4.7 Article

Correlation of daptomycin bactericidal activity and membrane depolarization in Staphylococcus aureus

Journal

ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
Volume 47, Issue 8, Pages 2538-2544

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.47.8.2538-2544.2003

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Funding

  1. NIAID NIH HHS [AI48354] Funding Source: Medline

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The objective of this study was to further elucidate the role of membrane potential in the mechanism of action of daptomycin, a novel lipopeptide antibiotic. Membrane depolarization was measured by both fluorimetric and flow cytometric assays. Adding daptomycin (5 mug/ml) to Staphylococcus aureus gradually dissipated membrane potential. In both assays, cell viability was reduced by >99% and membrane potential was reduced by >90% within 30 min of adding daptomycin. Cell viability decreased in parallel with changes in membrane potential, demonstrating a temporal correlation between bactericidal activity and membrane depolarization. Decreases in viability and potential also showed a dose-dependent correlation. Depolarization is indicative of ion movement across the cytoplasmic membrane. Fluorescent probes were used to demonstrate Ca2+-dependent, daptomycin-triggered potassium release from S. aureus. Potassium release was also correlated with bactericidal activity. This study demonstrates a clear correlation between dissipation of membrane potential and the bactericidal activity of daptomycin. A multistep model for daptomycin's mechanism of action is proposed.

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