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本文引用的文献

1
Precise Exchange of the Helper-Component Proteinase Cistron Between and : Impact on Virus Viability and Host Range Specificity.和之间辅助组分蛋白酶原基因的精确交换:对病毒存活能力和宿主范围特异性的影响。
Phytopathology. 2020 Jan;110(1):206-214. doi: 10.1094/PHYTO-06-19-0193-FI. Epub 2019 Nov 12.
2
First Report of Transmission of Soybean mosaic virus and Alfalfa mosaic virus by Aphis glycines in the New World.新世界中豆蚜传播大豆花叶病毒和苜蓿花叶病毒的首次报道。
Plant Dis. 2001 May;85(5):561. doi: 10.1094/PDIS.2001.85.5.561C.
3
Effect of Aphid Behavior on Efficiency of Transmission of Soybean mosaic virus by the Soybean-Colonizing Aphid, Aphis glycines.蚜虫行为对大豆定居蚜虫——大豆蚜传播大豆花叶病毒效率的影响
Plant Dis. 2002 Nov;86(11):1260-1264. doi: 10.1094/PDIS.2002.86.11.1260.
4
Transmissibility of Field Isolates of Soybean Viruses by Aphis glycines.大豆蚜传播大豆病毒田间分离株的能力
Plant Dis. 2002 Nov;86(11):1219-1222. doi: 10.1094/PDIS.2002.86.11.1219.
5
G7H, a New Soybean mosaic virus Strain: Its Virulence and Nucleotide Sequence of CI Gene.G7H,一种新的大豆花叶病毒株系:其毒力及CI基因的核苷酸序列
Plant Dis. 2003 Nov;87(11):1372-1375. doi: 10.1094/PDIS.2003.87.11.1372.
6
Occurrence of Seed Coat Mottling in Soybean Plants Inoculated with Bean pod mottle virus and Soybean mosaic virus.接种菜豆荚斑驳病毒和大豆花叶病毒的大豆植株种皮斑驳的发生情况
Plant Dis. 2003 Nov;87(11):1333-1336. doi: 10.1094/PDIS.2003.87.11.1333.
7
The Relationship Between Aphis glycines and Soybean mosaic virus Incidence in Different Pest Management Systems.不同害虫管理系统中大豆蚜与大豆花叶病毒发病率之间的关系
Plant Dis. 2005 Sep;89(9):926-934. doi: 10.1094/PD-89-0926.
8
Similarities in Seed and Aphid Transmission Among Soybean mosaic virus Isolates.大豆花叶病毒分离株在种子和蚜虫传播方面的相似性。
Plant Dis. 2007 May;91(5):546-550. doi: 10.1094/PDIS-91-5-0546.
9
Potential for Integrated Management of Soybean Virus Disease.大豆病毒病综合管理的潜力
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10
Identification and Distribution of Soybean mosaic virus Strains in Southern China.中国南方大豆花叶病毒株系的鉴定与分布
Plant Dis. 2010 Mar;94(3):351-357. doi: 10.1094/PDIS-94-3-0351.

大豆花叶病毒:一种分布广泛但自然宿主范围有限的成功的马铃薯 Y 病毒属病毒。

Soybean mosaic virus: a successful potyvirus with a wide distribution but restricted natural host range.

机构信息

Department of Entomology and Plant Pathology, The University of Tennessee, Knoxville, TN 37996, USA.

United States Department of Agriculture-Agricultural Research Service and Department of Crop Sciences, University of Illinois, Urbana, IL 61801, USA.

出版信息

Mol Plant Pathol. 2018 Jul;19(7):1563-1579. doi: 10.1111/mpp.12644. Epub 2018 Feb 14.

DOI:10.1111/mpp.12644
PMID:29134790
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6638002/
Abstract

TAXONOMY

Soybean mosaic virus (SMV) is a species within the genus Potyvirus, family Potyviridae, which includes almost one-quarter of all known plant RNA viruses affecting agriculturally important plants. The Potyvirus genus is the largest of all genera of plant RNA viruses with 160 species.

