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在海豚中鉴定出具有大基因组的新型环曲病毒谱系。

Novel lineage of anelloviruses with large genomes identified in dolphins.

作者信息

De Koch Matthew D, Krupovic Mart, Fielding Russell, Smith Kendal, Schiavone Kelsie, Hall Katharine R, Reid Vincent S, Boyea Diallo, Smith Emma L, Schmidlin Kara, Fontenele Rafaela S, Koonin Eugene V, Martin Darren P, Kraberger Simona, Varsani Arvind

机构信息

The Biodesign Center for Fundamental and Applied Microbiomics, Center for Evolution and Medicine, School of Life Sciences, Arizona State University, Tempe, Arizona, USA.

Institut Pasteur, Université Paris Cité, CNRS UMR6047, Archaeal Virology Unit, Paris, France.

出版信息

J Virol. 2025 Jan 31;99(1):e0137024. doi: 10.1128/jvi.01370-24. Epub 2024 Dec 12.

DOI:10.1128/jvi.01370-24
PMID:39665547
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11784456/
Abstract

UNLABELLED

Anellovirus infections are ubiquitous in mammals but lack any clear disease association, suggesting a commensal virus-host relationship. Although anelloviruses have been identified in numerous mammalian hosts, their presence in members of the family Delphinidae has yet to be reported. Here, using a metagenomic approach, we characterize complete anellovirus genomes ( = 69) from four Delphinidae host species: short-finned pilot whale (, = 19), killer whale (, = 9), false killer whale (, = 6), and pantropical spotted dolphin (, = 1). Sequence comparison of the open reading frame 1 (ORF1) encoding the capsid protein, the only conserved gene shared by all anelloviruses, shows that the Delphinidae anelloviruses form a novel genus-level clade that encompasses 22 unique species-level groupings. We provide evidence that different Delphinidae species can be co-infected by multiple anelloviruses belonging to distinct species groupings. Notably, the ORF1 protein of the Delphinidae anelloviruses is considerably larger than those encoded by all previously described anelloviruses from other hosts (spanning 14 vertebrate orders and including 27 families). Comprehensive analysis of the ORF1 sequences and predicted protein structures showed that the increased size of these proteins results from divergent elaborations within the capsid-distal P2 subdomain and elongation of the C-terminal domain of ORF1. Comparative structural and phylogenetic analyses suggest that acquisition of the P2 subdomain and its diversification occurred convergently in the anelloviruses associated with primate and Delphinidae hosts. Collectively, our results further the appreciation of diversity and evolution of the ubiquitous and enigmatic viruses in the family .

IMPORTANCE

Anelloviruses are ubiquitous in mammals, but their infection has not yet been linked to any disease, suggesting a commensal virus-host relationship. Here, we describe the first anelloviruses associated with diverse species of dolphins. The dolphinid anelloviruses represent a new genus (tentatively named "Qoptorquevirus") and encode open reading frame 1 (ORF1) (capsid) proteins that are considerably larger than those encoded by previously described anelloviruses from other hosts. Comprehensive analysis of the ORF1 sequences and predicted protein structures revealed the underlying structural basis for such an extravagant ORF1 size and suggested that ORF1 size increased convergently in the anelloviruses associated with primate and Delphinidae hosts, respectively. Collectively, our results provide insights into the diversity and evolution of . Further exploration of the anellovirus diversity, especially in the host species that have not yet been sampled, is expected to further clarify their evolutionary trajectory and explain the unusual virus-host commensal relationship.

摘要

未标注

环曲病毒感染在哺乳动物中普遍存在,但缺乏任何明确的疾病关联,提示病毒与宿主为共生关系。尽管已在众多哺乳动物宿主中鉴定出环曲病毒,但尚未有其在海豚科动物中存在的报道。在此,我们采用宏基因组学方法,对来自四种海豚科宿主物种的完整环曲病毒基因组(n = 69)进行了特征分析:短鳍领航鲸(Globicephala macrorhynchus,n = 19)、虎鲸(Orcinus orca,n = 9)、伪虎鲸(Pseudorca crassidens,n = 6)和泛热带斑海豚(Stenella attenuata,n = 1)。对编码衣壳蛋白的开放阅读框1(ORF1)进行序列比较,该基因是所有环曲病毒共有的唯一保守基因,结果表明海豚科环曲病毒形成了一个新的属级分支,包含22个独特的物种级分组。我们提供的证据表明,不同的海豚科物种可能会被属于不同物种分组的多种环曲病毒共同感染。值得注意的是,海豚科环曲病毒的ORF1蛋白比所有先前描述的来自其他宿主(涵盖14个脊椎动物目,包括27个科)的环曲病毒所编码的蛋白要大得多。对ORF1序列和预测的蛋白质结构进行综合分析表明,这些蛋白质大小的增加是由于衣壳远端P2亚结构域内的不同修饰以及ORF1 C末端结构域的延长。比较结构和系统发育分析表明,P2亚结构域的获得及其多样化在与灵长类和海豚科宿主相关的环曲病毒中是趋同发生的。总体而言,我们的结果进一步加深了对该科普遍存在且神秘的病毒的多样性和进化的认识。

重要性

环曲病毒在哺乳动物中普遍存在,但其感染尚未与任何疾病相关联,提示病毒与宿主为共生关系。在此,我们描述了首批与多种海豚物种相关的环曲病毒。海豚科环曲病毒代表一个新的属(暂命名为“Qoptorquevirus”),其编码的开放阅读框1(ORF1)(衣壳)蛋白比先前描述的来自其他宿主的环曲病毒所编码的蛋白要大得多。对ORF1序列和预测的蛋白质结构进行综合分析,揭示了这种ORF1异常大小的潜在结构基础,并表明ORF1大小分别在与灵长类和海豚科宿主相关的环曲病毒中趋同增加。总体而言,我们的结果为环曲病毒的多样性和进化提供了见解。预计对环曲病毒多样性的进一步探索,尤其是在尚未采样的宿主物种中,将进一步阐明其进化轨迹,并解释这种不寻常的病毒与宿主共生关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e03/11784456/224da57d8905/jvi.01370-24.f008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e03/11784456/224da57d8905/jvi.01370-24.f008.jpg

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