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红腿蝗昆虫痘病毒的基因组

The genome of Melanoplus sanguinipes entomopoxvirus.

作者信息

Afonso C L, Tulman E R, Lu Z, Oma E, Kutish G F, Rock D L

机构信息

Plum Island Animal Disease Center, Agricultural Research Service, U. S. Department of Agriculture, Greenport, New York 11944, USA.

出版信息

J Virol. 1999 Jan;73(1):533-52. doi: 10.1128/JVI.73.1.533-552.1999.

Abstract

The family Poxviridae contains two subfamilies: the Entomopoxvirinae (poxviruses of insects) and the Chordopoxvirinae (poxviruses of vertebrates). Here we present the first characterization of the genome of an entomopoxvirus (EPV) which infects the North American migratory grasshopper Melanoplus sanguinipes and other important orthopteran pests. The 236-kbp M. sanguinipes EPV (MsEPV) genome consists of a central coding region bounded by 7-kbp inverted terminal repeats and contains 267 open reading frames (ORFs), of which 107 exhibit similarity to previously described genes. The presence of genes not previously described in poxviruses, and in some cases in any other known virus, suggests significant viral adaptation to the arthropod host and the external environment. Genes predicting interactions with host cellular mechanisms include homologues of the inhibitor of apoptosis protein, stress response protein phosphatase 2C, extracellular matrixin metalloproteases, ubiquitin, calcium binding EF-hand protein, glycosyltransferase, and a triacylglyceride lipase. MsEPV genes with putative functions in prevention and repair of DNA damage include a complete base excision repair pathway (uracil DNA glycosylase, AP endonuclease, DNA polymerase beta, and an NAD+-dependent DNA ligase), a photoreactivation repair pathway (cyclobutane pyrimidine dimer photolyase), a LINE-type reverse transcriptase, and a mutT homologue. The presence of these specific repair pathways may represent viral adaptation for repair of environmentally induced DNA damage. The absence of previously described poxvirus enzymes involved in nucleotide metabolism and the presence of a novel thymidylate synthase homologue suggest that MsEPV is heavily reliant on host cell nucleotide pools and the de novo nucleotide biosynthesis pathway. MsEPV and lepidopteran genus B EPVs lack genome colinearity and exhibit a low level of amino acid identity among homologous genes (20 to 59%), perhaps reflecting a significant evolutionary distance between lepidopteran and orthopteran viruses. Divergence between MsEPV and the Chordopoxvirinae is indicated by the presence of only 49 identifiable chordopoxvirus homologues, low-level amino acid identity among these genes (20 to 48%), and the presence in MsEPV of 43 novel ORFs in five gene families. Genes common to both poxvirus subfamilies, which include those encoding enzymes involved in RNA transcription and modification, DNA replication, protein processing, virion assembly, and virion structural proteins, define the genetic core of the Poxviridae.

摘要

痘病毒科包含两个亚科

昆虫痘病毒亚科(昆虫痘病毒)和脊椎动物痘病毒亚科(脊椎动物痘病毒)。在此,我们首次对一种感染北美迁徙蝗虫红翅蝗以及其他重要直翅目害虫的昆虫痘病毒(EPV)的基因组进行了特征分析。红翅蝗EPV(MsEPV)基因组大小为236 kbp,由一个中央编码区组成,该编码区两侧为7 kbp的反向末端重复序列,包含267个开放阅读框(ORF),其中107个与先前描述的基因具有相似性。痘病毒中先前未描述的基因,以及在某些情况下任何其他已知病毒中都未描述的基因的存在,表明病毒对节肢动物宿主和外部环境有显著的适应性。预测与宿主细胞机制相互作用的基因包括凋亡抑制蛋白、应激反应蛋白磷酸酶2C、细胞外基质金属蛋白酶、泛素、钙结合EF手蛋白、糖基转移酶和三酰甘油脂肪酶的同源物。MsEPV中具有在预防和修复DNA损伤方面推定功能的基因包括一个完整的碱基切除修复途径(尿嘧啶DNA糖基化酶、AP内切核酸酶、DNA聚合酶β和一个NAD⁺依赖性DNA连接酶)、一个光复活修复途径(环丁烷嘧啶二聚体光解酶)、一个LINE型逆转录酶和一个mutT同源物。这些特定修复途径的存在可能代表病毒为修复环境诱导的DNA损伤而进行的适应性变化。缺乏先前描述的参与核苷酸代谢的痘病毒酶以及存在一种新型胸苷酸合成酶同源物表明MsEPV严重依赖宿主细胞核苷酸库和从头核苷酸生物合成途径。MsEPV和鳞翅目B属EPV缺乏基因组共线性,并且同源基因之间的氨基酸同一性水平较低(20%至59%),这可能反映了鳞翅目病毒和直翅目病毒之间存在显著的进化距离。MsEPV与脊椎动物痘病毒亚科之间的差异表现为仅存在49个可识别的脊椎动物痘病毒同源物、这些基因之间的低水平氨基酸同一性(20%至48%)以及MsEPV在五个基因家族中存在43个新的ORF。痘病毒两个亚科共有的基因,包括那些编码参与RNA转录和修饰、DNA复制、蛋白质加工、病毒粒子组装以及病毒粒子结构蛋白的酶的基因,定义了痘病毒科的遗传核心。

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