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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society Publishing
2018
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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 |
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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 |
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