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本文引用的文献

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Ratification vote on taxonomic proposals to the International Committee on Taxonomy of Viruses (2016).对提交给国际病毒分类委员会的分类学提案的批准投票(2016年)
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Arterivirus nsp12 versus the coronavirus nsp16 2'-O-methyltransferase: comparison of the C-terminal cleavage products of two nidovirus pp1ab polyproteins.动脉炎病毒非结构蛋白12与冠状病毒非结构蛋白16 2'-O-甲基转移酶:两种巢病毒多聚蛋白pp1ab C末端裂解产物的比较
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动脉炎病毒基因组高度分化的5'编码区的结构组织与进化,包括新型负鼠正粘病毒

Domain Organization and Evolution of the Highly Divergent 5' Coding Region of Genomes of Arteriviruses, Including the Novel Possum Nidovirus.

作者信息

Gulyaeva Anastasia, Dunowska Magdalena, Hoogendoorn Erik, Giles Julia, Samborskiy Dmitry, Gorbalenya Alexander E

机构信息

Department of Medical Microbiology, Leiden University Medical Center, Leiden, the Netherlands.

Institute of Veterinary, Animal and Biomedical Sciences, Massey University, Palmerston North, New Zealand

出版信息

J Virol. 2017 Feb 28;91(6). doi: 10.1128/JVI.02096-16. Print 2017 Mar 15.

DOI:10.1128/JVI.02096-16
PMID:28053107
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5331827/
Abstract

In five experimentally characterized arterivirus species, the 5'-end genome coding region encodes the most divergent nonstructural proteins (nsp's), nsp1 and nsp2, which include papain-like proteases (PLPs) and other poorly characterized domains. These are involved in regulation of transcription, polyprotein processing, and virus-host interaction. Here we present results of a bioinformatics analysis of this region of 14 arterivirus species, including that of the most distantly related virus, wobbly possum disease virus (WPDV), determined by a modified 5' rapid amplification of cDNA ends (RACE) protocol. By combining profile-profile comparisons and phylogeny reconstruction, we identified an association of the four distinct domain layouts of nsp1-nsp2 with major phylogenetic lineages, implicating domain gain, including duplication, and loss in the early nsp1 evolution. Specifically, WPDV encodes highly divergent homologs of PLP1a, PLP1b, PLP1c, and PLP2, with PLP1a lacking the catalytic Cys residue, but does not encode nsp1 Zn finger (ZnF) and "nuclease" domains, which are conserved in other arteriviruses. Unexpectedly, our analysis revealed that the only catalytically active nsp1 PLP of equine arteritis virus (EAV), known as PLP1b, is most similar to PLP1c and thus is likely to be a PLP1b paralog. In all non-WPDV arteriviruses, PLP1b/c and PLP1a show contrasting patterns of conservation, with the N- and C-terminal subdomains, respectively, being enriched with conserved residues, which is indicative of different functional specializations. The least conserved domain of nsp2, the hypervariable region (HVR), has its size varied 5-fold and includes up to four copies of a novel PxPxPR motif that is potentially recognized by SH3 domain-containing proteins. Apparently, only EAV lacks the signal that directs -2 ribosomal frameshifting in the nsp2 coding region. Arteriviruses comprise a family of mammalian enveloped positive-strand RNA viruses that include some of the most economically important pathogens of swine. Most of our knowledge about this family has been obtained through characterization of viruses from five species: , , , , and Here we present the results of comparative genomics analyses of viruses from all known 14 arterivirus species, including the most distantly related virus, WPDV, whose genome sequence was completed in this study. Our analysis focused on the multifunctional 5'-end genome coding region that encodes multidomain nonstructural proteins 1 and 2. Using diverse bioinformatics techniques, we identified many patterns of evolutionary conservation that are specific to members of distinct arterivirus species, both characterized and novel, or their groups. They are likely associated with structural and functional determinants important for virus replication and virus-host interaction.

摘要

在五个已通过实验表征的动脉炎病毒种中,5'-端基因组编码区编码了最具差异的非结构蛋白(nsp),即nsp1和nsp2,其中包括木瓜蛋白酶样蛋白酶(PLP)和其他特征不明的结构域。这些蛋白参与转录调控、多聚蛋白加工以及病毒与宿主的相互作用。在此,我们展示了对14种动脉炎病毒该区域的生物信息学分析结果,其中包括关系最远的病毒——晃荡负鼠病病毒(WPDV),其序列是通过改良的5' cDNA末端快速扩增(RACE)方案确定的。通过结合图谱-图谱比较和系统发育重建,我们确定了nsp1-nsp2的四种不同结构域布局与主要系统发育谱系的关联,这意味着在nsp1早期进化过程中存在结构域的获得,包括重复,以及结构域的丢失。具体而言,WPDV编码高度差异的PLP1a、PLP1b、PLP1c和PLP2同源物,其中PLP1a缺乏催化性半胱氨酸残基,但不编码nsp1锌指(ZnF)和“核酸酶”结构域,而这些结构域在其他动脉炎病毒中是保守的。出乎意料的是,我们的分析表明,马动脉炎病毒(EAV)唯一具有催化活性的nsp1 PLP,即PLP-1b,与PLP1c最为相似,因此可能是PLP1b的旁系同源物。在所有非WPDV动脉炎病毒中,PLP1b/c和PLP1a表现出相反的保守模式,其N端和C端亚结构域分别富含保守残基,这表明它们具有不同的功能特化。nsp2最不保守的结构域,即高变区(HVR),其大小变化了5倍,并且包含多达四个新型PxPxPR基序拷贝,这些基序可能被含SH3结构域的蛋白识别。显然,只有EAV在nsp2编码区缺乏引导-2核糖体移码的信号。动脉炎病毒是一类哺乳动物有包膜正链RNA病毒,其中包括一些对猪来说经济上最重要的病原体。我们对这个病毒家族的大部分了解是通过对五个种的病毒进行表征获得的: 、 、 、 以及 。在此,我们展示了对所有已知的14种动脉炎病毒进行比较基因组学分析的结果,其中包括关系最远的病毒WPDV(其基因组序列在本研究中完成)。我们的分析集中在多功能的5'-端基因组编码区,该区域编码多结构域非结构蛋白1和2。使用多种生物信息学技术,我们确定了许多进化保守模式,这些模式是不同动脉炎病毒种(包括已表征的和新发现的种)或其群体所特有的。它们可能与对病毒复制和病毒-宿主相互作用至关重要的结构和功能决定因素相关。