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Disentangling serology to elucidate henipa- and filovirus transmission in Madagascar fruit bats

Authors :
Alison J. Peel
Jean-Michel Heraud
Cara E. Brook
Christopher C. Broder
C. Jessica E. Metcalf
Louise Gibson
Andrew A. Cunningham
Hafaliana Christian Ranaivoson
Andrew P. Dobson
James L. N. Wood
Brook, Cara E [0000-0003-4276-073X]
Cunningham, Andrew A [0000-0002-3543-6504]
Peel, Alison J [0000-0003-3538-3550]
Wood, James LN [0000-0002-0258-3188]
Metcalf, C Jessica [0000-0003-3166-7521]
Dobson, Andrew P [0000-0002-9678-1694]
Apollo - University of Cambridge Repository
Princeton University
Unité de Virologie [Antananarivo, Madagascar] (IPM)
Institut Pasteur de Madagascar
Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)
Université d'Antananarivo
Uniformed Services University of the Health Sciences (USUHS)
Zoological Society of London - ZSL (UNITED KINGDOM)
Griffith University [Brisbane]
University of Cambridge [UK] (CAM)
Biological Defense Research Directorate (CCB)
AI054715 (CCB)
MR/P025226/1 (JLNW)
Veterinary Research Grant (JLNW)
Accelerate Postdoctoral Research Fellowship (AJP)
Center for Health and Well-being Research Grant (CJEM)
Doctoral Dissertation Improvement (CEB). Grant Number: 1600980
Graduate Research Fellowship Program (CEB)
R01-AI129822-01 (JMH)
Young Explorer's Grant (CEB). Grant Number: YEG-9269-13
Waitt Grant (CEB). Grant Number: W376-15
Walbridge Graduate Research Fund (CEB)
Source :
Journal of Animal Ecology, Journal of Animal Ecology, Wiley, 2019, 88 (7), pp.1001-1016. ⟨10.1111/1365-2656.12985⟩
Publication Year :
2019
Publisher :
Wiley, 2019.

Abstract

International audience; Bats are reservoirs for emerging human pathogens, including Hendra and Nipah henipaviruses and Ebola and Marburg filoviruses. These viruses demonstrate predictable patterns in seasonality and age structure across multiple systems; previous work suggests that they may circulate in Madagascar's endemic fruit bats, which are widely consumed as human food. We aimed to (a) document the extent of henipa- and filovirus exposure among Malagasy fruit bats, (b) explore seasonality in seroprevalence and serostatus in these bat populations and (c) compare mechanistic hypotheses for possible transmission dynamics underlying these data. To this end, we amassed and analysed a unique dataset documenting longitudinal serological henipa- and filovirus dynamics in three Madagascar fruit bat species. We uncovered serological evidence of exposure to Hendra-/Nipah-related henipaviruses in Eidolon dupreanum, Pteropus rufus and Rousettus madagascariensis, to Cedar-related henipaviruses in E. dupreanum and R. madagascariensis and to Ebola-related filoviruses in P. rufus and R. madagascariensis. We demonstrated significant seasonality in population-level seroprevalence and individual serostatus for multiple viruses across these species, linked to the female reproductive calendar. An age-structured subset of the data highlighted evidence of waning maternal antibodies in neonates, increasing seroprevalence in young and decreasing seroprevalence late in life. Comparison of mechanistic epidemiological models fit to these data offered support for transmission hypotheses permitting waning antibodies but retained immunity in adult-age bats. Our findings suggest that bats may seasonally modulate mechanisms of pathogen control, with consequences for population-level transmission. Additionally, we narrow the field of candidate transmission hypotheses by which bats are presumed to host and transmit potentially zoonotic viruses globally.

Details

ISSN :
00218790 and 13652656
Database :
OpenAIRE
Journal :
Journal of Animal Ecology, Journal of Animal Ecology, Wiley, 2019, 88 (7), pp.1001-1016. ⟨10.1111/1365-2656.12985⟩
Accession number :
edsair.doi.dedup.....cc186917825b9868da68755dd7b796b6
Full Text :
https://doi.org/10.1111/1365-2656.12985⟩