Zha Zhiqiang, Jia Chunhong, Zhou Ruisi, Yin Qinlan, Hu Yu, Huang Zhipeng, Peng Linyu, Zhang Yichi, Qiu Xiaowei, Chen Ying, Zhong Yawen, Wang Yu, Pang Menglan, Lu Shijing, Sheng Chao, Huang Liping
Department of Obstetrics and Gynecology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Department of Neonatology, Guangzhou Key Laboratory of Neonatal Intestinal Diseases, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
NPJ Biofilms Microbiomes. 2024 Dec 31;10(1):158. doi: 10.1038/s41522-024-00630-5.
Fetal growth restriction (FGR) is a common complication of pregnancy, which seriously endangers fetal health and still lacks effective therapeutic targets. Clostridium difficile (C. difficile) is associated with fetal birth weight, and its membrane vesicles (MVs) are pathogenic vectors. However, the role of C. difficile and its MVs in FGR remains unclear. Here we found that supplementation with C. difficile altered the characteristics of gut microbiota and reduced the birth weight in mice. Interestingly, C. difficile MVs entered placenta, inhibited trophoblast motility, and induced fetal weight loss in mice. Mechanistically, C. difficile MVs activated the PPAR pathway via enhancing the transcriptional activity of PPARγ promoter, consequently inhibiting trophoblast motility. Moreover, PPARγ expression was significantly elevated in FGR placenta, and negatively correlated with fetal birth weight. Together, our findings reveal the significance of C. difficile and its MVs in FGR, providing new insights into the mechanisms of FGR development.
胎儿生长受限(FGR)是一种常见的妊娠并发症,严重危及胎儿健康,且仍缺乏有效的治疗靶点。艰难梭菌(C. difficile)与胎儿出生体重有关,其膜泡(MVs)是致病载体。然而,艰难梭菌及其膜泡在FGR中的作用仍不清楚。在此,我们发现补充艰难梭菌会改变肠道微生物群的特征,并降低小鼠的出生体重。有趣的是,艰难梭菌膜泡进入胎盘,抑制滋养层细胞的运动,并导致小鼠胎儿体重减轻。机制上,艰难梭菌膜泡通过增强PPARγ启动子的转录活性激活PPAR途径,从而抑制滋养层细胞的运动。此外,PPARγ在FGR胎盘组织中的表达显著升高,且与胎儿出生体重呈负相关。总之,我们的研究结果揭示了艰难梭菌及其膜泡在FGR中的重要性,为FGR发生发展的机制提供了新的见解。