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Pathogen-derived mechanical cues potentiate the spatio-temporal implementation of plant defense

BACKGROUND: The ongoing adaptation of plants to their environment is the basis for their survival. In this adaptation, mechanoperception of gravity and local curvature plays a role of prime importance in finely regulating growth and ensuring a dynamic balance preventing buckling. However, the abioti...

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Autores principales: Léger, Ophélie, Garcia, Frédérick, Khafif, Mehdi, Carrere, Sebastien, Leblanc-Fournier, Nathalie, Duclos, Aroune, Tournat, Vincent, Badel, Eric, Didelon, Marie, Le Ru, Aurélie, Raffaele, Sylvain, Barbacci, Adelin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795618/
https://www.ncbi.nlm.nih.gov/pubmed/36575418
http://dx.doi.org/10.1186/s12915-022-01495-w
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author Léger, Ophélie
Garcia, Frédérick
Khafif, Mehdi
Carrere, Sebastien
Leblanc-Fournier, Nathalie
Duclos, Aroune
Tournat, Vincent
Badel, Eric
Didelon, Marie
Le Ru, Aurélie
Raffaele, Sylvain
Barbacci, Adelin
author_facet Léger, Ophélie
Garcia, Frédérick
Khafif, Mehdi
Carrere, Sebastien
Leblanc-Fournier, Nathalie
Duclos, Aroune
Tournat, Vincent
Badel, Eric
Didelon, Marie
Le Ru, Aurélie
Raffaele, Sylvain
Barbacci, Adelin
author_sort Léger, Ophélie
collection PubMed
description BACKGROUND: The ongoing adaptation of plants to their environment is the basis for their survival. In this adaptation, mechanoperception of gravity and local curvature plays a role of prime importance in finely regulating growth and ensuring a dynamic balance preventing buckling. However, the abiotic environment is not the exclusive cause of mechanical stimuli. Biotic interactions between plants and microorganisms also involve physical forces and potentially mechanoperception. Whether pathogens trigger mechanoperception in plants and the impact of mechanotransduction on the regulation of plant defense remains however elusive. RESULTS: Here, we found that the perception of pathogen-derived mechanical cues by microtubules potentiates the spatio-temporal implementation of plant immunity to fungus. By combining biomechanics modeling and image analysis of the post-invasion stage, we reveal that fungal colonization releases plant cell wall-born tension locally, causing fluctuations of tensile stress in walls of healthy cells distant from the infection site. In healthy cells, the pathogen-derived mechanical cues guide the reorganization of mechanosensing cortical microtubules (CMT). The anisotropic patterning of CMTs is required for the regulation of immunity-related genes in distal cells. The CMT-mediated mechanotransduction of pathogen-derived cues increases Arabidopsis disease resistance by 40% when challenged with the fungus Sclerotinia sclerotiorum. CONCLUSIONS: CMT anisotropic patterning triggered by pathogen-derived mechanical cues activates the implementation of early plant defense in cells distant from the infection site. We propose that the mechano-signaling triggered immunity (MTI) complements the molecular signals involved in pattern and effector-triggered immunity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01495-w.
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spelling pubmed-97956182022-12-29 Pathogen-derived mechanical cues potentiate the spatio-temporal implementation of plant defense Léger, Ophélie Garcia, Frédérick Khafif, Mehdi Carrere, Sebastien Leblanc-Fournier, Nathalie Duclos, Aroune Tournat, Vincent Badel, Eric Didelon, Marie Le Ru, Aurélie Raffaele, Sylvain Barbacci, Adelin BMC Biol Research Article BACKGROUND: The ongoing adaptation of plants to their environment is the basis for their survival. In this adaptation, mechanoperception of gravity and local curvature plays a role of prime importance in finely regulating growth and ensuring a dynamic balance preventing buckling. However, the abiotic environment is not the exclusive cause of mechanical stimuli. Biotic interactions between plants and microorganisms also involve physical forces and potentially mechanoperception. Whether pathogens trigger mechanoperception in plants and the impact of mechanotransduction on the regulation of plant defense remains however elusive. RESULTS: Here, we found that the perception of pathogen-derived mechanical cues by microtubules potentiates the spatio-temporal implementation of plant immunity to fungus. By combining biomechanics modeling and image analysis of the post-invasion stage, we reveal that fungal colonization releases plant cell wall-born tension locally, causing fluctuations of tensile stress in walls of healthy cells distant from the infection site. In healthy cells, the pathogen-derived mechanical cues guide the reorganization of mechanosensing cortical microtubules (CMT). The anisotropic patterning of CMTs is required for the regulation of immunity-related genes in distal cells. The CMT-mediated mechanotransduction of pathogen-derived cues increases Arabidopsis disease resistance by 40% when challenged with the fungus Sclerotinia sclerotiorum. CONCLUSIONS: CMT anisotropic patterning triggered by pathogen-derived mechanical cues activates the implementation of early plant defense in cells distant from the infection site. We propose that the mechano-signaling triggered immunity (MTI) complements the molecular signals involved in pattern and effector-triggered immunity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01495-w. BioMed Central 2022-12-27 /pmc/articles/PMC9795618/ /pubmed/36575418 http://dx.doi.org/10.1186/s12915-022-01495-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Léger, Ophélie
Garcia, Frédérick
Khafif, Mehdi
Carrere, Sebastien
Leblanc-Fournier, Nathalie
Duclos, Aroune
Tournat, Vincent
Badel, Eric
Didelon, Marie
Le Ru, Aurélie
Raffaele, Sylvain
Barbacci, Adelin
Pathogen-derived mechanical cues potentiate the spatio-temporal implementation of plant defense
title Pathogen-derived mechanical cues potentiate the spatio-temporal implementation of plant defense
title_full Pathogen-derived mechanical cues potentiate the spatio-temporal implementation of plant defense
title_fullStr Pathogen-derived mechanical cues potentiate the spatio-temporal implementation of plant defense
title_full_unstemmed Pathogen-derived mechanical cues potentiate the spatio-temporal implementation of plant defense
title_short Pathogen-derived mechanical cues potentiate the spatio-temporal implementation of plant defense
title_sort pathogen-derived mechanical cues potentiate the spatio-temporal implementation of plant defense
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795618/
https://www.ncbi.nlm.nih.gov/pubmed/36575418
http://dx.doi.org/10.1186/s12915-022-01495-w
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