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

被引:169
作者
Wei, Qing [1 ,2 ]
Phu Nguyen Le Minh [1 ]
Doetsch, Andreas [3 ,4 ,5 ]
Hildebrand, Falk [1 ,2 ]
Panmanee, Warunya [6 ]
Elfarash, Ameer [1 ,2 ]
Schulz, Sebastian [3 ,4 ,5 ]
Plaisance, Stephane [7 ]
Charlier, Daniel [1 ]
Haessett, Daniel [6 ]
Haussler, Susanne [3 ,4 ,5 ]
Cornelis, Pierre [1 ,2 ]
机构
[1] Vrije Univ Brussel, Dept Bioengn Sci, Microbiol Res Grp, B-1050 Brussels, Belgium
[2] Vrije Univ Brussel, VIB Dept Struct Biol, B-1050 Brussels, Belgium
[3] Helmholtz Ctr Infect Res, Chron Pseudomonas Infect Res Grp, D-38124 Braunschweig, Germany
[4] Twincore, Ctr Expt & Clin Infect Res, Hannover, Germany
[5] Hannover Med Sch, D-3000 Hannover, Germany
[6] Univ Cincinnati, Coll Med, Dept Mol Genet Biochem & Microbiol, Cincinnati, OH 45267 USA
[7] BITS VIB, B-9052 Ghent, Belgium
关键词
PSEUDOMONAS-AERUGINOSA-OXYR; OXIDATIVE STRESS-RESPONSE; DISULFIDE BOND FORMATION; HYDROGEN-PEROXIDE; ESCHERICHIA-COLI; TRANSCRIPTION FACTOR; BIOFILM COMMUNITIES; GENOMIC ANALYSIS; CROSS-LINKING; PROTEIN;
D O I
10.1093/nar/gks017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:4320 / 4333
页数:14
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