Department of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI 53706, USA.
Integrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious Diseases, NIH, Frederick, MD 21702, USA.
Cell Rep. 2019 Nov 19;29(8):2175-2183.e4. doi: 10.1016/j.celrep.2019.10.064.
All viruses balance interactions between cellular machinery co-opted to support replication and host factors deployed to halt the infection. We use gene correlation analysis to perform an unbiased screen for host factors involved in influenza A virus (FLUAV) infection. Our screen identifies the cellular factor epidermal growth factor receptor pathway substrate 8 (EPS8) as the highest confidence pro-viral candidate. Knockout and overexpression of EPS8 confirm its importance in enhancing FLUAV infection and titers. Loss of EPS8 does not affect virion attachment, uptake, or fusion. Rather, our data show that EPS8 specifically functions during virion uncoating. EPS8 physically associates with incoming virion components, and subsequent nuclear import of released ribonucleoprotein complexes is significantly delayed in the absence of EPS8. Our study identifies EPS8 as a host factor important for uncoating, a crucial step of FLUAV infection during which the interface between the virus and host is still being discovered.
所有病毒都在平衡着被细胞机制劫持来支持复制的相互作用,以及被宿主用来阻止感染的因素。我们使用基因相关性分析,对参与甲型流感病毒(FLUAV)感染的宿主因素进行了无偏见的筛选。我们的筛选确定了细胞因子表皮生长因子受体途径底物 8(EPS8)是最有信心的促病毒候选物。EPS8 的敲除和过表达证实了它在增强 FLUAV 感染和滴度方面的重要性。EPS8 的缺失并不影响病毒粒子的附着、摄取或融合。相反,我们的数据表明,EPS8 专门在病毒粒子脱壳期间发挥作用。EPS8 与进入的病毒粒子成分物理结合,在没有 EPS8 的情况下,释放的核糖核蛋白复合物的核内导入显著延迟。我们的研究确定 EPS8 是一个对脱壳很重要的宿主因子,这是 FLUAV 感染的一个关键步骤,在此过程中,病毒与宿主之间的界面仍在被发现。