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A sulfur-containing volatile emitted by potato-associated bacteria confers protection against late blight through direct anti-oomycete activity
Plant diseases are a major cause for yield losses and new strategies to control them without harming the environment are urgently needed. Plant-associated bacteria contribute to their host’s health in diverse ways, among which the emission of disease-inhibiting volatile organic compounds (VOCs). We...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937334/ https://www.ncbi.nlm.nih.gov/pubmed/31889050 http://dx.doi.org/10.1038/s41598-019-55218-3 |
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author | Chinchilla, Delphine Bruisson, Sébastien Meyer, Silvan Zühlke, Daniela Hirschfeld, Claudia Joller, Charlotte L’Haridon, Floriane Mène-Saffrané, Laurent Riedel, Katharina Weisskopf, Laure |
author_facet | Chinchilla, Delphine Bruisson, Sébastien Meyer, Silvan Zühlke, Daniela Hirschfeld, Claudia Joller, Charlotte L’Haridon, Floriane Mène-Saffrané, Laurent Riedel, Katharina Weisskopf, Laure |
author_sort | Chinchilla, Delphine |
collection | PubMed |
description | Plant diseases are a major cause for yield losses and new strategies to control them without harming the environment are urgently needed. Plant-associated bacteria contribute to their host’s health in diverse ways, among which the emission of disease-inhibiting volatile organic compounds (VOCs). We have previously reported that VOCs emitted by potato-associated bacteria caused strong in vitro growth inhibition of the late blight causing agent Phytophthora infestans. This work focuses on sulfur-containing VOCs (sVOCs) and demonstrates the high in planta protective potential of S-methyl methane thiosulfonate (MMTS), which fully prevented late blight disease in potato leaves and plantlets without phytotoxic effects, in contrast to other sVOCs. Short exposure times were sufficient to protect plants against infection. We further showed that MMTS’s protective activity was not mediated by the plant immune system but lied in its anti-oomycete activity. Using quantitative proteomics, we determined that different sVOCs caused specific proteome changes in P. infestans, indicating perturbations in sulfur metabolism, protein translation and redox balance. This work brings new perspectives for plant protection against the devastating Irish Famine pathogen, while opening new research avenues on the role of sVOCs in the interaction between plants and their microbiome. |
format | Online Article Text |
id | pubmed-6937334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69373342020-01-06 A sulfur-containing volatile emitted by potato-associated bacteria confers protection against late blight through direct anti-oomycete activity Chinchilla, Delphine Bruisson, Sébastien Meyer, Silvan Zühlke, Daniela Hirschfeld, Claudia Joller, Charlotte L’Haridon, Floriane Mène-Saffrané, Laurent Riedel, Katharina Weisskopf, Laure Sci Rep Article Plant diseases are a major cause for yield losses and new strategies to control them without harming the environment are urgently needed. Plant-associated bacteria contribute to their host’s health in diverse ways, among which the emission of disease-inhibiting volatile organic compounds (VOCs). We have previously reported that VOCs emitted by potato-associated bacteria caused strong in vitro growth inhibition of the late blight causing agent Phytophthora infestans. This work focuses on sulfur-containing VOCs (sVOCs) and demonstrates the high in planta protective potential of S-methyl methane thiosulfonate (MMTS), which fully prevented late blight disease in potato leaves and plantlets without phytotoxic effects, in contrast to other sVOCs. Short exposure times were sufficient to protect plants against infection. We further showed that MMTS’s protective activity was not mediated by the plant immune system but lied in its anti-oomycete activity. Using quantitative proteomics, we determined that different sVOCs caused specific proteome changes in P. infestans, indicating perturbations in sulfur metabolism, protein translation and redox balance. This work brings new perspectives for plant protection against the devastating Irish Famine pathogen, while opening new research avenues on the role of sVOCs in the interaction between plants and their microbiome. Nature Publishing Group UK 2019-12-30 /pmc/articles/PMC6937334/ /pubmed/31889050 http://dx.doi.org/10.1038/s41598-019-55218-3 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 Chinchilla, Delphine Bruisson, Sébastien Meyer, Silvan Zühlke, Daniela Hirschfeld, Claudia Joller, Charlotte L’Haridon, Floriane Mène-Saffrané, Laurent Riedel, Katharina Weisskopf, Laure A sulfur-containing volatile emitted by potato-associated bacteria confers protection against late blight through direct anti-oomycete activity |
title | A sulfur-containing volatile emitted by potato-associated bacteria confers protection against late blight through direct anti-oomycete activity |
title_full | A sulfur-containing volatile emitted by potato-associated bacteria confers protection against late blight through direct anti-oomycete activity |
title_fullStr | A sulfur-containing volatile emitted by potato-associated bacteria confers protection against late blight through direct anti-oomycete activity |
title_full_unstemmed | A sulfur-containing volatile emitted by potato-associated bacteria confers protection against late blight through direct anti-oomycete activity |
title_short | A sulfur-containing volatile emitted by potato-associated bacteria confers protection against late blight through direct anti-oomycete activity |
title_sort | sulfur-containing volatile emitted by potato-associated bacteria confers protection against late blight through direct anti-oomycete activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937334/ https://www.ncbi.nlm.nih.gov/pubmed/31889050 http://dx.doi.org/10.1038/s41598-019-55218-3 |
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