Gut microbiota impacts bone via Bacteroides vulgatus-valeric acid-related pathways

Author:

Lin XuORCID,Xiao Hong-MeiORCID,Liu Hui-Min,Lv Wan-QiangORCID,Greenbaum Jonathan,Gong RuiORCID,Zhang Qiang,Chen Yuan-Cheng,Peng ChengORCID,Xu Xue-JuanORCID,Pan Dao-YanORCID,Chen ZhiORCID,Li Zhang-FangORCID,Zhou Rou,Wang Xia-Fang,Lu Jun-Min,Ao Zeng-Xin,Song Yu-Qian,Zhang Yin-Hua,Su Kuan-JuiORCID,Meng Xiang-HeORCID,Ge Chang-LiORCID,Lv Feng-Ye,Luo ZheORCID,Shi Xing-MingORCID,Zhao QiORCID,Guo Bo-YiORCID,Yi Neng-Jun,Shen HuiORCID,Papasian Christopher J.ORCID,Shen JieORCID,Deng Hong-WenORCID

Abstract

AbstractAlthough the gut microbiota has been reported to influence osteoporosis risk, the individual species involved, and underlying mechanisms, remain largely unknown. We performed integrative analyses in a Chinese cohort of peri-/post-menopausal women with metagenomics/targeted metabolomics/whole-genome sequencing to identify novel microbiome-related biomarkers for bone health. Bacteroides vulgatus was found to be negatively associated with bone mineral density (BMD), which was validated in US white people. Serum valeric acid (VA), a microbiota derived metabolite, was positively associated with BMD and causally downregulated by B. vulgatus. Ovariectomized mice fed B. vulgatus demonstrated increased bone resorption and poorer bone micro-structure, while those fed VA demonstrated reduced bone resorption and better bone micro-structure. VA suppressed RELA protein production (pro-inflammatory), and enhanced IL10 mRNA expression (anti-inflammatory), leading to suppressed maturation of osteoclast-like cells and enhanced maturation of osteoblasts in vitro. The findings suggest that B. vulgatus and VA may represent promising targets for osteoporosis prevention/treatment.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

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