Luo, Xiumei, Tian, Tingting, Feng, Li, Yang, Xingyong, Li, Linxuan, Tan, Xue, Wu, Wenxian, Li, Zhengguo, Treves, Haim, Serneels, Francois, Ng, I-Son, Tanaka, Kan, and Ren, Maozhi
The potato- Phytophthora infestans system was used as a model to investigate how PR1 proteins protect plants against oomycete pathogens. Results showed that upon pathogen infection, PR1 proteins were induced, and secreted PR1 translocated into pathogen cells to target AMPK kinase complex, thus inhibiting vegetative growth and pathogenicity. Question marks and dotted lines represent scientific problems which need more detailed proofs. NPR1, nonexpressor of pathogenesis-related genes 1; TGA, TGACG-binding factor; SNF1, Sucrose non-fermenting 1; RxLR, the amino acid (Arg-x-Leu-Arg) of conserved motif in effector, where x is any amino acid. [Display omitted] • Upon infecting by P. infestans , StPR1 expression was induced in host and secretory StPR1 proteins translocated into pathogen. • The translocated PR1 proteins target AMPK complex in P. infestans , and impaired the AMPK activation to downstream targets. • StPR1 prevented ROS homeostasis and inhibited the expression of RxLR effector-encoding genes in P. infestans. During the arms race between plants and pathogens, pathogenesis-related proteins (PR) in host plants play a crucial role in disease resistance, especially PR1. PR1 constitute a secretory peptide family, and their role in plant defense has been widely demonstrated in both hosts and in vitro. However, the mechanisms by which they control host-pathogen interactions and the nature of their targets within the pathogen remain poorly understood. The present study was aimed to investigate the anti-oomycete activity of secretory PR1 proteins and elaborate their underlying mechanisms. This study was conducted in the potato- Phytophthora infestans pathosystem. After being induced by the pathogen infection, the cross-kingdom translocation of secretory PR1 was demonstrated by histochemical assays and western blot, and their targets in P. infestans were identified by yeast-two-hybrid assays, bimolecular fluorescence complementation assays, and co-immunoprecipitation assay. The results showed that the expression of secretory PR1-encoding genes was induced during pathogen infection, and the host could deliver PR1 into P. infestans to inhibit its vegetative growth and pathogenicity. The translocated secretory PR1 targeted the subunits of the AMPK kinase complex in P. infestans , thus affecting the AMPK-driven phosphorylation of downstream target proteins, preventing ROS homeostasis, and down-regulating the expression of RxLR effectors. The results provide novel insights into the molecular function of PR1 in protecting plants against pathogen infection, and uncover a potential target for preventing pre- and post-harvest late blight. [ABSTRACT FROM AUTHOR]