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Light prevents pathogen-induced aqueous microenvironments via potentiation of salicylic acid signaling

Many plant pathogens induce water-soaked lesions in infected tissues. In the case of Pseudomonas syringae (Pst), water-soaking effectors stimulate abscisic acid (ABA) production and signaling, resulting in stomatal closure. This reduces transpiration, increases water accumulation, and induces an apo...

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Autores principales: Lajeunesse, Gaële, Roussin-Léveillée, Charles, Boutin, Sophie, Fortin, Élodie, Laforest-Lapointe, Isabelle, Moffett, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911384/
https://www.ncbi.nlm.nih.gov/pubmed/36759607
http://dx.doi.org/10.1038/s41467-023-36382-7
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author Lajeunesse, Gaële
Roussin-Léveillée, Charles
Boutin, Sophie
Fortin, Élodie
Laforest-Lapointe, Isabelle
Moffett, Peter
author_facet Lajeunesse, Gaële
Roussin-Léveillée, Charles
Boutin, Sophie
Fortin, Élodie
Laforest-Lapointe, Isabelle
Moffett, Peter
author_sort Lajeunesse, Gaële
collection PubMed
description Many plant pathogens induce water-soaked lesions in infected tissues. In the case of Pseudomonas syringae (Pst), water-soaking effectors stimulate abscisic acid (ABA) production and signaling, resulting in stomatal closure. This reduces transpiration, increases water accumulation, and induces an apoplastic microenvironment favorable for bacterial growth. Stomata are sensitive to environmental conditions, including light. Here, we show that a period of darkness is required for water-soaking, and that a constant light regime abrogates stomatal closure by Pst. We find that constant light induces resistance to Pst, and that this effect requires salicylic acid (SA). Constant light did not alter effector-induced accumulation of ABA, but induced greater SA production, promoting stomatal opening despite the presence of ABA. Furthermore, application of a SA analog was sufficient to prevent pathogen-induced stomatal closure and water-soaking. Our results suggest potential approaches for interfering with a common virulence strategy, as well as providing a physiological mechanism by which SA functions in defense against pathogens.
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spelling pubmed-99113842023-02-11 Light prevents pathogen-induced aqueous microenvironments via potentiation of salicylic acid signaling Lajeunesse, Gaële Roussin-Léveillée, Charles Boutin, Sophie Fortin, Élodie Laforest-Lapointe, Isabelle Moffett, Peter Nat Commun Article Many plant pathogens induce water-soaked lesions in infected tissues. In the case of Pseudomonas syringae (Pst), water-soaking effectors stimulate abscisic acid (ABA) production and signaling, resulting in stomatal closure. This reduces transpiration, increases water accumulation, and induces an apoplastic microenvironment favorable for bacterial growth. Stomata are sensitive to environmental conditions, including light. Here, we show that a period of darkness is required for water-soaking, and that a constant light regime abrogates stomatal closure by Pst. We find that constant light induces resistance to Pst, and that this effect requires salicylic acid (SA). Constant light did not alter effector-induced accumulation of ABA, but induced greater SA production, promoting stomatal opening despite the presence of ABA. Furthermore, application of a SA analog was sufficient to prevent pathogen-induced stomatal closure and water-soaking. Our results suggest potential approaches for interfering with a common virulence strategy, as well as providing a physiological mechanism by which SA functions in defense against pathogens. Nature Publishing Group UK 2023-02-09 /pmc/articles/PMC9911384/ /pubmed/36759607 http://dx.doi.org/10.1038/s41467-023-36382-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lajeunesse, Gaële
Roussin-Léveillée, Charles
Boutin, Sophie
Fortin, Élodie
Laforest-Lapointe, Isabelle
Moffett, Peter
Light prevents pathogen-induced aqueous microenvironments via potentiation of salicylic acid signaling
title Light prevents pathogen-induced aqueous microenvironments via potentiation of salicylic acid signaling
title_full Light prevents pathogen-induced aqueous microenvironments via potentiation of salicylic acid signaling
title_fullStr Light prevents pathogen-induced aqueous microenvironments via potentiation of salicylic acid signaling
title_full_unstemmed Light prevents pathogen-induced aqueous microenvironments via potentiation of salicylic acid signaling
title_short Light prevents pathogen-induced aqueous microenvironments via potentiation of salicylic acid signaling
title_sort light prevents pathogen-induced aqueous microenvironments via potentiation of salicylic acid signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911384/
https://www.ncbi.nlm.nih.gov/pubmed/36759607
http://dx.doi.org/10.1038/s41467-023-36382-7
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