A multiregional serosurvey of RNA virus-reactive antibodies in bats and rodents reveals the enzootic presence of flavi- and paramyxoviruses in African Pteropodidae.

Jackson Emanuel1,2 Jan Papies1,2 Leonie Meiners1,2 Talitha Veith1,2 Victor M Corman1,2 Tabea Binger3 Erik Lattwein4 Beate M Kümmerer5,6 Susanne Zweerink7,8 Kai Fechner4 Florian Gloza-Rausch9,10 Veronika Cottontail11,12 Gaël D Maganga13,14 Jonas Schmidt-Chanasit15,16 Peter Vallo17 Samuel K Oppong18 Marco Tschapka12,19 Chantal B E M Reusken20,21 Rainer G Ulrich22 Eric M Leroy23 Jan Felix Drexler1,2 Terry C Jones1,2,24 Christian Drosten1,2 Marcel A Müller1,2
Affiliations 24 institutions
  1. Institute of Virology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
  2. German Centre for Infection Research (DZIF), Berlin, Germany.
  3. International Vaccine Institute (IVI), Seoul, Korea.
  4. Institute for Experimental Immunology, affiliated to EUROIMMUN Medizinische Labordiagnostika AG, Lübeck, Germany.
  5. Institute of Virology, Medical Faculty, University of Bonn, Bonn, Germany.
  6. German Centre for Infection Research, Partner Site Bonn-Cologne, Bonn, Germany.
  7. Department of Gastroenterology and Hepatology, Faculty of Medicine and University Hospital of Cologne, University of Cologne, Cologne, Germany.
  8. Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
  9. Museum für Naturkunde, Leibniz Institute for Evolution and Biodiversity Science, Berlin, Germany.
  10. Fledermaus-Rausch-Umweltgutachten, Flintbek, Germany.
  11. Department of Medicine II, Division of Infectious Diseases and Tropical Medicine, University Hospital Würzburg, Würzburg, Germany.
  12. Smithsonian Tropical Research Institute, Ancon, Panama.
  13. Centre Interdisciplinaire de Recherches Médicales de Franceville (CIRMF), Franceville, Gabon.
  14. Institut National Supérieur d'Agronomie et de Biotechnologies (INSAB), Université des Sciences et Techniques de Masuku (USTM), Franceville, Gabon.
  15. Department of Arbovirology and Entomology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
  16. Faculty of Mathematics, Informatics and Natural Sciences, Universität Hamburg, Hamburg, Germany.
  17. Institute of Vertebrate Biology, Czech Academy of Sciences, Brno, Czech Republic.
  18. Department of Wildlife and Range Management, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
  19. Institute of Evolutionary Ecology and Conservation Genomics, University of Ulm, Ulm, Germany.
  20. Centre for infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.
  21. Division Infectious Diseases and Immunology, Department Biomolecular Health Sciences, Faculty Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.
  22. Institute of Novel and Emerging Infectious Diseases, Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany.
  23. Recherches translationnelles sur le VIH et les maladies infectieuses (TransVIHMI), Université de Montpellier-IRD-Inserm, Montpellier, France.
  24. Centre for Pathogen Evolution, Department of Zoology, University of Cambridge, Cambridge, United Kingdom.
Active Last checked 2026-10-10 03:30:25 Source: NCBI PubMed

