Cao Yalei, Wang Haojie, Jin Zirun, Hang Jing, Jiang Hui, Wu Huajun, Zhang Zhe
Department of Urology, Peking University Third Hospital, Beijing 100191, China.
Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
J Clin Med. 2023 Jan 16;12(2):701. doi: 10.3390/jcm12020701.
(1) Background: Non-obstructive azoospermia (NOA) is a complex multifactorial disease and the causes of most NOA cases remain unknown. (2) Methods: Here, we performed comprehensive clinical analyses and gut microbial profiling using shotgun metagenomic sequencing in patients with NOA and control individuals. (3) Results: The gut microbial alpha and beta diversity significantly differed between patients with NOA and controls. Several microbial strains, including and , were significantly more abundant in the NOA group, whereas and sp. were enriched in the control group. Moreover, functional pathway analysis suggested that the altered microbiota in NOA suppressed the carbohydrate metabolism pathway, while amino acid metabolism and methane metabolism pathways were enhanced. We observed that the differential microbial species, such as , had a strong correlation with clinical parameters, including age, body mass index, testosterone, and follicle-stimulating hormone. Communication and interplay among microbial genera were significantly increased in NOA than in the control group. (4) Conclusions: Altered microbial composition and functional pathways in the NOA group were revealed, which highlight the utility of gut microbiota in understanding microbiota-related pathogenesis of NOA and might be helpful to the clinical management of NOA.
(1) 背景:非梗阻性无精子症(NOA)是一种复杂的多因素疾病,大多数NOA病例的病因仍不清楚。(2) 方法:在此,我们对NOA患者和对照个体进行了全面的临床分析,并使用鸟枪法宏基因组测序对肠道微生物进行了分析。(3) 结果:NOA患者和对照个体之间的肠道微生物α和β多样性存在显著差异。包括[具体菌株1]和[具体菌株2]在内的几种微生物菌株在NOA组中显著更为丰富,而[具体菌株3]和[具体菌株4]在对照组中更为富集。此外,功能通路分析表明,NOA中改变的微生物群抑制了碳水化合物代谢通路,而氨基酸代谢和甲烷代谢通路增强。我们观察到,诸如[具体微生物物种]等差异微生物物种与年龄、体重指数、睾酮和促卵泡激素等临床参数具有很强的相关性。与对照组相比,NOA中微生物属之间的交流和相互作用显著增加。(4) 结论:揭示了NOA组中微生物组成和功能通路的改变,这突出了肠道微生物群在理解NOA的微生物群相关发病机制中的作用,可能有助于NOA的临床管理。