Aly AbdelRahman Mahmoud, Adel AbdelReheem, El-Gendy Ahmed Osama, Essam Tamer M, Aziz Ramy K
Faculty of Post Graduate Studies for Advanced Sciences, Beni-Suef University, Beni-Suef, 62511 Egypt.
Department of Microbiology and Immunology, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, 62511 Egypt.
Gut Pathog. 2016 Sep 13;8(1):42. doi: 10.1186/s13099-016-0124-2. eCollection 2016.
Hepatitis C virus (HCV) causes debilitating liver diseases, which may progress to cirrhosis and cancer, and claims 500,000 annual lives worldwide. While HCV epidemiology, pathophysiology, and therapy are being deeply studied, rare attention is given to reciprocal interactions between HCV infection , HCV-induced chronic liver diseases, and the human gut microbiome. As Egypt has the world's highest prevalence of HCV infections, we launched this study to monitor differences in the gut microbial community composition of Egyptian HCV patients that may affect, or result from, the patients' liver state.
To this end, we analyzed stool samples from six stage 4-HCV patients and eight healthy individuals by high-throughput 16S rRNA gene sequencing using Illumina MiSeq. Overall, the alpha-diversity of the healthy persons' gut microbiomes was higher than those of the HCV patients. Whereas members of phylum Bacteroidetes were more abundant in HCV patients, healthy individuals had higher abundance of Firmicutes, Proteobacteria, and Actinobacteria. Genus-level analysis showed differential abundance of Prevotella and Faecalibacterium (higher in HCV patients) vs. Ruminococcus and Clostridium (healthy group), indicating that the higher abundance of Bacteroidetes in HCV patients is most likely due to Prevotella overabundance. The probiotic genus, Bifidobacterium, was only observed in the microbiotas of healthy individuals.
To the best of our knowledge, this study provides a first overview of major phyla and genera differentiating stage 4-HCV patients from healthy individuals and suggests possible microbiome remodeling in chronic hepatitis C, possibly shaped by bacterial translocation as well as the liver's impaired role in digestion and protein synthesis. Future studies will investigate the microbiome composition and functional capabilities in more patients while tracing some potential biomarker taxa (e.g., Prevotella, Faecalibacterium vs. Bifidobacterium).
丙型肝炎病毒(HCV)可引发使人衰弱的肝脏疾病,这些疾病可能会发展为肝硬化和癌症,在全球每年导致50万人死亡。虽然对HCV的流行病学、病理生理学和治疗方法进行了深入研究,但HCV感染、HCV引发的慢性肝病与人类肠道微生物群之间的相互作用却很少受到关注。由于埃及是全球HCV感染率最高的国家,我们开展了这项研究,以监测可能影响埃及HCV患者肝脏状态或由其肝脏状态导致的肠道微生物群落组成差异。
为此,我们使用Illumina MiSeq通过高通量16S rRNA基因测序分析了6名4期HCV患者和8名健康个体的粪便样本。总体而言,健康人的肠道微生物群α多样性高于HCV患者。拟杆菌门成员在HCV患者中更为丰富,而健康个体中厚壁菌门、变形菌门和放线菌门的丰度更高。属水平分析显示,普氏菌属和粪杆菌属(在HCV患者中丰度更高)与瘤胃球菌属和梭菌属(健康组)的丰度存在差异,这表明HCV患者中拟杆菌门丰度较高很可能是由于普氏菌属过度增殖所致。益生菌属双歧杆菌仅在健康个体的微生物群中被观察到。
据我们所知,本研究首次概述了区分4期HCV患者与健康个体的主要门和属,并提示慢性丙型肝炎可能存在微生物群重塑,这可能是由细菌易位以及肝脏在消化和蛋白质合成方面的功能受损所导致的。未来的研究将在追踪一些潜在生物标志物分类群(如普氏菌属、粪杆菌属与双歧杆菌属)时,对更多患者的微生物群组成和功能能力进行研究。