Thézé Julien, Lowes Sophia, Parker Joe, Pybus Oliver G
Department of Zoology, University of Oxford, United Kingdom.
Biodiversity Informatics and Spatial Analysis, The Jodrell Laboratory, Royal Botanic Gardens, Kew, United Kingdom.
Genome Biol Evol. 2015 Oct 21;7(11):2996-3008. doi: 10.1093/gbe/evv202.
The known genetic diversity of the hepaciviruses and pegiviruses has increased greatly in recent years through the discovery of viruses related to hepatitis C virus and human pegivirus in bats, bovines, equines, primates, and rodents. Analysis of these new species is important for research into animal models of hepatitis C virus infection and into the zoonotic origins of human viruses. Here, we provide the first systematic phylogenetic and evolutionary analysis of these two genera at the whole-genome level. Phylogenies confirmed that hepatitis C virus is most closely related to viruses from horses whereas human pegiviruses clustered with viruses from African primates. Within each genus, several well-supported lineages were identified and viral diversity was structured by both host species and location of sampling. Recombination analyses provided evidence of interspecific recombination in hepaciviruses, but none in the pegiviruses. Putative mosaic genome structures were identified in NS5B gene region and were supported by multiple tests. The identification of interspecific recombination in the hepaciviruses represents an important evolutionary event that could be clarified by future sampling of novel viruses. We also identified parallel amino acid changes shared by distantly related lineages that infect similar types of host. Notable parallel changes were clustered in the NS3 and NS4B genes and provide a useful starting point for experimental studies of the evolution of Hepacivirus host-virus interactions.
近年来,通过在蝙蝠、牛、马、灵长类动物和啮齿动物中发现与丙型肝炎病毒和人pegivirus相关的病毒,已知的肝炎病毒属和pegivirus属的遗传多样性大幅增加。对这些新物种的分析对于丙型肝炎病毒感染动物模型以及人类病毒人畜共患病起源的研究至关重要。在此,我们在全基因组水平上对这两个属进行了首次系统的系统发育和进化分析。系统发育分析证实,丙型肝炎病毒与来自马的病毒关系最为密切,而人pegivirus与来自非洲灵长类动物的病毒聚集在一起。在每个属内,确定了几个得到充分支持的谱系,病毒多样性由宿主物种和采样地点构成。重组分析提供了肝炎病毒属种间重组的证据,但pegivirus属没有。在NS5B基因区域鉴定出推定的嵌合基因组结构,并得到多项测试的支持。肝炎病毒属种间重组的鉴定代表了一个重要的进化事件,未来对新型病毒的采样可能会阐明这一事件。我们还鉴定出感染相似类型宿主的远缘谱系共有的平行氨基酸变化。显著的平行变化集中在NS3和NS4B基因中,为肝炎病毒宿主-病毒相互作用进化的实验研究提供了有用的起点。