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Genome-centric investigation of bile acid metabolizing microbiota of dairy cows and associated diet-induced functional implications

Although the importance of bile acid (BA)-related microbial strains and enzymes is increasingly recognized for monogastric animals, a lack of knowledge about BA metabolism in dairy cows limits functional applications aimed at the targeted modulation of microbe–host interactions for animal production...

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Autores principales: Lin, Limei, Lai, Zheng, Yang, Huisheng, Zhang, Jiyou, Qi, Weibiao, Xie, Fei, Mao, Shengyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9750977/
https://www.ncbi.nlm.nih.gov/pubmed/36261508
http://dx.doi.org/10.1038/s41396-022-01333-5
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author Lin, Limei
Lai, Zheng
Yang, Huisheng
Zhang, Jiyou
Qi, Weibiao
Xie, Fei
Mao, Shengyong
author_facet Lin, Limei
Lai, Zheng
Yang, Huisheng
Zhang, Jiyou
Qi, Weibiao
Xie, Fei
Mao, Shengyong
author_sort Lin, Limei
collection PubMed
description Although the importance of bile acid (BA)-related microbial strains and enzymes is increasingly recognized for monogastric animals, a lack of knowledge about BA metabolism in dairy cows limits functional applications aimed at the targeted modulation of microbe–host interactions for animal production and health. In the present study, 108 content samples from six intestinal regions of dairy cows were used for shotgun metagenomic sequencing. Overall, 372 high-quality metagenome-assembled genomes (MAGs) were involved in BA deconjugation, oxidation, and dehydroxylation pathways. Furthermore, the BA-metabolizing microbiome predominately occurred in the large intestine, resulting in the accumulation of secondary unconjugated BAs. Comparative genomic analysis revealed that the bile salt hydrolase (BSH)-carrying microbial populations managed with the selective environment of the dairy cow intestine by adopting numerous host mucin glycan-degrading abilities. A sequence similarity network analysis classified 439 BSH homologs into 12 clusters and identified different clusters with diverse evolution, taxonomy, signal peptides, and ecological niches. Our omics data further revealed that the strains of Firmicutes bacterium CAG-110 processed the increased abundance of BSHs from Cluster 1, coinciding with the changes in the colon cholic acid concentration after grain introduction, and were intricately related to intestinal inflammation. This study is the first to use a genome-centric approach and whole intestine-targeted metabolomics to reveal microbial BA metabolism and its diet-induced functional implications in dairy cows. These findings provide insight into the manipulation of intestinal microorganisms for improving host health.
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spelling pubmed-97509772022-12-16 Genome-centric investigation of bile acid metabolizing microbiota of dairy cows and associated diet-induced functional implications Lin, Limei Lai, Zheng Yang, Huisheng Zhang, Jiyou Qi, Weibiao Xie, Fei Mao, Shengyong ISME J Article Although the importance of bile acid (BA)-related microbial strains and enzymes is increasingly recognized for monogastric animals, a lack of knowledge about BA metabolism in dairy cows limits functional applications aimed at the targeted modulation of microbe–host interactions for animal production and health. In the present study, 108 content samples from six intestinal regions of dairy cows were used for shotgun metagenomic sequencing. Overall, 372 high-quality metagenome-assembled genomes (MAGs) were involved in BA deconjugation, oxidation, and dehydroxylation pathways. Furthermore, the BA-metabolizing microbiome predominately occurred in the large intestine, resulting in the accumulation of secondary unconjugated BAs. Comparative genomic analysis revealed that the bile salt hydrolase (BSH)-carrying microbial populations managed with the selective environment of the dairy cow intestine by adopting numerous host mucin glycan-degrading abilities. A sequence similarity network analysis classified 439 BSH homologs into 12 clusters and identified different clusters with diverse evolution, taxonomy, signal peptides, and ecological niches. Our omics data further revealed that the strains of Firmicutes bacterium CAG-110 processed the increased abundance of BSHs from Cluster 1, coinciding with the changes in the colon cholic acid concentration after grain introduction, and were intricately related to intestinal inflammation. This study is the first to use a genome-centric approach and whole intestine-targeted metabolomics to reveal microbial BA metabolism and its diet-induced functional implications in dairy cows. These findings provide insight into the manipulation of intestinal microorganisms for improving host health. Nature Publishing Group UK 2022-10-19 2023-01 /pmc/articles/PMC9750977/ /pubmed/36261508 http://dx.doi.org/10.1038/s41396-022-01333-5 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
Lin, Limei
Lai, Zheng
Yang, Huisheng
Zhang, Jiyou
Qi, Weibiao
Xie, Fei
Mao, Shengyong
Genome-centric investigation of bile acid metabolizing microbiota of dairy cows and associated diet-induced functional implications
title Genome-centric investigation of bile acid metabolizing microbiota of dairy cows and associated diet-induced functional implications
title_full Genome-centric investigation of bile acid metabolizing microbiota of dairy cows and associated diet-induced functional implications
title_fullStr Genome-centric investigation of bile acid metabolizing microbiota of dairy cows and associated diet-induced functional implications
title_full_unstemmed Genome-centric investigation of bile acid metabolizing microbiota of dairy cows and associated diet-induced functional implications
title_short Genome-centric investigation of bile acid metabolizing microbiota of dairy cows and associated diet-induced functional implications
title_sort genome-centric investigation of bile acid metabolizing microbiota of dairy cows and associated diet-induced functional implications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9750977/
https://www.ncbi.nlm.nih.gov/pubmed/36261508
http://dx.doi.org/10.1038/s41396-022-01333-5
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