Maize miR167-ARF3/30-polyamine oxidase 1 module-regulated H2O2 production confers resistance to maize chlorotic mottle virus

Maize employs a signaling mechanism mediated by microR167-auxin response factor 3 and 30-polyamine oxidase 1 for defense and counterdefense against maize chlorotic mottle virus. Maize chlorotic mottle virus (MCMV) is the key pathogen causing maize lethal necrosis (MLN). Due to the sharply increased incidence of MLN in many countries, there is an urgent need to identify resistant lines and uncover the underlying resistance mechanism. Here, we showed that the abundance of maize (Zea mays) microR167 (Zma-miR167) positively modulates the degree of resistance to MCMV. Zma-miR167 directly targets Auxin Response Factor3 (ZmARF3) and ZmARF30, both of which negatively regulate resistance to MCMV. RNA-sequencing coupled with gene expression assays revealed that both ZmARF3 and ZmARF30 directly bind the promoter of Polyamine Oxidase 1 (ZmPAO1) and activate its expression. Knockdown or inhibition of enzymatic activity of ZmPAO1 suppressed MCMV infection. Nevertheless, MCMV-encoded p31 protein directly targets ZmPAO1 and enhances the enzyme activity to counteract Zma-miR167-mediated defense to some degree. We uncovered a role of the Zma-miR167-ZmARF3/30 module for restricting MCMV infection by regulating ZmPAO1 expression, while MCMV employs p31 to counteract this defense.

Automated summary

Maize employs a signaling mechanism mediated by microR167-auxin response factor 3 and 30-polyamine oxidase 1 for defense and counterdefense against maize chlorotic mottle virus. The study showed that Zma-miR167 positively modulates the degree of resistance to MCMV by targeting ZmARF3 and ZmARF30, which negatively regulate resistance. However, MCMV uses p31 protein to counteract Zma-miR167-mediated defense. The results reveal the role of Zma-miR167-ZmARF3/30 module in restricting MCMV infection.