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首页> 外文期刊>Cereal Research Communications >Rapid detection of Fusarium graminearum complex in wheat seeds using species-specific PCR primer designed based on a microsatellite region.
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Rapid detection of Fusarium graminearum complex in wheat seeds using species-specific PCR primer designed based on a microsatellite region.

机译:使用基于微卫星区域设计的物种特异性PCR引物,快速检测小麦种子中的禾谷镰刀菌复合物。

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摘要

Fusarium head blight disease (FHB) in wheat, caused by Fusarium graminearum species complex (Fg complex), is a very serious disease threatening wheat production worldwide. Polymerase chain reaction (PCR) based methods have been established for rapid and quantitative detection of many plant pathogens. In this study, a specific pair of primers was designed based on the sequence of DNA fragment (740 bp) amplified by a microsatellite primer M13 from Fg complex isolates. This pair of primers was able to amplify a 380 bp fragment from all Fg complex isolates but not from any other tested fungal species. Using this pair of primers, a real-time PCR assay was developed to quantitatively detect small amounts of Fg complex in wheat seeds. This sensitive and quantitative detection assay could be useful in epidemiological studies and assessment of mycotoxin contamination in wheat seeds.
机译:由禾谷镰刀菌(Fusarium graminearum)种复合物(Fgar复合体)引起的小麦镰刀菌枯萎病(FHB)是一种非常严重的疾病,威胁着全世界的小麦生产。已经建立了基于聚合酶链反应(PCR)的方法来快速定量检测许多植物病原体。在这项研究中,根据微卫星引物M13从 Fg 复杂分离物中扩增的DNA片段(740 bp)的序列,设计了一对特异性引物。这对引物能够从所有 Fg 复杂分离物中扩增出380 bp的片段,但不能从任何其他测试的真菌物种中扩增出。使用这对引物,开发了一种实时PCR分析方法,可以定量检测小麦种子中的少量 Fg 复合物。这种灵敏和定量的检测方法可用于流行病学研究和评估小麦种子中的霉菌毒素污染。

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