Cargando…

Transcriptomic analysis of Pseudomonas ogarae F113 reveals the antagonistic roles of AmrZ and FleQ during rhizosphere adaption

Rhizosphere colonization by bacteria involves molecular and cellular mechanisms, such as motility and chemotaxis, biofilm formation, metabolic versatility, or biosynthesis of secondary metabolites, among others. Nonetheless, there is limited knowledge concerning the main regulatory factors that driv...

Descripción completa

Detalles Bibliográficos
Autores principales: Blanco-Romero, Esther, Durán, David, Garrido-Sanz, Daniel, Rivilla, Rafael, Martín, Marta, Redondo-Nieto, Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8914362/
https://www.ncbi.nlm.nih.gov/pubmed/35012704
http://dx.doi.org/10.1099/mgen.0.000750
_version_ 1784667688344223744
author Blanco-Romero, Esther
Durán, David
Garrido-Sanz, Daniel
Rivilla, Rafael
Martín, Marta
Redondo-Nieto, Miguel
author_facet Blanco-Romero, Esther
Durán, David
Garrido-Sanz, Daniel
Rivilla, Rafael
Martín, Marta
Redondo-Nieto, Miguel
author_sort Blanco-Romero, Esther
collection PubMed
description Rhizosphere colonization by bacteria involves molecular and cellular mechanisms, such as motility and chemotaxis, biofilm formation, metabolic versatility, or biosynthesis of secondary metabolites, among others. Nonetheless, there is limited knowledge concerning the main regulatory factors that drive the rhizosphere colonization process. Here we show the importance of the AmrZ and FleQ transcription factors for adaption in the plant growth-promoting rhizobacterium (PGPR) and rhizosphere colonization model Pseudomonas ogarae F113. RNA-Seq analyses of P. ogarae F113 grown in liquid cultures either in exponential and stationary growth phase, and rhizosphere conditions, revealed that rhizosphere is a key driver of global changes in gene expression in this bacterium. Regarding the genetic background, this work has revealed that a mutation in fleQ causes considerably more alterations in the gene expression profile of this bacterium than a mutation in amrZ under rhizosphere conditions. The functional analysis has revealed that in P. ogarae F113, the transcription factors AmrZ and FleQ regulate genes involved in diverse bacterial functions. Notably, in the rhizosphere, these transcription factors antagonistically regulate genes related to motility, biofilm formation, nitrogen, sulfur, and amino acid metabolism, transport, signalling, and secretion, especially the type VI secretion systems. These results define the regulon of two important bifunctional transcriptional regulators in pseudomonads during the process of rhizosphere colonization.
format Online
Article
Text
id pubmed-8914362
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Microbiology Society
record_format MEDLINE/PubMed
spelling pubmed-89143622022-03-11 Transcriptomic analysis of Pseudomonas ogarae F113 reveals the antagonistic roles of AmrZ and FleQ during rhizosphere adaption Blanco-Romero, Esther Durán, David Garrido-Sanz, Daniel Rivilla, Rafael Martín, Marta Redondo-Nieto, Miguel Microb Genom Research Articles Rhizosphere colonization by bacteria involves molecular and cellular mechanisms, such as motility and chemotaxis, biofilm formation, metabolic versatility, or biosynthesis of secondary metabolites, among others. Nonetheless, there is limited knowledge concerning the main regulatory factors that drive the rhizosphere colonization process. Here we show the importance of the AmrZ and FleQ transcription factors for adaption in the plant growth-promoting rhizobacterium (PGPR) and rhizosphere colonization model Pseudomonas ogarae F113. RNA-Seq analyses of P. ogarae F113 grown in liquid cultures either in exponential and stationary growth phase, and rhizosphere conditions, revealed that rhizosphere is a key driver of global changes in gene expression in this bacterium. Regarding the genetic background, this work has revealed that a mutation in fleQ causes considerably more alterations in the gene expression profile of this bacterium than a mutation in amrZ under rhizosphere conditions. The functional analysis has revealed that in P. ogarae F113, the transcription factors AmrZ and FleQ regulate genes involved in diverse bacterial functions. Notably, in the rhizosphere, these transcription factors antagonistically regulate genes related to motility, biofilm formation, nitrogen, sulfur, and amino acid metabolism, transport, signalling, and secretion, especially the type VI secretion systems. These results define the regulon of two important bifunctional transcriptional regulators in pseudomonads during the process of rhizosphere colonization. Microbiology Society 2022-01-11 /pmc/articles/PMC8914362/ /pubmed/35012704 http://dx.doi.org/10.1099/mgen.0.000750 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial License.
spellingShingle Research Articles
Blanco-Romero, Esther
Durán, David
Garrido-Sanz, Daniel
Rivilla, Rafael
Martín, Marta
Redondo-Nieto, Miguel
Transcriptomic analysis of Pseudomonas ogarae F113 reveals the antagonistic roles of AmrZ and FleQ during rhizosphere adaption
title Transcriptomic analysis of Pseudomonas ogarae F113 reveals the antagonistic roles of AmrZ and FleQ during rhizosphere adaption
title_full Transcriptomic analysis of Pseudomonas ogarae F113 reveals the antagonistic roles of AmrZ and FleQ during rhizosphere adaption
title_fullStr Transcriptomic analysis of Pseudomonas ogarae F113 reveals the antagonistic roles of AmrZ and FleQ during rhizosphere adaption
title_full_unstemmed Transcriptomic analysis of Pseudomonas ogarae F113 reveals the antagonistic roles of AmrZ and FleQ during rhizosphere adaption
title_short Transcriptomic analysis of Pseudomonas ogarae F113 reveals the antagonistic roles of AmrZ and FleQ during rhizosphere adaption
title_sort transcriptomic analysis of pseudomonas ogarae f113 reveals the antagonistic roles of amrz and fleq during rhizosphere adaption
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8914362/
https://www.ncbi.nlm.nih.gov/pubmed/35012704
http://dx.doi.org/10.1099/mgen.0.000750
work_keys_str_mv AT blancoromeroesther transcriptomicanalysisofpseudomonasogaraef113revealstheantagonisticrolesofamrzandfleqduringrhizosphereadaption
AT durandavid transcriptomicanalysisofpseudomonasogaraef113revealstheantagonisticrolesofamrzandfleqduringrhizosphereadaption
AT garridosanzdaniel transcriptomicanalysisofpseudomonasogaraef113revealstheantagonisticrolesofamrzandfleqduringrhizosphereadaption
AT rivillarafael transcriptomicanalysisofpseudomonasogaraef113revealstheantagonisticrolesofamrzandfleqduringrhizosphereadaption
AT martinmarta transcriptomicanalysisofpseudomonasogaraef113revealstheantagonisticrolesofamrzandfleqduringrhizosphereadaption
AT redondonietomiguel transcriptomicanalysisofpseudomonasogaraef113revealstheantagonisticrolesofamrzandfleqduringrhizosphereadaption