McWilliam Leitch E C, Bendig J, Cabrerizo M, Cardosa J, Hyypiä T, Ivanova O E, Kelly A, Kroes A C M, Lukashev A, MacAdam A, McMinn P, Roivainen M, Trallero G, Evans D J, Simmonds P
Centre for Infectious Diseases, University of Edinburgh, Summerhall, Edinburgh EH9 1QH, United Kingdom.
J Virol. 2009 Mar;83(5):2109-18. doi: 10.1128/JVI.02109-08. Epub 2008 Dec 17.
Globally, echovirus 30 (E30) is one of the most frequently identified enteroviruses and a major cause of meningitis. Despite its wide distribution, little is known about its transmission networks or the dynamics of its recombination and geographical spread. To address this, we have conducted an extensive molecular epidemiology and evolutionary study of E30 isolates collected over 8 years from a geographically wide sample base (11 European countries, Asia, and Australia). 3Dpol sequences fell into several distinct phylogenetic groups, interspersed with other species B serotypes, enabling E30 isolates to be classified into 38 recombinant forms (RFs). Substitutions in VP1 and 3Dpol regions occurred predominantly at synonymous sites (ratio of nonsynonymous to synonymous substitutions, 0.05) with VP1 showing a rapid substitution rate of 8.3 x 10(-3) substitutions per site per year. Recombination frequency was tightly correlated with VP1 divergence; viruses differing by evolutionary distances of >0.1 (or 6 years divergent evolution) almost invariably (>97%) had different 3Dpol groups. Frequencies of shared 3Dpol groups additionally correlated with geographical distances, with Europe and South Asia showing turnover of entirely distinct virus populations. Population turnover of E30 was characterized by repeated cycles of emergence, dominance, and disappearance of individual RFs over periods of 3 to 5 years, although the existence and nature of evolutionary selection underlying these population replacements remain unclear. The occurrence of frequent "sporadic" recombinants embedded within VP1 groupings of other RFs and the much greater number of 3Dpol groups than separately identifiable VP1 lineages suggest frequent recombination with an external diverse reservoir of non-E30 viruses.
在全球范围内,肠道病毒71型(E30)是最常被鉴定出的肠道病毒之一,也是脑膜炎的主要病因。尽管其分布广泛,但对其传播网络或重组及地理传播动态知之甚少。为了解决这一问题,我们对8年间从广泛的地理样本库(11个欧洲国家、亚洲和澳大利亚)收集的E30分离株进行了广泛的分子流行病学和进化研究。3Dpol序列分为几个不同的系统发育组,穿插在其他B种血清型之间,使E30分离株能够被分为38种重组形式(RFs)。VP1和3Dpol区域的替换主要发生在同义位点(非同义替换与同义替换的比率为0.05),VP1显示出每年每个位点8.3×10⁻³替换的快速替换率。重组频率与VP1分歧紧密相关;进化距离>0.1(或6年分歧进化)的病毒几乎总是(>97%)具有不同的3Dpol组。共享3Dpol组的频率还与地理距离相关,欧洲和南亚显示出完全不同的病毒种群更替。E30的种群更替特征是在3至5年的时间内,单个RFs反复出现、占主导地位和消失的周期,尽管这些种群替代背后的进化选择的存在和性质仍不清楚。在其他RFs的VP1分组中嵌入频繁的“散发性”重组体,以及3Dpol组的数量比可单独识别的VP1谱系多得多,这表明与非E30病毒的外部多样库频繁重组。