The Replicase Protein of Potato Virus X Is Able to Recognize and Trans-Replicate Its RNA Component.

IF 3.8 3区 医学 Q2 VIROLOGY
Viruses-Basel Pub Date : 2024-10-15 DOI:10.3390/v16101611
Pinky Dutta, Andres Lõhmus, Tero Ahola, Kristiina Mäkinen
{"title":"The Replicase Protein of Potato Virus X Is Able to Recognize and <i>Trans-</i>Replicate Its RNA Component.","authors":"Pinky Dutta, Andres Lõhmus, Tero Ahola, Kristiina Mäkinen","doi":"10.3390/v16101611","DOIUrl":null,"url":null,"abstract":"<p><p>The <i>trans-</i>replication system explores the concept of separating the viral RNA involved in the translation of the replicase protein from the replication of the viral genome and has been successfully used to study the replication mechanisms of alphaviruses. We tested the feasibility of this system with potato virus X (PVX), an alpha-like virus, <i>in planta</i>. A viral RNA template was designed which does not produce the replicase and prevents virion formation but remains recognizable by the replicase. The replicase construct encodes for the replicase protein, while lacking other virus-specific recognition sequences. Both the constructs were delivered into <i>Nicotiana benthamiana</i> leaves via <i>Agrobacterium</i>-mediated infiltration. Templates of various lengths were tested, with the longer templates not replicating at 4 and 6 days post inoculation, when the replicase protein was provided <i>in trans</i>. Co-expression of helper component proteinase with the short template led to its <i>trans-</i>replication. The cells where replication had been initiated were observed to be scattered across the leaf lamina. This study established that PVX is capable of <i>trans</i>-replicating and can likely be further optimized, and that the experimental freedom offered by the system can be utilized to delve deeper into understanding the replication mechanism of the virus.</p>","PeriodicalId":49328,"journal":{"name":"Viruses-Basel","volume":"16 10","pages":""},"PeriodicalIF":3.8000,"publicationDate":"2024-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11512358/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Viruses-Basel","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3390/v16101611","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"VIROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The trans-replication system explores the concept of separating the viral RNA involved in the translation of the replicase protein from the replication of the viral genome and has been successfully used to study the replication mechanisms of alphaviruses. We tested the feasibility of this system with potato virus X (PVX), an alpha-like virus, in planta. A viral RNA template was designed which does not produce the replicase and prevents virion formation but remains recognizable by the replicase. The replicase construct encodes for the replicase protein, while lacking other virus-specific recognition sequences. Both the constructs were delivered into Nicotiana benthamiana leaves via Agrobacterium-mediated infiltration. Templates of various lengths were tested, with the longer templates not replicating at 4 and 6 days post inoculation, when the replicase protein was provided in trans. Co-expression of helper component proteinase with the short template led to its trans-replication. The cells where replication had been initiated were observed to be scattered across the leaf lamina. This study established that PVX is capable of trans-replicating and can likely be further optimized, and that the experimental freedom offered by the system can be utilized to delve deeper into understanding the replication mechanism of the virus.

马铃薯病毒 X 的复制酶蛋白能够识别并转录其 RNA 成分。
反式复制系统探索了将参与复制酶蛋白翻译的病毒 RNA 与病毒基因组复制分离的概念,并已成功用于研究阿尔法病毒的复制机制。我们用马铃薯病毒 X(PVX)(一种α-类病毒)在植物体内测试了这一系统的可行性。我们设计了一种病毒 RNA 模板,它不产生复制酶,能阻止病毒体的形成,但仍能被复制酶识别。复制酶构建体编码复制酶蛋白,但缺乏其他病毒特异性识别序列。这两种构建体都是通过农杆菌介导的浸润法输送到烟草叶片中的。对不同长度的模板进行了测试,当反式提供复制酶蛋白时,较长的模板在接种后 4 天和 6 天不会复制。与短模板共表达辅助成分蛋白酶会导致其反式复制。据观察,开始复制的细胞散布在叶片上。这项研究证实,PVX 能够进行反式复制,并有可能进一步优化,而且可以利用该系统提供的实验自由度来深入了解病毒的复制机制。
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
Viruses-Basel
Viruses-Basel VIROLOGY-
CiteScore
7.30
自引率
12.80%
发文量
2445
审稿时长
1 months
期刊介绍: Viruses (ISSN 1999-4915) is an open access journal which provides an advanced forum for studies of viruses. It publishes reviews, regular research papers, communications, conference reports and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. We also encourage the publication of timely reviews and commentaries on topics of interest to the virology community and feature highlights from the virology literature in the ''News and Views'' section. Electronic files or software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material.
×
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