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Systemic acquired resistance networks amplify airborne defense cues
Salicylic acid (SA)-mediated innate immune responses are activated in plants perceiving volatile monoterpenes. Here, we show that monoterpene-associated responses are propagated in feed-forward loops involving the systemic acquired resistance (SAR) signaling components pipecolic acid, glycerol-3-pho...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707303/ https://www.ncbi.nlm.nih.gov/pubmed/31444353 http://dx.doi.org/10.1038/s41467-019-11798-2 |
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author | Wenig, Marion Ghirardo, Andrea Sales, Jennifer H. Pabst, Elisabeth S. Breitenbach, Heiko H. Antritter, Felix Weber, Baris Lange, Birgit Lenk, Miriam Cameron, Robin K. Schnitzler, Joerg-Peter Vlot, A. Corina |
author_facet | Wenig, Marion Ghirardo, Andrea Sales, Jennifer H. Pabst, Elisabeth S. Breitenbach, Heiko H. Antritter, Felix Weber, Baris Lange, Birgit Lenk, Miriam Cameron, Robin K. Schnitzler, Joerg-Peter Vlot, A. Corina |
author_sort | Wenig, Marion |
collection | PubMed |
description | Salicylic acid (SA)-mediated innate immune responses are activated in plants perceiving volatile monoterpenes. Here, we show that monoterpene-associated responses are propagated in feed-forward loops involving the systemic acquired resistance (SAR) signaling components pipecolic acid, glycerol-3-phosphate, and LEGUME LECTIN-LIKE PROTEIN1 (LLP1). In this cascade, LLP1 forms a key regulatory unit in both within-plant and between-plant propagation of immunity. The data integrate molecular components of SAR into systemic signaling networks that are separate from conventional, SA-associated innate immune mechanisms. These networks are central to plant-to-plant propagation of immunity, potentially raising SAR to the population level. In this process, monoterpenes act as microbe-inducible plant volatiles, which as part of plant-derived volatile blends have the potential to promote the generation of a wave of innate immune signaling within canopies or plant stands. Hence, plant-to-plant propagation of SAR holds significant potential to fortify future durable crop protection strategies following a single volatile trigger. |
format | Online Article Text |
id | pubmed-6707303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67073032019-08-26 Systemic acquired resistance networks amplify airborne defense cues Wenig, Marion Ghirardo, Andrea Sales, Jennifer H. Pabst, Elisabeth S. Breitenbach, Heiko H. Antritter, Felix Weber, Baris Lange, Birgit Lenk, Miriam Cameron, Robin K. Schnitzler, Joerg-Peter Vlot, A. Corina Nat Commun Article Salicylic acid (SA)-mediated innate immune responses are activated in plants perceiving volatile monoterpenes. Here, we show that monoterpene-associated responses are propagated in feed-forward loops involving the systemic acquired resistance (SAR) signaling components pipecolic acid, glycerol-3-phosphate, and LEGUME LECTIN-LIKE PROTEIN1 (LLP1). In this cascade, LLP1 forms a key regulatory unit in both within-plant and between-plant propagation of immunity. The data integrate molecular components of SAR into systemic signaling networks that are separate from conventional, SA-associated innate immune mechanisms. These networks are central to plant-to-plant propagation of immunity, potentially raising SAR to the population level. In this process, monoterpenes act as microbe-inducible plant volatiles, which as part of plant-derived volatile blends have the potential to promote the generation of a wave of innate immune signaling within canopies or plant stands. Hence, plant-to-plant propagation of SAR holds significant potential to fortify future durable crop protection strategies following a single volatile trigger. Nature Publishing Group UK 2019-08-23 /pmc/articles/PMC6707303/ /pubmed/31444353 http://dx.doi.org/10.1038/s41467-019-11798-2 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Wenig, Marion Ghirardo, Andrea Sales, Jennifer H. Pabst, Elisabeth S. Breitenbach, Heiko H. Antritter, Felix Weber, Baris Lange, Birgit Lenk, Miriam Cameron, Robin K. Schnitzler, Joerg-Peter Vlot, A. Corina Systemic acquired resistance networks amplify airborne defense cues |
title | Systemic acquired resistance networks amplify airborne defense cues |
title_full | Systemic acquired resistance networks amplify airborne defense cues |
title_fullStr | Systemic acquired resistance networks amplify airborne defense cues |
title_full_unstemmed | Systemic acquired resistance networks amplify airborne defense cues |
title_short | Systemic acquired resistance networks amplify airborne defense cues |
title_sort | systemic acquired resistance networks amplify airborne defense cues |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707303/ https://www.ncbi.nlm.nih.gov/pubmed/31444353 http://dx.doi.org/10.1038/s41467-019-11798-2 |
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