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Identification of Five Interferon-Induced Cellular Proteins That Inhibit West Nile Virus and Dengue Virus Infections

机译:鉴定抑制西尼罗河病毒和登革热病毒感染的五种干扰素诱导的细胞蛋白

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摘要

Interferons (IFNs) are key mediators of the host innate antiviral immune response. To identify IFN-stimulated genes (ISGs) that instigate an antiviral state against two medically important flaviviruses, West Nile virus (WNV) and dengue virus (DENV), we tested 36 ISGs that are commonly induced by IFN-α for antiviral activity against the two viruses. We discovered that five ISGs efficiently suppressed WNV and/or DENV infection when they were individually expressed in HEK293 cells. Mechanistic analyses revealed that two structurally related cell plasma membrane proteins, IFITM2 and IFITM3, disrupted early steps (entry and/or uncoating) of the viral infection. In contrast, three IFN-induced cellular enzymes, viperin, ISG20, and double-stranded-RNA-activated protein kinase, inhibited steps in viral proteins and/or RNA biosynthesis. Our results thus imply that the antiviral activity of IFN-α is collectively mediated by a panel of ISGs that disrupt multiple steps of the DENV and WNV life cycles.
机译:干扰素(IFN)是宿主先天性抗病毒免疫反应的关键介质。为了鉴定能激发针对两种医学上重要的黄病毒西尼罗河病毒(WNV)和登革热病毒(DENV)的IFN刺激基因(ISG),我们测试了通常由IFN-α诱导的36种ISG的抗病毒活性。两种病毒。我们发现,当五个ISG在HEK293细胞中单独表达时,它们可以有效抑制WNV和/或DENV感染。机理分析表明,两种结构相关的细胞质膜蛋白IFITM2和IFITM3破坏了病毒感染的早期步骤(进入和/或脱膜)。相反,三种IFN诱导的细胞酶,viperin,ISG20和双链RNA激活的蛋白激酶,抑制了病毒蛋白和/或RNA生物合成的步骤。因此,我们的结果表明,IFN-α的抗病毒活性是由一系列破坏DENV和WNV生命周期多个步骤的ISG共同介导的。

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