Influence of a functional sigB operon on the global regulators sar and agr in Staphylococcus aureus

被引:177
作者
Bischoff, M
Entenza, JM
Giachino, P
机构
[1] Univ Zurich, Dept Med Microbiol, CH-8028 Zurich, Switzerland
[2] CHU Vaudois, Dept Internal Med, Div Infect Dis, CH-1011 Lausanne, Switzerland
关键词
D O I
10.1128/JB.183.17.5171-5179.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The growth phase-dependent activity profile of the alternate transcription factor sigma (B) and its effects on the expression of sar and agr were examined in three different Staphylococcus aureus strains by Northern blot analyses and by the use of reporter gene fusion experiments. Significant sigma (B) activity was detectable only in the clinical isolates MSSA1112 and Newman, carrying the wild-type rsbU allele, but not in the NCTC8325 derivative BB255, which is defective in rsbU. sigma (B) activity peaked in the late exponential phase and diminished towards the stationary phase when bacteria were grown in Luria-Bertani medium. Transcriptional analysis and a sarP1-sarP2-sarP3 (sarP1-P2-P3)-driven firefly luciferase (luc+) reporter gene fusion demonstrated a strong sigma (B) activity- and growth phase-dependent increase in sar expression that was totally absent in either rsbU or Delta rsbUVWsigB mutants. In contrast, expression of the agr locus, as measured by RNAIII levels and by an hldp::luc+ fusion, was found to be higher in the absence of sigma (B) activity, such as in rsbU or Delta rsbUVWsigB mutants, than in wild-type strains. Overexpression of sigma (B) in BB255 derivatives resulted in a clear increase in sarP1-P2-P3::luc+ expression as well as a strong decrease in hldp::luc+ expression. The data presented here suggest that sigma (B) increases sar expression while simultaneously reducing the RNAIII level in a growth phase-dependent manner.
引用
收藏
页码:5171 / 5179
页数:9
相关论文
共 61 条
[1]   THE ACCESSORY GENE REGULATOR (AGR) CONTROLS STAPHYLOCOCCUS-AUREUS VIRULENCE IN A MURINE ARTHRITIS MODEL [J].
ABDELNOUR, A ;
ARVIDSON, S ;
BREMELL, T ;
RYDEN, C ;
TARKOWSKI, A .
INFECTION AND IMMUNITY, 1993, 61 (09) :3879-3885
[2]   Autoinducer of virulence as a target for vaccine and therapy against Staphylococcus aureus [J].
Balaban, N ;
Goldkorn, T ;
Nhan, RT ;
Dang, LB ;
Scott, S ;
Ridgley, RM ;
Rasooly, A ;
Wright, SC ;
Larrick, JW ;
Rasooly, R ;
Carlson, JR .
SCIENCE, 1998, 280 (5362) :438-440
[3]   The molecular architecture of the sar locus in Staphylococcus aureus [J].
Bayer, MG ;
Heinrichs, JH ;
Cheung, AL .
JOURNAL OF BACTERIOLOGY, 1996, 178 (15) :4563-4570
[4]  
BERGERBACHI B, 1983, J BACTERIOL, V154, P533
[5]   Teicoplanin stress-selected mutations increasing σB activity in Staphylococcus aureus [J].
Bischoff, M ;
Berger-Bächi, B .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (06) :1714-1720
[6]   Involvement of multiple genetic loci in Staphylococcus aureus teicoplanin resistance [J].
Bischoff, M ;
Roos, M ;
Putnik, J ;
Wada, A ;
Glanzmann, P ;
Giachino, P ;
Vaudaux, P ;
Berger-Bächi, B .
FEMS MICROBIOLOGY LETTERS, 2001, 194 (01) :77-82
[7]   The staphylococcal accessory regulator (sar) represses transcription of the Staphylococcus aureus collagen adhesin gene (cna) in an agr-independent manner [J].
Blevins, JS ;
Gillaspy, AF ;
Rechtin, TM ;
Hurlburt, BK ;
Smeltzer, MS .
MOLECULAR MICROBIOLOGY, 1999, 33 (02) :317-326
[8]   Staphylococcal accessory regulator (sar) in conjunction with agr contributes to Staphylococcus aureus virulence in endophthalmitis [J].
Booth, MC ;
Cheung, AL ;
Hatter, KL ;
Jett, BD ;
Callegan, MC ;
Gilmore, MS .
INFECTION AND IMMUNITY, 1997, 65 (04) :1550-1556
[9]  
Bruckner R, 1997, FEMS MICROBIOL LETT, V151, P1
[10]   SarA represses agr operon expression in a purified in vitro Staphylococcus aureus transcription system [J].
Chakrabarti, SK ;
Misra, TK .
JOURNAL OF BACTERIOLOGY, 2000, 182 (20) :5893-5897