Tay Douglas Jie Wen, Lew Zhe Zhang Ryan, Chu Justin Jang Hann, Tan Kai Sen
Biosafety Level 3 Core Facility, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Front Microbiol. 2022 Mar 23;13:844447. doi: 10.3389/fmicb.2022.844447. eCollection 2022.
The ongoing SARS-CoV-2 pandemic has tested the capabilities of public health and scientific community. Since the dawn of the twenty-first century, viruses have caused several outbreaks, with coronaviruses being responsible for 2: SARS-CoV in 2007 and MERS-CoV in 2013. As the border between wildlife and the urban population continue to shrink, it is highly likely that zoonotic viruses may emerge more frequently. Furthermore, it has been shown repeatedly that these viruses are able to efficiently evade the innate immune system through various strategies. The strong and abundant antiviral innate immunity evasion strategies shown by SARS-CoV-2 has laid out shortcomings in our approach to quickly identify and modulate these mechanisms. It is thus imperative that there be a systematic framework for the study of the immune evasion strategies of these viruses, to guide development of therapeutics and curtail transmission. In this review, we first provide a brief overview of general viral evasion strategies against the innate immune system. Then, we utilize SARS-CoV-2 as a case study to highlight the methods used to identify the mechanisms of innate immune evasion, and pinpoint the shortcomings in the current paradigm with its focus on overexpression and protein-protein interactions. Finally, we provide a recommendation for future work to unravel viral innate immune evasion strategies and suitable methods to aid in the study of virus-host interactions. The insights provided from this review may then be applied to other viruses with outbreak potential to remain ahead in the arms race against viral diseases.
持续的新型冠状病毒肺炎疫情考验了公共卫生和科学界的能力。自21世纪初以来,病毒已引发多次疫情,其中冠状病毒导致了两次疫情:2007年的严重急性呼吸综合征冠状病毒(SARS-CoV)和2013年的中东呼吸综合征冠状病毒(MERS-CoV)。随着野生动物与城市人口之间的界限不断缩小,人畜共患病毒很可能会更频繁地出现。此外,反复研究表明,这些病毒能够通过各种策略有效逃避先天性免疫系统。新型冠状病毒肺炎所展现出的强大且丰富的抗病毒先天性免疫逃避策略,暴露出我们在快速识别和调控这些机制的方法上存在不足。因此,必须有一个系统框架来研究这些病毒的免疫逃避策略,以指导治疗方法的开发并遏制病毒传播。在这篇综述中,我们首先简要概述病毒针对先天性免疫系统的一般逃避策略。然后,我们以新型冠状病毒肺炎为例,突出用于识别先天性免疫逃避机制的方法,并指出当前以过表达和蛋白质-蛋白质相互作用为重点的模式存在的不足。最后,我们为未来的工作提供建议,以揭示病毒先天性免疫逃避策略以及有助于研究病毒-宿主相互作用的合适方法。这篇综述所提供的见解随后可应用于其他具有爆发潜力的病毒,以便在与病毒性疾病的斗争中保持领先。