Disruption of PAMP-Induced MAP Kinase Cascade by a Pseudomonas syringae Effector Activates Plant Immunity Mediated by the NB-LRR Protein SUMM2

Pathogen-associated molecular pattern (PAMP)-triggered immunity (PTI) serves as a primary plant defense response against microbial pathogens, with MEKK1, MKK1/MKK2, and MPK4 functioning as a MAP kinase cascade downstream of PAMP receptors. Plant Resistance (R) proteins sense specific pathogen effect...

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Published inCell host & microbe Vol. 11; no. 3; pp. 253 - 263
Main Authors Zhang, Zhibin, Wu, Yaling, Gao, Minghui, Zhang, Jie, Kong, Qing, Liu, Yanan, Ba, Hongping, Zhou, Jianmin, Zhang, Yuelin
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 15.03.2012
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Summary:Pathogen-associated molecular pattern (PAMP)-triggered immunity (PTI) serves as a primary plant defense response against microbial pathogens, with MEKK1, MKK1/MKK2, and MPK4 functioning as a MAP kinase cascade downstream of PAMP receptors. Plant Resistance (R) proteins sense specific pathogen effectors to initiate a second defense mechanism, termed effector-triggered immunity (ETI). In a screen for suppressors of the mkk1 mkk2 autoimmune phenotype, we identify the nucleotide-binding leucine-rich repeat (NB-LRR) protein SUMM2 and find that the MEKK1-MKK1/MKK2-MPK4 cascade negatively regulates SUMM2-mediated immunity. Further, the MEKK1-MKK1/MKK2-MPK4 cascade positively regulates basal defense targeted by the Pseudomonas syringae pathogenic effector HopAI1, which inhibits MPK4 kinase activity. Inactivation of MPK4 by HopAI1 results in activation of SUMM2-mediated defense responses. Our data suggest that SUMM2 is an R protein that becomes active when the MEKK1-MKK1/MKK2-MPK4 cascade is disrupted by pathogens, supporting the hypothesis that R proteins evolved to protect plants when microbial effectors suppress basal resistance. ► The MEKK1-MKK1/MKK2-MPK4 kinase cascade is required for basal defense ► MEKK1-MKK1/MKK2-MPK4 cascade negatively regulates NB-LRR protein SUMM2-mediated immunity ► The bacterial pathogenic effector HopAI1 targets MPK4 kinase activity ► Inactivation of MPK4 by HopAI1 activates SUMM2-mediated immune responses
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ISSN:1931-3128
1934-6069
1934-6069
DOI:10.1016/j.chom.2012.01.015