• 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

植物病毒韧皮部运输涉及的病毒和细胞因子。

Viral and cellular factors involved in Phloem transport of plant viruses.

机构信息

UMR INRA-UDS Virus-Vection Group Colmar, France.

出版信息

Front Plant Sci. 2013 May 24;4:154. doi: 10.3389/fpls.2013.00154. eCollection 2013.

DOI:10.3389/fpls.2013.00154
PMID:23745125
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3662875/
Abstract

Phloem transport of plant viruses is an essential step in the setting-up of a complete infection of a host plant. After an initial replication step in the first cells, viruses spread from cell-to-cell through mesophyll cells, until they reach the vasculature where they rapidly move to distant sites in order to establish the infection of the whole plant. This last step is referred to as systemic transport, or long-distance movement, and involves virus crossings through several cellular barriers: bundle sheath, vascular parenchyma, and companion cells for virus loading into sieve elements (SE). Viruses are then passively transported within the source-to-sink flow of photoassimilates and are unloaded from SE into sink tissues. However, the molecular mechanisms governing virus long-distance movement are far from being understood. While most viruses seem to move systemically as virus particles, some viruses are transported in SE as viral ribonucleoprotein complexes (RNP). The nature of the cellular and viral factors constituting these RNPs is still poorly known. The topic of this review will mainly focus on the host and viral factors that facilitate or restrict virus long-distance movement.

摘要

植物病毒的韧皮部运输是建立宿主植物完整感染的一个必要步骤。在最初的细胞内复制步骤之后,病毒通过叶肉细胞从一个细胞传播到另一个细胞,直到它们到达维管束,在那里它们迅速移动到遥远的部位,以建立对整个植物的感染。这最后一步被称为系统运输或长距离运动,涉及病毒穿过几个细胞屏障:束鞘、维管束薄壁组织和伴细胞,以便将病毒装载到筛管中 (SE)。然后,病毒在光产物的源到汇流中被动运输,并从 SE 卸载到汇组织中。然而,控制病毒长距离运动的分子机制远未被理解。虽然大多数病毒似乎作为病毒颗粒系统性地移动,但有些病毒作为病毒核糖核蛋白复合物 (RNP) 在 SE 中运输。构成这些 RNP 的细胞和病毒因子的性质仍然知之甚少。这篇综述的主题将主要集中在促进或限制病毒长距离运动的宿主和病毒因素上。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a0/3662875/21bbd115484a/fpls-04-00154-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a0/3662875/21bbd115484a/fpls-04-00154-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a0/3662875/21bbd115484a/fpls-04-00154-g001.jpg

相似文献

1
Viral and cellular factors involved in Phloem transport of plant viruses.植物病毒韧皮部运输涉及的病毒和细胞因子。
Front Plant Sci. 2013 May 24;4:154. doi: 10.3389/fpls.2013.00154. eCollection 2013.
2
Mutations in viral movement protein alter systemic infection and identify an intercellular barrier to entry into the phloem long-distance transport system.病毒运动蛋白的突变会改变系统感染,并确定了进入韧皮部长距离运输系统的细胞间屏障。
Virology. 1998 May 25;245(1):75-89. doi: 10.1006/viro.1998.9154.
3
Viral infection enables phloem loading of GFP and long-distance trafficking of the protein.病毒感染可使绿色荧光蛋白(GFP)在韧皮部中装载并进行蛋白质的长距离运输。
Plant J. 2007 Jul;51(2):165-72. doi: 10.1111/j.1365-313X.2007.03128.x. Epub 2007 Jun 8.
4
Phloem loading and unloading of Cowpea mosaic virus in Vigna unguiculata.豇豆花叶病毒在豇豆中的韧皮部装载与卸载
J Gen Virol. 2002 Jun;83(Pt 6):1493-1504. doi: 10.1099/0022-1317-83-6-1493.
5
Viral Hacks of the Plant Vasculature: The Role of Phloem Alterations in Systemic Virus Infection.病毒对植物维管束的劫持:韧皮部改变在系统性病毒感染中的作用。
Annu Rev Virol. 2020 Sep 29;7(1):351-370. doi: 10.1146/annurev-virology-010320-072410. Epub 2020 May 26.
6
Factors involved in the systemic transport of plant RNA viruses: the emerging role of the nucleus.植物 RNA 病毒系统转运涉及的因素:核的新兴作用。
J Exp Bot. 2014 Apr;65(7):1689-97. doi: 10.1093/jxb/ert449. Epub 2014 Jan 13.
7
A Distinct, Non-Virion Plant Virus Movement Protein Encoded by a Crinivirus Essential for Systemic Infection.一种独特的、非病毒粒子的植物病毒运动蛋白,由克鲁尼病毒编码,对系统感染至关重要。
mBio. 2018 Nov 20;9(6):e02230-18. doi: 10.1128/mBio.02230-18.
8
Membrane-associated virus replication complexes locate to plant conducting tubes.膜相关病毒复制复合体定位于植物导管。
Plant Signal Behav. 2015;10(8):e1042639. doi: 10.1080/15592324.2015.1042639.
9
Long-distance trafficking of macromolecules in the phloem.韧皮部中大分子的远距离运输。
Plant Signal Behav. 2008 Apr;3(4):260-2. doi: 10.4161/psb.3.4.5196.
10
Hitchhikers, highway tolls and roadworks: the interactions of plant viruses with the phloem.搭便车者、高速公路通行费和道路工程:植物病毒与韧皮部的相互作用。
Curr Opin Plant Biol. 2018 Jun;43:82-88. doi: 10.1016/j.pbi.2018.02.001. Epub 2018 Feb 21.

