• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

论微小双RNA病毒的本质

On the nature of picobirnaviruses.

作者信息

Kashnikov A Yu, Epifanova N V, Novikova N A

机构信息

I.N. Blokhina Nizhny Novgorod Research Institute of Epidemiology and Microbiology, Nizhny Novgorod, Russia.

出版信息

Vavilovskii Zhurnal Genet Selektsii. 2023 Jun;27(3):264-275. doi: 10.18699/VJGB-23-32.

DOI:10.18699/VJGB-23-32
PMID:37293447
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10244588/
Abstract

The picobirnaviruses (Picobirnaviridae, Picobirnavirus, PBVs) are currently thought to be animal viruses, as they are usually found in animal stool samples. However, no animal model or cell culture for their propagation has yet been found. In 2018, a hypothetical assumption about PBVs belonging to prokaryotic viruses was put forward and experimentally substantiated. This hypothesis is based on the presence of Shine-Dalgarno sequences in the genome of all PBVs before three reading frames (ORF) at the ribosomal binding site, with which the prokaryotic genome is saturated, while in the eukaryotic genome such regions occur with low frequency. The genome saturation with the Shine-Dalgarno sequences, as well as the preservation of this saturation in the progeny, according to scientists, allows us to attribute PBVs to prokaryotic viruses. On the other hand, there is a possibility that PBVs belong to viruses of eukaryotic hosts - fungi or invertebrates, since PBV-like sequences similar to the genome of fungal viruses from the families of mitoviruses and partitiviruses have been identified. In this regard, the idea arose that, in terms of reproduction mode, PBVs resemble fungal viruses. The divergence of views on the true PBV host(s) has sparked discussions among scientists and required further research to elucidate their nature. The review highlights the results of the search for a PBV host. The reasons for the occurrence of atypical sequences among the PBV genome sequences that use an alternative mitochondrial code of lower eukaryotes (fungi and invertebrates) for the translation of viral RNA-dependent RNA polymerase (RdRp) instead of the standard genetic code are analyzed. The purpose of the review was to collect arguments in support of the hypothesis about the phage nature of PBVs and to find the most realistic explanation of the reasons for identifying non-standard genomic sequences for PBVs. Based on the hypothesis about the genealogical relationship of PBVs with RNA viruses from other families with similar segmented genomes, such as Reoviridae, Cystoviridae, Totiviridae and Partitiviridae, virologists support the assumption of a decisive role in the origin of atypical PBV-like reassortment strains between PBVs and viruses of the listed families. The collected arguments given in this review indicate a high probability of a phage nature of PBVs. The data presented in the review show that the belonging of PBV-like progeny to prokaryotic or eukaryotic viruses is determined not only by its genome saturation level with a prokaryotic motif, standard or mitochondrial genetic code. The primary structure of the gene encoding the viral capsid protein responsible for the presence or absence of specific proteolytic properties of the virus that determine its ability for independent horizontal transmission into new cells may also be a decisive factor.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/437d/10244588/384522929199/VJGB-27-2332-Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/437d/10244588/384522929199/VJGB-27-2332-Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/437d/10244588/ac2422ad454f/VJGB-27-2332-Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/437d/10244588/818468f49a7b/VJGB-27-2332-Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/437d/10244588/8a0e9ee35b01/VJGB-27-2332-Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/437d/10244588/384522929199/VJGB-27-2332-Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/437d/10244588/384522929199/VJGB-27-2332-Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/437d/10244588/ac2422ad454f/VJGB-27-2332-Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/437d/10244588/818468f49a7b/VJGB-27-2332-Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/437d/10244588/8a0e9ee35b01/VJGB-27-2332-Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/437d/10244588/384522929199/VJGB-27-2332-Fig1.jpg
摘要

