基因组
肠道菌群
胆汁酸
串扰
细菌
遗传关联
新陈代谢
生物化学
微生物遗传学
生物
微生物代谢
微生物群
化学
遗传学
G蛋白偶联胆汁酸受体
微生物学
肝肠循环
计算生物学
基因
基因型
单核苷酸多态性
物理
光学
作者
Daoming Wang,Marwah Doestzada,Long Qing Chen,Sergio Andreu-Sánchez,Inge C.L. van den Munckhof,Hannah E. Augustijn,Martijn Koehorst,Vincent W. Bloks,Niels P. Riksen,Joost H.W. Rutten,Mihai G. Netea,Alexandra Zhernakova,Folkert Kuipers,J. Fu
出处
期刊:Social Science Research Network
[Social Science Electronic Publishing]
日期:2021-01-01
摘要
Bile acids (BAs) facilitate intestinal fat absorption and act as important signaling molecules in host‒gut microbiota crosstalk. BA-metabolizing pathways in the microbial community have been identified, but how the highly variable genomes of gut bacteria interact with host BA metabolism remains largely unknown. We characterized 8,282 structural variants (SVs) of 55 bacterial species in the gut microbiomes of 1,437 individuals from two Dutch cohorts and performed a systematic association study with 39 plasma BA parameters. Both variations in SV-based continuous genetic makeup and discrete subspecies showed correlations with BA metabolism. Metagenome-wide association analysis identified 797 replicable associations between bacterial SVs and BAs and SV regulators that mediate the effects of lifestyle factors on BA metabolism. This is the first large-scale microbial genetic association analysis to demonstrate the impact of bacterial SVs on human BA composition, and highlights the potential of targeting gut microbiota to regulate BA metabolism through lifestyle intervention.
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