Cargando…

The Pepper Mitogen-Activated Protein Kinase CaMAPK7 Acts as a Positive Regulator in Response to Ralstonia solanacearum Infection

Mitogen-activated protein kinase (MAPK) pathways play a vital role in multiple plant processes, including growth, development, and stress signaling, but their involvement in response to Ralstonia solanacearum is poorly understood, particularly in pepper plants. Herein, CaMAPK7 was identified from th...

Descripción completa

Detalles Bibliográficos
Autores principales: Shi, Lanping, Zhang, Kan, Xie, Linjing, Yang, Mingxing, Xie, Baixue, He, Shuilin, Liu, Zhiqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290481/
https://www.ncbi.nlm.nih.gov/pubmed/34295316
http://dx.doi.org/10.3389/fmicb.2021.664926
_version_ 1783724502303113216
author Shi, Lanping
Zhang, Kan
Xie, Linjing
Yang, Mingxing
Xie, Baixue
He, Shuilin
Liu, Zhiqin
author_facet Shi, Lanping
Zhang, Kan
Xie, Linjing
Yang, Mingxing
Xie, Baixue
He, Shuilin
Liu, Zhiqin
author_sort Shi, Lanping
collection PubMed
description Mitogen-activated protein kinase (MAPK) pathways play a vital role in multiple plant processes, including growth, development, and stress signaling, but their involvement in response to Ralstonia solanacearum is poorly understood, particularly in pepper plants. Herein, CaMAPK7 was identified from the pepper genome and functionally analyzed. The accumulations of CaMAPK7 transcripts and promoter activities were both significantly induced in response to R. solanacearum strain FJC100301 infection, and exogenously applied phytohormones, including methyl jasmonate (MeJA), brassinolide (BR), salicylic acid (SA), and ethephon (ETN), were decreased by abscisic acid (ABA) treatment. Virus-induced gene silencing (VIGS) of CaMAPK7 significantly enhanced the susceptibility of pepper plants to infection by R. solanacearum and downregulated the defense-related marker genes, including CaDEF1, CaPO2, CaSAR82A, and CaWRKY40. In contrast, the ectopic overexpression of CaMAPK7 in transgenic tobacco enhanced resistance to R. solanacearum and upregulated the defense-associated marker genes, including NtHSR201, NtHSR203, NtPR4, PR1a/c, NtPR1b, NtCAT1, and NtACC. Furthermore, transient overexpression of CaMAPK7 in pepper leaves triggered intensive hypersensitive response (HR)-like cell death, H(2)O(2) accumulation, and enriched CaWRKY40 at the promoters of its target genes and drove their transcript accumulations, including CaDEF1, CaPO2, and CaSAR82A. Taken together, these data indicate that R. solanacearum infection induced the expression of CaMAPK7, which indirectly modifies the binding of CaWRKY40 to its downstream targets, including CaDEF1, CaPO2, and CaSAR82A, ultimately leading to the activation of pepper immunity against R. solanacearum. The protein that responds to CaMAPK7 in pepper plants should be isolated in the future to build a signaling bridge between CaMAPK7 and CaWRKY40.
format Online
Article
Text
id pubmed-8290481
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-82904812021-07-21 The Pepper Mitogen-Activated Protein Kinase CaMAPK7 Acts as a Positive Regulator in Response to Ralstonia solanacearum Infection Shi, Lanping Zhang, Kan Xie, Linjing Yang, Mingxing Xie, Baixue He, Shuilin Liu, Zhiqin Front Microbiol Microbiology Mitogen-activated protein kinase (MAPK) pathways play a vital role in multiple plant processes, including growth, development, and stress signaling, but their involvement in response to Ralstonia solanacearum is poorly understood, particularly in pepper plants. Herein, CaMAPK7 was identified from the pepper genome and functionally analyzed. The accumulations of CaMAPK7 transcripts and promoter activities were both significantly induced in response to R. solanacearum strain FJC100301 infection, and exogenously applied phytohormones, including methyl jasmonate (MeJA), brassinolide (BR), salicylic acid (SA), and ethephon (ETN), were decreased by abscisic acid (ABA) treatment. Virus-induced gene silencing (VIGS) of CaMAPK7 significantly enhanced the susceptibility of pepper plants to infection by R. solanacearum and downregulated the defense-related marker genes, including CaDEF1, CaPO2, CaSAR82A, and