Impairment of spermatogenesis and sperm motility by the high-fat diet-induced dysbiosis of gut microbes

Author:

Ding NingORCID,Zhang Xin,Zhang Xue Di,Jing Jun,Liu Shan Shan,Mu Yun Ping,Peng Li LiORCID,Yan Yun Jing,Xiao Geng Miao,Bi Xin Yun,Chen Hao,Li Fang Hong,Yao Bing,Zhao Allan Z

Abstract

ObjectiveHigh-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.DesignFaecal 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.ResultsTransplantation 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.ConclusionWe 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 numberNCT03634644.

Funder

the Guangdong Innovative Research Team Program

the Startup R&D Funding of Guangdong University of Technology

the National Key Research and Development Program of China

National Natural Science Foundation of China

the National Program on Key Basic Research Project of China

National Key R&D Program of China

China Postdoctoral Science Foundation

Publisher

BMJ

Subject

Gastroenterology

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