全基因组 RNAi 筛选鉴定出流感病毒复制所必需的人类宿主因子。
Genome-wide RNAi screen identifies human host factors crucial for influenza virus replication.
机构信息
Molecular Biology Department, Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany.
出版信息
Nature. 2010 Feb 11;463(7282):818-22. doi: 10.1038/nature08760. Epub 2010 Jan 17.
Influenza A virus, being responsible for seasonal epidemics and reoccurring pandemics, represents a worldwide threat to public health. High mutation rates facilitate the generation of viral escape mutants, rendering vaccines and drugs directed against virus-encoded targets potentially ineffective. In contrast, targeting host cell determinants temporarily dispensable for the host but crucial for virus replication could prevent viral escape. Here we report the discovery of 287 human host cell genes influencing influenza A virus replication in a genome-wide RNA interference (RNAi) screen. Using an independent assay we confirmed 168 hits (59%) inhibiting either the endemic H1N1 (119 hits) or the current pandemic swine-origin (121 hits) influenza A virus strains, with an overlap of 60%. Notably, a subset of these common hits was also essential for replication of a highly pathogenic avian H5N1 strain. In-depth analyses of several factors provided insights into their infection stage relevance. Notably, SON DNA binding protein (SON) was found to be important for normal trafficking of influenza virions to late endosomes early in infection. We also show that a small molecule inhibitor of CDC-like kinase 1 (CLK1) reduces influenza virus replication by more than two orders of magnitude, an effect connected with impaired splicing of the viral M2 messenger RNA. Furthermore, influenza-virus-infected p27(-/-) (cyclin-dependent kinase inhibitor 1B; Cdkn1b) mice accumulated significantly lower viral titres in the lung, providing in vivo evidence for the importance of this gene. Thus, our results highlight the potency of genome-wide RNAi screening for the dissection of virus-host interactions and the identification of drug targets for a broad range of influenza viruses.
甲型流感病毒是造成季节性流行和反复大流行的罪魁祸首,对全球公共卫生构成严重威胁。高突变率促使病毒逃避免疫的能力增强,使得针对病毒编码靶点的疫苗和药物可能失去效果。相比之下,针对宿主细胞中那些对宿主暂时非必需但对病毒复制至关重要的决定因素,可能会阻止病毒发生逃逸。在此,我们报告了在全基因组 RNA 干扰(RNAi)筛选中发现 287 个人类宿主细胞基因会影响甲型流感病毒的复制。我们使用独立的检测方法验证了 168 个(59%)抑制地方性 H1N1(119 个)或当前流行的猪源(121 个)甲型流感病毒株的作用,两者有 60%的重叠。值得注意的是,这些共同作用的靶点中有一部分对于高致病性禽流感 H5N1 株的复制也是必需的。对几种因素的深入分析提供了其感染阶段相关性的深入了解。特别地,SON 核酸结合蛋白(SON)对于感染早期流感病毒颗粒向晚期内体的正常转运是重要的。我们还表明,CDC 样蛋白激酶 1(CLK1)的小分子抑制剂可使流感病毒复制减少两个以上数量级,其效果与病毒 M2 信使 RNA 的剪接受损有关。此外,在感染流感病毒的 p27(-/-)(细胞周期蛋白依赖性激酶抑制剂 1B;Cdkn1b)小鼠中,肺部病毒滴度显著降低,这为该基因的重要性提供了体内证据。因此,我们的研究结果突出了全基因组 RNAi 筛选在解析病毒-宿主相互作用和鉴定针对广泛流感病毒的药物靶标方面的潜力。