Key Laboratory of Molecular Biology of Infectious Diseases (Chinese Ministry of Education), Department of Infectious Diseases, The Second Affiliated Hospital, Institute for Viral Hepatitis, Chongqing Medical University, Chongqing, People's Republic of China.
Department of Neurosurgery, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, People's Republic of China.
Emerg Microbes Infect. 2021 Dec;10(1):196-205. doi: 10.1080/22221751.2021.1872353.
Following outbreaks of severe acute respiratory syndrome coronavirus (SARS-CoV) and the Middle East respiratory syndrome coronavirus (MERS-CoV) in 2002 and 2012, respectively, the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the third highly pathogenic emerging human coronavirus (hCoV). SARS-CoV-2 is currently causing the global coronavirus disease 2019 (COVID-19) pandemic. CoV infections in target cells may stimulate the formation of numerous double-membrane autophagosomes and induce autophagy. Several studies provided evidence that hCoV infections are closely related to various cellular aspects associated with autophagy. Autophagy may even promote hCoV infection and replication. However, so far it is unclear how hCoV infections induce autophagy and whether the autophagic machinery is necessary for viral propagation. Here, we summarize the most recent advances concerning the mutual interplay between the autophagic machinery and the three emerging hCoVs, SARS-CoV, MERS-CoV, and SARS-CoV-2 and the model system mouse hepatitis virus. We also discuss the applicability of approved and well-tolerated drugs targeting autophagy as a potential treatment against COVID-19.
继 2002 年和 2012 年分别暴发严重急性呼吸综合征冠状病毒(SARS-CoV)和中东呼吸综合征冠状病毒(MERS-CoV)后,严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)是第三种高致病性新兴人类冠状病毒(hCoV)。SARS-CoV-2 目前正在引发全球 2019 年冠状病毒病(COVID-19)大流行。CoV 在靶细胞中的感染可能会刺激大量双层自噬体的形成,并诱导自噬。有几项研究提供了证据表明,hCoV 感染与自噬相关的各种细胞方面密切相关。自噬甚至可能促进 hCoV 感染和复制。然而,到目前为止,hCoV 感染如何诱导自噬以及自噬机制是否对病毒传播是必需的,这些问题仍不清楚。在这里,我们总结了关于自噬机制与三种新兴的 hCoV(SARS-CoV、MERS-CoV 和 SARS-CoV-2)以及模式系统鼠肝炎病毒之间相互作用的最新进展。我们还讨论了靶向自噬的已批准且耐受良好的药物作为 COVID-19 潜在治疗方法的适用性。