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Transcriptional Basis of Drought-Induced Susceptibility to the Rice Blast Fungus Magnaporthe oryzae
Plants are often facing several stresses simultaneously. Understanding how they react and the way pathogens adapt to such combinational stresses is poorly documented. Here, we developed an experimental system mimicking field intermittent drought on rice followed by inoculation by the pathogenic fung...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5081564/ https://www.ncbi.nlm.nih.gov/pubmed/27833621 http://dx.doi.org/10.3389/fpls.2016.01558 |
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author | Bidzinski, Przemyslaw Ballini, Elsa Ducasse, Aurélie Michel, Corinne Zuluaga, Paola Genga, Annamaria Chiozzotto, Remo Morel, Jean-Benoit |
author_facet | Bidzinski, Przemyslaw Ballini, Elsa Ducasse, Aurélie Michel, Corinne Zuluaga, Paola Genga, Annamaria Chiozzotto, Remo Morel, Jean-Benoit |
author_sort | Bidzinski, Przemyslaw |
collection | PubMed |
description | Plants are often facing several stresses simultaneously. Understanding how they react and the way pathogens adapt to such combinational stresses is poorly documented. Here, we developed an experimental system mimicking field intermittent drought on rice followed by inoculation by the pathogenic fungus Magnaporthe oryzae. This experimental system triggers an enhancement of susceptibility that could be correlated with the dampening of several aspects of plant immunity, namely the oxidative burst and the transcription of several pathogenesis-related genes. Quite strikingly, the analysis of fungal transcription by RNASeq analysis under drought reveals that the fungus is greatly modifying its virulence program: genes coding for small secreted proteins were massively repressed in droughted plants compared to unstressed ones whereas genes coding for enzymes involved in degradation of cell-wall were induced. We also show that drought can lead to the partial breakdown of several major resistance genes by affecting R plant gene and/or pathogen effector expression. We propose a model where a yet unknown plant signal can trigger a change in the virulence program of the pathogen to adapt to a plant host that was affected by drought prior to infection. |
format | Online Article Text |
id | pubmed-5081564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50815642016-11-10 Transcriptional Basis of Drought-Induced Susceptibility to the Rice Blast Fungus Magnaporthe oryzae Bidzinski, Przemyslaw Ballini, Elsa Ducasse, Aurélie Michel, Corinne Zuluaga, Paola Genga, Annamaria Chiozzotto, Remo Morel, Jean-Benoit Front Plant Sci Plant Science Plants are often facing several stresses simultaneously. Understanding how they react and the way pathogens adapt to such combinational stresses is poorly documented. Here, we developed an experimental system mimicking field intermittent drought on rice followed by inoculation by the pathogenic fungus Magnaporthe oryzae. This experimental system triggers an enhancement of susceptibility that could be correlated with the dampening of several aspects of plant immunity, namely the oxidative burst and the transcription of several pathogenesis-related genes. Quite strikingly, the analysis of fungal transcription by RNASeq analysis under drought reveals that the fungus is greatly modifying its virulence program: genes coding for small secreted proteins were massively repressed in droughted plants compared to unstressed ones whereas genes coding for enzymes involved in degradation of cell-wall were induced. We also show that drought can lead to the partial breakdown of several major resistance genes by affecting R plant gene and/or pathogen effector expression. We propose a model where a yet unknown plant signal can trigger a change in the virulence program of the pathogen to adapt to a plant host that was affected by drought prior to infection. Frontiers Media S.A. 2016-10-27 /pmc/articles/PMC5081564/ /pubmed/27833621 http://dx.doi.org/10.3389/fpls.2016.01558 Text en Copyright © 2016 Bidzinski, Ballini, Ducasse, Michel, Zuluaga, Genga, Chiozzotto and Morel. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Bidzinski, Przemyslaw Ballini, Elsa Ducasse, Aurélie Michel, Corinne Zuluaga, Paola Genga, Annamaria Chiozzotto, Remo Morel, Jean-Benoit Transcriptional Basis of Drought-Induced Susceptibility to the Rice Blast Fungus Magnaporthe oryzae |
title | Transcriptional Basis of Drought-Induced Susceptibility to the Rice Blast Fungus Magnaporthe oryzae |
title_full | Transcriptional Basis of Drought-Induced Susceptibility to the Rice Blast Fungus Magnaporthe oryzae |
title_fullStr | Transcriptional Basis of Drought-Induced Susceptibility to the Rice Blast Fungus Magnaporthe oryzae |
title_full_unstemmed | Transcriptional Basis of Drought-Induced Susceptibility to the Rice Blast Fungus Magnaporthe oryzae |
title_short | Transcriptional Basis of Drought-Induced Susceptibility to the Rice Blast Fungus Magnaporthe oryzae |
title_sort | transcriptional basis of drought-induced susceptibility to the rice blast fungus magnaporthe oryzae |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5081564/ https://www.ncbi.nlm.nih.gov/pubmed/27833621 http://dx.doi.org/10.3389/fpls.2016.01558 |
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