme* | FAT, RT-PCR, phylogenetics | A |
| France | 1989–2013 | 2,447 | 48 (1.96%) | — | EBLV-1, BBLV | *E. serotinus*, *M. nattereri* | FAT, RTCIT, RT-PCR | A |
| UK | 1987–2016 | ~15,500 | 15 (all EBLV-2) | 1–5% *M. dau* (active) | EBLV-2 | *Myotis daubentonii* | FAT, RT-qPCR, RFFIT | A |
| Spain | 1977–2016 | >3,500+ | >60 (RNA); antibodies in 13 species | 20.7% (active) | EBLV-1 | *E. serotinus*, *E. isabellinus*, *M.* spp. | FAT, RT-PCR, RFFIT, serology | A |
| Denmark | 1985–2024 | N/A (~several hundreds) | >154 (1985–2009) | — | EBLV-1, EBLV-2 | *E. serotinus*, *M. dasycneme* | FAT, RT-PCR | B |
| Poland | 1972–2018 | 115 (systematic) + historical | 55+ historically; 2 (2012–2018) | 30.4% (ELISA) | EBLV-1, BBLV | *E. serotinus*, *M. nattereri* | FAT, RT-PCR, ELISA, RFFIT | B |
| Switzerland | 1976–2009 | 837 | 3–4 | 3 (2009) | EBLV-2 | *M. daubentonii* | FAT, RT-PCR, RFFIT | B |
| Finland | 1985–2012 | 1,156 | 1 (2009) | Antibodies in *M. dau* | EBLV-2 | *M. daubentonii* | RT-PCR, serology | B |
| Norway | 2015–present | 1 (documented) | 1 (2015) | — | EBLV-2 | *M. daubentonii* | PCR, sequencing, isolation | C |
| Italy | 1986–2017 | 296 (passive) + >1,000 (active) | 0 | 3 species seropositive | EBLV-1 (serologically) | *M. myotis*, *M. blythii*, *T. teniotis* | FAT, RT-PCR, RFFIT | B |
| Sweden | 2008–2013 | 452 | 0 | 14/452 (VNA) | EBLV (antibodies) | *M. daubentonii* | Neutralization, RT-PCR | B |
| Belgium | 2016–2018 | 124 (passive) + 200 (active) | 2 (1.61%) | 32% | EBLV-1 | *E. serotinus* | RT-PCR, neutralization | B |
---
Trend Analysis: Causes of Apparent Changes
Table 14. Factors Explaining Apparent Changes in the Number of Detected Cases
| Country | Observed trend | Main explanatory factor | Factor type | Justification |
|---|---|---|---|---|
| France | 17-fold increase in samples (2001–2013 vs 1989–2000) with stable positivity (~2%) in *E. serotinus* | ↑ Surveillance intensity | Surveillance artifact | SFEPM network + lab network strengthening since 2000; share of positives among serotines is stable [8] |
| Germany | Increase in documented cases from 1970s to 2000s; then normalization | ↑ Diagnostic improvement + ↑ coverage | Surveillance artifact | Introduction of PCR alongside FAT; network expansion; real number of EBLV-1 cases in *E. serotinus* stable [2,4] |
| UK | Slow but continuous increase in submitted samples; 15 confirmed cases since 1987 | ↑ Surveillance intensity + geographic expansion | Surveillance artifact + ecology | Increase in samples; identification of focal endemism (Stokesay Castle); no signs of true new appearance [10] |
| Belgium | No historical data → first cases from 2016 | Start of systematic surveillance | Surveillance artifact | No targeted testing before 2016; EBLV-1 in *E. serotinus* likely present [25] |
| Norway | Zero → 1 case (2015) | Single finding in passive surveillance | Possibly true appearance or lack of surveillance | No systematic surveillance; cannot exclude introduction from Denmark/Germany or longstanding circulation [22] |
| Poland | Stable EBLV-1 case numbers; new BBLV in 2018 | Expanded diagnostic panel (BBLV-PCR) | Diagnostic factor | BBLV was not searched for previously; real BBLV ecology in *M. nattereri* is stable [18] |
| Italy | 0 virus-positive despite seropositivity | Main host species (*E. serotinus*) not entering surveillance | Surveillance artifact | *E. serotinus* not represented in Italian laboratories; seropositivity in *M. myotis* confirms exposure [23] |
| Denmark | Mass detection 1986–1987 → decrease after 1990s | Decrease in surveillance intensity + initial "burst" from monitoring start | Surveillance artifact + possible ecological changes | Decrease in sample submission activity; endemicity persists (PEP recipients) [12,13] |
| Netherlands | High initial positivity decreased after 1994 | From 1994 — only biting/suspicious bats, not all dead | Surveillance protocol change | Shift to "high-risk cases" overestimated prior prevalence [5,6] |
| Spain, Germany, Netherlands | Seroprevalence significantly exceeds virus positivity | Subclinical infectious state and serological criterion | Biological + diagnostic | Seroprevalence reflects exposure, not active shedding; gap grows with transition from FAT to serology [15,4] |
---
Methodological Notes
- Passive vs active surveillance: Passive surveillance is systematically biased toward large, easily noticed species (*E. serotinus*, synanthropic Pipistrellus), which people more often find and submit. Active capture provides more representative data but is labor-intensive.
- FAT vs PCR: FAT requires fresh brain material and detects antigen (active infection). RT-PCR is more sensitive for decomposed samples and allows lyssavirus typing. Introduction of PCR increases detectability without changing true prevalence.
