牦牛多组学揭示了微生物组对宿主新陈代谢的重要贡献。

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY npj Biofilms and Microbiomes Pub Date : 2024-11-21 DOI:10.1038/s41522-024-00609-2
Shuli Yang, Jieyi Zheng, Huaming Mao, Paramintra Vinitchaikul, Dongwang Wu, Jianmin Chai
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引用次数: 0

摘要

集约化饲养系统可能会改善牦牛的生产周期。然而,集约化饲养系统如何促进牦牛生长尚不清楚。在此,我们进行了多组学研究,包括瘤胃元基因组学、瘤胃和血浆代谢组学,以对密集饲养系统对牦牛的调控机制进行分类。观察到牦牛的生长性能有所提高。瘤胃元基因组学显示,密集饲养牦牛的梭状芽孢杆菌、甲烷杆菌、螺旋霉菌和厌氧霉菌增加,促进了氨基酸和碳水化合物的代谢。放牧牦牛则有更多的纤维素分解微生物。这些微生物群与 "丙氨酸天冬氨酸和谷氨酸代谢 "和 "丙酮酸代谢 "途径相关。密集饲养增加了甲烷降解功能,而放牧牦牛则有更多与甲烷生产相关的甲基代谢物。这些瘤胃微生物组及其代谢物导致血浆代谢组发生变化,最终影响牦牛的生长。因此,密集饲养系统改变了瘤胃微生物组和代谢以及宿主代谢,从而改善了牦牛的生长。
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Multiomics of yaks reveals significant contribution of microbiome into host metabolism.

An intensive feeding system might improve the production cycle of yaks. However, how intensive feeding system contributes to yak growth is unclear. Here, multi-omics, including rumen metagenomics, rumen and plasma metabolomics, were performed to classify the regulatory mechanisms of intensive feeding system on yaks. Increased growth performance were observed. Rumen metagenomics revealed that Clostridium, Methanobrevibacter, Piromyces and Anaeromyces increased in the intensively fed yaks, contributing to amino acid and carbohydrate metabolism. The grazing yaks had more cellulolytic microbes. These microbiomes were correlated with the pathways of "Alanine aspartate and glutamate metabolism" and "Pyruvate metabolism". Intensive feeding increased methane degradation functions, while grazing yaks had higher methyl metabolites associated with methane production. These rumen microbiomes and their metabolites resulted in changes in plasma metabolome, finally influencing yaks' growth. Thus, an intensive feeding system altered the rumen microbiome and metabolism as well as host metabolism, resulting in improvements of yak growth.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
期刊最新文献
Unlocking gut-liver-brain axis communication metabolites: energy metabolism, immunity and barriers. Viruses in the female lower reproductive tract: a systematic descriptive review of metagenomic investigations. NMFGOT: a multi-view learning framework for the microbiome and metabolome integrative analysis with optimal transport plan. Diversity of bacteria within the human gut and its contribution to the functional unity of holobionts. Multiomics of yaks reveals significant contribution of microbiome into host metabolism.
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