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Antimicrobial Agents and Chemotherapy, June 2009, p. 2636-2637, Vol. 53, No. 6
0066-4804/09/$08.00+0 doi:10.1128/AAC.01415-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Los Angeles Biomedical Research Institute, Torrance, California,1 Department of Medicine, Division of Infectious Diseases, Harbor-UCLA Medical Center, Torrance, California,2 Geffen School of Medicine at UCLA, Los Angeles, California,3 Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska,4 Department of Internal Medicine, University Hospitals, Geneva, Switzerland,5 Cellular and Molecular Microbiology, Medical Microbiology and Hygiene, University of Tübingen, Germany6
Received 21 October 2008/ Returned for modification 24 January 2009/ Accepted 7 March 2009
We used a well-characterized isogenic set of clinical bloodstream Staphylococcus aureus strains to study (i) regulation of mprF-mediated phosphatidylglycerol lysinylation in the contexts of in vitro daptomycin (DAP) nonsuceptibility and (ii) the role of mprF mutation in endovascular virulence. We observed a correlation between increased expression of a mutant mprF gene and reduced in vitro DAP susceptibility. There were no detectable fitness differences between strains in experimental infective endocarditis.
Published ahead of print on 16 March 2009.
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