Dybas Joseph M, Lum Krystal K, Kulej Katarzyna, Reyes Emigdio D, Lauman Richard, Charman Matthew, Purman Caitlin E, Steinbock Robert T, Grams Nicholas, Price Alexander M, Mendoza Lydia, Garcia Benjamin A, Weitzman Matthew D
Division of Protective Immunity and Division of Cancer Pathobiology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
mSystems. 2021 Aug 31:e0046821. doi: 10.1128/mSystems.00468-21.
Viral infections are associated with extensive remodeling of the cellular proteome. Viruses encode gene products that manipulate host proteins to redirect cellular processes or subvert antiviral immune responses. Adenovirus (AdV) encodes proteins from the early E4 region which are necessary for productive infection. Some cellular antiviral proteins are known to be targeted by AdV E4 gene products, resulting in their degradation or mislocalization. However, the full repertoire of host proteome changes induced by viral E4 proteins has not been defined. To identify cellular proteins and processes manipulated by viral products, we developed a global, unbiased proteomics approach to analyze changes to the host proteome during infection with adenovirus serotype 5 (Ad5) virus. We used whole-cell proteomics to measure total protein abundances in the proteome during Ad5 infection. Since host antiviral proteins can antagonize viral infection by associating with viral genomes and inhibiting essential viral processes, we used Isolation of Proteins on Nascent DNA (iPOND) proteomics to identify proteins associated with viral genomes during infection with wild-type Ad5 or an E4 mutant virus. By integrating these proteomics data sets, we identified cellular factors that are degraded in an E4-dependent manner or are associated with the viral genome in the absence of E4 proteins. We further show that some identified proteins exert inhibitory effects on Ad5 infection. Our systems-level analysis reveals cellular processes that are manipulated during Ad5 infection and points to host factors counteracted by early viral proteins as they remodel the host proteome to promote efficient infection. Viral infections induce myriad changes to the host cell proteome. As viruses harness cellular processes and counteract host defenses, they impact abundance, post-translational modifications, interactions, or localization of cellular proteins. Elucidating the dynamic changes to the cellular proteome during viral replication is integral to understanding how virus-host interactions influence the outcome of infection. Adenovirus encodes early gene products from the E4 genomic region that are known to alter host response pathways and promote replication, but the full extent of proteome modifications they mediate is not known. We used an integrated proteomics approach to quantitate protein abundance and protein associations with viral DNA during virus infection. Systems-level analysis identifies cellular proteins and processes impacted in an E4-dependent manner, suggesting ways that adenovirus counteracts potentially inhibitory host defenses. This study provides a global view of adenovirus-mediated proteome remodeling, which can serve as a model to investigate virus-host interactions of DNA viruses.
病毒感染与细胞蛋白质组的广泛重塑有关。病毒编码的基因产物可操纵宿主蛋白,以重定向细胞进程或颠覆抗病毒免疫反应。腺病毒(AdV)从早期E4区域编码蛋白质,这些蛋白质是有效感染所必需的。已知一些细胞抗病毒蛋白是腺病毒E4基因产物的作用靶点,导致它们降解或定位错误。然而,病毒E4蛋白诱导的宿主蛋白质组变化的完整清单尚未确定。为了鉴定被病毒产物操纵的细胞蛋白和进程,我们开发了一种全局性、无偏差的蛋白质组学方法,以分析在5型腺病毒(Ad5)感染期间宿主蛋白质组的变化。我们使用全细胞蛋白质组学来测量Ad5感染期间蛋白质组中总蛋白的丰度。由于宿主抗病毒蛋白可通过与病毒基因组结合并抑制基本的病毒进程来拮抗病毒感染,我们使用新生DNA上蛋白质分离(iPOND)蛋白质组学来鉴定在野生型Ad5或E4突变病毒感染期间与病毒基因组相关的蛋白质。通过整合这些蛋白质组学数据集,我们鉴定出了以E4依赖方式降解或在没有E4蛋白时与病毒基因组相关的细胞因子。我们进一步表明,一些鉴定出的蛋白对Ad5感染具有抑制作用。我们的系统水平分析揭示了Ad5感染期间被操纵的细胞进程,并指出了早期病毒蛋白在重塑宿主蛋白质组以促进有效感染时所抵消的宿主因子。病毒感染会引起宿主细胞蛋白质组的无数变化。由于病毒利用细胞进程并对抗宿主防御,它们会影响细胞蛋白的丰度、翻译后修饰、相互作用或定位。阐明病毒复制期间细胞蛋白质组的动态变化对于理解病毒 - 宿主相互作用如何影响感染结果至关重要。腺病毒从E4基因组区域编码早期基因产物,已知这些产物会改变宿主反应途径并促进复制,但它们介导的蛋白质组修饰的全部范围尚不清楚。我们使用综合蛋白质组学方法来定量病毒感染期间蛋白质的丰度以及蛋白质与病毒DNA的关联。系统水平分析鉴定出以E4依赖方式受到影响的细胞蛋白和进程,提示了腺病毒对抗潜在抑制性宿主防御的方式。这项研究提供了腺病毒介导的蛋白质组重塑的全局视图,可作为研究DNA病毒的病毒 - 宿主相互作用的模型。