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Rapid detection of Magnaporthe oryzae chrysovirus 1-A from fungal colonies on agar plates and lesions of rice blast

机译:从琼脂平板上的真菌菌落和稻瘟病灶快速检测稻瘟病菌Chrysovirus 1-A

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摘要

Mycoviruses associated with hypovirulent phenotypes have been reported for many plant pathogenic fungi. Common techniques to detect mycoviruses depend on the presence of dsRNA elements. These techniques require cultivation of the host fungus, extraction of nucleic acids and purification of dsRNA. These procedures are time-consuming steps and use organic solvents. Here we developed a simple and rapid method detect Magnaporthe oryzae chrysovirus 1-A by direct one-step RT-PCR in samples picked using a sterilized toothpick from fungal colonies growing on plate media. This method could be applied for direct detection of mycoviruses from lesions caused by virus-infected plant pathogenic fungi.
机译:已经报道了许多植物致病真菌与低毒表型相关的分枝杆菌病毒。检测分枝杆菌病毒的常用技术取决于dsRNA元件的存在。这些技术需要宿主真菌的培养,核酸的提取和dsRNA的纯化。这些步骤是耗时的步骤,并且使用有机溶剂。在这里,我们开发了一种简单快速的方法,通过直接一步一步RT-PCR在使用无菌牙签从平板培养基上生长的真菌菌落中采集的样品中检测稻瘟病毒1A。该方法可用于直接检测病毒感染的植物病原真菌引起的病变中的分枝杆菌病毒。

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