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Plant metabolism of nematode pheromones mediates plant-nematode interactions
Microorganisms and nematodes in the rhizosphere profoundly impact plant health, and small-molecule signaling is presumed to play a central role in plant rhizosphere interactions. However, the nature of the signals and underlying mechanisms are poorly understood. Here we show that the ascaroside ascr...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954178/ https://www.ncbi.nlm.nih.gov/pubmed/31924834 http://dx.doi.org/10.1038/s41467-019-14104-2 |
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author | Manohar, Murli Tenjo-Castano, Francisco Chen, Shiyan Zhang, Ying K. Kumari, Anshu Williamson, Valerie M. Wang, Xiaohong Klessig, Daniel F. Schroeder, Frank C. |
author_facet | Manohar, Murli Tenjo-Castano, Francisco Chen, Shiyan Zhang, Ying K. Kumari, Anshu Williamson, Valerie M. Wang, Xiaohong Klessig, Daniel F. Schroeder, Frank C. |
author_sort | Manohar, Murli |
collection | PubMed |
description | Microorganisms and nematodes in the rhizosphere profoundly impact plant health, and small-molecule signaling is presumed to play a central role in plant rhizosphere interactions. However, the nature of the signals and underlying mechanisms are poorly understood. Here we show that the ascaroside ascr#18, a pheromone secreted by plant-parasitic nematodes, is metabolized by plants to generate chemical signals that repel nematodes and reduce infection. Comparative metabolomics of plant tissues and excretions revealed that ascr#18 is converted into shorter side-chained ascarosides that confer repellency. An Arabidopsis mutant defective in two peroxisomal acyl-CoA oxidases does not metabolize ascr#18 and does not repel nematodes, indicating that plants, like nematodes, employ conserved peroxisomal β-oxidation to edit ascarosides and change their message. Our results suggest that plant-editing of nematode pheromones serves as a defense mechanism that acts in parallel to conventional pattern-triggered immunity, demonstrating that plants may actively manipulate chemical signaling of soil organisms. |
format | Online Article Text |
id | pubmed-6954178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69541782020-01-13 Plant metabolism of nematode pheromones mediates plant-nematode interactions Manohar, Murli Tenjo-Castano, Francisco Chen, Shiyan Zhang, Ying K. Kumari, Anshu Williamson, Valerie M. Wang, Xiaohong Klessig, Daniel F. Schroeder, Frank C. Nat Commun Article Microorganisms and nematodes in the rhizosphere profoundly impact plant health, and small-molecule signaling is presumed to play a central role in plant rhizosphere interactions. However, the nature of the signals and underlying mechanisms are poorly understood. Here we show that the ascaroside ascr#18, a pheromone secreted by plant-parasitic nematodes, is metabolized by plants to generate chemical signals that repel nematodes and reduce infection. Comparative metabolomics of plant tissues and excretions revealed that ascr#18 is converted into shorter side-chained ascarosides that confer repellency. An Arabidopsis mutant defective in two peroxisomal acyl-CoA oxidases does not metabolize ascr#18 and does not repel nematodes, indicating that plants, like nematodes, employ conserved peroxisomal β-oxidation to edit ascarosides and change their message. Our results suggest that plant-editing of nematode pheromones serves as a defense mechanism that acts in parallel to conventional pattern-triggered immunity, demonstrating that plants may actively manipulate chemical signaling of soil organisms. Nature Publishing Group UK 2020-01-10 /pmc/articles/PMC6954178/ /pubmed/31924834 http://dx.doi.org/10.1038/s41467-019-14104-2 Text en © The Author(s) 2020 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 Manohar, Murli Tenjo-Castano, Francisco Chen, Shiyan Zhang, Ying K. Kumari, Anshu Williamson, Valerie M. Wang, Xiaohong Klessig, Daniel F. Schroeder, Frank C. Plant metabolism of nematode pheromones mediates plant-nematode interactions |
title | Plant metabolism of nematode pheromones mediates plant-nematode interactions |
title_full | Plant metabolism of nematode pheromones mediates plant-nematode interactions |
title_fullStr | Plant metabolism of nematode pheromones mediates plant-nematode interactions |
title_full_unstemmed | Plant metabolism of nematode pheromones mediates plant-nematode interactions |
title_short | Plant metabolism of nematode pheromones mediates plant-nematode interactions |
title_sort | plant metabolism of nematode pheromones mediates plant-nematode interactions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954178/ https://www.ncbi.nlm.nih.gov/pubmed/31924834 http://dx.doi.org/10.1038/s41467-019-14104-2 |
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