Expanding the genomic diversity of human anelloviruses.

IF 5.5 2区 医学 Q1 VIROLOGY Virus Evolution Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI:10.1093/ve/veaf002
Sejal Modha, Joseph Hughes, Richard J Orton, Spyros Lytras
{"title":"Expanding the genomic diversity of human anelloviruses.","authors":"Sejal Modha, Joseph Hughes, Richard J Orton, Spyros Lytras","doi":"10.1093/ve/veaf002","DOIUrl":null,"url":null,"abstract":"<p><p>Anelloviruses are a group of small, circular, single-stranded DNA viruses that are found ubiquitously across mammalian hosts. Here, we explored a large number of publicly available human microbiome datasets and retrieved a total of 829 anellovirus genomes, substantially expanding the known diversity of these viruses. The majority of new genomes fall within the three major human anellovirus genera: <i>Alphatorquevirus, Betatorquevirus</i>, and <i>Gammatorquevirus</i>, while we also present new genomes of the under-sampled <i>Hetorquevirus, Memtorquevirus</i>, and <i>Samektorquevirus</i> genera. We performed recombination analysis and show evidence of extensive recombination across all human anelloviruses. Interestingly, more than 95% of the detected events are between members of the same genus and only 15 inter-genus recombination events were detected. The breakpoints of recombination cluster in hotspots at the ends and outside of the ORF1 gene, while a recombination coldspot was detected within the gene. Our analysis suggests that anellovirus evolution is governed by homologous recombination; however, events between distant viruses or ones producing chimaeric ORF1s likely lead to nonviable recombinants. The large number of genomes further allowed us to examine how essential genomic features vary across anelloviruses. These include functional domains in the ORF1 protein and the nucleotide motif of the replication loop region, required for the viruses' rolling-circle replication. A subset of the genomes assembled in both this and previous studies are completely lacking these essential elements, opening up the possibility that anellovirus intracellular populations contain nonstandard viral genomes. However, low-read depth of the metagenomically assembled contigs may partly explain the lack of some features. Overall, our study highlights key features of anellovirus genomics and evolution, a largely understudied group of viruses whose potential in virus-based therapeutics is recently being explored.</p>","PeriodicalId":56026,"journal":{"name":"Virus Evolution","volume":"11 1","pages":"veaf002"},"PeriodicalIF":5.5000,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11749082/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virus Evolution","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/ve/veaf002","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"VIROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Anelloviruses are a group of small, circular, single-stranded DNA viruses that are found ubiquitously across mammalian hosts. Here, we explored a large number of publicly available human microbiome datasets and retrieved a total of 829 anellovirus genomes, substantially expanding the known diversity of these viruses. The majority of new genomes fall within the three major human anellovirus genera: Alphatorquevirus, Betatorquevirus, and Gammatorquevirus, while we also present new genomes of the under-sampled Hetorquevirus, Memtorquevirus, and Samektorquevirus genera. We performed recombination analysis and show evidence of extensive recombination across all human anelloviruses. Interestingly, more than 95% of the detected events are between members of the same genus and only 15 inter-genus recombination events were detected. The breakpoints of recombination cluster in hotspots at the ends and outside of the ORF1 gene, while a recombination coldspot was detected within the gene. Our analysis suggests that anellovirus evolution is governed by homologous recombination; however, events between distant viruses or ones producing chimaeric ORF1s likely lead to nonviable recombinants. The large number of genomes further allowed us to examine how essential genomic features vary across anelloviruses. These include functional domains in the ORF1 protein and the nucleotide motif of the replication loop region, required for the viruses' rolling-circle replication. A subset of the genomes assembled in both this and previous studies are completely lacking these essential elements, opening up the possibility that anellovirus intracellular populations contain nonstandard viral genomes. However, low-read depth of the metagenomically assembled contigs may partly explain the lack of some features. Overall, our study highlights key features of anellovirus genomics and evolution, a largely understudied group of viruses whose potential in virus-based therapeutics is recently being explored.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
扩大人类类线虫病毒的基因组多样性。
线虫病毒是一组小的、圆形的单链DNA病毒,在哺乳动物宿主中无处不在。在这里,我们探索了大量公开可用的人类微生物组数据集,并检索了总共829个样病毒基因组,大大扩展了这些病毒的已知多样性。大多数新基因组属于三种主要的人类无线虫病毒属:甲型托尔克病毒、倍托尔克病毒和伽玛托尔克病毒,同时我们也提出了样本不足的hetorquevus、memtorquevus和samektorquevus属的新基因组。我们进行了重组分析,并显示了在所有人类类病毒中广泛重组的证据。有趣的是,超过95%的检测事件发生在同一属成员之间,仅检测到15个属间重组事件。重组断点集中在ORF1基因末端和外侧的热点区域,基因内部存在重组冷点。我们的分析表明,无线虫病毒的进化是由同源重组控制的;然而,远距离病毒之间的事件或产生嵌合orf1的病毒之间的事件可能导致无法存活的重组。大量的基因组进一步使我们能够研究不同类病毒的基本基因组特征是如何变化的。这些包括ORF1蛋白的功能域和复制环区的核苷酸基序,这是病毒滚圈复制所必需的。在本研究和之前的研究中组装的基因组的一个子集完全缺乏这些基本元素,这就打开了蛔虫病毒细胞内群体包含非标准病毒基因组的可能性。然而,宏基因组组装的低读取深度可能部分解释了某些特征的缺乏。总的来说,我们的研究突出了无绒病毒基因组学和进化的关键特征,这是一组在很大程度上未被充分研究的病毒,其基于病毒的治疗方法的潜力最近正在探索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
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.
期刊最新文献
Correction to: Going beyond consensus genome sequences: An innovative SNP-based methodology reconstructs different Ugandan cassava brown streak virus haplotypes at a nationwide scale in Rwanda. Dispersal dynamics and introduction patterns of SARS-CoV-2 lineages in Iran. Genome sizes of animal RNA viruses reflect phylogenetic constraints. SARS-CoV-2 CoCoPUTs: analyzing GISAID and NCBI data to obtain codon statistics, mutations, and free energy over a multiyear period. Expanding the genomic diversity of human anelloviruses.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1