Agr-independent regulation of fibronectin-binding protein(s) by the regulatory locus sar in Staphylococcus aureus

被引:105
作者
Wolz, C
Pöhlmann-Dietze, P
Steinhuber, A
Chien, YT
Manna, A
van Wamel, W
Cheung, A
机构
[1] Rockefeller Univ, Lab Bacterial Pathogenesis & Immunol, New York, NY 10021 USA
[2] Univ Tubingen, Dept Gen & Environm Hyg, D-72074 Tubingen, Germany
[3] Dartmouth Coll, Sch Med, Dept Microbiol, Hanover, NH 03755 USA
关键词
D O I
10.1046/j.1365-2958.2000.01853.x
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
Fibronectin-binding proteins (FnBPs) are thought to be important for the attachment of Staphylococcus aureus during infection. The regulation of the genes fnbA and fnbB by the global regulatory loci sar and agr was examined using site-specific regulatory mutants of S. aureus strain Newman. The results from binding assays using both aqueous and solid-phase fibronectin as well as ligand blotting with biotinylated fibronectin showed that the expression of FnBPA is enhanced in the agr mutant but inhibited in the sar mutant and the sar-agr double mutant. The same regulatory pattern was observed in Northern blot analysis using fnbA-specific probes. The introduction of sar on a multicopy plasmid increased the already enhanced fnbA transcription of the agr mutant. FnBPB was not detectable by ligand blotting and the fnbB promoter activity in promoter fusion assays was not affected by either sar or agr. The sequence encompassing ORF3 located upstream of sarA was found to be essential for the activation of fnbA transcription. We hypothesize that this sequence may modulate SarA expression and/or activity on the post-transcriptional level. Gel shift assays demonstrated that SarA binds to the fnbA promoter fragments, probably as a dimer. DNase I footprinting assays with SarA revealed a protected area of 102 bp upstream of fnbA.
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页码:230 / 243
页数:14
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