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利用实时定量聚合酶链反应快速准确检测和定量水稻中的稻瘟病菌

Quick and Accurate Detection and Quantification of Magnaporthe oryzae in Rice Using Real-Time Quantitative Polymerase Chain Reaction.

作者信息

Sun Geng, Liu Jinliang, Li Guihua, Zhang Xianghui, Chen Tingting, Chen Jingyuan, Zhang Hao, Wang Dongping, Sun Fengjie, Pan Hongyu

机构信息

College of Plant Sciences, Jilin University, Jilin, Changchun 130062, China, and State Key Laboratory of the Discovery and Development of Novel Pesticide, Shenyang Research Institute of Chemical Industry Co., Ltd., Shenyang 110021, China.

College of Plant Sciences, Jilin University.

出版信息

Plant Dis. 2015 Feb;99(2):219-224. doi: 10.1094/PDIS-05-14-0485-RE.

Abstract

Rice blast, caused by Magnaporthe oryzae, is one of the most severe fungal diseases in rice worldwide. In this study, we developed methods to quickly and accurately detect and quantify M. oryzae in the pure cultures of the fungus, rice plants, and rice seed by using SYBR Green I of the real-time quantitative polymerase chain reaction (qPCR). Results of absolute qPCR show that Magnaporthe oryzae can be detected at as low as 6.9 × 10 ng of genomic DNA. Results also show that all 10 varieties of rice seed examined in this study contain this fungus, indicating that M. oryzae is generally widespread in rice seed. We report the quantification of DNA of M. oryzae in rice leaves collected in the field, instead of in the lab, using relative qPCR by using rice actin gene as a housekeeping gene. Our results show great practical significance because we would know the potential fungal infection even before planting.

摘要

由稻瘟病菌引起的稻瘟病是全球水稻最严重的真菌病害之一。在本研究中,我们开发了利用实时定量聚合酶链反应(qPCR)的SYBR Green I快速准确地检测和定量稻瘟病菌在该真菌的纯培养物、水稻植株及水稻种子中的方法。绝对定量PCR结果表明,低至6.9×10 ng的基因组DNA就能检测到稻瘟病菌。结果还表明,本研究中检测的所有10个水稻品种种子均含有这种真菌,这表明稻瘟病菌在水稻种子中普遍存在。我们报告了以水稻肌动蛋白基因作为管家基因,采用相对定量PCR在田间而非实验室采集的水稻叶片中对稻瘟病菌DNA进行定量。我们的结果具有重大的实际意义,因为在种植前就能了解潜在的真菌感染情况。

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