{"title":"从瘤胃微生物组深入了解胆汁酸代谢和宿主代谢调节。","authors":"Boyan Zhang, Xianzhe Jiang, Yue Yu, Yimeng Cui, Wei Wang, Hailing Luo, Sokratis Stergiadis, Bing Wang","doi":"10.1093/ismejo/wrae098","DOIUrl":null,"url":null,"abstract":"<p><p>Gut microbes play a crucial role in transforming primary bile acids (BAs) into secondary forms, which influence systemic metabolic processes. The rumen, a distinctive and critical microbial habitat in ruminants, boasts a diverse array of microbial species with multifaceted metabolic capabilities. There remains a gap in our understanding of BA metabolism within this ecosystem. Herein, through the analysis of 9371 metagenome-assembled genomes and 329 cultured organisms from the rumen, we identified two enzymes integral to BA metabolism: 3-dehydro-bile acid delta4,6-reductase (baiN) and the bile acid:Na + symporter family (BASS). Both in vitro and in vivo experiments were employed by introducing exogenous BAs. 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引用次数: 0
摘要
肠道微生物在将初级胆汁酸(BA)转化为次级形式的过程中发挥着至关重要的作用,而次级形式的胆汁酸会影响全身代谢过程。瘤胃是反刍动物独特而重要的微生物栖息地,拥有多种多样的微生物物种,具有多方面的代谢能力。我们对这一生态系统中 BA 代谢的了解仍然存在差距。在此,我们通过分析 9371 个元基因组组装的基因组和 329 个来自瘤胃的培养生物,确定了两种与 BA 代谢密不可分的酶:3-脱氢胆汁酸 delta4,6 还原酶(baiN)和胆汁酸:Na + 合成酶家族(BASS)。我们通过引入外源 BA 进行了体外和体内实验。我们发现了瘤胃中 BAs 的转化,并发现了一个酶集群,包括 L-ribulose-5-phosphate 3-epimerase 和 dihydroorotate dehydrogenase。该酶簇与之前已知的负责 7α 脱羟基的 BA 诱导操作子不同,它表明一种之前未被认识的途径有可能将原生 BA 转化为次生 BA。此外,我们的体内实验表明,在瘤胃中施用微生物 BA 可调节氨基酸和脂质代谢,核心次生 BA 及其代谢产物对系统的影响尤为突出。我们的研究深入揭示了瘤胃微生物组在 BA 代谢中的作用,揭示了 BA 生物转化的复杂微生物途径及其对宿主代谢途径的影响,包括对葡萄糖、氨基酸和脂质代谢途径的影响。这项研究不仅增进了我们对微生物乙酰胆碱代谢的了解,还强调了其对代谢调节的广泛影响,为改善动物和潜在的人类健康提供了机会。
Rumen microbiome-driven insight into bile acid metabolism and host metabolic regulation.
Gut microbes play a crucial role in transforming primary bile acids (BAs) into secondary forms, which influence systemic metabolic processes. The rumen, a distinctive and critical microbial habitat in ruminants, boasts a diverse array of microbial species with multifaceted metabolic capabilities. There remains a gap in our understanding of BA metabolism within this ecosystem. Herein, through the analysis of 9371 metagenome-assembled genomes and 329 cultured organisms from the rumen, we identified two enzymes integral to BA metabolism: 3-dehydro-bile acid delta4,6-reductase (baiN) and the bile acid:Na + symporter family (BASS). Both in vitro and in vivo experiments were employed by introducing exogenous BAs. We revealed a transformation of BAs in rumen and found an enzyme cluster, including L-ribulose-5-phosphate 3-epimerase and dihydroorotate dehydrogenase. This cluster, distinct from the previously known BA-inducible operon responsible for 7α-dehydroxylation, suggests a previously unrecognized pathway potentially converting primary BAs into secondary BAs. Moreover, our in vivo experiments indicated that microbial BA administration in the rumen can modulate amino acid and lipid metabolism, with systemic impacts underscored by core secondary BAs and their metabolites. Our study provides insights into the rumen microbiome's role in BA metabolism, revealing a complex microbial pathway for BA biotransformation and its subsequent effect on host metabolic pathways, including those for glucose, amino acids, and lipids. This research not only advances our understanding of microbial BA metabolism but also underscores its wider implications for metabolic regulation, offering opportunities for improving animal and potentially human health.
期刊介绍:
The ISME Journal covers the diverse and integrated areas of microbial ecology. We encourage contributions that represent major advances for the study of microbial ecosystems, communities, and interactions of microorganisms in the environment. Articles in The ISME Journal describe pioneering discoveries of wide appeal that enhance our understanding of functional and mechanistic relationships among microorganisms, their communities, and their habitats.