Discovery and characterization of complete genomes of 38 head-tailed proviruses in four predominant phyla of archaea.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
Tianqi Xu, Yimin Ni, Hailing Li, Shuang Wu, Shuling Yan, Lanming Chen, Yongxin Yu, Yongjie Wang
{"title":"Discovery and characterization of complete genomes of 38 head-tailed proviruses in four predominant phyla of archaea.","authors":"Tianqi Xu, Yimin Ni, Hailing Li, Shuang Wu, Shuling Yan, Lanming Chen, Yongxin Yu, Yongjie Wang","doi":"10.1128/spectrum.00492-24","DOIUrl":null,"url":null,"abstract":"<p><p>Archaea play a significant role in natural ecosystems and the human body. Archaeal viruses exert a considerable influence on the structure and composition of archaeal communities and their associated ecological environments. The present study revealed the complete genomes of 38 archaeal head-tailed proviruses through comprehensive data mining. The hosts of these proviruses were identified as belonging to the following four dominant phyla: <i>Halobacteriota</i>, <i>Thermoplasmatota</i>, <i>Thermoproteota</i>, and <i>Nanoarchaeota</i>. In addition to the 14 proviruses of halophilic archaea related to the <i>Graaviviridae</i> family, the remaining proviruses exhibited limited genetic similarities to known (pro)viruses, suggesting the existence of 14 potential novel families. Of the 38 archaeal proviruses, 30 have the potential to lyse host cells. Eleven proviruses contain genes linked to antiviral defense mechanisms, including those involved in restriction modification (RM), clustered regularly interspaced short palindromic repeat (CRISPR)-associated (CRISPR-Cas) nucleases, defense island system associated with restriction-modification (DISARM), and DNA degradation (Dnd). Moreover, auxiliary metabolic genes were identified in the proviruses of <i>Bathyarchaeia</i> and <i>Halobacteriota</i> archaea, including those involved in carbohydrate and amino acid metabolism. Our findings indicate the diversity of archaeal viruses, their interactions with archaeal hosts, and their roles in the adaptation of the host.IMPORTANCEThe field of archaeal virology has seen a rapid expansion through the use of metagenomics, yet the diversity of these viruses remains largely uncharted. In this study, the complete genomes of 38 novel archaeal proviruses were identified for the following four dominant phyla: <i>Halobacteriota</i>, <i>Thermoplasmatota</i>, <i>Thermoproteota</i>, and <i>Nanoarchaeota</i>. Two families and six genera of Archaea were the first to be identified as hosts for viruses. The proviruses were found to contain diverse genes that were involved in distinct adaptation strategies of viruses to hosts. Our findings contribute to the expansion of the lineages of archaeal viruses and highlight their intricate interactions and essential roles in enabling host survival and adaptation to diverse environmental conditions.</p>","PeriodicalId":18670,"journal":{"name":"Microbiology spectrum","volume":" ","pages":"e0049224"},"PeriodicalIF":3.7000,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiology spectrum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/spectrum.00492-24","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Archaea play a significant role in natural ecosystems and the human body. Archaeal viruses exert a considerable influence on the structure and composition of archaeal communities and their associated ecological environments. The present study revealed the complete genomes of 38 archaeal head-tailed proviruses through comprehensive data mining. The hosts of these proviruses were identified as belonging to the following four dominant phyla: Halobacteriota, Thermoplasmatota, Thermoproteota, and Nanoarchaeota. In addition to the 14 proviruses of halophilic archaea related to the Graaviviridae family, the remaining proviruses exhibited limited genetic similarities to known (pro)viruses, suggesting the existence of 14 potential novel families. Of the 38 archaeal proviruses, 30 have the potential to lyse host cells. Eleven proviruses contain genes linked to antiviral defense mechanisms, including those involved in restriction modification (RM), clustered regularly interspaced short palindromic repeat (CRISPR)-associated (CRISPR-Cas) nucleases, defense island system associated with restriction-modification (DISARM), and DNA degradation (Dnd). Moreover, auxiliary metabolic genes were identified in the proviruses of Bathyarchaeia and Halobacteriota archaea, including those involved in carbohydrate and amino acid metabolism. Our findings indicate the diversity of archaeal viruses, their interactions with archaeal hosts, and their roles in the adaptation of the host.IMPORTANCEThe field of archaeal virology has seen a rapid expansion through the use of metagenomics, yet the diversity of these viruses remains largely uncharted. In this study, the complete genomes of 38 novel archaeal proviruses were identified for the following four dominant phyla: Halobacteriota, Thermoplasmatota, Thermoproteota, and Nanoarchaeota. Two families and six genera of Archaea were the first to be identified as hosts for viruses. The proviruses were found to contain diverse genes that were involved in distinct adaptation strategies of viruses to hosts. Our findings contribute to the expansion of the lineages of archaeal viruses and highlight their intricate interactions and essential roles in enabling host survival and adaptation to diverse environmental conditions.

发现古细菌四个主要门类中 38 种头尾状病毒的完整基因组并确定其特征。
古菌在自然生态系统和人体中发挥着重要作用。古菌病毒对古菌群落及其相关生态环境的结构和组成有相当大的影响。本研究通过全面的数据挖掘,揭示了38种古细菌头尾病毒的完整基因组。经鉴定,这些病毒的宿主属于以下四个主要门类:卤杆菌门(Halobacteriota)、热原生动物门(Thermoplasmatota)、热蛋白门(Thermoproteota)和纳米古动物门(Nanoarchaeota)。除了 14 种与 Graaviviridae 科相关的嗜卤古细菌病毒外,其余病毒与已知(原)病毒的遗传相似性有限,这表明存在 14 个潜在的新科。在 38 种古细菌前病毒中,有 30 种具有裂解宿主细胞的潜能。11个前病毒含有与抗病毒防御机制相关的基因,包括参与限制性修饰(RM)、聚类规则间隔短回文重复(CRISPR)-相关(CRISPR-Cas)核酸酶、与限制性修饰相关的防御岛系统(DISARM)和DNA降解(Dnd)的基因。此外,我们还在Bathyarchaeia和Halobacteriota古菌的前病毒中发现了辅助代谢基因,包括参与碳水化合物和氨基酸代谢的基因。我们的研究结果表明了古细菌病毒的多样性、它们与古细菌宿主的相互作用以及它们在宿主适应过程中的作用。重要意义通过使用元基因组学,古细菌病毒学领域得到了迅速扩展,但这些病毒的多样性在很大程度上仍是未知的。本研究鉴定了以下四个主要门类的 38 种新型古细菌病毒的完整基因组:卤杆菌门、热原生动物门、热蛋白门和纳米古细菌门。古细菌中有两科六属首次被鉴定为病毒宿主。研究发现,病毒的前体含有多种基因,这些基因参与了病毒对宿主的不同适应策略。我们的发现有助于扩大古细菌病毒的谱系,并突出了它们之间错综复杂的相互作用以及在使宿主生存和适应不同环境条件方面的重要作用。
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 求助全文
来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信