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小麦多重 RT-PCR 检测技术同时检测小麦丛矮病毒、禾谷镶嵌病毒、大麦黄花叶病毒和水稻齿叶矮缩病毒。

Simultaneous detection of wheat dwarf virus, northern cereal mosaic virus, barley yellow striate mosaic virus and rice black-streaked dwarf virus in wheat by multiplex RT-PCR.

机构信息

State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, No. 2, West Yuan Ming Yuan Road, Beijing, 100193, China; Laboratory of Phytopathology, University of Liège, Gembloux Agro-Bio Tech, Passage des déportés, 2, 5030, Gembloux, Belgium.

State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, No. 2, West Yuan Ming Yuan Road, Beijing, 100193, China.

出版信息

J Virol Methods. 2017 Nov;249:170-174. doi: 10.1016/j.jviromet.2017.09.010. Epub 2017 Sep 14.

Abstract

Wheat dwarf virus (WDV), barley yellow striate mosaic virus (BYSMV), rice black-streaked dwarf virus (RBSDV) and northern cereal mosaic virus (NCMV) are four viruses infecting wheat and causing similar symptoms. In this paper, a multiplex reverse transcription polymerase chain reaction (m-RT-PCR) method has been developed for the simultaneous detection and discrimination of these viruses. The protocol uses specific primer set for each virus and produces four distinct fragments (273, 565, 783 and 1296bp), detecting the presence of RBSDV, BYSMV, WDV and NCMV, respectively. Annealing temperature, concentrations of dNTP, Taq polymerase and Mg were optimized for the m-RT-PCR. The detection limit of the assay was up to 10 dilution. The amplification specificity of these primers was tested against a range of field samples from different regions of China, where RBSDV, BYSMV, WDV have been detected. This study fulfills the need for a rapid and specific wheat virus detection that also has the potential for investigating the epidemiology of these new viral diseases.

摘要

小麦矮缩病毒(WDV)、大麦黄花叶条纹病毒(BYSMV)、水稻黑条矮缩病毒(RBSDV)和北方禾谷花叶病毒(NCMV)是侵染小麦并引起相似症状的四种病毒。本文建立了一种同时检测和区分这四种病毒的多重反转录聚合酶链反应(m-RT-PCR)方法。该方案使用针对每种病毒的特异性引物组,分别产生四个不同的片段(273、565、783 和 1296bp),检测 RBSDV、BYSMV、WDV 和 NCMV 的存在。对 m-RT-PCR 的退火温度、dNTP、Taq 聚合酶和 Mg 浓度进行了优化。该检测方法的检测限低至 10 倍稀释。这些引物的扩增特异性已通过来自中国不同地区的一系列田间样本进行了测试,其中已检测到 RBSDV、BYSMV、WDV。该研究满足了对小麦病毒进行快速和特异性检测的需求,同时也有潜力调查这些新病毒性疾病的流行病学。

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