Centre for Infectious Diseases, University of Edinburgh, Summerhall, Edinburgh, UK.
J Gen Virol. 2010 May;91(Pt 5):1229-38. doi: 10.1099/vir.0.018747-0. Epub 2010 Jan 20.
Human parechoviruses (HPeVs) are highly prevalent RNA viruses classified in the family Picornaviridae. Several antigenically distinct types circulate in human populations worldwide, whilst recombination additionally contributes to the genetic heterogeneity of the virus. To investigate factors influencing the likelihood of recombination and to compare its dynamics among types, 154 variants collected from four widely geographically separated referral centres (UK, The Netherlands, Thailand and Brazil) were typed by VP3/VP1 amplification/sequencing with recombination groups assigned by analysis of 3Dpol sequences. HPeV1B and HPeV3 were the most frequently detected types in each referral region, but with marked geographical differences in the frequencies of different recombinant forms (RFs) of types 1B, 5 and 6. HPeV1B showed more frequent recombination than HPeV3, in terms both of evolutionary divergence and of temporal/geographical indicators of population separation. HPeV1 variants showing between 10 and 20% divergence in VP3/VP1 almost invariably fell into different recombination groups, compared with only one-third of similarly divergent HPeV3 variants. Substitution rates calculated by beast in the VP3/VP1 region of HPeV1 and HPeV3 allowed half-lives of the RFs of 4 and 20 years, respectively, to be calculated, estimates fitting closely with their observed lifespans based on population sampling. The variability in recombination dynamics between HPeV1B and HPeV3 offers an intriguing link with their markedly different seasonal patterns of transmission, age distributions of infection and clinical outcomes. Future investigation of the epidemiological and biological opportunities and constraints on intertypic recombination will provide more information about its influence on the longer term evolution and pathogenicity of parechoviruses.
人类肠道孤儿病毒(HPeV)是一种高度流行的 RNA 病毒,属于小 RNA 病毒科。世界范围内存在多种具有不同抗原性的亚型,而重组则进一步增加了病毒的遗传异质性。为了研究影响重组可能性的因素,并比较不同类型之间的重组动态,我们对从四个地理位置相距甚远的转诊中心(英国、荷兰、泰国和巴西)收集的 154 个变异株进行了 VP3/VP1 扩增/测序分型,并通过 3Dpol 序列分析分配重组群。在每个转诊地区,HPeV1B 和 HPeV3 是最常检测到的类型,但不同 1B、5 和 6 型的重组形式(RF)的频率存在明显的地理差异。就进化分歧和种群分离的时间/地理指标而言,HPeV1B 的重组频率高于 HPeV3。HPeV1 变异株在 VP3/VP1 区显示 10-20%的差异,几乎总是属于不同的重组群,而类似差异的 HPeV3 变异株只有三分之一属于不同的重组群。Beast 在 HPeV1 和 HPeV3 的 VP3/VP1 区计算的替代率允许分别计算出 RF 的半衰期为 4 年和 20 年,这些估计值与根据人群抽样观察到的 RF 寿命非常吻合。HPeV1B 和 HPeV3 之间重组动态的差异与它们明显不同的传播季节模式、感染年龄分布和临床结果之间存在有趣的联系。未来对 HPeV 间重组的流行病学和生物学机会和限制的研究将提供更多关于其对肠道孤儿病毒长期进化和致病性影响的信息。