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Differential Regulation of Genes for Cyclic-di-GMP Metabolism Orchestrates Adaptive Changes During Rhizosphere Colonization by Pseudomonas fluorescens

Bacteria belonging to the Pseudomonas genus are highly successful colonizers of the plant rhizosphere. The ability of different Pseudomonas species to live either commensal lifestyles or to act as agents of plant-growth promotion or disease is reflected in a large, highly flexible accessory genome....

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Autores principales: Little, Richard H., Woodcock, Stuart D., Campilongo, Rosaria, Fung, Rowena K. Y., Heal, Robert, Humphries, Libby, Pacheco-Moreno, Alba, Paulusch, Stefan, Stigliano, Egidio, Vikeli, Eleni, Ward, Danny, Malone, Jacob G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531821/
https://www.ncbi.nlm.nih.gov/pubmed/31156596
http://dx.doi.org/10.3389/fmicb.2019.01089
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author Little, Richard H.
Woodcock, Stuart D.
Campilongo, Rosaria
Fung, Rowena K. Y.
Heal, Robert
Humphries, Libby
Pacheco-Moreno, Alba
Paulusch, Stefan
Stigliano, Egidio
Vikeli, Eleni
Ward, Danny
Malone, Jacob G.
author_facet Little, Richard H.
Woodcock, Stuart D.
Campilongo, Rosaria
Fung, Rowena K. Y.
Heal, Robert
Humphries, Libby
Pacheco-Moreno, Alba
Paulusch, Stefan
Stigliano, Egidio
Vikeli, Eleni
Ward, Danny
Malone, Jacob G.
author_sort Little, Richard H.
collection PubMed
description Bacteria belonging to the Pseudomonas genus are highly successful colonizers of the plant rhizosphere. The ability of different Pseudomonas species to live either commensal lifestyles or to act as agents of plant-growth promotion or disease is reflected in a large, highly flexible accessory genome. Nevertheless, adaptation to the plant environment involves a commonality of phenotypic outputs such as changes to motility, coupled with synthesis of nutrient uptake systems, stress-response molecules and adherence factors including exopolysaccharides. Cyclic-di-GMP (cdG) is a highly important second messenger involved in the integration of environmental signals with appropriate adaptive responses and is known to play a central role in mediating effective rhizosphere colonization. In this study, we examined the transcription of multiple, reportedly plant-upregulated cdG metabolism genes during colonization of the wheat rhizosphere by the plant-growth-promoting strain P. fluorescens SBW25. While transcription of the tested genes generally increased in the rhizosphere environment, we additionally observed a tightly orchestrated response to environmental cues, with a distinct transcriptional pattern seen for each gene throughout the colonization process. Extensive phenotypical analysis of deletion and overexpression strains was then conducted and used to propose cellular functions for individual cdG signaling genes. Finally, in-depth genetic analysis of an important rhizosphere colonization regulator revealed a link between cdG control of growth, motility and stress response, and the carbon sources available in the rhizosphere.
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spelling pubmed-65318212019-05-31 Differential Regulation of Genes for Cyclic-di-GMP Metabolism Orchestrates Adaptive Changes During Rhizosphere Colonization by Pseudomonas fluorescens Little, Richard H. Woodcock, Stuart D. Campilongo, Rosaria Fung, Rowena K. Y. Heal, Robert Humphries, Libby Pacheco-Moreno, Alba Paulusch, Stefan Stigliano, Egidio Vikeli, Eleni Ward, Danny Malone, Jacob G. Front Microbiol Microbiology Bacteria belonging to the Pseudomonas genus are highly successful colonizers of the plant rhizosphere. The ability of different Pseudomonas species to live either commensal lifestyles or to act as agents of plant-growth promotion or disease is reflected in a large, highly flexible accessory genome. Nevertheless, adaptation to the plant environment involves a commonality of phenotypic outputs such as changes to motility, coupled with synthesis of nutrient uptake systems, stress-response molecules and adherence factors including exopolysaccharides. Cyclic-di-GMP (cdG) is a highly important second messenger involved in the integration of environmental signals with appropriate adaptive responses and is known to play a central role in mediating effective rhizosphere colonization. In this study, we examined the transcription of multiple, reportedly plant-upregulated cdG metabolism genes during colonization of the wheat rhizosphere by the plant-growth-promoting strain P. fluorescens SBW25. While transcription of the tested genes generally increased in the rhizosphere environment, we additionally observed a tightly orchestrated response to environmental cues, with a distinct transcriptional pattern seen for each gene throughout the colonization process. Extensive phenotypical analysis of deletion and overexpression strains was then conducted and used to propose cellular functions for individual cdG signaling genes. Finally, in-depth genetic analysis of an important rhizosphere colonization regulator revealed a link between cdG control of growth, motility and stress response, and the carbon sources available in the rhizosphere. Frontiers Media S.A. 2019-05-16 /pmc/articles/PMC6531821/ /pubmed/31156596 http://dx.doi.org/10.3389/fmicb.2019.01089 Text en Copyright © 2019 Little, Woodcock, Campilongo, Fung, Heal, Humphries, Pacheco-Moreno, Paulusch, Stigliano, Vikeli, Ward and Malone. 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) and the copyright owner(s) 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 Microbiology
Little, Richard H.
Woodcock, Stuart D.
Campilongo, Rosaria
Fung, Rowena K. Y.
Heal, Robert
Humphries, Libby
Pacheco-Moreno, Alba
Paulusch, Stefan
Stigliano, Egidio
Vikeli, Eleni
Ward, Danny
Malone, Jacob G.
Differential Regulation of Genes for Cyclic-di-GMP Metabolism Orchestrates Adaptive Changes During Rhizosphere Colonization by Pseudomonas fluorescens
title Differential Regulation of Genes for Cyclic-di-GMP Metabolism Orchestrates Adaptive Changes During Rhizosphere Colonization by Pseudomonas fluorescens
title_full Differential Regulation of Genes for Cyclic-di-GMP Metabolism Orchestrates Adaptive Changes During Rhizosphere Colonization by Pseudomonas fluorescens
title_fullStr Differential Regulation of Genes for Cyclic-di-GMP Metabolism Orchestrates Adaptive Changes During Rhizosphere Colonization by Pseudomonas fluorescens
title_full_unstemmed Differential Regulation of Genes for Cyclic-di-GMP Metabolism Orchestrates Adaptive Changes During Rhizosphere Colonization by Pseudomonas fluorescens
title_short Differential Regulation of Genes for Cyclic-di-GMP Metabolism Orchestrates Adaptive Changes During Rhizosphere Colonization by Pseudomonas fluorescens
title_sort differential regulation of genes for cyclic-di-gmp metabolism orchestrates adaptive changes during rhizosphere colonization by pseudomonas fluorescens
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531821/
https://www.ncbi.nlm.nih.gov/pubmed/31156596
http://dx.doi.org/10.3389/fmicb.2019.01089
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