- Serology: Antibodies (RFFIT/FAVN/ELISA) indicate past exposure, not active shedding. Seroprevalence is higher than virus positivity in all countries — this is biologically normal and does not mean growth in the number of infected animals.
- Evidence grade scale:
- A — Long-term (≥10 years) systematic monitoring; national or WHO/OIE reference laboratory; peer-reviewed publications with complete methods and numerical data.
- B — Systematic monitoring <10 years or significant data gap; peer-reviewed publications with limited temporal/spatial coverage.
- C — Single finding; no systematic surveillance; data from abstracts or grey sources.
---
List of Main Sources with URLs
| # | Reference | URL |
|---|---|---|
| 1 | King et al. 2004. Lyssaviruses in European bats | https://pmc.ncbi.nlm.nih.gov/articles/PMC7096730/ |
| 2 | Freuling et al. 2013. Retrospective Enhanced Bat Lyssavirus Surveillance Germany | https://pmc.ncbi.nlm.nih.gov/articles/PMC8402685/ |
| 3 | Freuling et al. 2014. PLOS NTD Enhanced Passive Bat Rabies Surveillance Germany | https://journals.plos.org/plosntds/article?id=10.1371%2Fjournal.pntd.0002835 |
| 4 | Pikula/Freuling 2014. Twenty years active bat rabies surveillance Germany | https://www.cambridge.org/core/journals/epidemiology-and-infection/article/twenty-years-of-active-bat-rabies-surveillance-in-germany-a-detailed-analysis-and-future-perspectives/E7EC32DF6231629E199F4CA82CFA5B16 |
| 5 | Van der Poel et al. 2005. European Bat Lyssaviruses, the Netherlands (CDC EID) | https://wwwnc.cdc.gov/eid/article/11/12/04-1200_article |
| 6 | Willems et al. 2012. European Bat Lyssaviruses, Netherlands PMC3367619 | https://pmc.ncbi.nlm.nih.gov/articles/PMC3367619/ |
| 7 | Eurosurveillance 2025. EBLV-1 in a cat, Netherlands | https://www.eurosurveillance.org/content/10.2807/1560-7917.ES.2025.30.10.2500154 |
| 8 | Picard-Meyer et al. 2014. Bat Rabies France 24-year PMC4044004 | https://pmc.ncbi.nlm.nih.gov/articles/PMC4044004/ |
| 9 | Harris et al. 2006. Passive surveillance UK bats 1987–2004 | https://pmc.ncbi.nlm.nih.gov/articles/PMC7096730/ |
| 10 | Brookes/Fooks et al. 2022. Passive surveillance UK bats 2005–2015 | https://pmc.ncbi.nlm.nih.gov/articles/PMC9148805/ |
| 11 | PMC7096730. European bat lyssaviruses distribution prevalence review | https://pmc.ncbi.nlm.nih.gov/articles/PMC7096730/ |
| 12 | SSI Denmark Rabies Annual Report 2018 | https://en.ssi.dk/surveillance-and-preparedness/surveillance-in-denmark/annual-reports-on-disease-incidence/r/rabies---annual-report-2018 |
| 13 | SSI Denmark Rabies 2024 | https://en.ssi.dk/surveillance-and-preparedness/surveillance-in-denmark/annual-reports-on-disease-incidence/r/rabies-2024 |
| 14 | Serra-Cobo et al. 2002. EBLV Spanish bat populations | https://pmc.ncbi.nlm.nih.gov/articles/PMC2600403/ |
| 15 | Echevarria et al. 2001 / PMC2600403 endemic Spain | https://pmc.ncbi.nlm.nih.gov/articles/PMC2600403/ |
| 16 | PLOS ONE 2013. Ecological factors EBLV Spain 2001–2011 | https://journals.plos.org/plosone/article?id=10.1371%2Fjournal.pone.0064467 |
| 17 | PLOS NTD 2018. First EBLV-1 Eptesicus serotinus south Pyrenees Spain | https://journals.plos.org/plosntds/article?id=10.1371%2Fjournal.pntd.0006290 |
| 18 | Smreczak et al. 2020. Serological survey lyssaviruses Polish bats PMC7150987 | https://pmc.ncbi.nlm.nih.gov/articles/PMC7150987/ |
| 19 | PMC3846527. Nordahl 2014. Lyssavirus Scandinavia/Switzerland | https://pmc.ncbi.nlm.nih.gov/articles/PMC3846527/ |
| 20 | Lumio et al. 1986. Human rabies bat origin Europe (Finland) | https://pubmed.ncbi.nlm.nih.gov/20196902/ |
| 21 | Nokireki 2017. EBLV-2 Finland (dissertation) | https://www.ruokavirasto.fi/globalassets/yhteisot/tieteellinen-tutkimus/vaitoskirjat/2017-nokireki.pdf |
| 22 | PMC5504624. First detection EBLV-2 Norway | https://pmc.ncbi.nlm.nih.gov/articles/PMC5504624/ |
| 23 | Sacchi et al. 2019. Active passive surveillance Italy PMC6518613 | https://pmc.ncbi.nlm.nih.gov/articles/PMC6518613/ |
| 24 | Westin et al. 2016. Lyssavirus-reactive antibodies Swedish bats PMC5156864 | https://pmc.ncbi.nlm.nih.gov/articles/PMC5156864/ |
| 25 | Sciensano 2024. EBLV-1 Belgian bats | https://www.sciensano.be/sites/default/files/tropicalmed-09-00151-v2.pdf |