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The gastrointestinal microbiome in dairy cattle is constrained by the deterministic driver of the region and the modified effect of diet

BACKGROUND: Dairy cattle (Bos taurus), especially Holstein cows, which are the highest-producing dairy animals and are widely bred to provide milk products to humans, rely critically on their associated gastrointestinal tract (GIT) microbiota to digest plant feed. However, the region-specific taxono...

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Autores principales: Lin, Limei, Lai, Zheng, Zhang, Jiyou, Zhu, Weiyun, Mao, Shengyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9863278/
https://www.ncbi.nlm.nih.gov/pubmed/36670455
http://dx.doi.org/10.1186/s40168-022-01453-2
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author Lin, Limei
Lai, Zheng
Zhang, Jiyou
Zhu, Weiyun
Mao, Shengyong
author_facet Lin, Limei
Lai, Zheng
Zhang, Jiyou
Zhu, Weiyun
Mao, Shengyong
author_sort Lin, Limei
collection PubMed
description BACKGROUND: Dairy cattle (Bos taurus), especially Holstein cows, which are the highest-producing dairy animals and are widely bred to provide milk products to humans, rely critically on their associated gastrointestinal tract (GIT) microbiota to digest plant feed. However, the region-specific taxonomic composition and function of the GIT microbiome in dairy cattle and the mechanistic basis for the diet-induced effects remain to be elucidated.  RESULTS: We collected 120 digesta samples from 10 GIT regions of 12 Holstein cows fed forage- and grain-based diets and characterized their GIT microbiome via functional shotgun metagenomics and the resolution of metagenome-assembled genomes. Our results demonstrated that the GIT microbiome was mainly partitioned into three distinct clusters, four-chambered stomach, small intestine, and large intestine. Moreover, we found that the four-chambered stomach microbiome with the highest diversity had a strong ability to degrade recalcitrant polysaccharide substrates, underpinned by the prevalence of potential cellulosome-­producing and plant-derived polysaccharide utilization loci-encoding consortia. In contrast, the post-gastric intestinal microbiome orchestrated alternative fermentation pathways to adapt to nutrient availability and energy acquisition. Diet shifts selectively modified the metabolic cascades of the microbiome in specific GIT regions, evidenced by the loss of fiber-degrading taxa and increased hydrogen sinks in propionate after grain introduction. CONCLUSIONS: Our findings provide new insights into GIT microbial organization and function in dairy cattle by GIT regions and diet regimes, which offers clues for improving animal production and health in the future. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01453-2.
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spelling pubmed-98632782023-01-22 The gastrointestinal microbiome in dairy cattle is constrained by the deterministic driver of the region and the modified effect of diet Lin, Limei Lai, Zheng Zhang, Jiyou Zhu, Weiyun Mao, Shengyong Microbiome Research BACKGROUND: Dairy cattle (Bos taurus), especially Holstein cows, which are the highest-producing dairy animals and are widely bred to provide milk products to humans, rely critically on their associated gastrointestinal tract (GIT) microbiota to digest plant feed. However, the region-specific taxonomic composition and function of the GIT microbiome in dairy cattle and the mechanistic basis for the diet-induced effects remain to be elucidated.  RESULTS: We collected 120 digesta samples from 10 GIT regions of 12 Holstein cows fed forage- and grain-based diets and characterized their GIT microbiome via functional shotgun metagenomics and the resolution of metagenome-assembled genomes. Our results demonstrated that the GIT microbiome was mainly partitioned into three distinct clusters, four-chambered stomach, small intestine, and large intestine. Moreover, we found that the four-chambered stomach microbiome with the highest diversity had a strong ability to degrade recalcitrant polysaccharide substrates, underpinned by the prevalence of potential cellulosome-­producing and plant-derived polysaccharide utilization loci-encoding consortia. In contrast, the post-gastric intestinal microbiome orchestrated alternative fermentation pathways to adapt to nutrient availability and energy acquisition. Diet shifts selectively modified the metabolic cascades of the microbiome in specific GIT regions, evidenced by the loss of fiber-degrading taxa and increased hydrogen sinks in propionate after grain introduction. CONCLUSIONS: Our findings provide new insights into GIT microbial organization and function in dairy cattle by GIT regions and diet regimes, which offers clues for improving animal production and health in the future. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01453-2. BioMed Central 2023-01-20 /pmc/articles/PMC9863278/ /pubmed/36670455 http://dx.doi.org/10.1186/s40168-022-01453-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Lin, Limei
Lai, Zheng
Zhang, Jiyou
Zhu, Weiyun
Mao, Shengyong
The gastrointestinal microbiome in dairy cattle is constrained by the deterministic driver of the region and the modified effect of diet
title The gastrointestinal microbiome in dairy cattle is constrained by the deterministic driver of the region and the modified effect of diet
title_full The gastrointestinal microbiome in dairy cattle is constrained by the deterministic driver of the region and the modified effect of diet
title_fullStr The gastrointestinal microbiome in dairy cattle is constrained by the deterministic driver of the region and the modified effect of diet
title_full_unstemmed The gastrointestinal microbiome in dairy cattle is constrained by the deterministic driver of the region and the modified effect of diet
title_short The gastrointestinal microbiome in dairy cattle is constrained by the deterministic driver of the region and the modified effect of diet
title_sort gastrointestinal microbiome in dairy cattle is constrained by the deterministic driver of the region and the modified effect of diet
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9863278/
https://www.ncbi.nlm.nih.gov/pubmed/36670455
http://dx.doi.org/10.1186/s40168-022-01453-2
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