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Synchronicity of viral shedding in molossid bat maternity colonies

Infection dynamics in vertebrates are driven by biological and ecological processes. For bats, population structure and reproductive cycles have major effects on RNA virus transmission. On Reunion Island, previous studies have shown that parturition of pregnant females and aggregation of juvenile Re...

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Autores principales: Hoarau, Axel O. G., Köster, Marie, Dietrich, Muriel, Le Minter, Gildas, Joffrin, Léa, Ramanantsalama, Riana V., Mavingui, Patrick, Lebarbenchon, Camille
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052574/
https://www.ncbi.nlm.nih.gov/pubmed/36750225
http://dx.doi.org/10.1017/S0950268823000171
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author Hoarau, Axel O. G.
Köster, Marie
Dietrich, Muriel
Le Minter, Gildas
Joffrin, Léa
Ramanantsalama, Riana V.
Mavingui, Patrick
Lebarbenchon, Camille
author_facet Hoarau, Axel O. G.
Köster, Marie
Dietrich, Muriel
Le Minter, Gildas
Joffrin, Léa
Ramanantsalama, Riana V.
Mavingui, Patrick
Lebarbenchon, Camille
author_sort Hoarau, Axel O. G.
collection PubMed
description Infection dynamics in vertebrates are driven by biological and ecological processes. For bats, population structure and reproductive cycles have major effects on RNA virus transmission. On Reunion Island, previous studies have shown that parturition of pregnant females and aggregation of juvenile Reunion free-tailed bats (Mormopterus francoismoutoui) are associated with major increase in the prevalence of bats shedding RNA viruses. The synchronicity of such shedding pulses, however, is yet to be assessed between viruses but also maternity colonies. Based on 3422 fresh faeces collected every 2–5 weeks during four consecutive birthing seasons, we report the prevalence of bats shedding astroviruses (AstVs), coronaviruses (CoVs) and paramyxoviruses (PMVs) in two maternity colonies on Reunion Island. We found that the proportion of bats shedding viruses is highly influenced by sampling collection periods, and therefore by the evolution of the population age structure. We highlight that virus shedding patterns are consistent among years and colonies for CoVs and to a lesser extent for PMVs, but not for AstVs. We also report that 1% of bats harbour co-infections, with two but not three of the viruses, and most co-infections were due to CoVs and PMVs.
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spelling pubmed-100525742023-03-30 Synchronicity of viral shedding in molossid bat maternity colonies Hoarau, Axel O. G. Köster, Marie Dietrich, Muriel Le Minter, Gildas Joffrin, Léa Ramanantsalama, Riana V. Mavingui, Patrick Lebarbenchon, Camille Epidemiol Infect Original Paper Infection dynamics in vertebrates are driven by biological and ecological processes. For bats, population structure and reproductive cycles have major effects on RNA virus transmission. On Reunion Island, previous studies have shown that parturition of pregnant females and aggregation of juvenile Reunion free-tailed bats (Mormopterus francoismoutoui) are associated with major increase in the prevalence of bats shedding RNA viruses. The synchronicity of such shedding pulses, however, is yet to be assessed between viruses but also maternity colonies. Based on 3422 fresh faeces collected every 2–5 weeks during four consecutive birthing seasons, we report the prevalence of bats shedding astroviruses (AstVs), coronaviruses (CoVs) and paramyxoviruses (PMVs) in two maternity colonies on Reunion Island. We found that the proportion of bats shedding viruses is highly influenced by sampling collection periods, and therefore by the evolution of the population age structure. We highlight that virus shedding patterns are consistent among years and colonies for CoVs and to a lesser extent for PMVs, but not for AstVs. We also report that 1% of bats harbour co-infections, with two but not three of the viruses, and most co-infections were due to CoVs and PMVs. Cambridge University Press 2023-02-08 /pmc/articles/PMC10052574/ /pubmed/36750225 http://dx.doi.org/10.1017/S0950268823000171 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
spellingShingle Original Paper
Hoarau, Axel O. G.
Köster, Marie
Dietrich, Muriel
Le Minter, Gildas
Joffrin, Léa
Ramanantsalama, Riana V.
Mavingui, Patrick
Lebarbenchon, Camille
Synchronicity of viral shedding in molossid bat maternity colonies
title Synchronicity of viral shedding in molossid bat maternity colonies
title_full Synchronicity of viral shedding in molossid bat maternity colonies
title_fullStr Synchronicity of viral shedding in molossid bat maternity colonies
title_full_unstemmed Synchronicity of viral shedding in molossid bat maternity colonies
title_short Synchronicity of viral shedding in molossid bat maternity colonies
title_sort synchronicity of viral shedding in molossid bat maternity colonies
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052574/
https://www.ncbi.nlm.nih.gov/pubmed/36750225
http://dx.doi.org/10.1017/S0950268823000171
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