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Multi-Omics Revealed Molecular Mechanisms Underlying Guard Cell Systemic Acquired Resistance
Systemic Acquired Resistance (SAR) improves immunity of plant systemic tissue after local exposure to a pathogen. Guard cells that form stomatal pores on leaf surfaces recognize bacterial pathogens via pattern recognition receptors, such as Flagellin Sensitive 2 (FLS2). However, how SAR affects stom...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7795379/ https://www.ncbi.nlm.nih.gov/pubmed/33375472 http://dx.doi.org/10.3390/ijms22010191 |
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author | David, Lisa Kang, Jianing Dufresne, Daniel Zhu, Dan Chen, Sixue |
author_facet | David, Lisa Kang, Jianing Dufresne, Daniel Zhu, Dan Chen, Sixue |
author_sort | David, Lisa |
collection | PubMed |
description | Systemic Acquired Resistance (SAR) improves immunity of plant systemic tissue after local exposure to a pathogen. Guard cells that form stomatal pores on leaf surfaces recognize bacterial pathogens via pattern recognition receptors, such as Flagellin Sensitive 2 (FLS2). However, how SAR affects stomatal immunity is not known. In this study, we aim to reveal molecular mechanisms underlying the guard cell response to SAR using multi-omics of proteins, metabolites and lipids. Arabidopsis plants previously exposed to pathogenic bacteria Pseudomonas syringae pv. tomato DC3000 (Pst) exhibit an altered stomatal response compared to control plants when they are later exposed to the bacteria. Reduced stomatal apertures of SAR primed plants lead to decreased number of bacteria in leaves. Multi-omics has revealed molecular components of SAR response specific to guard cells functions, including potential roles of reactive oxygen species (ROS) and fatty acid signaling. Our results show an increase in palmitic acid and its derivative in the primed guard cells. Palmitic acid may play a role as an activator of FLS2, which initiates stomatal immune response. Improved understanding of how SAR signals affect stomatal immunity can aid biotechnology and marker-based breeding of crops for enhanced disease resistance. |
format | Online Article Text |
id | pubmed-7795379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77953792021-01-10 Multi-Omics Revealed Molecular Mechanisms Underlying Guard Cell Systemic Acquired Resistance David, Lisa Kang, Jianing Dufresne, Daniel Zhu, Dan Chen, Sixue Int J Mol Sci Article Systemic Acquired Resistance (SAR) improves immunity of plant systemic tissue after local exposure to a pathogen. Guard cells that form stomatal pores on leaf surfaces recognize bacterial pathogens via pattern recognition receptors, such as Flagellin Sensitive 2 (FLS2). However, how SAR affects stomatal immunity is not known. In this study, we aim to reveal molecular mechanisms underlying the guard cell response to SAR using multi-omics of proteins, metabolites and lipids. Arabidopsis plants previously exposed to pathogenic bacteria Pseudomonas syringae pv. tomato DC3000 (Pst) exhibit an altered stomatal response compared to control plants when they are later exposed to the bacteria. Reduced stomatal apertures of SAR primed plants lead to decreased number of bacteria in leaves. Multi-omics has revealed molecular components of SAR response specific to guard cells functions, including potential roles of reactive oxygen species (ROS) and fatty acid signaling. Our results show an increase in palmitic acid and its derivative in the primed guard cells. Palmitic acid may play a role as an activator of FLS2, which initiates stomatal immune response. Improved understanding of how SAR signals affect stomatal immunity can aid biotechnology and marker-based breeding of crops for enhanced disease resistance. MDPI 2020-12-27 /pmc/articles/PMC7795379/ /pubmed/33375472 http://dx.doi.org/10.3390/ijms22010191 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article David, Lisa Kang, Jianing Dufresne, Daniel Zhu, Dan Chen, Sixue Multi-Omics Revealed Molecular Mechanisms Underlying Guard Cell Systemic Acquired Resistance |
title | Multi-Omics Revealed Molecular Mechanisms Underlying Guard Cell Systemic Acquired Resistance |
title_full | Multi-Omics Revealed Molecular Mechanisms Underlying Guard Cell Systemic Acquired Resistance |
title_fullStr | Multi-Omics Revealed Molecular Mechanisms Underlying Guard Cell Systemic Acquired Resistance |
title_full_unstemmed | Multi-Omics Revealed Molecular Mechanisms Underlying Guard Cell Systemic Acquired Resistance |
title_short | Multi-Omics Revealed Molecular Mechanisms Underlying Guard Cell Systemic Acquired Resistance |
title_sort | multi-omics revealed molecular mechanisms underlying guard cell systemic acquired resistance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7795379/ https://www.ncbi.nlm.nih.gov/pubmed/33375472 http://dx.doi.org/10.3390/ijms22010191 |
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