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重复的肠道病毒 30 型到肠道病毒 6 型谱系的基因组转移表明,两种人肠道病毒血清型的流行人群存在共同进化。

Repeated genomic transfers from echovirus 30 to echovirus 6 lineages indicate co-divergence between co-circulating populations of the two human enterovirus serotypes.

机构信息

Clermont Université, Université d'Auvergne, EA 3843, BP 10448, F-63000 Clermont-Ferrand, France.

出版信息

Infect Genet Evol. 2011 Mar;11(2):276-89. doi: 10.1016/j.meegid.2010.06.019. Epub 2010 Jul 6.

DOI:10.1016/j.meegid.2010.06.019
PMID:20615482
Abstract

Human echovirus types 6 (E-6) and 30 (E-30) cause seasonal epidemics of aseptic meningitis. These two enteroviruses are frequently observed in co-circulation, an epidemiological pattern that is prerequisite for the occurrence of dual infections, which can lead to recombination between co-infecting virus strains. Viral sequences were determined at loci 1D (VP1 capsid protein) and 3CD (non structural proteins) in 49 E-6 strains recovered in a single geographical region in France from 1999 to 2007, during the epidemiological survey of enterovirus infections. They were compared with previously recorded sequences of E-30 strains to investigate their evolutionary histories and possible recombination patterns. Phylogenetic analyses identified two distinct E-6 populations and different subpopulations. Assuming a relaxed molecular clock model and a Bayesian skyline demographic model in coalescent analyses with the BEAST program, the substitution rate in E-6 was estimated at 8.597×10(-3) and 6.252×10(-3) substitution/site/year for loci 1D and 3CD respectively. Consistent estimates of divergence times (t(MRCA)) were obtained for loci 1D and 3CD indicating that two distinct E-6 populations originated in 1997 and 1999. Incongruent phylogenetic patterns inferred for the two loci were indicative of recombination events between the two populations. Phylogenies including the E-30 3CD sequences showed close genetic relationships between E-6 and discrete E-30 subpopulations. Recombination breakpoints were located with statistical significance in E-6 and E-30 genomes. Estimates of t(MRCA) of phylogenetic recombinant clades indicated directional genetic transfers from E-30 to E-6 populations and their co-divergence over the time period studied.

摘要

人肠道病毒 6 型(E-6)和 30 型(E-30)引起无菌性脑膜炎的季节性流行。这两种肠道病毒经常共同循环出现,这种流行病学模式是双重感染发生的前提,这可能导致共感染病毒株之间的重组。在法国一个单一地理区域从 1999 年至 2007 年进行肠道病毒感染的流行病学调查期间,在 49 株 E-6 分离株中确定了 1D(VP1 衣壳蛋白)和 3CD(非结构蛋白)基因座的病毒序列。将它们与先前记录的 E-30 株序列进行比较,以研究它们的进化历史和可能的重组模式。系统进化分析确定了两个不同的 E-6 群体和不同的亚群。在 BEAST 程序的合并分析中,假设一个宽松的分子钟模型和贝叶斯天空线人口模型,E-6 的替换率在 1D 和 3CD 基因座分别估计为 8.597×10(-3)和 6.252×10(-3)替换/位点/年。1D 和 3CD 基因座的分歧时间(t(MRCA))得到了一致的估计,表明两个不同的 E-6 群体起源于 1997 年和 1999 年。两个基因座推断的不一致系统发育模式表明两个群体之间发生了重组事件。包括 E-30 3CD 序列的系统发育表明,E-6 和离散 E-30 亚群之间存在密切的遗传关系。在 E-6 和 E-30 基因组中,重组断点具有统计学意义。系统发育重组枝的 t(MRCA)估计表明,从 E-30 到 E-6 群体的定向遗传转移及其在研究期间的共同分化。

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