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Dietary shifts and social interactions drive temporal fluctuations of the gut microbiome from wild redfronted lemurs

Animals living in highly seasonal environments adapt their diets accordingly to changes in food availability. The gut microbiome as an active participant in the metabolization of the host’s diet should adapt and change with temporal diet fluctuations, but dietary shifts can be short-term and, hence,...

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Autores principales: Murillo, Tatiana, Schneider, Dominik, Fichtel, Claudia, Daniel, Rolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723586/
https://www.ncbi.nlm.nih.gov/pubmed/37938637
http://dx.doi.org/10.1038/s43705-021-00086-0
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author Murillo, Tatiana
Schneider, Dominik
Fichtel, Claudia
Daniel, Rolf
author_facet Murillo, Tatiana
Schneider, Dominik
Fichtel, Claudia
Daniel, Rolf
author_sort Murillo, Tatiana
collection PubMed
description Animals living in highly seasonal environments adapt their diets accordingly to changes in food availability. The gut microbiome as an active participant in the metabolization of the host’s diet should adapt and change with temporal diet fluctuations, but dietary shifts can be short-term and, hence, difficult to detect in cross-sectional studies. Therefore, we performed a longitudinal study combining repeated sampling of fecal samples with observations of feeding behavior in wild redfronted lemurs. We amplified taxonomical marker genes for assessing the bacteria, archaea, protozoa, helminths, and fungi, as well as the active bacterial community inhabiting their gut. We found that the most abundant protozoans were Trichostomatia and Trichomonadida, and the most abundant helminths were Chromadorea. We detected known members of the gut mycobiome from humans but in low abundances. The archaeal community is composed only of members of Methanomethylophilaceae. The predominant phyla in the entire bacterial community were Bacteroidota and Firmicutes while the most abundant genera harbor so far unknown bacteria. Temporal fluctuations at the entire community level were driven by consumption of fruits and flowers, and affiliative interactions. Changes in alpha diversity correlated only with the consumption of flowers and leaves. The composition of the entire and active bacterial community was not significantly different, but the most abundant taxa differed. Our study revealed that monthly changes in the bacterial community composition were linked to fruit and flower consumption and affiliative interactions. Thus, portraying the importance of longitudinal studies for understanding the adaptations and alterations of the gut microbiome to temporal fluctuations.
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spelling pubmed-97235862023-01-04 Dietary shifts and social interactions drive temporal fluctuations of the gut microbiome from wild redfronted lemurs Murillo, Tatiana Schneider, Dominik Fichtel, Claudia Daniel, Rolf ISME Commun Article Animals living in highly seasonal environments adapt their diets accordingly to changes in food availability. The gut microbiome as an active participant in the metabolization of the host’s diet should adapt and change with temporal diet fluctuations, but dietary shifts can be short-term and, hence, difficult to detect in cross-sectional studies. Therefore, we performed a longitudinal study combining repeated sampling of fecal samples with observations of feeding behavior in wild redfronted lemurs. We amplified taxonomical marker genes for assessing the bacteria, archaea, protozoa, helminths, and fungi, as well as the active bacterial community inhabiting their gut. We found that the most abundant protozoans were Trichostomatia and Trichomonadida, and the most abundant helminths were Chromadorea. We detected known members of the gut mycobiome from humans but in low abundances. The archaeal community is composed only of members of Methanomethylophilaceae. The predominant phyla in the entire bacterial community were Bacteroidota and Firmicutes while the most abundant genera harbor so far unknown bacteria. Temporal fluctuations at the entire community level were driven by consumption of fruits and flowers, and affiliative interactions. Changes in alpha diversity correlated only with the consumption of flowers and leaves. The composition of the entire and active bacterial community was not significantly different, but the most abundant taxa differed. Our study revealed that monthly changes in the bacterial community composition were linked to fruit and flower consumption and affiliative interactions. Thus, portraying the importance of longitudinal studies for understanding the adaptations and alterations of the gut microbiome to temporal fluctuations. Nature Publishing Group UK 2022-01-19 /pmc/articles/PMC9723586/ /pubmed/37938637 http://dx.doi.org/10.1038/s43705-021-00086-0 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Murillo, Tatiana
Schneider, Dominik
Fichtel, Claudia
Daniel, Rolf
Dietary shifts and social interactions drive temporal fluctuations of the gut microbiome from wild redfronted lemurs
title Dietary shifts and social interactions drive temporal fluctuations of the gut microbiome from wild redfronted lemurs
title_full Dietary shifts and social interactions drive temporal fluctuations of the gut microbiome from wild redfronted lemurs
title_fullStr Dietary shifts and social interactions drive temporal fluctuations of the gut microbiome from wild redfronted lemurs
title_full_unstemmed Dietary shifts and social interactions drive temporal fluctuations of the gut microbiome from wild redfronted lemurs
title_short Dietary shifts and social interactions drive temporal fluctuations of the gut microbiome from wild redfronted lemurs
title_sort dietary shifts and social interactions drive temporal fluctuations of the gut microbiome from wild redfronted lemurs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723586/
https://www.ncbi.nlm.nih.gov/pubmed/37938637
http://dx.doi.org/10.1038/s43705-021-00086-0
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