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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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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. |
format | Online Article Text |
id | pubmed-9795618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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