Simmonds Peter, Welch Jon
Virus Evolution Group, Centre for Infectious Diseases, University of Edinburgh, Summerhall, Edinburgh EH9 1QH, United Kingdom.
J Virol. 2006 Jan;80(1):483-93. doi: 10.1128/JVI.80.1.483-493.2006.
Enteroviruses are members of the family Picornaviridae that cause widespread infections in human and other mammalian populations. Enteroviruses are genetically and antigenically highly variable, and recombination within and between serotypes contributes to their genetic diversity. To investigate the dynamics of the recombination process, sequence phylogenies between three regions of the genome (VP4, VP1, and 3Dpol) were compared among species A and B enterovirus variants detected in a human population-based survey in Scotland between 2000 and 2001, along with contemporary virus isolates collected in the same geographical region. This analysis used novel bioinformatic methods to quantify phylogenetic compatibility and correlations with serotype assignments of evolutionary trees constructed for different regions of the enterovirus genome. Species B enteroviruses showed much more frequent, time-correlated recombination events than those found for species A, despite the equivalence in population sampling, concordant with a linkage analysis of previously characterized enterovirus sequences obtained over longer collection periods. An analysis of recombination among complete genome sequences by computation of a phylogenetic compatibility matrix (PCM) demonstrated sharply defined boundaries between the VP2/VP3/VP1 block and sequences to either side in phylogenetic compatibility. The PCM also revealed equivalent or frequently greater degrees of incompatibility between different parts within the nonstructural region (2A-3D), indicating the occurrence of extensive recombination events in the past evolution of this part of the genome. Together, these findings provide new insights into the dynamics of species A and B enterovirus recombination and evolution and into the contribution of structured sampling to documenting reservoirs, emergence, and spread of novel recombinant forms in human populations.
肠道病毒是小核糖核酸病毒科的成员,可在人类和其他哺乳动物群体中引起广泛感染。肠道病毒在基因和抗原方面具有高度变异性,血清型内部和之间的重组促成了它们的遗传多样性。为了研究重组过程的动态变化,在2000年至2001年苏格兰一项基于人群的调查中检测到的A种和B种肠道病毒变体之间,比较了基因组三个区域(VP4、VP1和3Dpol)的序列系统发育,同时还比较了在同一地理区域收集的当代病毒分离株。该分析使用了新颖的生物信息学方法,以量化系统发育兼容性以及与为肠道病毒基因组不同区域构建的进化树血清型分配的相关性。尽管在人群抽样方面相当,但B种肠道病毒显示出比A种更频繁、与时间相关的重组事件,这与对更长收集期内获得的先前特征化肠道病毒序列的连锁分析一致。通过计算系统发育兼容性矩阵(PCM)对完整基因组序列之间的重组进行分析,结果表明VP2/VP3/VP1区域与系统发育兼容性两侧的序列之间存在明确界定的边界。PCM还揭示了非结构区域(2A - 3D)内不同部分之间同等或通常更大程度的不兼容性,表明在该基因组部分的过去进化中发生了广泛的重组事件。这些发现共同为A种和B种肠道病毒重组和进化的动态变化以及结构化抽样对记录人类群体中新型重组形式的储存库、出现和传播的贡献提供了新的见解。