The Second School of Clinical Medicine, Southern Medical University, Guangzhou, 510000, China.
Department of Obstetrics and Gynecology, The Sixth Medical Center of PLA General Hospital, No. 6 Fucheng Road, Haidian District, Beijing, 100000, China.
Sci Rep. 2024 May 30;14(1):12455. doi: 10.1038/s41598-024-63382-4.
Chronic endometritis is associated with the imbalance of female reproductive tract microbiota and pathogenic microbial infection. This study aimed to identify the specific changes in the endometrial microbiome in patients with endometritis and to explore how Clostridium tyrobutyricum (C.t) influences the progression of endometritis in mice for further elucidating endometritis pathogenesis. For this purpose, endometrial tissues from 100 participants were collected and divided into positive, weakly positive, and negative groups based on CD138 levels, while endometrial microbiome differences were detected and analyzed using 16S rRNA gene sequencing. Staphylococcus aureus (S. aureus)-induced endometritis mouse model was established, followed by treatment with C.t, and inflammatory response, epithelial barrier, and TLR4/NF-κB pathway were evaluated. Results showed that α- and β-diversity was significantly lower in the positive group compared with the weakly positive or negative groups, where the negative group had more unique operational taxonomic units. The abundance of Proteobacteria was found to be increased, while that of Actinobacteria, Firmicutes, and Bacteroidetes was found to be reduced in the positive group, while the area under the curve value was found to be 0.664. Furthermore, C.t treatment resulted in the alleviation of S. aureus-induced inflammatory response, epithelial barrier damage, and activation of the TLR4/NF-κB pathway in mice. Clinical samples analysis revealed that the diversity and abundance of microbiota were altered in patients with endometritis having positive CD138 levels, while mechanistic investigations revealed C.t alleviated S. aureus-induced endometritis by inactivating TLR4/NF-κB pathway. The findings of this study are envisaged to provide a diagnostic and therapeutic potential of microbiota in endometritis.
慢性子宫内膜炎与女性生殖道微生物群落失衡和病原微生物感染有关。本研究旨在确定子宫内膜炎患者子宫内膜微生物组的具体变化,并探讨丁酸梭菌(C.t)如何影响小鼠子宫内膜炎的进展,以进一步阐明子宫内膜炎的发病机制。为此,收集了 100 名参与者的子宫内膜组织,根据 CD138 水平将其分为阳性、弱阳性和阴性组,同时使用 16S rRNA 基因测序检测和分析子宫内膜微生物组差异。建立了金黄色葡萄球菌(S. aureus)诱导的子宫内膜炎小鼠模型,然后用 C.t 进行治疗,并评估炎症反应、上皮屏障和 TLR4/NF-κB 通路。结果表明,与弱阳性或阴性组相比,阳性组的α-和β-多样性显著降低,其中阴性组具有更多独特的操作分类单元。结果发现,阳性组中变形菌门的丰度增加,而放线菌门、厚壁菌门和拟杆菌门的丰度减少,曲线下面积值为 0.664。此外,C.t 治疗可减轻 S. aureus 诱导的小鼠炎症反应、上皮屏障损伤和 TLR4/NF-κB 通路激活。临床样本分析显示,CD138 水平阳性的子宫内膜炎患者的微生物多样性和丰度发生改变,而机制研究表明 C.t 通过抑制 TLR4/NF-κB 通路减轻 S. aureus 诱导的子宫内膜炎。本研究的结果预计将为子宫内膜炎的微生物诊断和治疗提供潜力。