Department of Microbiology and Immunology, Loyola University Chicagogrid.164971.c, Maywood, Illinois, USA.
mBio. 2022 Jun 28;13(3):e0044522. doi: 10.1128/mbio.00445-22. Epub 2022 May 17.
To successfully infect, viruses must respond to cues that promote their genome delivery into host cells. These keys to virus entry frequently reside inside endocytic vesicles. In a recent mBio article, Poston et al. (D. Poston, Y. Weisblum, A. Hobbs, and P. D. Bieniasz, mBio 13:e0300221, 2022, https://doi.org/10.1128/mbio.03002-21) identified and characterized protein complexes generating endocytic environments favorable for virus entry. These included retromer-associated vacuolar protein sorting 29 (VPS29) proteins. Without VPS29, endosomes lacked cathepsin activities, making them incapable of supporting those viruses in which endosomal proteolysis triggers entry. These protease-dependent viruses encompass several zoonotic filoviruses and coronaviruses, including recent SARS-CoV-2 variants of concern. The valuable findings of Poston et al. reveal retromer complexes as master keys for select endosomal virus entry processes and raise the possibility that threatening coronaviruses might be resisted through targeted inactivation of components controlling endosome structure and function.
为了成功感染,病毒必须对促进其基因组进入宿主细胞的信号做出反应。这些进入病毒的关键通常位于内体小泡内。在最近的一篇 mBio 文章中,Poston 等人(D. Poston、Y. Weisblum、A. Hobbs 和 P. D. Bieniasz,mBio 13:e0300221,2022,https://doi.org/10.1128/mBio.03002-21)鉴定并描述了产生有利于病毒进入的内吞环境的蛋白质复合物。其中包括与逆行体相关的液泡蛋白分选 29(VPS29)蛋白。没有 VPS29,内体就缺乏组织蛋白酶活性,使它们无法支持那些需要内体蛋白水解触发进入的病毒。这些依赖蛋白酶的病毒包括几种人畜共患的丝状病毒和冠状病毒,包括最近引起关注的 SARS-CoV-2 变体。Poston 等人的有价值发现揭示了逆行体复合物作为选择内体病毒进入过程的主钥匙,并提出了通过靶向失活控制内体结构和功能的成分来抵抗威胁性冠状病毒的可能性。