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泛素蛋白酶体系统与甲型流感病毒PB2聚合酶蛋白相互作用的比较分析:重现人类病毒进化过程

Comparative Profiling of Ubiquitin Proteasome System Interplay with Influenza A Virus PB2 Polymerase Protein Recapitulating Virus Evolution in Humans.

作者信息

Biquand Elise, Poirson Juline, Karim Marwah, Declercq Marion, Malausse Nicolas, Cassonnet Patricia, Barbezange Cyril, Straub Marie-Laure, Jones Louis, Munier Sandie, Naffakh Nadia, van der Werf Sylvie, Jacob Yves, Masson Murielle, Demeret Caroline

机构信息

Molecular Genetics of RNA Viruses, CNRS UMR 3569, Université Paris Diderot, Sorbonne Paris Cité, Institut Pasteur, Paris, France.

Ecole Supérieure de Biotechnologie Strasbourg, UMR-7242, CNRS, Université de Strasbourg, Illkirch, France.

出版信息

mSphere. 2017 Nov 22;2(6). doi: 10.1128/mSphere.00330-17. eCollection 2017 Nov-Dec.

Abstract

The optimized exploitation of cell resources is one cornerstone of a successful infection. Differential mapping of host-pathogen protein-protein interactions (PPIs) on the basis of comparative interactomics of multiple strains is an effective strategy to highlight correlations between host proteome hijacking and biological or pathogenic traits. Here, we developed an interactomic pipeline to deliver high-confidence comparative maps of PPIs between a given pathogen and the human ubiquitin proteasome system (UPS). This subarray of the human proteome represents a range of essential cellular functions and promiscuous targets for many viruses. The screening pipeline was applied to the influenza A virus (IAV) PB2 polymerase proteins of five strains representing different levels of virulence in humans. An extensive PB2-UPS interplay has been detected that recapitulates the evolution of IAVs in humans. Functional validation with several IAV strains, including the seasonal H1N1 and H3N2 viruses, confirmed the biological relevance of most identified UPS factors and revealed strain-independent and strain-specific effects of UPS factor invalidation on IAV infection. This strategy is applicable to proteins from any other virus or pathogen, providing a valuable resource with which to explore the UPS-pathogen interplay and its relationship with pathogenicity. Influenza A viruses (IAVs) are responsible for mild-to-severe seasonal respiratory illness of public health concern worldwide, and the risk of avian strain outbreaks in humans is a constant threat. Elucidating the requisites of IAV adaptation to humans is thus of prime importance. In this study, we explored how PB2 replication proteins of IAV strains with different levels of virulence in humans hijack a major protein modification pathway of the human host cell, the ubiquitin proteasome system (UPS). We found that the PB2 protein engages in an extended interplay with the UPS that evolved along with the virus's adaptation to humans. This suggests that UPS hijacking underlies the efficient infection of humans and can be used as an indicator for evaluation of the potential of avian IAVs to infect humans. Several UPS factors were found to be necessary for infection with circulating IAV strains, pointing to potential targets for therapeutic approaches.

摘要

细胞资源的优化利用是成功感染的基石之一。基于多菌株比较相互作用组学对宿主 - 病原体蛋白质 - 蛋白质相互作用(PPI)进行差异图谱分析,是突出宿主蛋白质组劫持与生物学或致病性状之间相关性的有效策略。在此,我们开发了一种相互作用组学流程,以提供给定病原体与人类泛素蛋白酶体系统(UPS)之间高可信度的PPI比较图谱。人类蛋白质组的这一子阵列代表了一系列基本细胞功能以及许多病毒的混杂靶点。该筛选流程应用于代表人类不同毒力水平的五种甲型流感病毒(IAV)PB2聚合酶蛋白。已检测到广泛的PB2 - UPS相互作用,概括了IAV在人类中的进化。对包括季节性H1N1和H3N2病毒在内的几种IAV菌株进行功能验证,证实了大多数已鉴定的UPS因子的生物学相关性,并揭示了UPS因子无效对IAV感染的菌株非依赖性和菌株特异性影响。该策略适用于任何其他病毒或病原体的蛋白质,为探索UPS - 病原体相互作用及其与致病性的关系提供了宝贵资源。甲型流感病毒(IAV)导致全球范围内从轻度到重度的季节性呼吸道疾病,对公共卫生构成威胁,而禽流感毒株在人类中爆发的风险始终存在。因此,阐明IAV适应人类的必要条件至关重要。在本研究中,我们探讨了人类中不同毒力水平的IAV菌株的PB2复制蛋白如何劫持人类宿主细胞的主要蛋白质修饰途径——泛素蛋白酶体系统(UPS)。我们发现PB2蛋白与UPS进行了广泛的相互作用,这种相互作用随着病毒对人类的适应而进化。这表明UPS劫持是人类有效感染的基础,可作为评估禽流感病毒感染人类潜力的指标。发现几种UPS因子对于循环IAV菌株的感染是必需的,这为治疗方法指出了潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc4a/5700371/fdd6860a4d9e/sph0061724110001.jpg

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