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Testing novel anti-viral strategies in plants

Testing novel anti-viral strategies in plants
在植物中测试新型抗病毒策略
批准号:
BB/L022095/1
负责人:
Peter Stockley
金额:
$58.08万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2014
资助国家:
英国
项目状态:
已结题
起止时间:
2014 至 --

项目摘要

项目成果

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中文摘要
翻译
单链RNA病毒是主要的病原体,气候变化和流动性增加等因素意味着这种类型的新病毒将更频繁地出现,带来巨大的社会挑战。这些病毒感染植物,导致作物产量严重下降。它们也会感染牲畜,最近英国爆发的口蹄疫病毒说明了它们可能对农业经济造成的潜在破坏性影响。其他病毒将成为英国常见的病原体,因为它们的载体,主要是咬人的昆虫,正变得越来越广泛。因此,病毒对扩大和确保世界粮食供应的努力构成重大威胁。尽管它们很重要,但除了接种疫苗之外,几乎没有解决病毒感染的办法,这对植物病毒来说是不可能的,因此迫切需要新的策略。基于我们对ssRNA病毒组装和拆卸机制的独特见解,我们提议在此测试几种针对病毒生命周期组装和拆卸阶段的新型抗病毒策略。我们最近的工作改变了我们对病毒组装的理解,即用由病毒外壳蛋白亚基组成的保护壳包围病毒RNA基因组的过程。我们已经证明,这些基本运输载体的有效构建关键取决于病毒RNA中的多个短序列,称为包装信号(ps),以及它们与病毒外壳蛋白亚基的相互作用。我们已经定义并确定了ps在多种ssRNA病毒中的作用,并建议将这项工作扩展到精心挑选的模型ssRNA植物病毒。我们将确定PS组对这些病毒衣壳组装的协同影响,并测试通过表达靶向PS活性的诱饵rna来干扰有效衣壳形成的策略。此外,我们将利用特定衣壳成分在拆卸和感染中的重要性。ssRNA病毒已被深入研究,其保护蛋白衣壳的高度对称结构已被很好地理解。然而,结构病毒学的成功掩盖了一个基本问题:许多病毒并非真正的二十面体。它们有独特的、非对称的组成部分,这对它们的生物学至关重要,包括它们的基因组,但这些通常在使用对称平均的结构模型中缺失。这些独特的成分对病毒生物学是绝对必要的,因为它们允许病毒对环境做出动态反应,并将稳定的保护性结构转变为准备将其遗传信息释放到细胞中并开始感染的结构。
英文摘要
Single-stranded (ss) RNA viruses are major pathogens, and factors such as climate change and increased mobility mean that new viruses of this type will emerge more frequently, presenting enormous societal challenges. These viruses infect plants and cause severe reductions in crop yields. They also infect livestock, and the recent UK outbreak of Foot & Mouth Disease Virus illustrates the potentially devastating effects they can have on the agricultural economy. Other viruses will become common UK pathogens because their vectors, mostly biting insects, are becoming more widespread. Viruses are thus a significant threat to efforts to expand and secure world food supply. Despite their importance, few solutions for viral infection exist beyond vaccination, which is not possible for plant viruses, and novel strategies are therefore urgently required. We are proposing to test here several novel anti-viral strategies that target the assembly and disassembly stage of the viral life cycle, and are based on our unique insights into the mechanisms of assembly and disassembly in ssRNA viruses. Our recent work has transformed our understanding of virus assembly, i.e. the process of surrounding the viral RNA genome with a protective shell made of viral coat protein sub-units. We have shown that the efficient construction of these essential transport vehicles depends critically on multiple short sequences within the viral RNA, termed packaging signals (PSs), and their interactions with the viral coat protein sub-units. We have defined and identified the roles of PSs in a wide range of ssRNA viruses, and are proposing to extend this work here to a carefully chosen selection of model ssRNA plant viruses. We will determine the cooperative impact of groups of PSs on capsid assembly in these viruses and test strategies to interfere with efficient capsid formation via expression of decoy RNAs targeting PS activity.Moreover, we will exploit the importance of specific capsid components in disassembly and infection. ssRNA viruses have been intensively studied, and the highly-symmetric structures of their protective protein capsids are well understood. However, successes in structural virology mask a fundamental problem: many of these viruses are not truly icosahedral. They have unique, non-symmetric components that are essential to their biology, including their genomes, but these are generally missing from structural models that use symmetry averaging. These unique components are absolutely essential to virus biology, because they allow viruses to respond dynamically to their environment and transform a stable, protective structure into one that is primed to release its genetic information into a cell and start an infection.
期刊论文(5)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1073/pnas.1706951114
发表时间: 2017-11-14
期刊: Proceedings of the National Academy of Sciences of the United States of America
影响因子: 11.1
作者: [Patel N, Wroblewski E, Leonov G, Phillips SEV, Tuma R, Twarock R, Stockley PG]
通讯作者: Stockley PG
DOI: 10.1016/j.jmb.2015.11.014
发表时间: 2016-01-29
期刊: Journal of molecular biology
影响因子: 5.6
作者: [Rolfsson Ó, Middleton S, Manfield IW, White SJ, Fan B, Vaughan R, Ranson NA, Dykeman E, Twarock R, Ford J, Kao CC, Stockley PG]
通讯作者: Stockley PG
DOI: 10.1080/21597081.2016.1157666
发表时间: 2016-01
期刊: Bacteriophage
影响因子: --
作者: [Stockley PG, White SJ, Dykeman E, Manfield I, Rolfsson O, Patel N, Bingham R, Barker A, Wroblewski E, Chandler-Bostock R, Weiß EU, Ranson NA, Tuma R, Twarock R]
通讯作者: Twarock R
Structural & Functional Investigations of Hepatitis B Virus Pol Activity in a Native-like Context
  • 批准号:
    BB/W017644/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $63.92万
  • 财政年份:
    2022
  • 负责人:
    Peter Stockley
  • 依托单位:
The roles of the pre-genomic RNA in Hepatitis B Virus nucleocapsid assembly.
  • 批准号:
    MR/N021517/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $43.9万
  • 财政年份:
    2016
  • 负责人:
    Peter Stockley
  • 依托单位:
Mathematical Virology: A new mathematical approach to viral evolution grounded in experiment
  • 批准号:
    EP/K027689/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $28.87万
  • 财政年份:
    2013
  • 负责人:
    Peter Stockley
  • 依托单位:
Single-molecule assays of the assembly/disassembly mechanisms of ssRNA viruses - Tools for screening novel anti-virals
  • 批准号:
    BB/J00667X/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $48.93万
  • 财政年份:
    2012
  • 负责人:
    Peter Stockley
  • 依托单位:
国内基金
海外基金
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  • 项目类别:
    省市级项目
  • 资助金额:
    10.0万元
  • 批准年份:
    2025
  • 负责人:
    崔文晓
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novel-miR75靶向OPR2,CA2和STK基因调控人参真菌胁迫响应的分子机制研究
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    82304677
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    30.00万元
  • 批准年份:
    2023
  • 负责人:
    边兴博
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海南广藿香Novel17-GSO1响应p-HBA调控连作障碍的分子机制
  • 批准号:
    82304658
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    30万元
  • 批准年份:
    2023
  • 负责人:
    刘亚
  • 依托单位:
白术多糖通过novel-mir2双靶向TRADD/MLKL缓解免疫抑制雏鹅的胸腺程序性坏死
  • 批准号:
    32102747
  • 项目类别:
    青年科学基金项目(C类)
  • 资助金额:
    30.0万元
  • 批准年份:
    2021
  • 负责人:
    李婉雁
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