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Transcriptomic profiling of Brassica napus responses to Pseudomonas aeruginosa

Pseudomonas aeruginosa is an opportunistic bacterial pathogen of plants. Unlike the well-characterized plant defense responses to highly adapted bacterial phytopathogens, little is known about plant response to P. aeruginosa infection. In this study, we examined the Brassica napus (canola) tissue-sp...

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Autores principales: Cook, Jamie, Douglas, Gavin M, Zhang, Janie, Glick, Bernard R, Langille, Morgan G I, Liu, Kun-Hsiang, Cheng, Zhenyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7882811/
https://www.ncbi.nlm.nih.gov/pubmed/33353474
http://dx.doi.org/10.1177/1753425920980512
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author Cook, Jamie
Douglas, Gavin M
Zhang, Janie
Glick, Bernard R
Langille, Morgan G I
Liu, Kun-Hsiang
Cheng, Zhenyu
author_facet Cook, Jamie
Douglas, Gavin M
Zhang, Janie
Glick, Bernard R
Langille, Morgan G I
Liu, Kun-Hsiang
Cheng, Zhenyu
author_sort Cook, Jamie
collection PubMed
description Pseudomonas aeruginosa is an opportunistic bacterial pathogen of plants. Unlike the well-characterized plant defense responses to highly adapted bacterial phytopathogens, little is known about plant response to P. aeruginosa infection. In this study, we examined the Brassica napus (canola) tissue-specific response to P. aeruginosa infection using RNA sequencing. Transcriptomic analysis of canola seedlings over a 5 day P. aeruginosa infection revealed that many molecular processes involved in plant innate immunity were up-regulated, whereas photosynthesis was down-regulated. Phytohormones control many vital biological processes within plants, including growth and development, senescence, seed setting, fruit ripening, and innate immunity. The three main phytohormones involved in plant innate immunity are salicylic acid (SA), jasmonic acid (JA), and ethylene (ET). Many bacterial pathogens have evolved multiple strategies to manipulate these hormone responses in order to infect plants successfully. Interestingly, gene expression within all three phytohormone (SA, JA, and ET) signaling pathways was up-regulated in response to P. aeruginosa infection. This study identified a unique plant hormone response to the opportunistic bacterial pathogen P. aeruginosa infection.
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spelling pubmed-78828112021-02-23 Transcriptomic profiling of Brassica napus responses to Pseudomonas aeruginosa Cook, Jamie Douglas, Gavin M Zhang, Janie Glick, Bernard R Langille, Morgan G I Liu, Kun-Hsiang Cheng, Zhenyu Innate Immun Original Articles Pseudomonas aeruginosa is an opportunistic bacterial pathogen of plants. Unlike the well-characterized plant defense responses to highly adapted bacterial phytopathogens, little is known about plant response to P. aeruginosa infection. In this study, we examined the Brassica napus (canola) tissue-specific response to P. aeruginosa infection using RNA sequencing. Transcriptomic analysis of canola seedlings over a 5 day P. aeruginosa infection revealed that many molecular processes involved in plant innate immunity were up-regulated, whereas photosynthesis was down-regulated. Phytohormones control many vital biological processes within plants, including growth and development, senescence, seed setting, fruit ripening, and innate immunity. The three main phytohormones involved in plant innate immunity are salicylic acid (SA), jasmonic acid (JA), and ethylene (ET). Many bacterial pathogens have evolved multiple strategies to manipulate these hormone responses in order to infect plants successfully. Interestingly, gene expression within all three phytohormone (SA, JA, and ET) signaling pathways was up-regulated in response to P. aeruginosa infection. This study identified a unique plant hormone response to the opportunistic bacterial pathogen P. aeruginosa infection. SAGE Publications 2020-12-22 2021-02 /pmc/articles/PMC7882811/ /pubmed/33353474 http://dx.doi.org/10.1177/1753425920980512 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Cook, Jamie
Douglas, Gavin M
Zhang, Janie
Glick, Bernard R
Langille, Morgan G I
Liu, Kun-Hsiang
Cheng, Zhenyu
Transcriptomic profiling of Brassica napus responses to Pseudomonas aeruginosa
title Transcriptomic profiling of Brassica napus responses to Pseudomonas aeruginosa
title_full Transcriptomic profiling of Brassica napus responses to Pseudomonas aeruginosa
title_fullStr Transcriptomic profiling of Brassica napus responses to Pseudomonas aeruginosa
title_full_unstemmed Transcriptomic profiling of Brassica napus responses to Pseudomonas aeruginosa
title_short Transcriptomic profiling of Brassica napus responses to Pseudomonas aeruginosa
title_sort transcriptomic profiling of brassica napus responses to pseudomonas aeruginosa
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7882811/
https://www.ncbi.nlm.nih.gov/pubmed/33353474
http://dx.doi.org/10.1177/1753425920980512
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