Cargando…

The Pseudomonas aeruginosa PilSR Two-Component System Regulates Both Twitching and Swimming Motilities

Motility is an important virulence trait for many bacterial pathogens, allowing them to position themselves in appropriate locations at appropriate times. The motility structures type IV pili and flagella are also involved in sensing surface contact, which modulates pathogenicity. In Pseudomonas aer...

Descripción completa

Detalles Bibliográficos
Autores principales: Kilmury, Sara L. N., Burrows, Lori L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058289/
https://www.ncbi.nlm.nih.gov/pubmed/30042200
http://dx.doi.org/10.1128/mBio.01310-18
_version_ 1783341666544910336
author Kilmury, Sara L. N.
Burrows, Lori L.
author_facet Kilmury, Sara L. N.
Burrows, Lori L.
author_sort Kilmury, Sara L. N.
collection PubMed
description Motility is an important virulence trait for many bacterial pathogens, allowing them to position themselves in appropriate locations at appropriate times. The motility structures type IV pili and flagella are also involved in sensing surface contact, which modulates pathogenicity. In Pseudomonas aeruginosa, the PilS-PilR two-component system (TCS) regulates expression of the type IV pilus (T4P) major subunit PilA, while biosynthesis of the single polar flagellum is regulated by a hierarchical system that includes the FleSR TCS. Previous studies of Geobacter sulfurreducens and Dichelobacter nodosus implicated PilR in regulation of non-T4P-related genes, including some involved in flagellar biosynthesis. Here we used transcriptome sequencing (RNA-seq) analysis to identify genes in addition to pilA with changes in expression in the absence of pilR. Among the genes identified were 10 genes whose transcription increased in the pilA mutant but decreased in the pilR mutant, despite both mutants lacking T4P and pilus-related phenotypes. The products of these inversely dysregulated genes, many of which were hypothetical, may be important for virulence and surface-associated behaviors, as mutants had altered swarming motility, biofilm formation, type VI secretion system expression, and pathogenicity in a nematode model. Further, the PilSR TCS positively regulated transcription of fleSR, and thus many genes in the FleSR regulon. As a result, pilSR deletion mutants had defects in swimming motility that were independent of the loss of PilA. Together, these data suggest that in addition to controlling T4P expression, PilSR could have a broader role in the regulation of P. aeruginosa motility and surface sensing behaviors.
format Online
Article
Text
id pubmed-6058289
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-60582892018-07-27 The Pseudomonas aeruginosa PilSR Two-Component System Regulates Both Twitching and Swimming Motilities Kilmury, Sara L. N. Burrows, Lori L. mBio Research Article Motility is an important virulence trait for many bacterial pathogens, allowing them to position themselves in appropriate locations at appropriate times. The motility structures type IV pili and flagella are also involved in sensing surface contact, which modulates pathogenicity. In Pseudomonas aeruginosa, the PilS-PilR two-component system (TCS) regulates expression of the type IV pilus (T4P) major subunit PilA, while biosynthesis of the single polar flagellum is regulated by a hierarchical system that includes the FleSR TCS. Previous studies of Geobacter sulfurreducens and Dichelobacter nodosus implicated PilR in regulation of non-T4P-related genes, including some involved in flagellar biosynthesis. Here we used transcriptome sequencing (RNA-seq) analysis to identify genes in addition to pilA with changes in expression in the absence of pilR. Among the genes identified were 10 genes whose transcription increased in the pilA mutant but decreased in the pilR mutant, despite both mutants lacking T4P and pilus-related phenotypes. The products of these inversely dysregulated genes, many of which were hypothetical, may be important for virulence and surface-associated behaviors, as mutants had altered swarming motility, biofilm formation, type VI secretion system expression, and pathogenicity in a nematode model. Further, the PilSR TCS positively regulated transcription of fleSR, and thus many genes in the FleSR regulon. As a result, pilSR deletion mutants had defects in swimming motility that were independent of the loss of PilA. Together, these data suggest that in addition to controlling T4P expression, PilSR could have a broader role in the regulation of P. aeruginosa motility and surface sensing behaviors. American Society for Microbiology 2018-07-24 /pmc/articles/PMC6058289/ /pubmed/30042200 http://dx.doi.org/10.1128/mBio.01310-18 Text en Copyright © 2018 Kilmury and Burrows. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Kilmury, Sara L. N.
Burrows, Lori L.
The Pseudomonas aeruginosa PilSR Two-Component System Regulates Both Twitching and Swimming Motilities
title The Pseudomonas aeruginosa PilSR Two-Component System Regulates Both Twitching and Swimming Motilities
title_full The Pseudomonas aeruginosa PilSR Two-Component System Regulates Both Twitching and Swimming Motilities
title_fullStr The Pseudomonas aeruginosa PilSR Two-Component System Regulates Both Twitching and Swimming Motilities
title_full_unstemmed The Pseudomonas aeruginosa PilSR Two-Component System Regulates Both Twitching and Swimming Motilities
title_short The Pseudomonas aeruginosa PilSR Two-Component System Regulates Both Twitching and Swimming Motilities
title_sort pseudomonas aeruginosa pilsr two-component system regulates both twitching and swimming motilities
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058289/
https://www.ncbi.nlm.nih.gov/pubmed/30042200
http://dx.doi.org/10.1128/mBio.01310-18
work_keys_str_mv AT kilmurysaraln thepseudomonasaeruginosapilsrtwocomponentsystemregulatesbothtwitchingandswimmingmotilities
AT burrowsloril thepseudomonasaeruginosapilsrtwocomponentsystemregulatesbothtwitchingandswimmingmotilities
AT kilmurysaraln pseudomonasaeruginosapilsrtwocomponentsystemregulatesbothtwitchingandswimmingmotilities
AT burrowsloril pseudomonasaeruginosapilsrtwocomponentsystemregulatesbothtwitchingandswimmingmotilities