Control of Thioredoxin Reductase Gene (trxB) Transcription by SarA in Staphylococcus aureus

被引:45
作者
Ballal, Anand [2 ]
Manna, Adhar C. [1 ]
机构
[1] Univ S Dakota, Sanford Sch Med, Div Basic Biomed Sci, Vermillion, SD 57069 USA
[2] S Dakota State Univ, Ctr Infect Dis Res & Vaccinol, Brookings, SD 57007 USA
基金
美国国家卫生研究院;
关键词
OXIDATIVE STRESS RESISTANCE; GLOBAL REGULATOR; VIRULENCE DETERMINANTS; BACILLUS-SUBTILIS; PEROXIDE STRESS; AGR LOCUS; EXPRESSION; IDENTIFICATION; MECHANISM; MGRA;
D O I
10.1128/JB.01202-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Thioredoxin reductase (encoded by trxB) protects Staphylococcus aureus against oxygen or disulfide stress and is indispensable for growth. Among the different sarA family mutants analyzed, transcription of trxB was markedly elevated in the sarA mutant under conditions of aerobic as well as microaerophilic growth, indicating that SarA acts as a negative regulator of trxB expression. Gel shift analysis showed that purified SarA protein binds directly to the trxB promoter region DNA in vitro. DNA binding of SarA was essential for repression of trxB transcription in vivo in S. aureus. Northern blot analysis and DNA binding studies of the purified wild-type SarA and the mutant SarAC9G with oxidizing agents indicated that oxidation of Cys-9 reduced the binding of SarA to the trxB promoter DNA. Oxidizing agents, in particular diamide, could further enhance transcription of the trxB gene in the sarA mutant, suggesting the presence of a SarA-independent mode of trxB induction. Analysis of two oxidative stress-responsive sarA regulatory target genes, trxB and sodM, with various mutant sarA constructs showed a differential ability of the SarA to regulate expression of the two above-mentioned genes in vivo. The overall data demonstrate the important role played by SarA in modulating expression of genes involved in oxidative stress resistance in S. aureus.
引用
收藏
页码:336 / 345
页数:10
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