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Root defense analysis against Fusarium oxysporum reveals new regulators to confer resistance
Fusarium oxysporum is a root-infecting fungal pathogen that causes wilt disease on a broad range of plant species, including Arabidopsis thaliana. Investigation of the defense response against this pathogen had primarily been conducted using leaf tissue and little was known about the root defense re...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4083284/ https://www.ncbi.nlm.nih.gov/pubmed/24998294 http://dx.doi.org/10.1038/srep05584 |
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author | Chen, Yi Chung Wong, Chin Lin Muzzi, Frederico Vlaardingerbroek, Ido Kidd, Brendan N. Schenk, Peer M. |
author_facet | Chen, Yi Chung Wong, Chin Lin Muzzi, Frederico Vlaardingerbroek, Ido Kidd, Brendan N. Schenk, Peer M. |
author_sort | Chen, Yi Chung |
collection | PubMed |
description | Fusarium oxysporum is a root-infecting fungal pathogen that causes wilt disease on a broad range of plant species, including Arabidopsis thaliana. Investigation of the defense response against this pathogen had primarily been conducted using leaf tissue and little was known about the root defense response. In this study, we profiled the expression of root genes after infection with F. oxysporum by microarray analysis. In contrast to the leaf response, root tissue did not show a strong induction of defense-associated gene expression and instead showed a greater proportion of repressed genes. Screening insertion mutants from differentially expressed genes in the microarray uncovered a role for the transcription factor ETHYLENE RESPONSE FACTOR72 (ERF72) in susceptibility to F. oxysporum. Due to the role of ERF72 in suppressing programmed cell death and detoxifying reactive oxygen species (ROS), we examined the pub22/pub23/pub24 U-box type E3 ubiquitin ligase triple mutant which is known to possess enhanced ROS production in response to pathogen challenge. We found that the pub22/23/24 mutant is more resistant to F. oxysporum infection, suggesting that a heightened innate immune response provides protection against F. oxysporum. We conclude that root-mediated defenses against soil-borne pathogens can be provided at multiple levels. |
format | Online Article Text |
id | pubmed-4083284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-40832842014-07-08 Root defense analysis against Fusarium oxysporum reveals new regulators to confer resistance Chen, Yi Chung Wong, Chin Lin Muzzi, Frederico Vlaardingerbroek, Ido Kidd, Brendan N. Schenk, Peer M. Sci Rep Article Fusarium oxysporum is a root-infecting fungal pathogen that causes wilt disease on a broad range of plant species, including Arabidopsis thaliana. Investigation of the defense response against this pathogen had primarily been conducted using leaf tissue and little was known about the root defense response. In this study, we profiled the expression of root genes after infection with F. oxysporum by microarray analysis. In contrast to the leaf response, root tissue did not show a strong induction of defense-associated gene expression and instead showed a greater proportion of repressed genes. Screening insertion mutants from differentially expressed genes in the microarray uncovered a role for the transcription factor ETHYLENE RESPONSE FACTOR72 (ERF72) in susceptibility to F. oxysporum. Due to the role of ERF72 in suppressing programmed cell death and detoxifying reactive oxygen species (ROS), we examined the pub22/pub23/pub24 U-box type E3 ubiquitin ligase triple mutant which is known to possess enhanced ROS production in response to pathogen challenge. We found that the pub22/23/24 mutant is more resistant to F. oxysporum infection, suggesting that a heightened innate immune response provides protection against F. oxysporum. We conclude that root-mediated defenses against soil-borne pathogens can be provided at multiple levels. Nature Publishing Group 2014-07-07 /pmc/articles/PMC4083284/ /pubmed/24998294 http://dx.doi.org/10.1038/srep05584 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Chen, Yi Chung Wong, Chin Lin Muzzi, Frederico Vlaardingerbroek, Ido Kidd, Brendan N. Schenk, Peer M. Root defense analysis against Fusarium oxysporum reveals new regulators to confer resistance |
title | Root defense analysis against Fusarium oxysporum reveals new regulators to confer resistance |
title_full | Root defense analysis against Fusarium oxysporum reveals new regulators to confer resistance |
title_fullStr | Root defense analysis against Fusarium oxysporum reveals new regulators to confer resistance |
title_full_unstemmed | Root defense analysis against Fusarium oxysporum reveals new regulators to confer resistance |
title_short | Root defense analysis against Fusarium oxysporum reveals new regulators to confer resistance |
title_sort | root defense analysis against fusarium oxysporum reveals new regulators to confer resistance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4083284/ https://www.ncbi.nlm.nih.gov/pubmed/24998294 http://dx.doi.org/10.1038/srep05584 |
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