Altered faecal microbiota on the expression of Th cells responses in the exacerbation of patients with hepatitis E infection

生物 恶化 免疫学 戊型肝炎 微生物学 乳酸菌 维管菌 肝炎 厚壁菌 链球菌 细菌 基因型 16S核糖体RNA 遗传学 生物化学 基因
作者
Jian Wu,Fen Huang,Zongxin Ling,Shuangchun Liu,Jun Liu,Jun Fan,Jiong Yu,Wei Wang,Xiuyuan Jin,Yiling Meng,Hongcui Cao,Lanjuan Li
出处
期刊:Journal of Viral Hepatitis [Wiley]
卷期号:27 (11): 1243-1252 被引量:26
标识
DOI:10.1111/jvh.13344
摘要

Abstract Fulminant hepatitis E may lead to acute liver failure (ALF). Perturbations of intestinal microbiota are related to severe liver disease. To study the correlations between faecal microbiota and the occurrence and exacerbation of hepatitis E virus (HEV) infection, we characterized 24 faecal samples from 12 patients with acute hepatitis E (AHE) and 12 patients with HEV‐ALF using high‐throughput sequencing. We found both the alpha and beta diversity indices showed no significant differences between the AHE and HEV‐ALF groups. Several predominant taxa were significantly different between the AHE and HEV‐ALF groups. Most notably, the HEV‐ALF group had increased levels of Gammaproteobacteria , Proteobacteria , Xanthomonadceae and Stenotrophomonas , but reduced levels of Firmicutes , Streptococcus , Subdoligranulum and Lactobacillus , compared with the AHE group. The levels of Lactobacillaceae and Gammaproteobacteria could be used to distinguish patients with HEV‐ALF from those with AHE. In addition, the level of Th lymphocytes was significantly lower in the HEV‐ALF group than in the AHE group. The relative abundances of Lactobacillaceae and Gammaproteobacteria were positively correlated with Th lymphocytes, serum international normalized ratio (INR) and hepatic encephalopathy severity. Moreover, surviving patients had higher levels of Lactobacillus mucosae than deceased patients. Our study demonstrated that the presence of altered faecal microbiota is associated with exacerbation of HEV infection; this finding may be useful for exploring the interactions among faecal microbiota, immune responses, mechanisms of infection and progression in patients with HEV, as well as for the development of novel diagnostic and therapeutic strategies.
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