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CC BY V4.0, Open Access
Journal article
Molecular mechanisms of resistance and tolerance of Staphylococcus aureus to daptomycin
International journal of antimicrobial agents, Vol.67(1), 107678
2025
PMID: 41297715
Appears in Open Access via Read & Publish Agreements
Abstract
Daptomycin is a cyclic lipopeptide antimicrobial used against gram-positive pathogens, including Staphylococcus aureus. Daptomycin relies on physiological calcium to anchor onto bacterial membranes and sequester lipid II, overproducing reactive oxygen species resulting in cell death. Although daptomycin is thought to be effective against approximately 80% of S. aureus, treatment failure can arise from resistant or tolerant cells. Daptomycin-resistant S. aureus typically acquires mutations in the multiple peptide resistance factor (MprF) to overproduce cationic lysyl-phosphatidylglycerol located on the outer membrane. The increase in positive cell surface charge inhibits daptomycin binding via electrostatic repulsion. Upon exposure to higher daptomycin concentrations, S. aureus may undergo further peptidoglycan modifications to attenuate daptomycin activity. These alterations can also be driven by the crosstalk in the signal transduction systems. Furthermore, the pathways in daptomycin resistance appear to overlap with tolerance which is understudied in S. aureus. In this review, we explore the current understanding of the complex interplay of molecular mechanisms involved in daptomycin resistance and tolerance in S. aureus.
Details
- Title
- Molecular mechanisms of resistance and tolerance of Staphylococcus aureus to daptomycin
- Authors/Creators
- Candice Lim - School of Medical, Molecular, and Forensic Sciences, Murdoch University, AustraliaGeoffrey W. Coombs - Murdoch UniversityShakeel Mowlaboccus - School of Medical, Molecular, and Forensic Sciences, Murdoch University, Australia
- Publication Details
- International journal of antimicrobial agents, Vol.67(1), 107678
- Publisher
- Elsevier Ltd.
- Identifiers
- 991005830078807891
- Copyright
- © 2025 The Author(s)
- Murdoch Affiliation
- Centre for Biosecurity and One Health; School of Medical, Molecular and Forensic Sciences
- Language
- English
- Resource Type
- Journal article
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