PARTICLE

The filamentous particles of SMV, typical of potyviruses, are about 7500 Å long and 120 Å in diameter with a central hole of about 15 Å in diameter. Coat protein residues are arranged in helices of about 34 Å pitch having slightly less than nine subunits per turn.

GENOME

The SMV genome consists of a single-stranded, positive-sense, polyadenylated RNA of approximately 9.6 kb with a virus-encoded protein (VPg) linked at the 5' terminus. The genomic RNA contains a single large open reading frame (ORF). The polypeptide produced from the large ORF is processed proteolytically by three viral-encoded proteinases to yield about 10 functional proteins. A small ORF, partially overlapping the P3 cistron, pipo, is encoded as a fusion protein in the N-terminus of P3 (P3N + PIPO).

BIOLOGICAL PROPERTIES

SMV's host range is restricted mostly to two plant species of a single genus: Glycine max (cultivated soybean) and G. soja (wild soybean). SMV is transmitted by aphids non-persistently and by seeds. The variability of SMV is recognized by reactions on cultivars with dominant resistance (R) genes. Recessive resistance genes are not known.

GEOGRAPHICAL DISTRIBUTION AND ECONOMIC IMPORTANCE

As a consequence of its seed transmissibility, SMV is present in all soybean-growing areas of the world. SMV infections can reduce significantly seed quantity and quality (e.g. mottled seed coats, reduced seed size and viability, and altered chemical composition).

CONTROL

The most effective means of managing losses from SMV are the planting of virus-free seeds and cultivars containing single or multiple R genes.

KEY ATTRACTIONS

The interactions of SMV with soybean genotypes containing different dominant R genes and an understanding of the functional role(s) of SMV-encoded proteins in virulence, transmission and pathogenicity have been investigated intensively. The SMV-soybean pathosystem has become an excellent model for the examination of the genetics and genomics of a uniquely complex gene-for-gene resistance model in a crop of worldwide importance.

摘要

分类学

大豆花叶病毒(SMV)是马铃薯 Y 病毒属的一个种,属于马铃薯 Y 病毒科,该科包括近四分之一影响农业重要植物的已知植物 RNA 病毒。马铃薯 Y 病毒属是所有植物 RNA 病毒属中最大的一个属,有 160 个种。

粒子

SMV 的丝状粒子,是典型的马铃薯 Y 病毒粒子,长约 7500Å,直径 120Å,中央孔直径约 15Å。外壳蛋白残基排列成约 34Å螺距的螺旋,每圈有略少于 9 个亚基。

基因组

SMV 基因组由一条单链、正义、多聚腺苷酸化的 RNA 组成,约 9.6kb,在 5'末端连接有一个病毒编码的蛋白(VPg)。基因组 RNA 包含一个单一的大开放阅读框(ORF)。从大 ORF 翻译的多肽通过三个病毒编码的蛋白酶进行蛋白水解加工,产生约 10 个功能蛋白。一个小的 ORF,部分重叠 P3 顺反子,pipo,作为 P3(P3N+PIPO)N 端的融合蛋白编码。

生物学特性

SMV 的宿主范围主要局限于两个豆科植物属的两个植物种:大豆(栽培大豆)和野生大豆(野生大豆)。SMV 通过非持久的蚜虫和种子传播。SMV 的变异性通过对具有显性抗性(R)基因的品种的反应来识别。隐性抗性基因尚不清楚。

地理分布和经济重要性

由于其种子可传播性,SMV 存在于世界上所有种植大豆的地区。SMV 感染可显著降低种子数量和质量(如斑驳的种皮、种子变小和活力降低以及化学成分改变)。

控制

管理 SMV 损失的最有效方法是种植无病毒种子和含有单个或多个 R 基因的品种。

重点关注

SMV 与含有不同显性 R 基因的大豆基因型的相互作用以及对 SMV 编码蛋白在毒力、传播和致病性中的功能作用的理解已被广泛研究。SMV-大豆病理系统已成为一个极好的模型,用于研究一种在全球重要作物中具有独特复杂基因对基因抗性模型的遗传学和基因组学。