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Contribution of cell wall peroxidase‐ and NADPH oxidase‐derived reactive oxygen species to Alternaria brassicicola‐induced oxidative burst in Arabidopsis
Cell wall peroxidases and plasma membrane‐localized NADPH oxidases are considered to be the main sources of the apoplastic oxidative burst in plants attacked by microbial pathogens. In spite of this established doctrine, approaches attempting a comparative, side‐by‐side analysis of the functions of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637864/ https://www.ncbi.nlm.nih.gov/pubmed/30426643 http://dx.doi.org/10.1111/mpp.12769 |
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author | Kámán‐Tóth, Evelin Dankó, Tamás Gullner, Gábor Bozsó, Zoltán Palkovics, László Pogány, Miklós |
author_facet | Kámán‐Tóth, Evelin Dankó, Tamás Gullner, Gábor Bozsó, Zoltán Palkovics, László Pogány, Miklós |
author_sort | Kámán‐Tóth, Evelin |
collection | PubMed |
description | Cell wall peroxidases and plasma membrane‐localized NADPH oxidases are considered to be the main sources of the apoplastic oxidative burst in plants attacked by microbial pathogens. In spite of this established doctrine, approaches attempting a comparative, side‐by‐side analysis of the functions of extracellular reactive oxygen species (ROS) generated by the two enzymatic sources are scarce. Previously, we have reported the role of Arabidopsis NADPH oxidase RBOHD (respiratory burst oxidase homologue D) in plants challenged with the necrotrophic fungus Alternaria brassicicola. Here, we present results on the activity of apoplastic class III peroxidases PRX33 (At3g49110) and PRX34 (At3g49120) investigated in the same Arabidopsis–Alternaria pathosystem. ROS generated by Arabidopsis peroxidases PRX33 and PRX34 increase the necrotic symptoms and colonization success of A. brassicicola. In addition, the knockdown of PRX33 and PRX34 transcript levels leads to a reduced number of host cells showing an extracellular burst of ROS after inoculation with A. brassicicola. Our results also reveal an age‐dependent transcript distribution of ROS‐producing peroxidase and NADPH oxidase enzymes, and some potential new components of the RBOHD, PRX33 and PRX34 signalling networks. |
format | Online Article Text |
id | pubmed-6637864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66378642019-09-16 Contribution of cell wall peroxidase‐ and NADPH oxidase‐derived reactive oxygen species to Alternaria brassicicola‐induced oxidative burst in Arabidopsis Kámán‐Tóth, Evelin Dankó, Tamás Gullner, Gábor Bozsó, Zoltán Palkovics, László Pogány, Miklós Mol Plant Pathol Original Articles Cell wall peroxidases and plasma membrane‐localized NADPH oxidases are considered to be the main sources of the apoplastic oxidative burst in plants attacked by microbial pathogens. In spite of this established doctrine, approaches attempting a comparative, side‐by‐side analysis of the functions of extracellular reactive oxygen species (ROS) generated by the two enzymatic sources are scarce. Previously, we have reported the role of Arabidopsis NADPH oxidase RBOHD (respiratory burst oxidase homologue D) in plants challenged with the necrotrophic fungus Alternaria brassicicola. Here, we present results on the activity of apoplastic class III peroxidases PRX33 (At3g49110) and PRX34 (At3g49120) investigated in the same Arabidopsis–Alternaria pathosystem. ROS generated by Arabidopsis peroxidases PRX33 and PRX34 increase the necrotic symptoms and colonization success of A. brassicicola. In addition, the knockdown of PRX33 and PRX34 transcript levels leads to a reduced number of host cells showing an extracellular burst of ROS after inoculation with A. brassicicola. Our results also reveal an age‐dependent transcript distribution of ROS‐producing peroxidase and NADPH oxidase enzymes, and some potential new components of the RBOHD, PRX33 and PRX34 signalling networks. John Wiley and Sons Inc. 2019-02-08 /pmc/articles/PMC6637864/ /pubmed/30426643 http://dx.doi.org/10.1111/mpp.12769 Text en © 2018 The Authors. Molecular Plant Pathology published by BSPP and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Kámán‐Tóth, Evelin Dankó, Tamás Gullner, Gábor Bozsó, Zoltán Palkovics, László Pogány, Miklós Contribution of cell wall peroxidase‐ and NADPH oxidase‐derived reactive oxygen species to Alternaria brassicicola‐induced oxidative burst in Arabidopsis |
title | Contribution of cell wall peroxidase‐ and NADPH oxidase‐derived reactive oxygen species to Alternaria brassicicola‐induced oxidative burst in Arabidopsis
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title_full | Contribution of cell wall peroxidase‐ and NADPH oxidase‐derived reactive oxygen species to Alternaria brassicicola‐induced oxidative burst in Arabidopsis
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title_fullStr | Contribution of cell wall peroxidase‐ and NADPH oxidase‐derived reactive oxygen species to Alternaria brassicicola‐induced oxidative burst in Arabidopsis
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title_full_unstemmed | Contribution of cell wall peroxidase‐ and NADPH oxidase‐derived reactive oxygen species to Alternaria brassicicola‐induced oxidative burst in Arabidopsis
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title_short | Contribution of cell wall peroxidase‐ and NADPH oxidase‐derived reactive oxygen species to Alternaria brassicicola‐induced oxidative burst in Arabidopsis
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title_sort | contribution of cell wall peroxidase‐ and nadph oxidase‐derived reactive oxygen species to alternaria brassicicola‐induced oxidative burst in arabidopsis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637864/ https://www.ncbi.nlm.nih.gov/pubmed/30426643 http://dx.doi.org/10.1111/mpp.12769 |
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