微小双股RNA病毒(微小双股RNA病毒科,微小双股RNA病毒,PBVs)目前被认为是动物病毒,因为它们通常在动物粪便样本中被发现。然而,尚未找到用于其繁殖的动物模型或细胞培养方法。2018年,有人提出关于PBVs属于原核病毒的假设,并通过实验得到了证实。该假设基于所有PBVs基因组在核糖体结合位点的三个阅读框(ORF)之前存在Shine-Dalgarno序列,原核基因组富含这种序列,而在真核基因组中此类区域出现频率较低。科学家们认为,基因组中Shine-Dalgarno序列的饱和度以及子代中这种饱和度的保留,使我们能够将PBVs归为原核病毒。另一方面,PBVs有可能属于真核宿主——真菌或无脊椎动物的病毒,因为已经鉴定出与微小RNA病毒科和双分病毒科真菌病毒基因组相似的PBV样序列。在这方面,有人提出PBVs在繁殖模式上类似于真菌病毒。关于PBVs真正宿主的观点分歧引发了科学家们的讨论,需要进一步研究以阐明它们的本质。这篇综述强调了寻找PBV宿主的结果。分析了在PBV基因组序列中出现非典型序列的原因,这些序列使用低等真核生物(真菌和无脊椎动物)的替代线粒体密码子来翻译病毒RNA依赖的RNA聚合酶(RdRp),而不是标准遗传密码。这篇综述的目的是收集支持PBVs噬菌体性质假设的论据,并找到对PBVs鉴定出非标准基因组序列原因的最现实解释。基于关于PBVs与其他具有相似分段基因组的病毒科(如呼肠孤病毒科、噬菌体病毒科、全病毒科和双分病毒科)的RNA病毒谱系关系的假设,病毒学家支持PBVs与所列病毒科的病毒之间非典型PBV样重配株起源中起决定性作用的假设。这篇综述中收集的论据表明PBVs具有噬菌体性质的可能性很高。综述中呈现的数据表明,PBV样子代属于原核或真核病毒不仅取决于其基因组中与原核基序、标准或线粒体遗传密码的饱和度。编码病毒衣壳蛋白的基因的一级结构,该蛋白决定病毒是否具有特定的蛋白水解特性,从而决定其独立水平传播到新细胞的能力,也可能是一个决定性因素。

相似文献

1
On the nature of picobirnaviruses.论微小双RNA病毒的本质
Vavilovskii Zhurnal Genet Selektsii. 2023 Jun;27(3):264-275. doi: 10.18699/VJGB-23-32.
2
Detection and molecular characterization of picobirnaviruses in the wild birds: Identification of a novel picobirnavirus possessing yeast mitochondrial genetic code.野生鸟类中微小双股RNA病毒的检测与分子特征分析:一种具有酵母线粒体遗传密码的新型微小双股RNA病毒的鉴定
Virus Res. 2022 Jan 15;308:198624. doi: 10.1016/j.virusres.2021.198624. Epub 2021 Nov 9.
3
Detection and Molecular Characterization of Picobirnaviruses (PBVs) in the Mongoose: Identification of a Novel PBV Using an Alternative Genetic Code.检测貂体内的微小双核糖核酸病毒(PBVs)并对其进行分子特征分析:使用替代遗传密码鉴定新型 PBV。
Viruses. 2020 Jan 15;12(1):99. doi: 10.3390/v12010099.
4
The True Host/s of Picobirnaviruses.微小双股RNA病毒的真正宿主
Front Vet Sci. 2021 Jan 20;7:615293. doi: 10.3389/fvets.2020.615293. eCollection 2020.
5
Marmota himalayana in the Qinghai-Tibetan plateau as a special host for bi-segmented and unsegmented picobirnaviruses.青藏高原旱獭作为双节段和非节段微小 RNA 病毒的特殊宿主。
Emerg Microbes Infect. 2018 Mar 7;7(1):20. doi: 10.1038/s41426-018-0020-6.
6
Picobirnaviruses: prevalence, genetic diversity, detection methods.微小双股RNA病毒:流行情况、遗传多样性、检测方法
Vavilovskii Zhurnal Genet Selektsii. 2020 Oct;24(6):661-672. doi: 10.18699/VJ20.660.
7
Extensive conservation of prokaryotic ribosomal binding sites in known and novel picobirnaviruses.已知和新型双顺反子微小 RNA 病毒中细菌核糖体结合位点的广泛保守性。
Virology. 2018 Mar;516:108-114. doi: 10.1016/j.virol.2018.01.006. Epub 2018 Jan 12.
8
Epidemiology, phylogeny, and evolution of emerging enteric Picobirnaviruses of animal origin and their relationship to human strains.动物源新兴肠道微小双股RNA病毒的流行病学、系统发育和进化及其与人类毒株的关系。
Biomed Res Int. 2014;2014:780752. doi: 10.1155/2014/780752. Epub 2014 Jul 17.
9
Parallel evolution of picobirnaviruses from distinct ancestral origins.从不同的祖先起源平行进化的微小双核糖核酸病毒。
Microbiol Spectr. 2023 Dec 12;11(6):e0269323. doi: 10.1128/spectrum.02693-23. Epub 2023 Oct 27.
10
High detection rates and genetic diversity of picobirnaviruses (PBVs) in pigs on St. Kitts Island: Identification of a porcine PBV strain closely related to simian and human PBVs.圣基茨岛猪中微小双核糖核酸病毒(PBVs)的高检出率和遗传多样性:鉴定出一种与灵长类动物和人类 PBVs 密切相关的猪 PBV 株。
Infect Genet Evol. 2020 Oct;84:104383. doi: 10.1016/j.meegid.2020.104383. Epub 2020 May 27.