Molecular Mechanisms of Drug Resistance in <i>Staphylococcus aureus</i>

oleh: Beata Mlynarczyk-Bonikowska, Cezary Kowalewski, Aneta Krolak-Ulinska, Wojciech Marusza

Format: Article
Diterbitkan: MDPI AG 2022-07-01

Deskripsi

This paper discusses the mechanisms of <i>S. aureus</i> drug resistance including: (1) introduction. (2) resistance to beta-lactam antibiotics, with particular emphasis on the <i>mec</i> genes found in the <i>Staphylococcaceae</i> family, the structure and occurrence of SCC<i>mec</i> cassettes, as well as differences in the presence of some virulence genes and its expression in major epidemiological types and clones of HA-MRSA, CA-MRSA, and LA-MRSA strains. Other mechanisms of resistance to beta-lactam antibiotics will also be discussed, such as mutations in the <i>gdpP</i> gene, BORSA or MODSA phenotypes, as well as resistance to ceftobiprole and ceftaroline. (3) Resistance to glycopeptides (VRSA, VISA, hVISA strains, vancomycin tolerance). (4) Resistance to oxazolidinones (mutational and enzymatic resistance to linezolid). (5) Resistance to MLS-B (macrolides, lincosamides, ketolides, and streptogramin B). (6) Aminoglycosides and spectinomicin, including resistance genes, their regulation and localization (plasmids, transposons, class I integrons, SCC<i>mec</i>), and types and spectrum of enzymes that inactivate aminoglycosides. (7). Fluoroquinolones (8) Tetracyclines, including the mechanisms of active protection of the drug target site and active efflux of the drug from the bacterial cell. (9) Mupirocin. (10) Fusidic acid. (11) Daptomycin. (12) Resistance to other antibiotics and chemioterapeutics (e.g., streptogramins A, quinupristin/dalfopristin, chloramphenicol, rifampicin, fosfomycin, trimethoprim) (13) Molecular epidemiology of MRSA.