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Antimicrobial Agents and Chemotherapy, May 2009, p. 1832-1839, Vol. 53, No. 5
0066-4804/09/$08.00+0 doi:10.1128/AAC.01255-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.
B-Dependent yabJ-spoVG Operon in Staphylococcus aureus: Role in Methicillin and Glycopeptide Resistance
Institute of Medical Microbiology, University of Zürich, Zürich, Switzerland,1 Institute of Molecular Biology, Centre of Excellence for Molecular Medicine, Slovak Academy of Sciences, Bratislava, Slovak Republic,2 Institute of Medical Microbiology and Hygiene, University of Tübingen, Tübingen, Germany,3 Institute of Medical Microbiology and Hygiene, University of Saarland Hospital, Homburg/Saar, Germany4
Received 19 September 2008/ Returned for modification 7 December 2008/ Accepted 31 January 2009
The alternative sigma factor
B of Staphylococcus aureus controls the expression of multiple genes, including virulence determinants and global regulators; promotes capsule production; and increases the resistance levels of methicillin-resistant S. aureus (MRSA) and glycopeptide-intermediate-resistant S. aureus (GISA) strains. We show here that deletion of the
B-controlled yabJ-spoVG operon, which codes for potential downstream regulators of
B, abolished capsule synthesis and reduced resistance in MRSA and GISA to the same extent that
B inactivation did. Introduction of the yabJ-spoVG operon in trans restored the original phenotype. By genetic manipulations, we show that SpoVG but not YabJ is required for complementation. We therefore postulate that SpoVG is the major factor of the yabJ-spoVG operon required in S. aureus for capsule formation and antibiotic resistance.
Published ahead of print on 17 February 2009.
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