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The Relationship Between Gut Microbiome and Bile Acids in Primates With Diverse Diets

Primates have evolved a variety of feeding habits and intestinal physiological structure. Gut microbiome act as metabolic organs in many biological processes and play a vital role in adaptation to dietary niches. Gut microbiome also convert primary bile acids (BAs) to secondary. BAs profile and gut...

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Autores principales: Li, Xinyue, Wang, Xiaochen, Wang, Ziming, Zhang, Mingyi, Wang, Song, Xiang, Zuofu, Pan, Huijuan, Li, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130754/
https://www.ncbi.nlm.nih.gov/pubmed/35633689
http://dx.doi.org/10.3389/fmicb.2022.899102
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author Li, Xinyue
Wang, Xiaochen
Wang, Ziming
Zhang, Mingyi
Wang, Song
Xiang, Zuofu
Pan, Huijuan
Li, Ming
author_facet Li, Xinyue
Wang, Xiaochen
Wang, Ziming
Zhang, Mingyi
Wang, Song
Xiang, Zuofu
Pan, Huijuan
Li, Ming
author_sort Li, Xinyue
collection PubMed
description Primates have evolved a variety of feeding habits and intestinal physiological structure. Gut microbiome act as metabolic organs in many biological processes and play a vital role in adaptation to dietary niches. Gut microbiome also convert primary bile acids (BAs) to secondary. BAs profile and gut microbiome are together influenced by diets and play a significant role in nutrient absorption. The regulation between gut microbiome and BAs metabolism is bidirectional although the relationship in primates consuming diverse diets is still unclear. Here, we investigated gut microbiome structures, fecal BAs profile, and their relationship in primates preferring three distinct diets. We found that gut microbiome communities are well differentiated among dietary groups. Folivorous primates had higher Firmicutes abundance and lower Prevotella to Bacaeroides ratios, possibly related to fiber consumption. Frugivorous primates are colonized predominantly by Prevotella and Bacteroides, pointing to an increased adaptation to high-sugar and simple carbohydrate diets. Likewise, BA profiles differ according to diet in a manner predictable from the known effects of BAs on metabolism. Folivorous primates have high conjugated bile acid levels and low unconjugated to conjugated BA ratios, consistent with their fiber-rich leaf-eating diet. Much of the differentiation in secondary and unconjugated BAs is associated with microbiome composition shifts and individual bile acid concentrations are correlated with the abundance of distinct bacterial taxonomic groups. Omnivores have higher concentrations of secondary BAs, mainly lithocholic acid (LCA). These levels are significantly positively correlated with the presence of Clostrida species, showing that the digestion requirements of omnivores are different from plant-eating primates. In conclusion, gut microbiome and BAs can respond to changes in diet and are associated with nutrient component consumption in each diet primate group. Our study is the first to demonstrate BA profile differentiation among primates preferring diverse diets. BAs thus appear to work with gut microbiome to help primates adapt to their diet.
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spelling pubmed-91307542022-05-26 The Relationship Between Gut Microbiome and Bile Acids in Primates With Diverse Diets Li, Xinyue Wang, Xiaochen Wang, Ziming Zhang, Mingyi Wang, Song Xiang, Zuofu Pan, Huijuan Li, Ming Front Microbiol Microbiology Primates have evolved a variety of feeding habits and intestinal physiological structure. Gut microbiome act as metabolic organs in many biological processes and play a vital role in adaptation to dietary niches. Gut microbiome also convert primary bile acids (BAs) to secondary. BAs profile and gut microbiome are together influenced by diets and play a significant role in nutrient absorption. The regulation between gut microbiome and BAs metabolism is bidirectional although the relationship in primates consuming diverse diets is still unclear. Here, we investigated gut microbiome structures, fecal BAs profile, and their relationship in primates preferring three distinct diets. We found that gut microbiome communities are well differentiated among dietary groups. Folivorous primates had higher Firmicutes abundance and lower Prevotella to Bacaeroides ratios, possibly related to fiber consumption. Frugivorous primates are colonized predominantly by Prevotella and Bacteroides, pointing to an increased adaptation to high-sugar and simple carbohydrate diets. Likewise, BA profiles differ according to diet in a manner predictable from the known effects of BAs on metabolism. Folivorous primates have high conjugated bile acid levels and low unconjugated to conjugated BA ratios, consistent with their fiber-rich leaf-eating diet. Much of the differentiation in secondary and unconjugated BAs is associated with microbiome composition shifts and individual bile acid concentrations are correlated with the abundance of distinct bacterial taxonomic groups. Omnivores have higher concentrations of secondary BAs, mainly lithocholic acid (LCA). These levels are significantly positively correlated with the presence of Clostrida species, showing that the digestion requirements of omnivores are different from plant-eating primates. In conclusion, gut microbiome and BAs can respond to changes in diet and are associated with nutrient component consumption in each diet primate group. Our study is the first to demonstrate BA profile differentiation among primates preferring diverse diets. BAs thus appear to work with gut microbiome to help primates adapt to their diet. Frontiers Media S.A. 2022-05-11 /pmc/articles/PMC9130754/ /pubmed/35633689 http://dx.doi.org/10.3389/fmicb.2022.899102 Text en Copyright © 2022 Li, Wang, Wang, Zhang, Wang, Xiang, Pan and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Li, Xinyue
Wang, Xiaochen
Wang, Ziming
Zhang, Mingyi
Wang, Song
Xiang, Zuofu
Pan, Huijuan
Li, Ming
The Relationship Between Gut Microbiome and Bile Acids in Primates With Diverse Diets
title The Relationship Between Gut Microbiome and Bile Acids in Primates With Diverse Diets
title_full The Relationship Between Gut Microbiome and Bile Acids in Primates With Diverse Diets
title_fullStr The Relationship Between Gut Microbiome and Bile Acids in Primates With Diverse Diets
title_full_unstemmed The Relationship Between Gut Microbiome and Bile Acids in Primates With Diverse Diets
title_short The Relationship Between Gut Microbiome and Bile Acids in Primates With Diverse Diets
title_sort relationship between gut microbiome and bile acids in primates with diverse diets
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130754/
https://www.ncbi.nlm.nih.gov/pubmed/35633689
http://dx.doi.org/10.3389/fmicb.2022.899102
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