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Two nuclear effectors of the rice blast fungus modulate host immunity via transcriptional reprogramming.


ABSTRACT: Pathogens utilize multiple types of effectors to modulate plant immunity. Although many apoplastic and cytoplasmic effectors have been reported, nuclear effectors have not been well characterized in fungal pathogens. Here, we characterize two nuclear effectors of the rice blast pathogen Magnaporthe oryzae. Both nuclear effectors are secreted via the biotrophic interfacial complex, translocated into the nuclei of initially penetrated and surrounding cells, and reprogram the expression of immunity-associated genes by binding on effector binding elements in rice. Their expression in transgenic rice causes ambivalent immunity: increased susceptibility to M. oryzae and Xanthomonas oryzae pv. oryzae, hemibiotrophic pathogens, but enhanced resistance to Cochliobolus miyabeanus, a necrotrophic pathogen. Our findings help remedy a significant knowledge deficiency in the mechanism of M. oryzae-rice interactions and underscore how effector-mediated manipulation of plant immunity by one pathogen may also affect the disease severity by other pathogens.

SUBMITTER: Kim S 

PROVIDER: S-EPMC7672089 | biostudies-literature | 2020 Nov

REPOSITORIES: biostudies-literature

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Two nuclear effectors of the rice blast fungus modulate host immunity via transcriptional reprogramming.

Kim Seongbeom S   Kim Chi-Yeol CY   Park Sook-Young SY   Kim Ki-Tae KT   Jeon Jongbum J   Chung Hyunjung H   Choi Gobong G   Kwon Seomun S   Choi Jaeyoung J   Jeon Junhyun J   Jeon Jong-Seong JS   Khang Chang Hyun CH   Kang Seogchan S   Lee Yong-Hwan YH  

Nature communications 20201117 1


Pathogens utilize multiple types of effectors to modulate plant immunity. Although many apoplastic and cytoplasmic effectors have been reported, nuclear effectors have not been well characterized in fungal pathogens. Here, we characterize two nuclear effectors of the rice blast pathogen Magnaporthe oryzae. Both nuclear effectors are secreted via the biotrophic interfacial complex, translocated into the nuclei of initially penetrated and surrounding cells, and reprogram the expression of immunity  ...[more]

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