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

Author:

Sun Geng1,Liu Jinliang2,Li Guihua2,Zhang Xianghui2,Chen Tingting2,Chen Jingyuan2,Zhang Hao3,Wang Dongping4,Sun Fengjie5,Pan Hongyu2

Affiliation:

1. 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

2. College of Plant Sciences, Jilin University

3. College of Resource and Environment, Jilin Agricultural University

4. Bioscience Division, Los Alamos National Laboratory, Los Alamos, NM 87544

5. School of Science and Technology, Georgia Gwinnett College, Lawrenceville, GA 30043

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 × 10−5 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.

Publisher

Scientific Societies

Subject

Plant Science,Agronomy and Crop Science

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