Endomembrane remodeling in SARS-CoV-2 infection

• Published in: Cell insight Vol. 1; no. 3; p. 100031
• Main Authors: Chen, Di, Zhao, Yan G., Zhang, Hong
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.06.2022; The Author(s). Published by Elsevier B.V. on behalf of Wuhan University; Elsevier
• Subjects: Autophagy; Coronavirus; DMV; Endocytosis; Review; SARS-CoV-2; SARS-CoV-2; Endocytosis; Coronavirus; DMV; Autophagy
• ISSN: 2772-8927; 2772-8927
• DOI: 10.1016/j.cellin.2022.100031

During severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, the viral proteins intimately interact with host factors to remodel the endomembrane system at various steps of the viral lifecycle. The entry of SARS-CoV-2 can be mediated by endocytosis-mediated internalization. Virus-containing endosomes then fuse with lysosomes, in which the viral S protein is cleaved to trigger membrane fusion. Double-membrane vesicles generated from the ER serve as platforms for viral replication and transcription. Virions are assembled at the ER–Golgi intermediate compartment and released through the secretory pathway and/or lysosome-mediated exocytosis. In this review, we will focus on how SARS-CoV-2 viral proteins collaborate with host factors to remodel the endomembrane system for viral entry, replication, assembly and egress. We will also describe how viral proteins hijack the host cell surveillance system—the autophagic degradation pathway—to evade destruction and benefit virus production. Finally, potential antiviral therapies targeting the host cell endomembrane system will be discussed.