引用本文的文献

1
Cucumber mosaic virus infection does not increase the translocation of the green fluorescent protein from GM rootstock to non-GM scion in transgrafted plants.黄瓜花叶病毒感染不会增加转基因嫁接植物中绿色荧光蛋白从转基因砧木向非转基因接穗的转运。
Virus Genes. 2025 Jun 24. doi: 10.1007/s11262-025-02172-0.
2
Viral tropism in plants, reproductive tissues, and seeds.病毒在植物、生殖组织和种子中的嗜性。
Arch Microbiol. 2025 May 23;207(7):152. doi: 10.1007/s00203-025-04353-9.
3
The roles of movement and coat proteins in the transport of tobamoviruses between plant cells.

本文引用的文献

1
Differential requirements for Tombusvirus coat protein and P19 in plants following leaf versus root inoculation.叶片和根系接种后,番木瓜环斑病毒外壳蛋白和 P19 在植物中存在差异需求。
Virology. 2013 May 10;439(2):89-96. doi: 10.1016/j.virol.2013.01.011. Epub 2013 Mar 12.
2
Silencing of the host factor eIF(iso)4E gene confers plum pox virus resistance in plum.沉默宿主因子 eIF(iso)4E 基因赋予李树抗李痘病毒。
PLoS One. 2013;8(1):e50627. doi: 10.1371/journal.pone.0050627. Epub 2013 Jan 28.
3
Recent advances in research of plant virus movement mediated by triple gene block.
运动蛋白和外壳蛋白在烟草花叶病毒在植物细胞间运输中的作用。
Front Plant Sci. 2025 Apr 17;16:1580554. doi: 10.3389/fpls.2025.1580554. eCollection 2025.
4
Identification of host specificity determinants in brome mosaic virus for rice infection.雀麦花叶病毒中决定水稻感染的宿主特异性决定因素的鉴定。
Virus Res. 2025 May;355:199564. doi: 10.1016/j.virusres.2025.199564. Epub 2025 Mar 25.
5
Transmission, Spread, Longevity and Management of Hop Latent Viroid, a Widespread and Destructive Pathogen Affecting Cannabis ( L.) Plants in North America.北美一种影响大麻(L.)植物的广泛且具破坏性的病原体——啤酒花潜隐类病毒的传播、扩散、存活及管理
Plants (Basel). 2025 Mar 6;14(5):830. doi: 10.3390/plants14050830.
6
Tobacco Mosaic Virus Movement: From Capsid Disassembly to Transport Through Plasmodesmata.烟草花叶病毒的移动:从衣壳解体到通过胞间连丝的运输
Viruses. 2025 Jan 31;17(2):214. doi: 10.3390/v17020214.
7
Systemic infection of cowpea aphid-borne mosaic virus in Passiflora spp. occurs at the initial stage regardless of the species' resistance.无论西番莲属植物的抗性如何,豇豆蚜传花叶病毒在其侵染初期都会发生系统感染。
Arch Virol. 2025 Jan 29;170(2):43. doi: 10.1007/s00705-025-06230-8.
8
Transcriptional and hormonal profiling uncovers the interactions between plant developmental stages and RNA virus infection.转录组和激素谱分析揭示了植物发育阶段与 RNA 病毒感染之间的相互作用。
J Gen Virol. 2024 Sep;105(9). doi: 10.1099/jgv.0.002023.
9
Detection of exogenous siRNA inside sweet corn bundle sheath cells and the RNAi dynamics in the early stage of infection.甜玉米维管束鞘细胞中外源小干扰RNA的检测及感染早期的RNA干扰动态
