中国妊娠期肝内胆汁淤积症患者肠道微生物群的变化

IF 2.6 2区 生物学 Q3 CELL BIOLOGY
Xiaozhen Lei, Jiangyan Yu, Yan Huang, Hua Lai, Siming Xin, Xiaoming Zeng
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引用次数: 0

摘要

妊娠期肝内胆汁淤积症(ICP)是一种妊娠期特异性肝病,也是导致妊娠期黄疸的第二大原因,但其病因尚不清楚。通过采集中国 12 名健康孕妇(CON 组)和 32 名 ICP 患者(ICP 组)的血液和粪便样本,我们进行了 16s rRNA 基因测序并分析了微生物多样性。结果显示,ICP 组的物种丰富度较 CON 组有所下降,两组之间的物种多样性差异显著。差异分析显示了以下生物标志物:S__未分类__嗜血杆菌属(Megamonas)、G__嗜血杆菌属(Megamonas)、F__硒单胞菌科(Selenomonadaceae)、C__杆菌属(Bacilli)和O__乳杆菌科(Lactobacillales)。重要的是,我们发现在 ICP 患者中,科级的硒单胞菌科物种丰富度下降,类级的杆菌减少。我们据此进行了相关网络分析和功能基因预测。我们的数据提供了将微生物群与 ICP 联系起来的新信息,可能有助于对该疾病的进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Alterations in the Gut Microbiota in Chinese Patients With Intrahepatic Cholestasis of Pregnancy

Alterations in the Gut Microbiota in Chinese Patients With Intrahepatic Cholestasis of Pregnancy

Intrahepatic cholestasis of pregnancy (ICP) is a pregnancy-specific liver disease and the second most frequent cause of jaundice in pregnancy, but the etiology of it is poorly understood. By collecting blood and fecal samples from 12 healthy pregnant women (CON group) and 32 ICP patients (ICP group) in China, we performed 16s rRNA gene sequencing and analyzed microbial diversity. The results showed a decrease in species richness of the ICP group compared to that in the CON group, with a significant difference in species diversity between the two groups. Differential analysis revealed the following biomarkers: s__unclassified__Megamonas, g__Megamonas, f__Selenomonadaceae, c__Bacilli, and o__Lactobacillales. Importantly, we found a decrease in species richness of Selenomonadaceae at the family level and decreased bacilli at the class level in ICP patients. Correlation network analysis and functional gene prediction were performed accordingly. Our data provided new information linking microbiota and ICP, and are possibly helpful for further exploration of the disease.

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来源期刊
Cellular Microbiology
Cellular Microbiology 生物-微生物学
CiteScore
9.70
自引率
0.00%
发文量
26
审稿时长
3 months
期刊介绍: Cellular Microbiology aims to publish outstanding contributions to the understanding of interactions between microbes, prokaryotes and eukaryotes, and their host in the context of pathogenic or mutualistic relationships, including co-infections and microbiota. We welcome studies on single cells, animals and plants, and encourage the use of model hosts and organoid cultures. Submission on cell and molecular biological aspects of microbes, such as their intracellular organization or the establishment and maintenance of their architecture in relation to virulence and pathogenicity are also encouraged. Contributions must provide mechanistic insights supported by quantitative data obtained through imaging, cellular, biochemical, structural or genetic approaches.
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