首页> 美国卫生研究院文献>Journal of Virology >Naturally Occurring Hepatitis C Virus Subgenomic Deletion Mutants Replicate Efficiently in Huh-7 Cells and Are trans-Packaged In Vitro To Generate Infectious Defective Particles
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Naturally Occurring Hepatitis C Virus Subgenomic Deletion Mutants Replicate Efficiently in Huh-7 Cells and Are trans-Packaged In Vitro To Generate Infectious Defective Particles

机译:自然出现的丙型肝炎病毒亚基因组缺失突变体可在Huh-7细胞中高效复制并在体外进行转包装以产生感染性缺陷颗粒。

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摘要

Naturally occurring hepatitis C virus (HCV) subgenomic RNAs have been found in several HCV patients. These subgenomic deletion mutants, mostly lacking the genes encoding envelope glycoproteins, were found in both liver and serum, where their relatively high abundance suggests that they are capable of autonomous replication and can be packaged and secreted in viral particles, presumably harboring the envelope proteins from wild type virus coinfecting the same cell. We recapitulated some of these natural subgenomic deletions in the context of the isolate JFH-1 and confirmed these hypotheses in vitro. In Huh-7.5 cells, these deletion-containing genomes show robust replication and can be efficiently trans-packaged and infect naïve Huh-7.5 cells when cotransfected with the full-length wild-type J6/JFH genome. The genome structure of these natural subgenomic deletion mutants was dissected, and the maintenance of both core and NS2 regions was proven to be significant for efficient replication and trans-packaging. To further explore the requirements needed to achieve trans-complementation, we provided different combinations of structural proteins in trans. Optimal trans-complementation was obtained when fragments of the polyprotein encompassing core to p7 or E1 to NS2 were expressed. Finally, we generated a stable helper cell line, constitutively expressing the structural proteins from core to p7, which efficiently supports trans-complementation of a subgenomic deletion encompassing amino acids 284 to 732. This cell line can produce and be infected by defective particles, thus representing a powerful tool to investigate the life cycle and relevance of natural HCV subgenomic deletion mutants in vivo.
机译:在几位HCV患者中发现了天然存在的丙型肝炎病毒(HCV)亚基因组RNA。这些亚基因组缺失突变体大多缺乏编码包膜糖蛋白的基因,在肝脏和血清中均发现,它们的相对较高的丰度表明它们具有自主复制的能力,可以包装并分泌到病毒颗粒中,大概是从共同感染同一细胞的野生型病毒。我们在分离物JFH-1的背景下概括了其中的一些自然亚基因组缺失,并在体外证实了这些假设。在Huh-7.5细胞中,这些包含缺失的基因组显示出强大的复制能力,当与全长野生型J6 / JFH基因组共转染时,可以有效地包装并感染原始的Huh-7.5细胞。解剖了这些天然亚基因组缺失突变体的基因组结构,并且核心和NS2区域的维护被证明对有效复制和反包装具有重要意义。为了进一步探讨实现反式互补的要求,我们提供了反式结构蛋白的不同组合。当表达包围p7核心或E1到NS2的多蛋白片段时,可获得最佳的反式互补。最后,我们生成了一个稳定的辅助细胞系,从核心到p7组成型表达该结构蛋白,可有效支持包含284至732位氨基酸的亚基因组缺失的反式互补。该细胞系可产生并被有缺陷的颗粒感染,因此代表了研究天然HCV亚基因组缺失突变体在体内生命周期和相关性的有力工具。

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