Deng Xufang, Baker Susan C
Department of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago, Maywood, IL 60153, USA.
Department of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago, Maywood, IL 60153, USA.
Virology. 2018 Apr;517:157-163. doi: 10.1016/j.virol.2017.12.024. Epub 2018 Jan 4.
Here we review the evolving story of the coronavirus endoribonuclease (EndoU). Coronavirus EndoU is encoded within the sequence of nonstructural protein (nsp) 15, which was initially identified as a component of the viral replication complex. Biochemical and structural studies revealed the enzymatic nature of nsp15/EndoU, which was postulated to be essential for the unique replication cycle of viruses in the order Nidovirales. However, the role of nsp15 in coronavirus replication was enigmatic as EndoU-deficient coronaviruses were viable and replicated to near wild-type virus levels in fibroblast cells. A breakthrough in our understanding of the role of EndoU was revealed in recent studies, which showed that EndoU mediates the evasion of viral double-stranded RNA recognition by host sensors in macrophages. This new discovery of nsp15/EndoU function leads to new opportunities for investigating how a viral EndoU contributes to pathogenesis and exploiting this enzyme for therapeutics and vaccine design against pathogenic coronaviruses.
在此,我们回顾冠状病毒内切核糖核酸酶(EndoU)的演变历程。冠状病毒EndoU编码于非结构蛋白(nsp)15序列中,nsp15最初被鉴定为病毒复制复合体的一个组成部分。生化和结构研究揭示了nsp15/EndoU的酶学性质,据推测它对于尼多病毒目病毒独特的复制周期至关重要。然而,nsp15在冠状病毒复制中的作用却很神秘,因为缺乏EndoU的冠状病毒是有活力的,并且在成纤维细胞中能复制到接近野生型病毒的水平。最近的研究揭示了我们对EndoU作用理解上的一个突破,这些研究表明EndoU介导巨噬细胞中宿主传感器对病毒双链RNA识别的逃避。nsp15/EndoU功能的这一新发现为研究病毒EndoU如何促成发病机制以及利用这种酶进行针对致病性冠状病毒的治疗和疫苗设计带来了新机遇。