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小 RNA 病毒科的进化:系统发育关系和共进化分析。

Evolution of Picornaviridae: an examination of phylogenetic relationships and cophylogeny.

机构信息

Department of Biology, Brigham Young University, 401 WIDB, Provo, UT 84602, USA.

出版信息

Mol Phylogenet Evol. 2010 Mar;54(3):995-1005. doi: 10.1016/j.ympev.2009.10.015. Epub 2009 Oct 14.

DOI:10.1016/j.ympev.2009.10.015
PMID:19835964
Abstract

Picornaviruses are responsible for some of the most common and debilitating illnesses affecting humans and animals worldwide. To extend our knowledge of the evolution of picornaviruses and their molecular epidemiology, phylogenetic relationships among 11 genera and the unassigned seal picornavirus type 1 were estimated from the conserved proteins 2C, 3C(pro), and 3D(pol). Each gene was analyzed separately and as a combined dataset. Different tree topologies were recovered from each gene. However, their sequences were determined to be combinable based on our finding of no recombination among genera and failing to reject the hypothesis of homogeneity among datasets using ILD tests. The combined data tree topology was identical to the 3D(pol) gene tree; a topology largely consistent with previous phylogenetic hypotheses based on 3D(pol) and the coding genome. Phylogenetic trees estimated from six phenotypic characters were not congruent with those recovered from molecular datasets; further supporting the hypothesis that viral phenotypes are highly plastic. Finally, we tested the hypothesis of host-virus cophylogeny. Both global and individual tests of the relationships between host and virus trees failed to detect a significant association. These results emphasize the importance of horizontal transmission among host species for picornavirus diversification rather than vertical transmission accompanying speciation.

摘要

小核糖核酸病毒可引起全世界人类和动物的一些最常见和最严重的疾病。为了增进我们对小核糖核酸病毒进化及其分子流行病学的了解,我们从保守蛋白 2C、3C(pro) 和 3D(pol) 估计了 11 个属和未分配的海豹小核糖核酸病毒 1 之间的系统发育关系。分别分析了每个基因,并将其作为一个组合数据集进行分析。从每个基因中都恢复了不同的树拓扑结构。然而,根据我们在属之间没有发现重组以及使用 ILD 检验未能拒绝数据集之间同质性假设的结果,确定它们的序列是可组合的。组合数据集的树拓扑结构与 3D(pol) 基因树相同;这一拓扑结构与基于 3D(pol) 和编码基因组的先前系统发育假说基本一致。从六个表型特征估计的系统发育树与从分子数据集恢复的树不一致;这进一步支持了病毒表型高度可塑的假说。最后,我们测试了宿主-病毒共进化假说。宿主和病毒树之间关系的全局和个体测试均未检测到显著关联。这些结果强调了小核糖核酸病毒多样化过程中宿主种间水平传播的重要性,而不是伴随物种形成的垂直传播。

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