Université de Lorraine, Vandœuvre-lès-Nancy, France.
Laboratoire de Virologie, CHRU de Nancy Brabois, Vandœuvre-lès-Nancy, France.
Rev Med Virol. 2021 Jul;31(4):e2197. doi: 10.1002/rmv.2197. Epub 2020 Nov 22.
Among the five main viruses responsible for human hepatitis, hepatitis C virus (HCV) and hepatitis E virus (HEV) are different while sharing similarities. Both viruses can be transmitted by blood or derivatives whereas HEV can also follow environmental or zoonotic routes. These highly variable RNA viruses can cause chronic hepatitis potentially leading to hepatocarcinoma. HCV and HEV can develop new structures and functions under selective pressure to adapt to host immunity, human tissues, treatments or even various animal reservoirs. Elsewhere, with directly acting antiviral treatments, HCV can be eradicated whereas HEV is an emerging pathogen against which specific treatments have to be improved. As a unique molecular tool able to explore viral genomic plasticity, full-length genome (FLG) sequencing has become easier, faster and cheaper. The present review will show how FLG sequencing can explore these RNA viruses with the aim to investigate key genomics data to improve basic knowledge, patients' healthcare and preventive tools.
在导致人类肝炎的五种主要病毒中,丙型肝炎病毒(HCV)和戊型肝炎病毒(HEV)既存在相似之处,也有不同之处。这两种病毒都可以通过血液或血液制品传播,而 HEV 也可以通过环境或动物源途径传播。这些高度变异的 RNA 病毒可导致慢性肝炎,进而可能导致肝癌。HCV 和 HEV 在选择性压力下可产生新的结构和功能,以适应宿主免疫、人体组织、治疗方法甚至各种动物宿主。此外,针对 HCV 可以采用直接作用抗病毒治疗将其清除,而戊型肝炎病毒是一种新兴的病原体,针对它需要改进具体的治疗方法。全长基因组(FLG)测序作为一种独特的分子工具,能够探索病毒基因组的可塑性,它变得更容易、更快、更便宜。本综述将展示 FLG 测序如何探索这些 RNA 病毒,旨在研究关键基因组数据,以增进基础知识、改善患者医疗保健和预防工具。