Singh Neetu, Ranjan Priya, Cao Weiping, Patel Jenish, Gangappa Shivaprakash, Davidson Bruce A, Sullivan John M, Prasad Paras N, Knight Paul R, Sambhara Suryaprakash
Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30329, USA.
Department of Anesthesiology, State University of New York at Buffalo, Buffalo, NY 14203, USA; Department of Pathology and Anatomical Sciences, State University of New York at Buffalo, Buffalo, NY 14203, USA; Veterans Administration Western New York Healthcare System, Buffalo, NY 14215, USA.
Mol Ther Nucleic Acids. 2020 Mar 6;19:1413-1422. doi: 10.1016/j.omtn.2020.01.025. Epub 2020 Jan 31.
Retinoic acid-inducible gene-I (RIG-I) is a cytosolic pathogen sensor that is crucial against a number of viral infections. Many viruses have evolved to inhibit pathogen sensors to suppress host innate immune responses. In the case of influenza, nonstructural protein 1 (NS1) suppresses RIG-I function, leading to viral replication, morbidity, and mortality. We show that silencing NS1 with in-vitro-transcribed 5'-triphosphate containing NS1 short hairpin RNA (shRNA) (5'-PPP-NS1shRNA), designed using the conserved region of a number of influenza viruses, not only prevented NS1 expression but also induced RIG-I activation and type I interferon (IFN) expression, resulting in an antiviral state leading to inhibition of influenza virus replication in vitro. In addition, administration of 5'-PPP-NS1shRNA in prophylactic and therapeutic settings resulted in significant inhibition of viral replication following viral challenge in vivo in mice with corresponding increases of RIG-I, IFN-β, and IFN-λ, as well as a decrease in NS1 expression.
维甲酸诱导基因I(RIG-I)是一种胞质病原体传感器,对多种病毒感染至关重要。许多病毒已经进化出抑制病原体传感器的机制,以抑制宿主的先天免疫反应。就流感而言,非结构蛋白1(NS1)会抑制RIG-I的功能,导致病毒复制、发病和死亡。我们发现,使用针对多种流感病毒保守区域设计的体外转录含5'-三磷酸的NS1短发夹RNA(shRNA)(5'-PPP-NS1shRNA)沉默NS1,不仅能阻止NS1的表达,还能诱导RIG-I激活和I型干扰素(IFN)表达,从而形成抗病毒状态,导致流感病毒在体外的复制受到抑制。此外,在预防性和治疗性环境中给予5'-PPP-NS1shRNA,在小鼠体内病毒攻击后能显著抑制病毒复制,同时RIG-I、IFN-β和IFN-λ相应增加,NS1表达减少。