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非 GII 基因型 4(GII.4)诺如病毒的进化动态显示变体的有限和独立多样化。

Evolutionary dynamics of non-GII genotype 4 (GII.4) noroviruses reveal limited and independent diversification of variants.

机构信息

Division of Viral Products, Food and Drug Administration, Silver Spring, MD, USA.

出版信息

J Gen Virol. 2018 Aug;99(8):1027-1035. doi: 10.1099/jgv.0.001088. Epub 2018 Jun 19.

DOI:10.1099/jgv.0.001088
PMID:29916802
Abstract

Noroviruses are extremely diverse, with ≥30 genotypes infecting humans. GII genotype 4 (GII.4) noroviruses, the most prevalent genotype, present a constant accumulation of mutations on the major capsid protein (VP1), resulting in the chronological emergence of new variants every 2-8 years. On the other hand, non-GII.4 noroviruses present a limited number of changes on the capsid protein over time. Despite limited diversification, non-GII.4 viruses can also be associated with large outbreaks. To gain insights into the evolutionary dynamics of non-GII.4 viruses, we performed variant-specific phylogenetic analyses on a comprehensive dataset of 13 genotypes. Although the genotypes with a single variant presented a linear (clock-like) evolution, maximum-likelihood analyses revealed a lack of clock-like signals for the genotypes with ≥3 variants: GI.3, GII.6 and GII.17. Notably, the evolutionary pattern of non-GII.4 viruses showed clock-like signals when each variant was analysed separately. A minimal impact on the long-term clock-like evolution of VP1 was detected due to the exchange (recombination) of the polymerase types. The linear evolution, without replacement among variants, is explained by minimal changes at the protein level due to the higher ratio of synonymous compared to non-synonymous substitutions in their evolution. Taken together, these data indicate that (i) the variants of non-GII.4 noroviruses evolve and persist in the population independently, probably due to strong evolutionary constraints on VP1, and (ii) variant-specific analyses with robust sequence databases that cover long periods of surveillance are needed to limit the potential for misinterpretation of the evolutionary dynamics of non-GII.4 noroviruses.

摘要

诺如病毒具有极高的多样性,至少有 30 种基因型可感染人类。其中,感染人类最常见的基因型是 GII 型 4(GII.4)诺如病毒,其主要衣壳蛋白(VP1)不断积累突变,导致每隔 2-8 年就会出现新的变异株。另一方面,非 GII.4 诺如病毒的衣壳蛋白随时间变化的突变数量有限。尽管病毒多样化程度有限,但非 GII.4 病毒也可能引发大规模暴发。为了深入了解非 GII.4 病毒的进化动态,我们对 13 种基因型的综合数据集进行了变体特异性系统发育分析。尽管具有单一变体的基因型表现出线性(钟形)进化,但最大似然分析显示,具有≥3 个变体的基因型缺乏钟形信号:GI.3、GII.6 和 GII.17。值得注意的是,当分别分析每个变体时,非 GII.4 病毒的进化模式显示出钟形信号。由于聚合酶类型的交换(重组),对 VP1 的长期钟形进化的影响最小。由于在其进化过程中同义替换与非同义替换的比例较高,VP1 蛋白水平的微小变化导致没有变体间的替换,从而解释了线性进化。综上所述,这些数据表明:(i)非 GII.4 诺如病毒的变体独立地在人群中进化和持续存在,这可能是由于 VP1 受到强烈的进化限制;(ii)需要使用覆盖长时间监测的稳健序列数据库进行变体特异性分析,以限制对非 GII.4 诺如病毒进化动态的潜在误解。

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