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通过开发稳健的亚基因组 DBN3a 复制子揭示丙型肝炎病毒基因型 3 的独特特征。

Insights into the unique characteristics of hepatitis C virus genotype 3 revealed by development of a robust sub-genomic DBN3a replicon.

机构信息

School of Molecular and Cellular Biology, Faculty of Biological Sciences and Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS2 9JT, UK.

Present address: São Paulo State University, Institute of Biosciences, Languages and Exact Sciences, Cristóvão Colombo Street, 2265, Post Code 15054-000, São José do Rio Preto, São Paulo State, Brazil.

出版信息

J Gen Virol. 2020 Nov;101(11):1182-1190. doi: 10.1099/jgv.0.001486.

Abstract

Hepatitis C virus (HCV) is an important human pathogen causing 400 000 chronic liver disease-related deaths annually. Until recently, the majority of laboratory-based investigations into the biology of HCV have focused on the genotype 2 isolate, JFH-1, involving replicons and infectious cell culture systems. However, genotype 2 is one of eight major genotypes of HCV and there is great sequence variation among these genotypes (>30 % nucleotide divergence). In this regard, genotype 3 is the second most common genotype and accounts for 30 % of global HCV cases. Further, genotype 3 is associated with both high levels of inherent resistance to direct-acting antiviral (DAA) therapy, and a more rapid progression to chronic liver diseases. Neither of these two attributes are fully understood, thus robust genotype 3 culture systems to unravel viral replication are required. Here we describe the generation of robust genotype 3 sub-genomic replicons (SGRs) based on the adapted HCV NS3-NS5B replicase from the DBN3a cell culture infectious clone. Such infectious cell culture-adaptive mutations could potentially promote the development of robust SGRs for other HCV strains and genotypes. The novel genotype 3 SGRs have been used both transiently and to establish stable SGR-harbouring cell lines. We show that these resources can be used to investigate aspects of genotype 3 biology, including NS5A function and DAA resistance. They will be useful tools for these studies, circumventing the need to work under the biosafety level 3 (BSL3) containment required in many countries.

摘要

丙型肝炎病毒 (HCV) 是一种重要的人类病原体,每年导致 40 万人死于慢性肝病相关疾病。直到最近,大多数基于实验室的 HCV 生物学研究都集中在基因型 2 分离株 JFH-1 上,涉及复制子和感染性细胞培养系统。然而,基因型 2 是 HCV 的 8 种主要基因型之一,这些基因型之间存在很大的序列变异(>30%核苷酸差异)。在这方面,基因型 3 是第二常见的基因型,占全球 HCV 病例的 30%。此外,基因型 3 与直接作用抗病毒 (DAA) 治疗的固有耐药性水平高以及慢性肝病的快速进展有关。这两个属性都没有得到充分理解,因此需要建立强大的基因型 3 培养系统来阐明病毒复制。在这里,我们描述了基于 DBN3a 细胞培养感染性克隆中适应的 HCV NS3-NS5B 复制酶生成强大的基因型 3 亚基因组复制子 (SGR) 的方法。这些感染性细胞培养适应性突变可能有助于为其他 HCV 株和基因型开发强大的 SGR。新型基因型 3 SGR 已被用于瞬时和建立稳定的 SGR 携带细胞系。我们表明,这些资源可用于研究基因型 3 生物学的各个方面,包括 NS5A 功能和 DAA 耐药性。它们将是这些研究的有用工具,避免了在许多国家需要在生物安全级别 3 (BSL3) 控制下进行工作的需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f44/7879556/b7e6737f2fac/jgv-101-1182-g001.jpg

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