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β-诺达病毒的系统发育及其RNA聚合酶和衣壳蛋白的分子进化

Phylogeny of betanodaviruses and molecular evolution of their RNA polymerase and coat proteins.

作者信息

Toffolo Vania, Negrisolo Enrico, Maltese Chiara, Bovo Giuseppe, Belvedere Paola, Colombo Lorenzo, Dalla Valle Luisa

机构信息

Department of Biology, University of Padova, Via U. Bassi 58/B, 35131 Padova, Italy.

出版信息

Mol Phylogenet Evol. 2007 Apr;43(1):298-308. doi: 10.1016/j.ympev.2006.08.003. Epub 2006 Aug 11.

Abstract

The betanodaviruses are the causative agent of the disease viral nervous necrosis in fishes. Betanodavirus genome consists of two single-stranded positive-sense RNA molecules (RNA1 and RNA2). RNA1 gene encodes the RNA polymerase, named also protein A, while RNA2 encodes the coat protein precursor, the CPp protein. We investigated the evolutionary relationships among betanodaviruses working on partial sequences of both RNA1 and RNA2. Phylogenetic analyses were performed by applying a maximum likelihood approach. The phylogenetic relationships among the major betanodavirus clades SJNNV-IV, TPNNV-III, BFNNV-II and RGNNV-I were resolved differently in the trees obtained, respectively, from RNA1 and RNA2 multiple alignments. The alternative topologies were corroborated by strong bootstrap values. The molecular evolution of proteins A and CPp was also investigated. Protein A appeared to have evolved under strong purifying selection while the CPp protein was subject to both purifying and neutral selection in different amino acid residues. Intragenic recombination in RNA1 and RNA2 genes was investigated by applying several methods and was not detected. Conversely reassortment of RNA1 and RNA2 genes was demonstrated in some isolates. Finally RNA1 and RNA2 genes substitution rates do not follow a clock-like behavior thus impeding estimation of a possible origin time for Betanodavirus genus.

摘要

β诺达病毒是鱼类病毒性神经坏死疾病的病原体。β诺达病毒基因组由两个单链正义RNA分子(RNA1和RNA2)组成。RNA1基因编码RNA聚合酶,也称为蛋白A,而RNA2编码衣壳蛋白前体,即CPp蛋白。我们通过研究RNA1和RNA2的部分序列来探究β诺达病毒之间的进化关系。采用最大似然法进行系统发育分析。在分别从RNA1和RNA2多序列比对得到的树中,主要的β诺达病毒分支SJNNV-IV、TPNNV-III、BFNNV-II和RGNNV-I之间的系统发育关系得到了不同的解析。不同的拓扑结构得到了较高的自展值的支持。我们还研究了蛋白A和CPp的分子进化。蛋白A似乎在强烈的纯化选择下进化,而CPp蛋白在不同的氨基酸残基上受到纯化选择和中性选择。通过应用多种方法研究了RNA1和RNA2基因中的基因内重组,但未检测到。相反,在一些分离株中证实了RNA1和RNA2基因的重配。最后,RNA1和RNA2基因的替换率不遵循时钟样行为,因此阻碍了对β诺达病毒属可能起源时间的估计。

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