Genomics and evolutionary analysis of Chlorella variabilis-infecting viruses demarcate criteria for defining species of giant viruses.

IF 4 2区 医学 Q2 VIROLOGY
Journal of Virology Pub Date : 2024-11-19 Epub Date: 2024-10-15 DOI:10.1128/jvi.00361-24
João Victor R P Carvalho, Roger M Carlson, Jayadri Ghosh, Victória F Queiroz, Ellen G de Oliveira, Bruna B Botelho, Clécio A C Filho, Irina V Agarkova, O William McClung, James L Van Etten, David D Dunigan, Rodrigo A L Rodrigues
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引用次数: 0

Abstract

Chloroviruses exhibit a close relationship with their hosts with the phenotypic aspect of their ability to form lytic plaques having primarily guided the taxonomy. However, with the isolation of viruses that are only able to complete their replication cycle in one strain of Chlorella variabilis, systematic challenges emerged. In this study, we described the genomic features of 53 new chlorovirus isolates and used them to elucidate part of the evolutionary history and taxonomy of this clade. Our analysis revealed new chloroviruses with the largest genomes to date (>400 kbp) and indicated that four genomic features are statistically different in the viruses that only infect the Syngen 2-3 strain of C. variabilis (OSy viruses). We found large regions of dissimilarity in the genomes of viruses PBCV-1 and OSy-NE5 when compared with the other genomes. These regions contained genes related to the interaction with the host cell machinery and viral capsid proteins, which provided insights into the evolution of the replicative and structural modules in these giant viruses. Phylogenetic analysis using hallmark genes of Nucleocytoviricota revealed that OSy-viruses evolved from the NC64A-viruses, possibly emerging as a result of the strict relationship with their hosts. Merging phylogenetics and nucleotide identity analyses, we propose strategies to demarcate viral species, resulting in seven new species of chloroviruses. Collectively, our results show how genomic data can be used as lines of evidence to demarcate viral species. Using the chloroviruses as a case study, we expect that similar initiatives will emerge using the basis exhibited here.IMPORTANCEChloroviruses are a group of giant viruses with long dsDNA genomes that infect different species of Chlorella-like green algae. They are host-specific, and some isolates can only replicate within a single strain of Chlorella variabilis. The genomics of these viruses is still poorly explored, and the characterization of new isolates provides important data on their genetic diversity and evolution. In this work, we describe 53 new chlorovirus genomes, including many isolated from alkaline lakes for the first time. Through comparative genomics and molecular phylogeny, we provide evidence of genomic gigantism in chloroviruses and show that a subset of viruses became highly specific for their hosts at a particular point in evolutionary history. We propose criteria to demarcate species of chloroviruses, paving the way for an update in the taxonomy of other groups of viruses. This study is a new and important piece in the complex puzzle of giant algal viruses.

变色小球藻感染病毒的基因组学和进化分析为界定巨型病毒的种类划定了标准。
氯病毒与其宿主关系密切,其形成溶解斑块的表型能力是其分类的主要依据。然而,随着只能在一株变色小球藻中完成复制周期的病毒的分离,系统性的挑战出现了。在本研究中,我们描述了 53 个新分离到的氯病毒的基因组特征,并利用它们阐明了该支系的部分进化史和分类法。我们的分析揭示了迄今为止具有最大基因组(>400 kbp)的新氯病毒,并指出仅感染变种C. Syngen 2-3株的病毒(OSy病毒)的四个基因组特征在统计学上是不同的。我们发现,与其他基因组相比,PBCV-1 和 OSy-NE5 病毒的基因组存在较大的差异区域。这些区域包含与宿主细胞机制和病毒外壳蛋白相互作用相关的基因,有助于深入了解这些巨型病毒的复制和结构模块的进化过程。利用核ocytoviricota的标志基因进行的系统进化分析表明,OSy-病毒是从NC64A-病毒进化而来的,可能是由于与宿主的严格关系而出现的。结合系统发生学和核苷酸同一性分析,我们提出了划分病毒物种的策略,从而产生了 7 个氯病毒新物种。总之,我们的研究结果表明了如何利用基因组数据作为划分病毒种类的证据。以绿藻病毒为案例,我们希望在此基础上会出现类似的举措。绿藻病毒是一类具有长dsDNA基因组的巨型病毒,感染不同种类的绿藻。它们具有宿主特异性,有些分离株只能在变色小球藻的单一菌株中复制。对这些病毒的基因组学研究还很薄弱,新分离株的特征描述提供了有关其遗传多样性和进化的重要数据。在这项工作中,我们描述了 53 个新的氯病毒基因组,其中包括许多首次从碱性湖泊中分离出来的病毒。通过比较基因组学和分子系统学,我们提供了氯病毒基因组巨型化的证据,并表明在进化史上的某个特定时期,一部分病毒对宿主具有高度特异性。我们提出了划分氯病毒物种的标准,为更新其他类病毒的分类学铺平了道路。这项研究是巨藻病毒复杂谜题中新的重要一环。
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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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