无精子症患者精浆微生态动态变化及核心代谢物十六酰胺的机理影响

IF 23.7 Q1 MICROBIOLOGY
iMeta Pub Date : 2024-01-25 DOI:10.1002/imt2.166
Baoquan Han, Yongyong Wang, Wei Ge, Junjie Wang, Shuai Yu, Jiamao Yan, Lei Hua, Xiaoyuan Zhang, Zihui Yan, Lu Wang, Jinxin Zhao, Cong Huang, Bo Yang, Yan Wang, Qian Ma, Yong Zhao, Hui Jiang, Yunqi Zhang, Shaolin Liang, Jianjuan Zhao, Zhongyi Sun, Wei Shen, Yaoting Gui
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引用次数: 0

摘要

无精子症(AZS)是导致男性不育的一个普遍原因,其特点是精子活力大幅下降。近年来,大规模的研究探索了男性生殖系统微生态之间的相互作用及其对生殖健康的影响。然而,精液微生态与男性不育发病机制之间的直接联系仍无定论。本研究采用 16S rDNA 测序和多组学分析方法,对 AZS 患者的精液微生物群落和代谢物进行了全面调查。患者被分为四个不同的组别:正常组、轻度 AZS 组(AZS-I)、中度 AZS 组(AZS-II)和重度 AZS 组(AZS-III)。微生物组差异丰度分析显示,这些组别精浆中的微生物组成和代谢物谱存在显著差异。随后,患者被分为对照组(正常和 AZS-I)和 AZS 组(AZS-II 和 AZS-III)。相关性和交叉对比分析确定了不同的微生物属和代谢物。值得注意的是,AZS 组的精浆中假单胞菌、沙雷氏菌和甲基分支杆菌等细菌属的数量减少,这与核心差异代谢物(十六酰胺)呈正相关。相反,AZS 组显示 Uruburuella、弧菌和假交替单胞菌等细菌属的数量增加,与核心差异代谢物(十六酰胺)呈负相关。体外和体内实验证实,十六酰胺能显著增强精子活力。利用预测性代谢物靶基因分析和单细胞转录组测序,我们分析了候选靶基因 PAOX 和 CA2 的基因表达。蛋白免疫印迹技术验证了十六烷酰胺处理后精子样本中 PAOX 和 CA2 蛋白水平的上调,从而增强了精子的活力。总之,这项研究发现精浆中的六种微生物属与代谢物十六酰胺(与 AZS 有关)的含量之间存在显著相关性。十六酰胺能显著增强精子活力,这表明它有可能被纳入治疗AZS的临床策略中,为诊断和治疗的进步提供了一个基础框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Changes in seminal plasma microecological dynamics and the mechanistic impact of core metabolite hexadecanamide in asthenozoospermia patients

Changes in seminal plasma microecological dynamics and the mechanistic impact of core metabolite hexadecanamide in asthenozoospermia patients

Asthenozoospermia (AZS) is a prevalent contributor to male infertility, characterized by a substantial decline in sperm motility. In recent years, large-scale studies have explored the interplay between the male reproductive system's microecology and its implications for reproductive health. Nevertheless, the direct association between seminal microecology and male infertility pathogenesis remains inconclusive. This study used 16S rDNA sequencing and multi-omics analysis to conduct a comprehensive investigation of the seminal microbial community and metabolites in AZS patients. Patients were categorized into four distinct groups: Normal, mild AZS (AZS-I), moderate AZS (AZS-II), and severe AZS (AZS-III). Microbiome differential abundance analysis revealed significant differences in microbial composition and metabolite profiles within the seminal plasma of these groups. Subsequently, patients were classified into a control group (Normal and AZS-I) and an AZS group (AZS-II and AZS-III). Correlation and cross-reference analyses identified distinct microbial genera and metabolites. Notably, the AZS group exhibited a reduced abundance of bacterial genera such as Pseudomonas, Serratia, and Methylobacterium-Methylorubrum in seminal plasma, positively correlating with core differential metabolite (hexadecanamide). Conversely, the AZS group displayed an increased abundance of bacterial genera such as Uruburuella, Vibrio, and Pseudoalteromonas, with a negative correlation with core differential metabolite (hexadecanamide). In vitro and in vivo experiments validated that hexadecanamide significantly enhanced sperm motility. Using predictive metabolite-targeting gene analysis and single-cell transcriptome sequencing, we profiled the gene expression of candidate target genes PAOX and CA2. Protein immunoblotting techniques validated the upregulation protein levels of PAOX and CA2 in sperm samples after hexadecanamide treatment, enhancing sperm motility. In conclusion, this study uncovered a significant correlation between six microbial genera in seminal plasma and the content of the metabolite hexadecanamide, which is related to AZS. Hexadecanamide notably enhances sperm motility, suggesting its potential integration into clinical strategies for managing AZS, providing a foundational framework for diagnostic and therapeutic advancements.

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