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重组对浓核病毒系统发育的影响。

Effects of recombination on densovirus phylogeny.

作者信息

Martynova Elena U, Schal Coby, Mukha Dmitry V

机构信息

Vavilov Institute of General Genetics Russian Academy of Sciences, Moscow, 119991, Russia.

North Carolina State University, Raleigh, North Carolina, 27695-7613, USA.

出版信息

Arch Virol. 2016 Jan;161(1):63-75. doi: 10.1007/s00705-015-2642-5. Epub 2015 Oct 16.

DOI:10.1007/s00705-015-2642-5
PMID:26475154
Abstract

Densoviruses are a group of arthropod-infecting viruses with a small single-stranded linear DNA genome. These viruses constitute the subfamily Densovirinae of the family Parvoviridae. While recombination in between vertebrate-infecting parvoviruses has been investigated, to date, no systematic analysis of recombination has been carried out for densoviruses. The aim of the present work was to study possible recombination events in the evolutionary history of densoviruses and to assess possible effects of recombination on phylogenies inferred using amino acid sequences of nonstructural (NS) and capsid (viral protein, VP) proteins. For this purpose, the complete or nearly complete genome nucleotide sequences of 40 densoviruses from the GenBank database were used to construct a phylogenetic cladogram. The viruses under study clustered into five distinct groups corresponding to the five currently accepted genera. Recombination within each group was studied independently. The RDP4 software revealed three statistically highly credible recombination events, two of which involved viruses of the genus Ambidensovirus, and the other, viruses from the genus Iteradensovirus. These recombination events led to mismatches between phylogenetic trees constructed using comparison of amino acid sequences of proteins encoded by genome regions of recombinant and non-recombinant origin (regulatory NS1 and NS3 proteins and capsid VP protein).

摘要

浓核病毒是一类感染节肢动物的病毒,具有小的单链线性DNA基因组。这些病毒构成了细小病毒科的浓核病毒亚科。虽然已经对感染脊椎动物的细小病毒之间的重组进行了研究,但迄今为止,尚未对浓核病毒进行系统的重组分析。本研究的目的是研究浓核病毒进化史上可能的重组事件,并评估重组对使用非结构(NS)蛋白和衣壳(病毒蛋白,VP)蛋白的氨基酸序列推断的系统发育的可能影响。为此,使用来自GenBank数据库的40种浓核病毒的完整或近乎完整的基因组核苷酸序列构建系统发育分支图。所研究的病毒聚为五个不同的组,对应于目前公认的五个属。对每组内的重组进行了独立研究。RDP4软件揭示了三个统计学上高度可信的重组事件,其中两个涉及双浓核病毒属的病毒,另一个涉及迭代浓核病毒属的病毒。这些重组事件导致了使用重组和非重组来源的基因组区域(调节性NS1和NS3蛋白以及衣壳VP蛋白)编码的蛋白质的氨基酸序列比较构建的系统发育树之间的不匹配。

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