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The simultaneous perception of self- and non-self-danger signals potentiates plant innate immunity responses
The simultaneous perception of endogenous and exogenous danger signals potentiates PAMP-triggered immunity in tomato and other downstream defence responses depending on the origin of the signal. Abstract Plant cells perceive a pathogen invasion by recognising endogenous or exogenous extracellular si...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9192368/ https://www.ncbi.nlm.nih.gov/pubmed/35697869 http://dx.doi.org/10.1007/s00425-022-03918-y |
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author | Pastor, Victoria Cervero, Raquel Gamir, Jordi |
author_facet | Pastor, Victoria Cervero, Raquel Gamir, Jordi |
author_sort | Pastor, Victoria |
collection | PubMed |
description | The simultaneous perception of endogenous and exogenous danger signals potentiates PAMP-triggered immunity in tomato and other downstream defence responses depending on the origin of the signal. Abstract Plant cells perceive a pathogen invasion by recognising endogenous or exogenous extracellular signals such as Damage-Associated Molecular Patterns (DAMPs) or Pathogen-Associated Molecular Patterns (PAMPs). In particular, DAMPs are intracellular molecules or cell wall fragments passive or actively released to the apoplast, whose extracellular recognition by intact cells triggers specific immune signalling, the so-called DAMP-triggered immunity. The extracellular recognition of DAMPs and PAMPs leads to a very similar intracellular signalling, and this similarity has generated a biological need to know why plants perceive molecules with such different origins and with overlapped innate immunity responses. Here, we report that the simultaneous perception of DAMPs and a PAMP strengthens early and late plant defence responses. To this aim, we studied classical PTI responses such as the generation of ROS and MAPK phosphorylation, but we also monitored the biosynthesis of phytocytokines and performed a non-targeted metabolomic analysis. We demonstrate that co-application of the bacterial peptide flagellin with the DAMPs cyclic AMP or cellobiose amplifies PAMP-triggered immunity responses. Both co-applications enhanced the synthesis of phytocytokines, but only simultaneous treatments with cAMP strengthened the flagellin-dependent metabolomic responses. In addition, cAMP and cellobiose treatments induced resistance against the hemibiotrophic bacteria Pseudomonas syringae pv. tomato DC3000. Overall, these results indicate that the complex mixture of DAMPs and PAMPs carries specific information that potentiates plant defence responses. However, downstream responses seem more specific depending on the composition of the mixture. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00425-022-03918-y. |
format | Online Article Text |
id | pubmed-9192368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-91923682022-06-15 The simultaneous perception of self- and non-self-danger signals potentiates plant innate immunity responses Pastor, Victoria Cervero, Raquel Gamir, Jordi Planta Original Article The simultaneous perception of endogenous and exogenous danger signals potentiates PAMP-triggered immunity in tomato and other downstream defence responses depending on the origin of the signal. Abstract Plant cells perceive a pathogen invasion by recognising endogenous or exogenous extracellular signals such as Damage-Associated Molecular Patterns (DAMPs) or Pathogen-Associated Molecular Patterns (PAMPs). In particular, DAMPs are intracellular molecules or cell wall fragments passive or actively released to the apoplast, whose extracellular recognition by intact cells triggers specific immune signalling, the so-called DAMP-triggered immunity. The extracellular recognition of DAMPs and PAMPs leads to a very similar intracellular signalling, and this similarity has generated a biological need to know why plants perceive molecules with such different origins and with overlapped innate immunity responses. Here, we report that the simultaneous perception of DAMPs and a PAMP strengthens early and late plant defence responses. To this aim, we studied classical PTI responses such as the generation of ROS and MAPK phosphorylation, but we also monitored the biosynthesis of phytocytokines and performed a non-targeted metabolomic analysis. We demonstrate that co-application of the bacterial peptide flagellin with the DAMPs cyclic AMP or cellobiose amplifies PAMP-triggered immunity responses. Both co-applications enhanced the synthesis of phytocytokines, but only simultaneous treatments with cAMP strengthened the flagellin-dependent metabolomic responses. In addition, cAMP and cellobiose treatments induced resistance against the hemibiotrophic bacteria Pseudomonas syringae pv. tomato DC3000. Overall, these results indicate that the complex mixture of DAMPs and PAMPs carries specific information that potentiates plant defence responses. However, downstream responses seem more specific depending on the composition of the mixture. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00425-022-03918-y. Springer Berlin Heidelberg 2022-06-13 2022 /pmc/articles/PMC9192368/ /pubmed/35697869 http://dx.doi.org/10.1007/s00425-022-03918-y 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/) . |
spellingShingle | Original Article Pastor, Victoria Cervero, Raquel Gamir, Jordi The simultaneous perception of self- and non-self-danger signals potentiates plant innate immunity responses |
title | The simultaneous perception of self- and non-self-danger signals potentiates plant innate immunity responses |
title_full | The simultaneous perception of self- and non-self-danger signals potentiates plant innate immunity responses |
title_fullStr | The simultaneous perception of self- and non-self-danger signals potentiates plant innate immunity responses |
title_full_unstemmed | The simultaneous perception of self- and non-self-danger signals potentiates plant innate immunity responses |
title_short | The simultaneous perception of self- and non-self-danger signals potentiates plant innate immunity responses |
title_sort | simultaneous perception of self- and non-self-danger signals potentiates plant innate immunity responses |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9192368/ https://www.ncbi.nlm.nih.gov/pubmed/35697869 http://dx.doi.org/10.1007/s00425-022-03918-y |
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