古细菌病毒的结构与组装。

2区 医学 Q1 Medicine
Advances in Virus Research Pub Date : 2020-01-01 Epub Date: 2020-10-05 DOI:10.1016/bs.aivir.2020.09.004
Diana P Baquero, Ying Liu, Fengbin Wang, Edward H Egelman, David Prangishvili, Mart Krupovic
{"title":"古细菌病毒的结构与组装。","authors":"Diana P Baquero,&nbsp;Ying Liu,&nbsp;Fengbin Wang,&nbsp;Edward H Egelman,&nbsp;David Prangishvili,&nbsp;Mart Krupovic","doi":"10.1016/bs.aivir.2020.09.004","DOIUrl":null,"url":null,"abstract":"<p><p>Viruses of archaea represent one of the most enigmatic parts of the virosphere. Most of the characterized archaeal viruses infect extremophilic hosts and display remarkable diversity of virion morphotypes, many of which have never been observed among bacteriophages or viruses of eukaryotes. However, recent environmental studies have shown that archaeal viruses are widespread also in moderate ecosystems, where they play an important ecological role by influencing the turnover of microbial communities, with a global impact on the carbon and nitrogen cycles. In this review, we summarize recent advances in understanding the molecular details of virion organization and assembly of archaeal viruses. We start by briefly introducing the 20 officially recognized families of archaeal viruses and then outline the similarities and differences of archaeal virus assembly with the morphogenesis pathways used by bacterial and eukaryotic viruses, and discuss the evolutionary implications of these observations. Generally, the assembly of the icosahedral archaeal viruses closely follows the mechanisms employed by evolutionarily related bacterial and eukaryotic viruses with the HK97 fold and double jelly-roll major capsid proteins, emphasizing the overall conservation of these pathways over billions of years of evolution. By contrast, archaea-specific viruses employ unique virion assembly mechanisms. We also highlight some of the molecular adaptations underlying the stability of archaeal viruses in extreme environments. Despite considerable progress during the past few years, the archaeal virosphere continues to represent one of the least studied parts of the global virome, with many molecular features awaiting to be discovered and characterized.</p>","PeriodicalId":50977,"journal":{"name":"Advances in Virus Research","volume":"108 ","pages":"127-164"},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/bs.aivir.2020.09.004","citationCount":"21","resultStr":"{\"title\":\"Structure and assembly of archaeal viruses.\",\"authors\":\"Diana P Baquero,&nbsp;Ying Liu,&nbsp;Fengbin Wang,&nbsp;Edward H Egelman,&nbsp;David Prangishvili,&nbsp;Mart Krupovic\",\"doi\":\"10.1016/bs.aivir.2020.09.004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Viruses of archaea represent one of the most enigmatic parts of the virosphere. Most of the characterized archaeal viruses infect extremophilic hosts and display remarkable diversity of virion morphotypes, many of which have never been observed among bacteriophages or viruses of eukaryotes. However, recent environmental studies have shown that archaeal viruses are widespread also in moderate ecosystems, where they play an important ecological role by influencing the turnover of microbial communities, with a global impact on the carbon and nitrogen cycles. In this review, we summarize recent advances in understanding the molecular details of virion organization and assembly of archaeal viruses. We start by briefly introducing the 20 officially recognized families of archaeal viruses and then outline the similarities and differences of archaeal virus assembly with the morphogenesis pathways used by bacterial and eukaryotic viruses, and discuss the evolutionary implications of these observations. Generally, the assembly of the icosahedral archaeal viruses closely follows the mechanisms employed by evolutionarily related bacterial and eukaryotic viruses with the HK97 fold and double jelly-roll major capsid proteins, emphasizing the overall conservation of these pathways over billions of years of evolution. By contrast, archaea-specific viruses employ unique virion assembly mechanisms. We also highlight some of the molecular adaptations underlying the stability of archaeal viruses in extreme environments. Despite considerable progress during the past few years, the archaeal virosphere continues to represent one of the least studied parts of the global virome, with many molecular features awaiting to be discovered and characterized.</p>\",\"PeriodicalId\":50977,\"journal\":{\"name\":\"Advances in Virus Research\",\"volume\":\"108 \",\"pages\":\"127-164\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/bs.aivir.2020.09.004\",\"citationCount\":\"21\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advances in Virus Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/bs.aivir.2020.09.004\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2020/10/5 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Virus Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/bs.aivir.2020.09.004","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/10/5 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 21

摘要

古细菌的病毒是病毒圈中最神秘的部分之一。大多数具有特征的古细菌病毒感染嗜极性宿主,并表现出显著的病毒粒子形态多样性,其中许多从未在真核生物的噬菌体或病毒中观察到。然而,最近的环境研究表明,古细菌病毒也广泛存在于中等生态系统中,它们通过影响微生物群落的更替发挥重要的生态作用,对碳和氮循环产生全球性影响。本文综述了近年来在了解古细菌病毒粒子组织和组装的分子细节方面的研究进展。我们首先简要介绍了20个官方认可的古细菌病毒家族,然后概述了古细菌病毒与细菌和真核病毒的形态发生途径的异同,并讨论了这些观察结果的进化意义。一般来说,二十面体古细菌病毒的组装与进化相关的细菌和真核病毒的HK97折叠和双果冻卷主要衣壳蛋白的组装机制密切相关,强调了这些途径在数十亿年进化中的总体保守性。相比之下,古细菌特异性病毒采用独特的病毒粒子组装机制。我们还强调了古细菌病毒在极端环境中稳定性的一些分子适应。尽管在过去几年中取得了相当大的进展,但古细菌病毒圈仍然是全球病毒组中研究最少的部分之一,有许多分子特征有待发现和表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structure and assembly of archaeal viruses.

Viruses of archaea represent one of the most enigmatic parts of the virosphere. Most of the characterized archaeal viruses infect extremophilic hosts and display remarkable diversity of virion morphotypes, many of which have never been observed among bacteriophages or viruses of eukaryotes. However, recent environmental studies have shown that archaeal viruses are widespread also in moderate ecosystems, where they play an important ecological role by influencing the turnover of microbial communities, with a global impact on the carbon and nitrogen cycles. In this review, we summarize recent advances in understanding the molecular details of virion organization and assembly of archaeal viruses. We start by briefly introducing the 20 officially recognized families of archaeal viruses and then outline the similarities and differences of archaeal virus assembly with the morphogenesis pathways used by bacterial and eukaryotic viruses, and discuss the evolutionary implications of these observations. Generally, the assembly of the icosahedral archaeal viruses closely follows the mechanisms employed by evolutionarily related bacterial and eukaryotic viruses with the HK97 fold and double jelly-roll major capsid proteins, emphasizing the overall conservation of these pathways over billions of years of evolution. By contrast, archaea-specific viruses employ unique virion assembly mechanisms. We also highlight some of the molecular adaptations underlying the stability of archaeal viruses in extreme environments. Despite considerable progress during the past few years, the archaeal virosphere continues to represent one of the least studied parts of the global virome, with many molecular features awaiting to be discovered and characterized.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
7.10
自引率
0.00%
发文量
7
审稿时长
>12 weeks
×
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