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High prevalence of viruses in table grape from Spain detected by real-time RT-PCR

机译:实时RT-PCR检测到西班牙食用葡萄中病毒的高流行

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Table grapes from one of the most important growing area in Spain (Vinalopó, Alicante) protected by the Designation of Origin “Vinalopó bagged table grape”, were surveyed and analysed to determine the prevalence of the five viruses included in the Spanish certification program: Arabis mosaic virus (ArMV), Grapevine fanleaf virus (GFLV), Grapevine fleck virus (GFkV), Grapevine leafroll associated virus-1 (GLRaV-1) and Grapevine leafroll associated virus-3 (GLRaV-3). Ninety five sampling points were selected and the position of grapevine plants georeferenced. Samples were collected in two different vegetative periods and analyses were performed by ELISA and real-time RT-PCR. Purified RNA and immobilized viral targets from plant extracts on nylon membranes were used in parallel assays as templates for PCR assays. In order to analyse these five viral species by real-time RT-PCR, new specific primers and TaqMan probes were designed for detection of ArMV and GFkV. Real time RT-PCR from purified RNA was more sensitive than spot version and ELISA tests. The most prevalent virus was GFLV (95.8%) followed by GLRaV-3 (94.7%), GLRaV-1 (66.3%) and GFkV (65.3%). ArMV was not detected in any sample. The high level of viral infections and the presence of mixed infections suggest that initial infected plant material and uncontrolled traffic of propagation material have played an important role in the spread of viruses.
机译:对来自西班牙最重要的产区之一(维纳洛普,阿利坎特)的食用葡萄进行了调查和分析,以确定西班牙认证计划中包括的五种病毒的流行性:阿拉比斯酒花叶病毒(ArMV),葡萄扇叶病毒(GFLV),葡萄斑点病毒(GFkV),葡萄叶相关病毒1(GLRaV-1)和葡萄叶相关病毒3(GLRaV-3)。选择了95个采样点,并对葡萄植物的位置进行了地理定位。在两个不同的营养阶段收集样品,并通过ELISA和实时RT-PCR进行分析。来自植物提取物的纯化RNA和固定在尼龙膜上的病毒靶标在平行测定中用作PCR测定的模板。为了通过实时RT-PCR分析这五个病毒种类,设计了新的特异性引物和TaqMan探针来检测ArMV和GFkV。来自纯化RNA的实时RT-PCR比点样法和ELISA测试更敏感。最流行的病毒是GFLV(95.8%),其次是GLRaV-3(94.7%),GLRaV-1(66.3%)和GFkV(65.3%)。在任何样品中均未检测到ArMV。高水平的病毒感染和混合感染的存在表明,最初感染的植物材料和不受控制的繁殖材料运输在病毒传播中发挥了重要作用。

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