生物
精子
失调
精子发生
精子活力
附睾
男科
拟杆菌
运动性
肠道菌群
移植
普雷沃菌属
男性不育
免疫学
内科学
内分泌学
不育
遗传学
医学
细菌
怀孕
作者
Ning Ding,Xin Zhang,Xue Di Zhang,Jun Jing,Shan Shan Liu,Yun Mu,Li Li Peng,Yun Jing Yan,Geng Miao Xiao,Xinyun Bi,Hao Chen,Fang Hong Li,Bing Yao,Allan Z. Zhao
出处
期刊:Gut
[BMJ]
日期:2020-01-02
卷期号:69 (9): 1608-1619
被引量:191
标识
DOI:10.1136/gutjnl-2019-319127
摘要
Objective High-fat diet (HFD)-induced metabolic disorders can lead to impaired sperm production. We aim to investigate if HFD-induced gut microbiota dysbiosis can functionally influence spermatogenesis and sperm motility. Design Faecal microbes derived from the HFD-fed or normal diet (ND)-fed male mice were transplanted to the mice maintained on ND. The gut microbes, sperm count and motility were analysed. Human faecal/semen/blood samples were collected to assess microbiota, sperm quality and endotoxin. Results Transplantation of the HFD gut microbes into the ND-maintained (HFD-FMT) mice resulted in a significant decrease in spermatogenesis and sperm motility, whereas similar transplantation with the microbes from the ND-fed mice failed to do so. Analysis of the microbiota showed a profound increase in genus Bacteroides and Prevotella , both of which likely contributed to the metabolic endotoxaemia in the HFD-FMT mice. Interestingly, the gut microbes from clinical subjects revealed a strong negative correlation between the abundance of Bacteroides-Prevotella and sperm motility, and a positive correlation between blood endotoxin and Bacteroides abundance. Transplantation with HFD microbes also led to intestinal infiltration of T cells and macrophages as well as a significant increase of pro-inflammatory cytokines in the epididymis, suggesting that epididymal inflammation have likely contributed to the impairment of sperm motility. RNA-sequencing revealed significant reduction in the expression of those genes involved in gamete meiosis and testicular mitochondrial functions in the HFD-FMT mice. Conclusion We revealed an intimate linkage between HFD-induced microbiota dysbiosis and defect in spermatogenesis with elevated endotoxin, dysregulation of testicular gene expression and localised epididymal inflammation as the potential causes. Trial registration number NCT03634644 .
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