Authors
Longjie Gu, Yinwei Chen, Lei Jin, Yi Liu
Published in
Translational andrology and urology. Volume 15. Issue 9. Pages 350. Sep 30, 2026. Epub Aug 14, 2026.
Abstract
Infertility affects approximately 8-12% of couples worldwide, with male factors accounting for nearly half of all cases. The gut microbiota is widely recognized as a key regulator of host physiology, yet its specific role in male reproductive health remains to be elucidated. This narrative review synthesizes current evidence on the "gut microbiota-testis axis" and provides a critical evaluation of the strength of evidence derived from different study designs.
We conducted a comprehensive literature search in PubMed/MEDLINE up to May 2026 using Boolean search strategies combining terms related to the gut microbiota (e.g., "Gastrointestinal Microbiome", "gut microbiota", "gut microbiome") with terms related to male reproduction (e.g., "Semen Analysis", "Spermatozoa", "Infertility, Male", "semen quality", "sperm quality"). Separate search strategies were developed for human and animal studies. Literature screening and data extraction were performed independently by two reviewers according to predefined inclusion and exclusion criteria.
Although human studies remain preliminary, several genera, including Anaerotruncus, Bacteroides, and Faecalibacterium prausnitzii, have been reproducibly associated with semen quality, with microbial metabolites such as butyrate, trimethylamine-N-oxide (TMAO), and succinate potentially serving as important mediators. At the mechanistic level, microbiota-derived metabolic and inflammatory signals act on Leydig cells, Sertoli cells, and germ cells, thereby influencing testosterone synthesis and spermatogenesis. Fecal microbiota transplantation (FMT) experiments in animal models have provided direct evidence for these causal links.
The gut microbiota-testis axis has emerged as a critical physiological pathway linking the microbiome to male reproductive function. This review provides an evidence-based framework for understanding this axis and highlights key knowledge gaps that must be addressed. Future research should integrate large-scale longitudinal cohorts, mechanistic exploration, and randomized controlled trials with fertility outcomes as primary endpoints to advance the field from descriptive correlations toward mechanism-driven clinical translation.
PMID:
42866850
Bibliographic data and abstract were imported from PubMed on 14 Oct 2026.
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