Characteristics of gut microbiota in patients with asthenozoospermia: a Chinese pilot study

• Published in: BMC microbiology Vol. 24; no. 1; pp. 22 - 14
• Main Authors: Pan, Yang, Wang, Shangren, Liu, Li, Liu, Xiaoqiang
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 15.01.2024; BioMed Central; BMC
• Subjects: 16S rRNA; Asthenozoospermia; Bacteroidetes - genetics; Biosynthesis; China; Chronic illnesses; Complications and side effects; Composition; Digestive system; Diversity indices; Dysbacteriosis; Dysbiosis; Dysbiosis - microbiology; Feces; Gastrointestinal Microbiome - genetics; Gastrointestinal tract; Gene sequencing; Genetic testing; Gut microbiota; Humans; Infertility; Intestinal microflora; Intestine; Lifestyles; Male; Males; Meiosis; Microbiota; Microbiota (Symbiotic organisms); Microorganisms; Motility; Next-generation sequencing; Patients; Pilot Projects; RNA, Ribosomal, 16S - genetics; rRNA; Semen; Semen quality; Software; Sperm; Taxonomy; Testes; China; United States > US; Gut microbiota; 16S rRNA; Semen quality; Dysbiosis; Asthenozoospermia
• DOI: 10.1186/s12866-023-03173-5
• ISSN: 1471-2180

Identification of intestinal flora composition is significant for exploring the cause and pathogenic mechanisms of the gut-testis axis and clarifying the relationship between microbiota and infertility. Our study aimed to examine the alternation in gut microbiota composition and identify potential microbes associated with development of Asthenozoospermia (AS). A total of 580 males were recruited in the outpatient department of Tianjin Medical University General Hospital between September 2021 and March 2023. Sperm parameters were analyzed according to the WHO laboratory manual. The 16 S rRNA gene high-throughput sequencing was performed to detect the gut microbiota composition in fecal samples. LEfSe analysis was used to screen key microbiota. PICRUSt2 software was utilized to predict relevant pathways. After rigorous screening, 60 isolated AS patients (AS group) and 48 healthy men (NC group) were enrolled. No significant differences were observed in demographic characteristics (p > 0.05), semen volume (p = 0.718), sperm concentration (p = 0.109), or total sperm count (p = 0.200). Sperm total motility and progressive motility were significantly decreased in the AS group (p < 0.001). AS patients had significantly lower alpha diversity indices (Chao1, observed OTUs, and PD Whole-tree; p < 0.05). The beta-diversity of gut microbiota in AS patients significantly differed from NC men (PCoA analysis, p = 0.001). Firmicutes, Bacteroidota, Proteobacteria, and Actinobacteria were the primary phyla, with the dominant genera including Bacteroides, Prevotella, and Blautia. Eleven key genera such as Escherichia_Shigella and Prevotellaceae_UCG_001 were identified by LEfSe analysis. Most of these genera were negatively correlated with sperm mobility. Eighty-eight KEGG pathways, including steroid biosynthesis and meiosis, were significantly enriched between the two groups. It appears that gut microbiota composition in AS patients significantly differed from that in healthy men, and the development of AS might be associated with intestinal flora dysbiosis.