Physiol Mol Biol Plants. 2024 Aug;30(8):1265-1276. doi: 10.1007/s12298-024-01500-2. Epub 2024 Aug 14.
10
The C4 photosynthesis bifunctional enzymes, PDRPs, of maize are co-opted to cytoplasmic viral replication complexes to promote infection of a prevalent potyvirus sugarcane mosaic virus.玉米 C4 光合作用双功能酶 PDRPs 被募集到细胞质病毒复制复合物中,以促进一种流行的马铃薯 Y 病毒——甘蔗花叶病毒的感染。
Plant Biotechnol J. 2024 Jul;22(7):1812-1832. doi: 10.1111/pbi.14304. Epub 2024 Feb 10.
植物病毒三基因块介导运动蛋白的研究进展
Front Plant Sci. 2012 Dec 12;3:276. doi: 10.3389/fpls.2012.00276. eCollection 2012.
4
Circulating virus load determines the size of bottlenecks in viral populations progressing within a host.循环病毒载量决定了在宿主内进展的病毒群体中的瓶颈大小。
PLoS Pathog. 2012;8(11):e1003009. doi: 10.1371/journal.ppat.1003009. Epub 2012 Nov 1.
5
Cauliflower mosaic virus protein P6 inhibits signaling responses to salicylic acid and regulates innate immunity.花椰菜花叶病毒蛋白 P6 抑制水杨酸信号反应并调节先天免疫。
PLoS One. 2012;7(10):e47535. doi: 10.1371/journal.pone.0047535. Epub 2012 Oct 11.
6
The benyvirus RNA silencing suppressor is essential for long-distance movement, requires both zinc-finger and NoLS basic residues but not a nucleolar localization for its silencing-suppression activity.贝尼病毒 RNA 沉默抑制子对于长距离移动是必需的,其沉默抑制活性既需要锌指结构和无定位信号的碱性氨基酸残基,也需要核仁定位。
Mol Plant Microbe Interact. 2013 Feb;26(2):168-81. doi: 10.1094/MPMI-06-12-0142-R.
7
Family-based linkage and association mapping reveals novel genes affecting Plum pox virus infection in Arabidopsis thaliana.基于家系的连锁和关联作图揭示了影响拟南芥感染李痘病毒的新基因。
New Phytol. 2012 Nov;196(3):873-886. doi: 10.1111/j.1469-8137.2012.04289.x. Epub 2012 Sep 3.
8
Virus population bottlenecks during within-host progression and host-to-host transmission.病毒在宿主内进化和宿主间传播过程中的种群瓶颈。
Curr Opin Virol. 2012 Oct;2(5):546-55. doi: 10.1016/j.coviro.2012.08.001. Epub 2012 Aug 22.
9
Multifunctional roles for the N-terminal basic motif of Alfalfa mosaic virus coat protein: nucleolar/cytoplasmic shuttling, modulation of RNA-binding activity, and virion formation.紫花苜蓿花叶病毒外壳蛋白 N 端碱性基序的多功能作用:核仁/细胞质穿梭、调节 RNA 结合活性和病毒粒子形成。
Mol Plant Microbe Interact. 2012 Aug;25(8):1093-103. doi: 10.1094/MPMI-04-12-0079-R.
10
The RTM resistance to potyviruses in Arabidopsis thaliana: natural variation of the RTM genes and evidence for the implication of additional genes.拟南芥中 RTM 对马铃薯 Y 病毒的抗性:RTM 基因的自然变异及其他基因参与的证据。
PLoS One. 2012;7(6):e39169. doi: 10.1371/journal.pone.0039169. Epub 2012 Jun 18.