Suppr超能文献

两种细胞系中人肝癌衍生细胞系 Huh7.5.1-8 和非洲绿猴肾衍生细胞系 Vero 中黄病毒生产的比较表征。

Comparative characterization of flavivirus production in two cell lines: Human hepatoma-derived Huh7.5.1-8 and African green monkey kidney-derived Vero.

机构信息

Department of Biochemistry and Cell Biology, National Institute of Infectious Diseases, Shinjuku-ku, Tokyo, Japan.

Department of Virology II, National Institute of Infectious Diseases, Musashi-murayama-shi, Tokyo, Japan.

出版信息

PLoS One. 2020 Apr 24;15(4):e0232274. doi: 10.1371/journal.pone.0232274. eCollection 2020.

Abstract

The Flaviviridae is a family of enveloped viruses with a positive-sense single-stranded RNA genome. It contains many viruses that threaten human health, such as Japanese encephalitis virus (JEV) and yellow fever virus (YFV) of the genus Flavivirus as well as hepatitis C virus of the genus Hepacivirus. Cell culture systems highly permissive for the Flaviviridae viruses are very useful for their isolation, propagation, and diagnosis, an understanding of their biology, and the development of vaccines and antiviral agents. Previously, we isolated a human hepatoma HuH-7-derived cell clone, Huh7.5.1-8, which is highly permissive to hepatitis C virus infection. Here, we have characterized flavivirus infection in the Huh7.5.1-8 cell line by comparing with that in the African green monkey kidney-derived Vero cell line, which is permissive for a wide spectrum of viruses. Upon infection with JEV, Huh7.5.1-8 cells produced a higher amount of virus particles early in infection and were more susceptible to virus-induced cell death than Vero cells. Similar outcomes were obtained when the cells were infected with another flavivirus, YFV (17D-204 strain). Quantification of cellular and extracellular viral RNA revealed that high JEV production in Huh7.5.1-8 cells can be attributed to rapid viral replication kinetics and efficient virus release early in infection. In a plaque assay, Huh7.5.1-8 cells developed JEV plaques more rapidly than Vero cells. Although this was not the case with YFV plaques, Huh7.5.1-8 cells developed higher numbers of YFV plaques than Vero cells. Sequence analysis of cDNA encoding an antiviral RNA helicase, RIG-I, showed that Huh7.5.1-8 cells expressed not only a full-length RIG-I mRNA with a known dominant-negative missense mutation but also variants without the mutation. However, the latter mRNAs lacked exon 5/6-12, indicating functional loss of RIG-I in the cells. These characteristics of the Huh7.5.1-8 cell line are helpful for flavivirus detection, titration, and propagation.

摘要

黄病毒科是一类具有正链单股 RNA 基因组的包膜病毒。它包含许多威胁人类健康的病毒,如黄病毒属的日本脑炎病毒(JEV)和黄热病病毒(YFV)以及丙型肝炎病毒属的丙型肝炎病毒。对黄病毒高度易感的细胞培养系统对于它们的分离、繁殖和诊断、对其生物学的理解以及疫苗和抗病毒药物的开发非常有用。以前,我们分离了一个人肝癌 HuH-7 衍生的细胞克隆,Huh7.5.1-8,它对丙型肝炎病毒感染高度敏感。在这里,我们通过比较非洲绿猴肾衍生的 Vero 细胞系(允许广泛的病毒感染)来描述 Huh7.5.1-8 细胞系中的黄病毒感染。感染 JEV 后,Huh7.5.1-8 细胞在感染早期产生了更高量的病毒颗粒,并且比 Vero 细胞更容易受到病毒诱导的细胞死亡。当细胞感染另一种黄病毒 YFV(17D-204 株)时,也获得了类似的结果。细胞内和细胞外病毒 RNA 的定量表明,Huh7.5.1-8 细胞中 JEV 的高产量归因于快速的病毒复制动力学和感染早期有效的病毒释放。在噬斑试验中,Huh7.5.1-8 细胞比 Vero 细胞更快地形成 JEV 噬斑。虽然 YFV 噬斑不是这种情况,但 Huh7.5.1-8 细胞形成的 YFV 噬斑比 Vero 细胞多。抗病毒 RNA 解旋酶 RIG-I 的 cDNA 序列分析表明,Huh7.5.1-8 细胞不仅表达了具有已知显性错义突变的全长 RIG-I mRNA,还表达了没有突变的变体。然而,后一种 mRNA 缺乏外显子 5/6-12,表明 RIG-I 在细胞中功能丧失。Huh7.5.1-8 细胞系的这些特征有助于黄病毒的检测、滴定和繁殖。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验