CaWRKY40. In contrast, the ectopic overexpression of CaMAPK7 in transgenic tobacco enhanced resistance to R. solanacearum and upregulated the defense-associated marker genes, including NtHSR201, NtHSR203, NtPR4, PR1a/c, NtPR1b, NtCAT1, and NtACC. Furthermore, transient overexpression of CaMAPK7 in pepper leaves triggered intensive hypersensitive response (HR)-like cell death, H(2)O(2) accumulation, and enriched CaWRKY40 at the promoters of its target genes and drove their transcript accumulations, including CaDEF1, CaPO2, and CaSAR82A. Taken together, these data indicate that R. solanacearum infection induced the expression of CaMAPK7, which indirectly modifies the binding of CaWRKY40 to its downstream targets, including CaDEF1, CaPO2, and CaSAR82A, ultimately leading to the activation of pepper immunity against R. solanacearum. The protein that responds to CaMAPK7 in pepper plants should be isolated in the future to build a signaling bridge between CaMAPK7 and CaWRKY40. Frontiers Media S.A. 2021-07-06 /pmc/articles/PMC8290481/ /pubmed/34295316 http://dx.doi.org/10.3389/fmicb.2021.664926 Text en Copyright © 2021 Shi, Zhang, Xie, Yang, Xie, He and Liu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Shi, Lanping
Zhang, Kan
Xie, Linjing
Yang, Mingxing
Xie, Baixue
He, Shuilin
Liu, Zhiqin
The Pepper Mitogen-Activated Protein Kinase CaMAPK7 Acts as a Positive Regulator in Response to Ralstonia solanacearum Infection
title The Pepper Mitogen-Activated Protein Kinase CaMAPK7 Acts as a Positive Regulator in Response to Ralstonia solanacearum Infection
title_full The Pepper Mitogen-Activated Protein Kinase CaMAPK7 Acts as a Positive Regulator in Response to Ralstonia solanacearum Infection
title_fullStr The Pepper Mitogen-Activated Protein Kinase CaMAPK7 Acts as a Positive Regulator in Response to Ralstonia solanacearum Infection
title_full_unstemmed The Pepper Mitogen-Activated Protein Kinase CaMAPK7 Acts as a Positive Regulator in Response to Ralstonia solanacearum Infection
title_short The Pepper Mitogen-Activated Protein Kinase CaMAPK7 Acts as a Positive Regulator in Response to Ralstonia solanacearum Infection
title_sort pepper mitogen-activated protein kinase camapk7 acts as a positive regulator in response to ralstonia solanacearum infection
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290481/
https://www.ncbi.nlm.nih.gov/pubmed/34295316
http://dx.doi.org/10.3389/fmicb.2021.664926
work_keys_str_mv AT shilanping thepeppermitogenactivatedproteinkinasecamapk7actsasapositiveregulatorinresponsetoralstoniasolanacearuminfection
AT zhangkan thepeppermitogenactivatedproteinkinasecamapk7actsasapositiveregulatorinresponsetoralstoniasolanacearuminfection
AT xielinjing thepeppermitogenactivatedproteinkinasecamapk7actsasapositiveregulatorinresponsetoralstoniasolanacearuminfection
AT yangmingxing thepeppermitogenactivatedproteinkinasecamapk7actsasapositiveregulatorinresponsetoralstoniasolanacearuminfection
AT xiebaixue thepeppermitogenactivatedproteinkinasecamapk7actsasapositiveregulatorinresponsetoralstoniasolanacearuminfection
AT heshuilin thepeppermitogenactivatedproteinkinasecamapk7actsasapositiveregulatorinresponsetoralstoniasolanacearuminfection
AT liuzhiqin thepeppermitogenactivatedproteinkinasecamapk7actsasapositiveregulatorinresponsetoralstoniasolanacearuminfection
AT shilanping peppermitogenactivatedproteinkinasecamapk7actsasapositiveregulatorinresponsetoralstoniasolanacearuminfection
AT zhangkan peppermitogenactivatedproteinkinasecamapk7actsasapositiveregulatorinresponsetoralstoniasolanacearuminfection
AT xielinjing peppermitogenactivatedproteinkinasecamapk7actsasapositiveregulatorinresponsetoralstoniasolanacearuminfection
AT yangmingxing peppermitogenactivatedproteinkinasecamapk7actsasapositiveregulatorinresponsetoralstoniasolanacearuminfection
AT xiebaixue peppermitogenactivatedproteinkinasecamapk7actsasapositiveregulatorinresponsetoralstoniasolanacearuminfection
AT heshuilin peppermitogenactivatedproteinkinasecamapk7actsasapositiveregulatorinresponsetoralstoniasolanacearuminfection
AT liuzhiqin peppermitogenactivatedproteinkinasecamapk7actsasapositiveregulatorinresponsetoralstoniasolanacearuminfection