Cargando…

Seasonality of coronavirus shedding in tropical bats

Anticipating cross-species transmission of zoonotic diseases requires an understanding of pathogen infection dynamics within natural reservoir hosts. Although bats might be a source of coronaviruses (CoVs) for humans, the drivers of infection dynamics in bat populations have received limited attenti...

Descripción completa

Detalles Bibliográficos
Autores principales: Joffrin, Léa, Hoarau, Axel O. G., Lagadec, Erwan, Torrontegi, Olalla, Köster, Marie, Le Minter, Gildas, Dietrich, Muriel, Mavingui, Patrick, Lebarbenchon, Camille
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825989/
https://www.ncbi.nlm.nih.gov/pubmed/35154796
http://dx.doi.org/10.1098/rsos.211600
_version_ 1784647340325339136
author Joffrin, Léa
Hoarau, Axel O. G.
Lagadec, Erwan
Torrontegi, Olalla
Köster, Marie
Le Minter, Gildas
Dietrich, Muriel
Mavingui, Patrick
Lebarbenchon, Camille
author_facet Joffrin, Léa
Hoarau, Axel O. G.
Lagadec, Erwan
Torrontegi, Olalla
Köster, Marie
Le Minter, Gildas
Dietrich, Muriel
Mavingui, Patrick
Lebarbenchon, Camille
author_sort Joffrin, Léa
collection PubMed
description Anticipating cross-species transmission of zoonotic diseases requires an understanding of pathogen infection dynamics within natural reservoir hosts. Although bats might be a source of coronaviruses (CoVs) for humans, the drivers of infection dynamics in bat populations have received limited attention. We conducted a fine-scale 2-year longitudinal study of CoV infection dynamics in the largest colony of Reunion free-tailed bats (Mormopterus francoismoutoui), a tropical insectivorous species. Real-time PCR screening of 1080 fresh individual faeces samples collected during the two consecutive years revealed an extreme variation of the detection rate of bats shedding viruses over the birthing season (from 0% to 80%). Shedding pulses were repeatedly observed and occurred both during late pregnancy and within two months after parturition. An additional shedding pulse at the end of the second year suggests some inter-annual variations. We also detected viral RNA in bat guano up to three months after bats had left the cave. Our results highlight the importance of fine-scale longitudinal studies to capture the rapid change of bat CoV infection over months, and that CoV shedding pulses in bats may increase spillover risk.
format Online
Article
Text
id pubmed-8825989
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher The Royal Society
record_format MEDLINE/PubMed
spelling pubmed-88259892022-02-10 Seasonality of coronavirus shedding in tropical bats Joffrin, Léa Hoarau, Axel O. G. Lagadec, Erwan Torrontegi, Olalla Köster, Marie Le Minter, Gildas Dietrich, Muriel Mavingui, Patrick Lebarbenchon, Camille R Soc Open Sci Ecology, Conservation and Global Change Biology Anticipating cross-species transmission of zoonotic diseases requires an understanding of pathogen infection dynamics within natural reservoir hosts. Although bats might be a source of coronaviruses (CoVs) for humans, the drivers of infection dynamics in bat populations have received limited attention. We conducted a fine-scale 2-year longitudinal study of CoV infection dynamics in the largest colony of Reunion free-tailed bats (Mormopterus francoismoutoui), a tropical insectivorous species. Real-time PCR screening of 1080 fresh individual faeces samples collected during the two consecutive years revealed an extreme variation of the detection rate of bats shedding viruses over the birthing season (from 0% to 80%). Shedding pulses were repeatedly observed and occurred both during late pregnancy and within two months after parturition. An additional shedding pulse at the end of the second year suggests some inter-annual variations. We also detected viral RNA in bat guano up to three months after bats had left the cave. Our results highlight the importance of fine-scale longitudinal studies to capture the rapid change of bat CoV infection over months, and that CoV shedding pulses in bats may increase spillover risk. The Royal Society 2022-02-09 /pmc/articles/PMC8825989/ /pubmed/35154796 http://dx.doi.org/10.1098/rsos.211600 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Ecology, Conservation and Global Change Biology
Joffrin, Léa
Hoarau, Axel O. G.
Lagadec, Erwan
Torrontegi, Olalla
Köster, Marie
Le Minter, Gildas
Dietrich, Muriel
Mavingui, Patrick
Lebarbenchon, Camille
Seasonality of coronavirus shedding in tropical bats
title Seasonality of coronavirus shedding in tropical bats
title_full Seasonality of coronavirus shedding in tropical bats
title_fullStr Seasonality of coronavirus shedding in tropical bats
title_full_unstemmed Seasonality of coronavirus shedding in tropical bats
title_short Seasonality of coronavirus shedding in tropical bats
title_sort seasonality of coronavirus shedding in tropical bats
topic Ecology, Conservation and Global Change Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825989/
https://www.ncbi.nlm.nih.gov/pubmed/35154796
http://dx.doi.org/10.1098/rsos.211600
work_keys_str_mv AT joffrinlea seasonalityofcoronavirussheddingintropicalbats
AT hoarauaxelog seasonalityofcoronavirussheddingintropicalbats
AT lagadecerwan seasonalityofcoronavirussheddingintropicalbats
AT torrontegiolalla seasonalityofcoronavirussheddingintropicalbats
AT kostermarie seasonalityofcoronavirussheddingintropicalbats
AT lemintergildas seasonalityofcoronavirussheddingintropicalbats
AT dietrichmuriel seasonalityofcoronavirussheddingintropicalbats
AT mavinguipatrick seasonalityofcoronavirussheddingintropicalbats
AT lebarbenchoncamille seasonalityofcoronavirussheddingintropicalbats