Min Chul Kim

The rice blast fungus Magnaporthe oryzae is a devastating plant pathogen that threatens rice production worldwide. Host‐induced gene silencing (HIGS) has been effectively applied to study pathogenic gene function during host–microbe interactions and control fungal diseases in various crops. In this study, the HIGS system of M. oryzae was established using transgenic fungus expressing green fluorescence protein (GFP), KJ201:: eGFP and 35S::dsRNAi plants, which produce small interfering RNAs targeting fungal genes. Through this system, we verified the HIGS of rice blast fungus quantitatively and qualitatively in both Arabidopsis and rice. Then, we showed that the HIGS of M. oryzae 's pathogenic genes, including RGS1 , MgAPT2 and LHS1 , significantly alter its virulence. Both 35S::dsRNAi_ MgAPT2 and 35S::dsRNAi_ LHS1 plants showed a considerably enhanced fungal resistance, characterized by the formation of H 2 O 2 ‐containing defensive granules and induction of rice pathogenesis‐related ( PR ) genes. In addition, the enhanced susceptibility of 35S::dsRNAi_ RGS1 plants to blast fungus suggested a novel mode of action of this gene during fungal infection. Overall, the results of this study demonstrate that HIGS is a very effective and efficient biological tool not only to accurately characterize the functions of fungal pathogenic genes during rice‐ M. oryzae interactions, but also to control fungal disease and ensure a successful rice production.