Abstract

Bats and rodents have been identified as reservoir hosts of diverse RNA viruses that pose potential risks to humans. However, overall virus prevalence in wildlife and underlying factors determining the zoonotic potential of reservoir-borne viruses remain poorly characterized. Virus detection often relies on the identification of viral nucleotide sequences and may therefore be limited by variable virus concentration, tissue tropism, sample quality, and duration of infection. In this study, we applied a multiplex immunofluorescence assay to examine bat and rodent seroprevalence against 14 different human pathogenic RNA viruses spanning seven virus families (Coronaviridae, Flaviviridae, Hantaviridae, Paramyxoviridae, Phenuiviridae, Pneumoviridae, Togaviridae). We retrospectively analyzed 1,135 bat (16 species) and 454 rodent (15 species) blood or transudate specimens collected at 63 sites in seven countries. The tropical bats in our dataset exhibited notably high rates of seropositivity against certain virus families (Flaviviridae: 42.7%; Paramyxoviridae: 67.7%; Togaviridae: 7.5%). Although confounding factors and sparse data continue to pose challenges to identifying correlates of RNA virus infection in wildlife, multivariable logistic regression models were created to provisionally evaluate the association of tropical bat characteristics with seropositivity. Preliminary findings indicate that large colony size, found among species such as Eidolon helvum and Rousettus aegyptiacus, is a predictor within this dataset of orthoflavi- and orthorubulavirus seroprevalence, consistent with the communal spread of bat-adapted viruses.

Supporting text Virus Host Location

Evidence records

6 total
Zoonotic Surveillance
6 records · 2 evidence types
Evidence type
5 records
OVE12323
Key finding

Tropical bats showed 42.7% seropositivity to Flaviviridae.

Virus
Host
Natural host
Location
Not specified
Supporting text

The tropical bats in our dataset exhibited notably high rates of seropositivity against certain virus families (Flaviviridae: 42.7%).

Method
multiplex immunofluorescence assay
Sample type
blood | transudate
OVE12324
Key finding

Tropical bats showed 67.7% seropositivity to Paramyxoviridae.

Virus
Host
Natural host
Location
Not specified
Supporting text

The tropical bats in our dataset exhibited notably high rates of seropositivity against certain virus families (Flaviviridae: 42.7%; Paramyxoviridae: 67.7%; Togaviridae: 7.5%).

Method
multiplex immunofluorescence assay
Sample type
blood | transudate
OVE12325
Key finding

Tropical bats showed 7.5% seropositivity to Togaviridae.

Virus
Host
Natural host
Location
Not specified
Supporting text

The tropical bats in our dataset exhibited notably high rates of seropositivity against certain virus families (Flaviviridae: 42.7%; Paramyxoviridae: 67.7%; Togaviridae: 7.5%).

Method
multiplex immunofluorescence assay
Sample type
blood | transudate
OVE12326
Key finding

A multiplex immunofluorescence assay was used to screen bat and rodent seroprevalence against 14 RNA viruses across seven families.

Virus
Host
Location
Not specified
Supporting text

In this study, we applied a multiplex immunofluorescence assay to examine bat and rodent seroprevalence against 14 different human pathogenic RNA viruses spanning seven virus families (Coronaviridae, Flaviviridae, Hantaviridae, Paramyxoviridae, Phenuiviridae, Pneumoviridae, Togaviridae).

Method
multiplex immunofluorescence assay
Sample type
blood | transudate
OVE12327
Key finding

The serosurvey analyzed 1,135 bat and 454 rodent blood or transudate specimens.

Virus
Not specified
Host
Location
Not specified
Supporting text

We retrospectively analyzed 1,135 bat (16 species) and 454 rodent (15 species) blood or transudate specimens collected at 63 sites in seven countries.

Method
multiplex immunofluorescence assay
Sample type
blood | transudate
Evidence type
1 records
OVE12328
Key finding

In tropical bats, larger colony size—seen in species such as Eidolon helvum and Rousettus aegyptiacus—is associated with higher orthoflavi- and orthorubulavirus seroprevalence.

Virus
Host
Natural host
Location
Not specified
Supporting text

Preliminary findings indicate that large colony size, found among species such as Eidolon helvum and Rousettus aegyptiacus, is a predictor within this dataset of orthoflavi- and orthorubulavirus seroprevalence, consistent with the communal spread of bat-adapted viruses.

Method
multiplex immunofluorescence assay | multivariable logistic regression
Sample type
blood | transudate