School of Life Sciences, Lanzhou University, 730000, PR China; MOE Key Laboratory of Cell Activities and Stress Adaptations, School of Life Sciences, Lanzhou University, Lanzhou, 730000, PR China; Gansu Key Laboratory of Biomonitoring and Bioremediation for Environmental Pollution, Lanzhou University, Lanzhou, 73000, PR China.
School of Life Sciences, Lanzhou University, 730000, PR China; MOE Key Laboratory of Cell Activities and Stress Adaptations, School of Life Sciences, Lanzhou University, Lanzhou, 730000, PR China.
Microb Pathog. 2022 Oct;171:105739. doi: 10.1016/j.micpath.2022.105739. Epub 2022 Aug 31.
Gut microbial dysbiosis during the development of Hepatitis C virus and liver-related diseases is not well studied. Nowadays, HCV and liver cirrhosis are the major concerns that cause gut bacterial alteration, which leads to dysbiosis. For this purpose, the present study was aimed at correlating the gut bacterial community of the control group in comparison to HCV and liver cirrhotic patients. A total of 23 stool samples were collected, including control (9), liver cirrhotic (8), and HCV (6). The collected samples were subjected to 16 S rRNA Illumina gene sequencing. In comparison with control, a significant gut bacterial alteration was observed in the progression of HCV and liver cirrhosis. Overall, Firmicutes were significantly abundant in the whole study. No significant difference was observed in the alpha diversity of the control and patient studies. Additionally, the beta diversity based on non-metric multidimensional scaling (NMDS) has a significant difference (p = 0.005) (ANOSIM R = 0.14) in all groups. The discriminative results based on the LEfSe tool revealed that the HCV-infected patients had higher Enterobacteriaceae and Enterobacterial, as well as Lactobacillus and Bacilli in comparison than the liver-cirrhotic patients. These taxa were significantly different from the control group (p < 0.05). Regarding prospects, a detailed analysis of the function through metagenomics and transcriptomics is needed.
在丙型肝炎病毒和肝脏相关疾病的发展过程中,肠道微生物失调的情况尚未得到充分研究。目前,丙型肝炎病毒和肝硬化是导致肠道细菌改变进而引发失调的主要关注点。为此,本研究旨在比较对照组、丙型肝炎病毒感染组和肝硬化组的肠道细菌群落。共收集了 23 份粪便样本,包括对照组(9 份)、肝硬化组(8 份)和丙型肝炎病毒感染组(6 份)。对收集的样本进行了 16S rRNA 高通量测序。与对照组相比,丙型肝炎病毒感染和肝硬化的进展过程中观察到肠道细菌明显改变。总体而言,厚壁菌门在整个研究中明显丰富。对照组和患者组的α多样性无显著差异。此外,基于非度量多维尺度分析(NMDS)的β多样性有显著差异(p=0.005)(ANOSIM R=0.14)。LEfSe 工具的判别结果表明,与肝硬化患者相比,丙型肝炎病毒感染患者的肠杆菌科和肠杆菌以及乳杆菌和芽孢杆菌明显更高。这些分类群与对照组有显著差异(p<0.05)。关于前景,需要通过宏基因组学和转录组学对功能进行详细分析。