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Assessing the drivers of gut microbiome composition in wild redfronted lemurs via longitudinal metacommunity analysis

The gut microbiome influences host’s immunity, development, and metabolism and participates in the gut–brain axis, thus impacting the health of the host. It is a dynamic community varying between individuals and within individuals at different time points. Hence, determining the factors causing this...

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Autores principales: Murillo, Tatiana, Schneider, Dominik, Heistermann, Michael, Daniel, Rolf, Fichtel, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744850/
https://www.ncbi.nlm.nih.gov/pubmed/36509795
http://dx.doi.org/10.1038/s41598-022-25733-x
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author Murillo, Tatiana
Schneider, Dominik
Heistermann, Michael
Daniel, Rolf
Fichtel, Claudia
author_facet Murillo, Tatiana
Schneider, Dominik
Heistermann, Michael
Daniel, Rolf
Fichtel, Claudia
author_sort Murillo, Tatiana
collection PubMed
description The gut microbiome influences host’s immunity, development, and metabolism and participates in the gut–brain axis, thus impacting the health of the host. It is a dynamic community varying between individuals and within individuals at different time points. Hence, determining the factors causing this variability may elucidate their impact on host’s health. However, understanding the drivers of variation has proven difficult particularly as multiple interactions occur simultaneously in the gut microbiome. We investigated the factors shaping the gut microbiome by applying the metacommunity concept where the gut microbiome is considered as a microbial community shaped by the interactions within the community, with the host and microbial communities outside the host, this through a longitudinal study in a wild primate. Focal behavioral data were collected for 1 year in four groups of redfronted lemurs to determine individual social and feeding behaviors. In addition, regular fecal samples were collected to assess bacteria, protozoa, and helminths through marker gene analysis and to measure fecal glucocorticoid metabolite (fGCM) concentrations to investigate the impact of physiological stress on the gut microbiome. Higher consumption of leaves and elevated fGCM concentrations correlated with higher alpha diversity, which also differed among groups. The major drivers of variation in beta diversity were group membership, precipitation and fGCM concentrations. We found positive and negative associations between bacterial genera and almost all studied factors. Correlations between bacterial indicator networks and social networks indicate transmission of bacteria between interacting individuals. We detected that processes occurring inside the gut environment are shaping the gut microbiome. Host associated factors such as, HPA axis, dietary changes, and fluctuations in water availability had a greater impact than interactions within the microbial community. The interplay with microbial communities outside the host also shape the gut microbiome through the exchange of bacteria through social relationships between individuals and the acquisition of microorganisms from environmental water sources.
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spelling pubmed-97448502022-12-14 Assessing the drivers of gut microbiome composition in wild redfronted lemurs via longitudinal metacommunity analysis Murillo, Tatiana Schneider, Dominik Heistermann, Michael Daniel, Rolf Fichtel, Claudia Sci Rep Article The gut microbiome influences host’s immunity, development, and metabolism and participates in the gut–brain axis, thus impacting the health of the host. It is a dynamic community varying between individuals and within individuals at different time points. Hence, determining the factors causing this variability may elucidate their impact on host’s health. However, understanding the drivers of variation has proven difficult particularly as multiple interactions occur simultaneously in the gut microbiome. We investigated the factors shaping the gut microbiome by applying the metacommunity concept where the gut microbiome is considered as a microbial community shaped by the interactions within the community, with the host and microbial communities outside the host, this through a longitudinal study in a wild primate. Focal behavioral data were collected for 1 year in four groups of redfronted lemurs to determine individual social and feeding behaviors. In addition, regular fecal samples were collected to assess bacteria, protozoa, and helminths through marker gene analysis and to measure fecal glucocorticoid metabolite (fGCM) concentrations to investigate the impact of physiological stress on the gut microbiome. Higher consumption of leaves and elevated fGCM concentrations correlated with higher alpha diversity, which also differed among groups. The major drivers of variation in beta diversity were group membership, precipitation and fGCM concentrations. We found positive and negative associations between bacterial genera and almost all studied factors. Correlations between bacterial indicator networks and social networks indicate transmission of bacteria between interacting individuals. We detected that processes occurring inside the gut environment are shaping the gut microbiome. Host associated factors such as, HPA axis, dietary changes, and fluctuations in water availability had a greater impact than interactions within the microbial community. The interplay with microbial communities outside the host also shape the gut microbiome through the exchange of bacteria through social relationships between individuals and the acquisition of microorganisms from environmental water sources. Nature Publishing Group UK 2022-12-12 /pmc/articles/PMC9744850/ /pubmed/36509795 http://dx.doi.org/10.1038/s41598-022-25733-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Murillo, Tatiana
Schneider, Dominik
Heistermann, Michael
Daniel, Rolf
Fichtel, Claudia
Assessing the drivers of gut microbiome composition in wild redfronted lemurs via longitudinal metacommunity analysis
title Assessing the drivers of gut microbiome composition in wild redfronted lemurs via longitudinal metacommunity analysis
title_full Assessing the drivers of gut microbiome composition in wild redfronted lemurs via longitudinal metacommunity analysis
title_fullStr Assessing the drivers of gut microbiome composition in wild redfronted lemurs via longitudinal metacommunity analysis
title_full_unstemmed Assessing the drivers of gut microbiome composition in wild redfronted lemurs via longitudinal metacommunity analysis
title_short Assessing the drivers of gut microbiome composition in wild redfronted lemurs via longitudinal metacommunity analysis
title_sort assessing the drivers of gut microbiome composition in wild redfronted lemurs via longitudinal metacommunity analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744850/
https://www.ncbi.nlm.nih.gov/pubmed/36509795
http://dx.doi.org/10.1038/s41598-022-25733-x
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