Molecular Determinants of Antibiotic Resistance in Methicillin-Resistant Staphylococcus aureus (MRSA)
A special issue of Antibiotics (ISSN 2079-6382). This special issue belongs to the section "Mechanism and Evolution of Antibiotic Resistance".
Deadline for manuscript submissions: closed (30 December 2022) | Viewed by 9896
Special Issue Editor
Interests: methicillin-resistant S. aureus (MRSA); antimicrobial resistance; novel targets against MRSA; biofilm inhibition; quorum sensing inhibition (QSI)
Special Issues, Collections and Topics in MDPI journals
Special Issue Information
Dear Colleagues,
Methicillin-resistant Staphylococcus aureus (MRSA) is one of the most common human bacterial pathogens, causing simple soft skin infections to severe pneumonia. Several antibiotics with different mechanisms of action such as ceftaroline, vancomycin, linezolid, and daptomycin have been introduced to treat MRSA infections. However, antimicrobial resistance has emerged in many S. aureus clones around the world, in both hospital and community settings. This antibiotic resistance can be due to different mechanisms such as target modification where antibiotics bind (PBP2a), mutation of the target site (mutation in PBP4, PBP2a, gdpP), drug inactivation through enzymes (β-lactamase hydrolyzes penicillin), or the prevention of drug accumulation or efflux (decreased membrane permeability or increased efflux by efflux pump). Thus, understanding the molecular mechanisms of antibiotic resistance is important for the development of antibiotics with novel mechanisms of action and molecular detection methods of antibiotic resistance.
For this Special Issue, we invite you to contribute original research, case reports, and review papers elucidating the molecular basis of antibiotic resistance in S. aureus. Novel computational approaches for antimicrobial resistance determination and genomic characterization will also be considered.
Dr. Harshad Lade
Guest Editor
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Keywords
- Staphylococcus aureus
- MRSA
- antimicrobial resistance
- β-lactams
- mecA
- PBP2a
- efflux pump
- auxiliary factors
- antibiotic targets
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