Wu Chang-Jer, Huang Hui-Wen, Liu Chiu-Yi, Hong Cheng-Fong, Chan Yi-Lin
Department of Food Science, National Taiwan Ocean University, Keelung, Pei Ning Road, Keelung 202, Taiwan, ROC.
Antiviral Res. 2005 Jan;65(1):45-8. doi: 10.1016/j.antiviral.2004.09.005.
Serious outbreaks of severe acute respiratory syndrome (SARS), caused by the newly discovered coronavirus SARS-CoV, occurred between late 2002 and early 2003 and there is an urgent need for effective antiviral agents. RNA interference in animals and post-transcriptional gene silencing plants is mediated by small double-stranded RNA molecules named small interfering RNA (siRNA). Recently, siRNA-induced RNA interference(RNAi) may provide a new approach to therapy for pathogenic viruses, e.g. HIV and HCV. In this study, the silencing potential of seven synthetic siRNAs against SARS-CoV leader, TRS, 3'-UTR and Spike coding sequence have been applied to explore the possibility for prevention of SARS-CoV infection. We demonstrate that siRNAs directed against Spike sequences and the 3'-UTR can inhibit the replication of SARS-CoV in Vero-E6 cells, and holds out promise for the development of an effective antiviral agent against SARS-CoV.
由新发现的冠状病毒SARS-CoV引起的严重急性呼吸综合征(SARS)在2002年末至2003年初期间严重爆发,因此迫切需要有效的抗病毒药物。动物中的RNA干扰和植物中的转录后基因沉默由名为小干扰RNA(siRNA)的小双链RNA分子介导。最近,siRNA诱导的RNA干扰(RNAi)可能为治疗致病性病毒(如HIV和HCV)提供一种新方法。在本研究中,已应用针对SARS-CoV前导序列、TRS、3'-UTR和刺突编码序列的七种合成siRNA的沉默潜力,以探索预防SARS-CoV感染的可能性。我们证明,针对刺突序列和3'-UTR的siRNA可以抑制SARS-CoV在Vero-E6细胞中的复制,并为开发针对SARS-CoV的有效抗病毒药物带来希望。