Stationary phase-specific virulence factor overproduction by a lasR mutant of Pseudomonas aeruginosa.

Secreted virulence factors of the human pathogen Pseudomonas aeruginosa are often under quorum sensing control. Cells lacking the quorum-sensing regulator LasR show reduced virulence factor production under typical laboratory conditions and are hypo-virulent in short-term animal infection models, ye...

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Main Author: Matthew T Cabeen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3923063?pdf=render
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spelling doaj-a2622e789d804723b072bf520166366f2020-11-25T01:21:23ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0192e8874310.1371/journal.pone.0088743Stationary phase-specific virulence factor overproduction by a lasR mutant of Pseudomonas aeruginosa.Matthew T CabeenSecreted virulence factors of the human pathogen Pseudomonas aeruginosa are often under quorum sensing control. Cells lacking the quorum-sensing regulator LasR show reduced virulence factor production under typical laboratory conditions and are hypo-virulent in short-term animal infection models, yet lasR mutants are frequently associated with long-term infection in cystic fibrosis patients. Here, I show that in stationary-phase or slow-growth conditions, lasR cells continuously and strongly produce the important virulence factor pyocyanin while wild-type cells do not. Pyocyanin overproduction by lasR cells is permitted by loss of repression by RsaL, a LasR-dependent negative regulator. lasR cells also contribute pyocyanin in mixed cultures, even under "cheating" conditions where they depend on their wild-type neighbors for nutrients. Finally, some clinical P. aeruginosa isolates with lasR mutations can overproduce pyocyanin in the laboratory. These results imply that slow-growing clinical populations of lasR cells in chronic infections may contribute to virulence by producing pyocyanin under conditions where lasR⁺ cells do not.http://europepmc.org/articles/PMC3923063?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Matthew T Cabeen
spellingShingle Matthew T Cabeen
Stationary phase-specific virulence factor overproduction by a lasR mutant of Pseudomonas aeruginosa.
PLoS ONE
author_facet Matthew T Cabeen
author_sort Matthew T Cabeen
title Stationary phase-specific virulence factor overproduction by a lasR mutant of Pseudomonas aeruginosa.
title_short Stationary phase-specific virulence factor overproduction by a lasR mutant of Pseudomonas aeruginosa.
title_full Stationary phase-specific virulence factor overproduction by a lasR mutant of Pseudomonas aeruginosa.
title_fullStr Stationary phase-specific virulence factor overproduction by a lasR mutant of Pseudomonas aeruginosa.
title_full_unstemmed Stationary phase-specific virulence factor overproduction by a lasR mutant of Pseudomonas aeruginosa.
title_sort stationary phase-specific virulence factor overproduction by a lasr mutant of pseudomonas aeruginosa.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Secreted virulence factors of the human pathogen Pseudomonas aeruginosa are often under quorum sensing control. Cells lacking the quorum-sensing regulator LasR show reduced virulence factor production under typical laboratory conditions and are hypo-virulent in short-term animal infection models, yet lasR mutants are frequently associated with long-term infection in cystic fibrosis patients. Here, I show that in stationary-phase or slow-growth conditions, lasR cells continuously and strongly produce the important virulence factor pyocyanin while wild-type cells do not. Pyocyanin overproduction by lasR cells is permitted by loss of repression by RsaL, a LasR-dependent negative regulator. lasR cells also contribute pyocyanin in mixed cultures, even under "cheating" conditions where they depend on their wild-type neighbors for nutrients. Finally, some clinical P. aeruginosa isolates with lasR mutations can overproduce pyocyanin in the laboratory. These results imply that slow-growing clinical populations of lasR cells in chronic infections may contribute to virulence by producing pyocyanin under conditions where lasR⁺ cells do not.
url http://europepmc.org/articles/PMC3923063?pdf=render
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