J. Bacteriol. doi:10.1128/JB.00889-07
Copyright (c) 2007, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.
Transcriptomic analysis of the sulfate starvation response of Pseudomonas aeruginosa
Tewes Tralau,
Stéphane Vuilleumier,
Christelle Thibault,
Barry J. Campbell,
C. Anthony Hart,
and
Michael A. Kertesz*
Faculty of Life Sciences, University of Manchester, Oxford Rd, Manchester, M13 9PT, UK, Génétique Moléculaire, Génomique, Microbiologie, UMR 7156 Université Louis Pasteur - CNRS, F-67083 Strasbourg, France, and Faculty of Medicine, University of Liverpool, Liverpool L69 3GA, United Kingdom
* To whom correspondence should be addressed. Email:
michael.kertesz{at}manchester.ac.uk.
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Abstract |
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Pseudomonas aeruginosa is an opportunistic pathogen that causes a number of infections in humans, but is best known for its association with cystic fibrosis. It is able to use a wide range of sulfur compounds as sources of sulfur for growth. Gene expression in response to changes in sulfur supply was studied in P. aeruginosa E601, a cystic fibrosis isolate that displays mucin sulfatase activity, and in P. aeruginosa PAO1. A large family of genes was found to be upregulated by sulfate limitation in both isolates, encoding sulfatases and sulfonatases, transport systems, oxidative stress proteins, and a sulfate-regulated TonB/ExbBD complex. These genes were localized in five distinct islands on the genome, and encoded proteins with a significantly reduced content of cysteine and methionine. Growth of P. aeruginosa E601 with mucin as sulfur source led to a sulfate starvation response, but also to induction of genes involved with type III secretion systems.