Lin Yuhao, Sun Qiqi, Zhang Bao, Zhao Wei, Shen Chenguang
BSL-3 Laboratory (Guangdong), Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Department of Laboratory Medicine, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Front Cell Dev Biol. 2023 Jul 27;11:1229393. doi: 10.3389/fcell.2023.1229393. eCollection 2023.
The coronavirus disease 2019 (COVID-19) was a global endemic that continues to cause a large number of severe illnesses and fatalities. There is increasing evidence that non-coding RNAs (ncRNAs) are crucial regulators of viral infection and antiviral immune response and the role of non-coding RNAs in SARS-CoV-2 infection has now become the focus of scholarly inquiry. After SARS-CoV-2 infection, some ncRNAs' expression levels are regulated to indirectly control the expression of antiviral genes and viral gene replication. However, some other ncRNAs are hijacked by SARS-CoV-2 in order to help the virus evade the immune system by suppressing the expression of type I interferon (IFN-1) and controlling cytokine levels. In this review, we summarize the recent findings of long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) among non-coding RNAs in SARS-CoV-2 infection and antiviral response, discuss the potential mechanisms of actions, and prospects for the detection, treatment, prevention and future directions of SARS-CoV-2 infection research.
2019年冠状病毒病(COVID-19)是一种全球流行病,持续导致大量严重疾病和死亡。越来越多的证据表明,非编码RNA(ncRNAs)是病毒感染和抗病毒免疫反应的关键调节因子,非编码RNA在严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染中的作用现已成为学术研究的焦点。SARS-CoV-2感染后,一些ncRNAs的表达水平受到调节,以间接控制抗病毒基因的表达和病毒基因复制。然而,其他一些ncRNAs被SARS-CoV-2劫持,通过抑制I型干扰素(IFN-1)的表达和控制细胞因子水平来帮助病毒逃避免疫系统。在这篇综述中,我们总结了非编码RNA中长链非编码RNA(lncRNAs)和微小RNA(miRNAs)在SARS-CoV-2感染和抗病毒反应中的最新发现,讨论了潜在的作用机制,以及SARS-CoV-2感染研究的检测、治疗、预防和未来方向的前景。