4.8 Article

Global regulation of gene expression by OxyR in an important human opportunistic pathogen

Journal

NUCLEIC ACIDS RESEARCH
Volume 40, Issue 10, Pages 4320-4333

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gks017

Keywords

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Funding

  1. Fonds voor Wetenschappelijk Onderzoek (FWO-Vlaanderen) [G.0119.10N]
  2. Research Council of the Vrije Universiteit Brussel
  3. CSC-Vrije Universiteit Brussel
  4. FEMS
  5. Veteran's Administration

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Most bacteria control oxidative stress through the H2O2-responsive transactivator OxyR, a member of the LTTR family (LysR Type Transcriptional Regulators), which activates the expression of defensive genes such as those encoding catalases, alkyl hydroperoxide reductases and superoxide dismutases. In the human opportunistic pathogen Pseudomonas aeruginosa, OxyR positively regulates expression of the oxidative stress response genes katA, katB, ahpB and ahpCF. To identify additional targets of OxyR in P. aeruginosa PAO1, we performed chromatin immunoprecipitation in combination with whole genome tiling array analyses (ChIP-chip). We detected 56 genes including all the previously identified defensive genes and a battery of novel direct targets of OxyR. Electrophoretic mobility shift assays (EMSAs) for selected newly identified targets indicated that similar to 70% of those were bound by purified oxidized OxyR and their regulation was confirmed by quantitative real-time polymerase chain reaction. Furthermore, a thioredoxin system was identified to enzymatically reduce OxyR under oxidative stress. Functional classification analysis showed that OxyR controls a core regulon of oxidative stress defensive genes, and other genes involved in regulation of iron homeostasis (pvdS), quorum-sensing (rsaL), protein synthesis (rpsL) and oxidative phosphorylation (cyoA and snr1). Collectively, our results indicate that OxyR is involved in oxidative stress defense and regulates other aspects of cellular metabolism as well.

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