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量化一种豆科植物曲叶病毒,以评估大豆基因型对黄化花叶病的抗性。

Quantification of a legume begomovirus to evaluate soybean genotypes for resistance to yellow mosaic disease.

机构信息

ICAR-Indian Institute of Soybean Research, Khandwa Road, Indore, Madhya Pradesh, India.

ICAR-Indian Institute of Soybean Research, Khandwa Road, Indore, Madhya Pradesh, India.

出版信息

J Virol Methods. 2019 Jun;268:24-31. doi: 10.1016/j.jviromet.2019.03.002. Epub 2019 Mar 16.

DOI:10.1016/j.jviromet.2019.03.002
PMID:30890330
Abstract

Mungbean yellow mosaic India virus (MYMIV) infecting soybean and other legumes causes yellow mosaic disease (YMD). Evaluation of soybean genotypes for YMD resistance involves field screening at disease hot spots or in a protected environment using infectious clones or viruliferous whiteflies as sources of virus inocula. Development of efficient virus inoculation and quantification protocols to screen soybean genetic stocks against YMD is imperative for breeding resistant varieties. Binary plasmids harbouring complete, tandem dimeric genomic components DNA A and DNA B of MYMIV-soybean isolate were engineered. The infectivity of the clones was demonstrated in soybean genotypes JS335 and UPSM534 that display contrasting YMD resistance. As a follow-up, soybean germplasm lines, breeding lines, and representative cultivars that were initially screened at an YMD hot-spot were then subjected to Agrobacterium-based infection with MYMIV. Quantitative real time polymerase chain reaction (qRT-PCR) based copy number analysis of MYMIV genomic components allowed soybean genotypes to be classified into three discrete categories; resistant, moderately resistant and susceptible to the viral infection. Thus, a soybean germplasm disease screening system based on agro-infection and qRT-PCR based quantification of MYMIV was developed to facilitate breeding YMD resistant soybean. The implications of this study for obtaining YMD resistant soybean cultivars are discussed.

摘要

感染大豆和其他豆科植物的绿豆黄斑驳印度病毒 (MYMIV) 会导致黄斑驳病 (YMD)。评估大豆基因型对 YMD 的抗性需要在疾病热点地区或使用感染性克隆或带毒粉虱作为病毒接种物来源的保护环境中进行田间筛选。开发有效的病毒接种和定量方案来筛选抗 YMD 的大豆遗传品系对于培育抗性品种至关重要。构建了含有 MYMIV-大豆分离物完整串联二聚体基因组元件 DNA A 和 DNA B 的二元质粒。这些克隆在表现出相反 YMD 抗性的大豆基因型 JS335 和 UPSM534 中证明了其感染性。作为后续行动,最初在 YMD 热点地区进行筛选的大豆种质系、育种系和代表性品种随后用 MYMIV 进行了农杆菌感染。基于定量实时聚合酶链反应 (qRT-PCR) 的 MYMIV 基因组成分拷贝数分析使大豆基因型分为三个离散类别:抗性、中度抗性和易感性。因此,开发了基于农杆菌感染和 qRT-PCR 定量的大豆种质疾病筛选系统,以促进抗 YMD 大豆的培育。讨论了这项研究对获得抗 YMD 大豆品种的意义。

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