Gorbalenya Alexander E, Enjuanes Luis, Ziebuhr John, Snijder Eric J
Molecular Virology Laboratory, Department of Medical Microbiology, Leiden University Medical Center, LUMC E4-P, P.O. Box 9600, 2300 RC Leiden, The Netherlands.
Virus Res. 2006 Apr;117(1):17-37. doi: 10.1016/j.virusres.2006.01.017. Epub 2006 Feb 28.
This review focuses on the monophyletic group of animal RNA viruses united in the order Nidovirales. The order includes the distantly related coronaviruses, toroviruses, and roniviruses, which possess the largest known RNA genomes (from 26 to 32kb) and will therefore be called "large" nidoviruses in this review. They are compared with their arterivirus cousins, which also belong to the Nidovirales despite having a much smaller genome (13-16kb). Common and unique features that have been identified for either large or all nidoviruses are outlined. These include the nidovirus genetic plan and genome diversity, the composition of the replicase machinery and virus particles, virus-specific accessory genes, the mechanisms of RNA and protein synthesis, and the origin and evolution of nidoviruses with small and large genomes. Nidoviruses employ single-stranded, polycistronic RNA genomes of positive polarity that direct the synthesis of the subunits of the replicative complex, including the RNA-dependent RNA polymerase and helicase. Replicase gene expression is under the principal control of a ribosomal frameshifting signal and a chymotrypsin-like protease, which is assisted by one or more papain-like proteases. A nested set of subgenomic RNAs is synthesized to express the 3'-proximal ORFs that encode most conserved structural proteins and, in some large nidoviruses, also diverse accessory proteins that may promote virus adaptation to specific hosts. The replicase machinery includes a set of RNA-processing enzymes some of which are unique for either all or large nidoviruses. The acquisition of these enzymes may have improved the low fidelity of RNA replication to allow genome expansion and give rise to the ancestors of small and, subsequently, large nidoviruses.
本综述聚焦于归属于尼多病毒目(Nidovirales)的动物RNA病毒单系群。该目包括亲缘关系较远的冠状病毒、环曲病毒和罗氏病毒,它们拥有已知最大的RNA基因组(26至32kb),因此在本综述中将被称为“大型”尼多病毒。它们与动脉炎病毒亲属进行了比较,动脉炎病毒尽管基因组小得多(13 - 16kb),但也属于尼多病毒目。概述了已确定的大型或所有尼多病毒的共同和独特特征。这些包括尼多病毒的遗传规划和基因组多样性、复制酶机制和病毒粒子的组成、病毒特异性辅助基因、RNA和蛋白质合成机制,以及小基因组和大基因组尼多病毒的起源和进化。尼多病毒采用正链单链多顺反子RNA基因组,该基因组指导复制复合体亚基的合成,包括RNA依赖性RNA聚合酶和解旋酶。复制酶基因表达主要受核糖体移码信号和胰凝乳蛋白酶样蛋白酶的控制,后者由一种或多种木瓜蛋白酶样蛋白酶辅助。合成了一组嵌套的亚基因组RNA,以表达3'-近端开放阅读框,这些开放阅读框编码最保守的结构蛋白,并且在一些大型尼多病毒中,还编码多种辅助蛋白,这些辅助蛋白可能促进病毒对特定宿主的适应。复制酶机制包括一组RNA加工酶,其中一些对所有或大型尼多病毒而言是独特的。这些酶的获得可能提高了RNA复制的低保真性,从而允许基因组扩展,并产生了小基因组尼多病毒的祖先,随后是大基因组尼多病毒的祖先。