Genotype-specific acquisition, evolution and adaptation of characteristic mutations in hepatitis E virus

文献类型： 外文期刊

第一作者： Ikram, Aqsa

作者： Ikram, Aqsa;Hakim, Mohamad S.;Zhou, Jian-hua;Wang, Wenshi;Peppelenbosch, Maikel P.;Pan, Qiuwei;Ikram, Aqsa;Hakim, Mohamad S.;Zhou, Jian-hua

作者机构：

关键词： B and T cells;epitope;evolution;hepatitis E virus;mutation

期刊名称：VIRULENCE （ 影响因子：5.882； 五年影响因子：6.489 ）

ISSN： 2150-5594

年卷期： 2018 年 9 卷 1 期

页码：

收录情况： SCI

摘要： Hepatitis E virus (HEV) infection is a major cause of acute hepatitis but also provokes chronic infection in immunocompromised patients. Although the pathogenesis and treatment outcome involve complex interplay between the virus and host, the nature of adaptive responses of HEV to the host immune system remain obscure at best. In this study, we used large-scale proteomic bioinformatics to profile characteristic mutations in human HEV isolates associated to ribavirin treatment failure, chronic hepatitis, hepatic failure or altered immunoreactivity. The prevalence of specific mutations was examined in a large number of protein sequences of ORF1 and ORF2 regions of the 3 major human-derived HEV genotypes (1, 3 and 4). By analyzing potential B, CD4+ and CD8+ T cell epitopes, we found that many of these mutations overlap with the predicted epitopes and are frequently present among the 3 HEV genotypes. These overlapping mutations mediate reduced antigenicity. Finally, by delineation of diversification and evolution of the underlying epitopes, we observe that most of these variants apparently evolved earlier in genotype 1 when compared with genotypes 3 and 4. These results indicate that HEV is under substantial evolutionary pressure to develop mutations enabling evasion of the host immune response and resistance to antiviral treatment. This indicates the existence of an ongoing evolutionary arms race between human immunity, antiviral medication and HEV.

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