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Detection and Quantification of Rhizoctonia solani AG-1 IA, the Rice Sheath Blight Pathogen, in Rice Using Real-Time PC

机译:实时PC检测和定量检测水稻纹枯病病原菌solani Rhizoctonia solani AG-1 IA

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摘要

Rhizoctonia solani Kuehn is the causal organism of sheath blight, a major rice disease worldwide that severely impairs yield and quality. It is difficult to identify the pathogen in the early phase of the infection and to accurately quantify the fungal development based on visual inspection. Therefore, a rapid and reliable method is advantageous for the detection and quantification of the pathogen causing this important rice disease. In this study, a real-time, quantitative polymerase chain reaction (QPCR) assay was developed to detect and quantify R. solani AG-1 IA DNA from infected rice plants. A specific primer pair was designed based on the internal transcribed spacer region of the fungal ribosomal DNA. The specific detection of R. solani DNA was successful with quantities as low as 1 pg. The QPCR assay could be used for detecting the rice sheath blight pathogen, quantifying fungal aggressiveness, and evaluating the resistance level of rice cultivars.
机译:solani Kuehn枯萎病是鞘枯病的病原生物,鞘枯病是世界范围内的一种主要水稻疾病,严重损害产量和品质。难以在感染的早期阶段识别病原体,并且难以根据目视检查准确量化真菌的发育。因此,快速可靠的方法对于检测和定量引起这种重要水稻疾病的病原体是有利的。在这项研究中,开发了一种实时定量聚合酶链反应(QPCR)分析方法,用于检测和定量受感染水稻植株的茄尼(R. solani)AG-1 IA DNA。根据真菌核糖体DNA的内部转录间隔区设计特异性引物对。 solani solani DNA的特异性检测成功,量低至1 pg。 QPCR分析可用于检测水稻鞘枯病病原体,定量真菌侵袭性和评估水稻品种的抗性水平。

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