罗斯河病毒和巴马森林病毒中的独立重复突变表明,尽管存在持续的净化选择,但祖先种群中仍存在趋同进化和过去的正向选择

IF 5.5 2区 医学 Q1 VIROLOGY Virus Evolution Pub Date : 2024-09-14 DOI:10.1093/ve/veae080
Alyssa T Pyke, Daniel J Wilson, Alice Michie, John S Mackenzie, Allison Imrie, Jane Cameron, Stephen L Doggett, John Haniotis, Lara J Herrero, Leon Caly, Stacey E Lynch, Peter T Mee, Eugene T Madzokere, Ana L Ramirez, Devina Paramitha, Jody Hobson-Peters, David W Smith, Richard Weir, Mitchell Sullivan, Julian Druce, Lorna Melville, Jennifer Robson, Robert Gibb, Andrew F van den Hurk, Sebastian Duchene
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引用次数: 0

摘要

罗斯河病毒(RRV)和巴马森林病毒(BFV)是由节肢动物传播的致关节炎病毒(虫媒病毒),它们表现出通性宿主关联,共同分布于澳大利亚和巴布亚新几内亚(PNG)。利用随机图谱和离散性状系统发育分析,我们对 RRV 和 BFV 特征突变的独立进化进行了剖析。对186个RRV基因组和88个BFV基因组的分析表明,它们的病毒进化轨迹涉及突变的反复选择,尤其是在非结构蛋白1(nsP1)和包膜3(E3)基因中的突变,这表明它们是趋同进化的。RRV(残基 248 和 441)和 BFV(残基 297 和 447)的 nsP1 基因中的趋同突变可能与病毒 RNA 复制和封盖过程中的催化酶机制和宿主膜相互作用有关。趋同的 E3 突变(RRV 位点 59 和 BFV 位点 57)可能与酶促呋喃活性和 E3 从蛋白前体的裂解有关,有助于病毒的成熟和感染。鉴于它们需要在不同的昆虫和脊椎动物宿主体内复制,RRV 和 BFV 的趋同进化可能代表了它们选择性 "微调 "细胞内宿主相互作用的要求与病毒复制酶过程之间的动态联系。尽管有进化趋同的证据,但选择压力分析并未发现任何 RRV 或 BFV 氨基酸位点受到强正向选择,而非结构蛋白位点仅受到弱正向选择。这些发现可能表明,它们的α病毒祖先受到了正选择事件的影响,从而导致了持续的普遍趋同进化,这在很大程度上支持了RRV和BFV种群在蚊子和脊椎动物宿主体内复制期间持续的纯化选择。
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Independent repeated mutations within the alphaviruses Ross River virus and Barmah Forest virus indicates convergent evolution and past positive selection in ancestral populations despite ongoing purifying selection
Ross River virus (RRV) and Barmah Forest virus (BFV) are arthritogenic arthropod-borne viruses (arboviruses) that exhibit generalist host associations and share distributions in Australia and Papua New Guinea (PNG). Using stochastic mapping and discrete-trait phylogenetic analyses we profiled the independent evolution of RRV and BFV signature mutations. Analysis of 186 RRV and 88 BFV genomes demonstrated their viral evolution trajectories have involved repeated selection of mutations, particularly in the nonstructural protein 1 (nsP1) and envelope 3 (E3) genes suggesting convergent evolution. Convergent mutations in the nsP1 genes of RRV (residues 248 and 441) and BFV (residues 297 and 447) may be involved with catalytic enzyme mechanisms and host membrane interactions during viral RNA replication and capping. Convergent E3 mutations (RRV site 59 and BFV site 57) may be associated with enzymatic furin activity and cleavage of E3 from protein precursors assisting viral maturation and infectivity. Given their requirement to replicate in disparate insect and vertebrate hosts, convergent evolution in RRV and BFV may represent a dynamic link between their requirement to selectively ‘fine-tune’ intracellular host interactions and viral replicative enzymatic processes. Despite evidence of evolutionary convergence, selection pressure analyses did not reveal any RRV or BFV amino acid sites under strong positive selection and only weak positive selection for nonstructural protein sites. These findings may indicate that their alphavirus ancestors were subject to positive selection events which predisposed ongoing pervasive convergent evolution, and this largely supports continued purifying selection in RRV and BFV populations during their replication in mosquito and vertebrate hosts.
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来源期刊
Virus Evolution
Virus Evolution Immunology and Microbiology-Microbiology
CiteScore
10.50
自引率
5.70%
发文量
108
审稿时长
14 weeks
期刊介绍: Virus Evolution is a new Open Access journal focusing on the long-term evolution of viruses, viruses as a model system for studying evolutionary processes, viral molecular epidemiology and environmental virology. The aim of the journal is to provide a forum for original research papers, reviews, commentaries and a venue for in-depth discussion on the topics relevant to virus evolution.
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