Cargando…
Pathogenesis-related protein 1 suppresses oomycete pathogen by targeting against AMPK kinase complex
INTRODUCTION: 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 v...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811325/ https://www.ncbi.nlm.nih.gov/pubmed/36585103 http://dx.doi.org/10.1016/j.jare.2022.02.002 |
_version_ | 1784863509566193664 |
---|---|
author | 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 Ren, Maozhi |
author_facet | 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 Ren, Maozhi |
author_sort | Luo, Xiumei |
collection | PubMed |
description | INTRODUCTION: 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. OBJECTIVES: The present study was aimed to investigate the anti-oomycete activity of secretory PR1 proteins and elaborate their underlying mechanisms. METHODS: 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. RESULTS: 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. CONCLUSION: 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. |
format | Online Article Text |
id | pubmed-9811325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-98113252023-01-05 Pathogenesis-related protein 1 suppresses oomycete pathogen by targeting against AMPK kinase complex 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 Ren, Maozhi J Adv Res Original Article INTRODUCTION: 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. OBJECTIVES: The present study was aimed to investigate the anti-oomycete activity of secretory PR1 proteins and elaborate their underlying mechanisms. METHODS: 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. RESULTS: 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. CONCLUSION: 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. Elsevier 2022-02-09 /pmc/articles/PMC9811325/ /pubmed/36585103 http://dx.doi.org/10.1016/j.jare.2022.02.002 Text en © 2022 The Authors. Published by Elsevier B.V. on behalf of Cairo University. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article 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 Ren, Maozhi Pathogenesis-related protein 1 suppresses oomycete pathogen by targeting against AMPK kinase complex |
title | Pathogenesis-related protein 1 suppresses oomycete pathogen by targeting against AMPK kinase complex |
title_full | Pathogenesis-related protein 1 suppresses oomycete pathogen by targeting against AMPK kinase complex |
title_fullStr | Pathogenesis-related protein 1 suppresses oomycete pathogen by targeting against AMPK kinase complex |
title_full_unstemmed | Pathogenesis-related protein 1 suppresses oomycete pathogen by targeting against AMPK kinase complex |
title_short | Pathogenesis-related protein 1 suppresses oomycete pathogen by targeting against AMPK kinase complex |
title_sort | pathogenesis-related protein 1 suppresses oomycete pathogen by targeting against ampk kinase complex |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811325/ https://www.ncbi.nlm.nih.gov/pubmed/36585103 http://dx.doi.org/10.1016/j.jare.2022.02.002 |
work_keys_str_mv | AT luoxiumei pathogenesisrelatedprotein1suppressesoomycetepathogenbytargetingagainstampkkinasecomplex AT tiantingting pathogenesisrelatedprotein1suppressesoomycetepathogenbytargetingagainstampkkinasecomplex AT fengli pathogenesisrelatedprotein1suppressesoomycetepathogenbytargetingagainstampkkinasecomplex AT yangxingyong pathogenesisrelatedprotein1suppressesoomycetepathogenbytargetingagainstampkkinasecomplex AT lilinxuan pathogenesisrelatedprotein1suppressesoomycetepathogenbytargetingagainstampkkinasecomplex AT tanxue pathogenesisrelatedprotein1suppressesoomycetepathogenbytargetingagainstampkkinasecomplex AT wuwenxian pathogenesisrelatedprotein1suppressesoomycetepathogenbytargetingagainstampkkinasecomplex AT lizhengguo pathogenesisrelatedprotein1suppressesoomycetepathogenbytargetingagainstampkkinasecomplex AT treveshaim pathogenesisrelatedprotein1suppressesoomycetepathogenbytargetingagainstampkkinasecomplex AT serneelsfrancois pathogenesisrelatedprotein1suppressesoomycetepathogenbytargetingagainstampkkinasecomplex AT ngison pathogenesisrelatedprotein1suppressesoomycetepathogenbytargetingagainstampkkinasecomplex AT tanakakan pathogenesisrelatedprotein1suppressesoomycetepathogenbytargetingagainstampkkinasecomplex AT renmaozhi pathogenesisrelatedprotein1suppressesoomycetepathogenbytargetingagainstampkkinasecomplex |