1. Disentangling serology to elucidate henipa- and filovirus transmission in Madagascar fruit bats
- Author
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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, and Walbridge Graduate Research Fund (CEB)
- Subjects
0106 biological sciences ,age-seroprevalence ,MESH: Henipavirus Infections ,Force of infection ,01 natural sciences ,law.invention ,MESH: Madagascar ,[SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases ,law ,Seroepidemiologic Studies ,Chiroptera ,MESH: Animals ,Henipavirus Infections ,[SDV.MHEP.ME]Life Sciences [q-bio]/Human health and pathology/Emerging diseases ,education.field_of_study ,biology ,MESH: Infant, Newborn ,MESH: Chiroptera ,Pteropus ,3. Good health ,Transmission (mechanics) ,[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology ,Female ,Henipavirus ,force of infection ,filovirus ,henipavirus ,Population ,Zoology ,010603 evolutionary biology ,Article ,Madagascar ,Seroprevalence ,Animals ,Humans ,education ,Ecology, Evolution, Behavior and Systematics ,MESH: Humans ,MESH: Seroepidemiologic Studies ,010604 marine biology & hydrobiology ,Eidolon dupreanum ,Infant, Newborn ,[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology ,zoonosis ,biology.organism_classification ,Filoviridae ,flying fox ,MESH: Filoviridae ,Rousettus madagascariensis ,fruit bat ,[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie ,Animal Science and Zoology ,MESH: Female - 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.
- Published
- 2019
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