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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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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. |
format | Online Article Text |
id | pubmed-9911384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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