Cargando…

Synchronized shift of oral, faecal and urinary microbiotas in bats and natural infection dynamics during seasonal reproduction

Seasonal reproduction is a period of extreme physiological and behavioural changes, yet we know little about how it may affect host microbial communities (i.e. microbiota) and pathogen transmission. Here, we investigated shifts of the bacterial microbiota in saliva, urine and faeces during the seaso...

Descripción completa

Detalles Bibliográficos
Autores principales: Dietrich, Muriel, Kearney, Teresa, Seamark, Ernest C. J., Paweska, Janusz T., Markotter, Wanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990816/
https://www.ncbi.nlm.nih.gov/pubmed/29892443
http://dx.doi.org/10.1098/rsos.180041
_version_ 1783329657199788032
author Dietrich, Muriel
Kearney, Teresa
Seamark, Ernest C. J.
Paweska, Janusz T.
Markotter, Wanda
author_facet Dietrich, Muriel
Kearney, Teresa
Seamark, Ernest C. J.
Paweska, Janusz T.
Markotter, Wanda
author_sort Dietrich, Muriel
collection PubMed
description Seasonal reproduction is a period of extreme physiological and behavioural changes, yet we know little about how it may affect host microbial communities (i.e. microbiota) and pathogen transmission. Here, we investigated shifts of the bacterial microbiota in saliva, urine and faeces during the seasonal reproduction of bats in South Africa, and test for an interaction in shedding patterns of both bacterial (Leptospira) and viral (adeno- and herpesviruses) agents. Based on a comparative approach in two cave-dwelling bat species and high-throughput sequencing of the 16S rRNA gene, we demonstrated a clear signature in microbiota changes over the reproduction season, consistent across the multiple body habitats investigated, and associated with the sex, age and reproductive condition of bats. We observed in parallel highly dynamic shedding patterns for both bacteria and viruses, but did not find a significant association between viral shedding and bacterial microbiota composition. Indeed, only Leptospira shedding was associated with alterations in both the diversity and composition of the urinary microbiota. These results illustrate how seasonal reproduction in bats substantially affects microbiota composition and infection dynamics, and have broad implications for the understanding of disease ecology in important reservoir hosts, such as bats.
format Online
Article
Text
id pubmed-5990816
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher The Royal Society Publishing
record_format MEDLINE/PubMed
spelling pubmed-59908162018-06-11 Synchronized shift of oral, faecal and urinary microbiotas in bats and natural infection dynamics during seasonal reproduction Dietrich, Muriel Kearney, Teresa Seamark, Ernest C. J. Paweska, Janusz T. Markotter, Wanda R Soc Open Sci Biology (Whole Organism) Seasonal reproduction is a period of extreme physiological and behavioural changes, yet we know little about how it may affect host microbial communities (i.e. microbiota) and pathogen transmission. Here, we investigated shifts of the bacterial microbiota in saliva, urine and faeces during the seasonal reproduction of bats in South Africa, and test for an interaction in shedding patterns of both bacterial (Leptospira) and viral (adeno- and herpesviruses) agents. Based on a comparative approach in two cave-dwelling bat species and high-throughput sequencing of the 16S rRNA gene, we demonstrated a clear signature in microbiota changes over the reproduction season, consistent across the multiple body habitats investigated, and associated with the sex, age and reproductive condition of bats. We observed in parallel highly dynamic shedding patterns for both bacteria and viruses, but did not find a significant association between viral shedding and bacterial microbiota composition. Indeed, only Leptospira shedding was associated with alterations in both the diversity and composition of the urinary microbiota. These results illustrate how seasonal reproduction in bats substantially affects microbiota composition and infection dynamics, and have broad implications for the understanding of disease ecology in important reservoir hosts, such as bats. The Royal Society Publishing 2018-05-02 /pmc/articles/PMC5990816/ /pubmed/29892443 http://dx.doi.org/10.1098/rsos.180041 Text en © 2018 The Authors. http://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/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Biology (Whole Organism)
Dietrich, Muriel
Kearney, Teresa
Seamark, Ernest C. J.
Paweska, Janusz T.
Markotter, Wanda
Synchronized shift of oral, faecal and urinary microbiotas in bats and natural infection dynamics during seasonal reproduction
title Synchronized shift of oral, faecal and urinary microbiotas in bats and natural infection dynamics during seasonal reproduction
title_full Synchronized shift of oral, faecal and urinary microbiotas in bats and natural infection dynamics during seasonal reproduction
title_fullStr Synchronized shift of oral, faecal and urinary microbiotas in bats and natural infection dynamics during seasonal reproduction
title_full_unstemmed Synchronized shift of oral, faecal and urinary microbiotas in bats and natural infection dynamics during seasonal reproduction
title_short Synchronized shift of oral, faecal and urinary microbiotas in bats and natural infection dynamics during seasonal reproduction
title_sort synchronized shift of oral, faecal and urinary microbiotas in bats and natural infection dynamics during seasonal reproduction
topic Biology (Whole Organism)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990816/
https://www.ncbi.nlm.nih.gov/pubmed/29892443
http://dx.doi.org/10.1098/rsos.180041
work_keys_str_mv AT dietrichmuriel synchronizedshiftoforalfaecalandurinarymicrobiotasinbatsandnaturalinfectiondynamicsduringseasonalreproduction
AT kearneyteresa synchronizedshiftoforalfaecalandurinarymicrobiotasinbatsandnaturalinfectiondynamicsduringseasonalreproduction
AT seamarkernestcj synchronizedshiftoforalfaecalandurinarymicrobiotasinbatsandnaturalinfectiondynamicsduringseasonalreproduction
AT paweskajanuszt synchronizedshiftoforalfaecalandurinarymicrobiotasinbatsandnaturalinfectiondynamicsduringseasonalreproduction
AT markotterwanda synchronizedshiftoforalfaecalandurinarymicrobiotasinbatsandnaturalinfectiondynamicsduringseasonalreproduction