In vitro activity of telithromycin and quinupristin/dalfopristin against methicillin-resistant coagulase-negative staphylococci with defined resistance genotypes
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
18450221
DOI
10.1007/bf02932188
Knihovny.cz E-resources
- MeSH
- Anti-Bacterial Agents pharmacology MeSH
- Drug Resistance, Bacterial genetics MeSH
- Erythromycin pharmacology MeSH
- Ketolides pharmacology MeSH
- Clindamycin pharmacology MeSH
- Coagulase metabolism MeSH
- Macrolides pharmacology MeSH
- Microbial Sensitivity Tests MeSH
- Methicillin Resistance drug effects MeSH
- Staphylococcus drug effects MeSH
- Streptogramin A pharmacology MeSH
- Streptogramin B pharmacology MeSH
- Virginiamycin pharmacology MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Anti-Bacterial Agents MeSH
- Erythromycin MeSH
- Ketolides MeSH
- Clindamycin MeSH
- Coagulase MeSH
- Macrolides MeSH
- quinupristin-dalfopristin MeSH Browser
- Streptogramin A MeSH
- Streptogramin B MeSH
- telithromycin MeSH Browser
- Virginiamycin MeSH
We determined the activities of new antibiotics telithromycin (ketolide) and quinupristin/dalfopristin (streptogramins) against 88 macrolide and/or lincosamide resistant coagulase-negative staphylococci (CoNS) isolates with defined resistance gene status. Telithromycin susceptibility was determined only in erythromycin-sensitive isolates (15) indicating the same mechanisms of resistance. In contrast, all erythromycin-resistant isolates (73) were either constitutively resistant to telithromycin (13 isolates with constitutive erm genes) or demonstrated telithromycin D-shaped zone (60 isolates with inducible msr(A) and/or erm). However, the level of inducible resistance conferred by msr(A) (35 isolates) was borderline even after induction by erythromycin. No quinupristin/dalfopristin resistant isolate was observed if tested by disk-diffusion method (DDM) but 18 isolates were intermediate (MIC = 1-3 mg/L) and two isolates resistant (MIC = 8 mg/L) if tested by E-test. All these isolates were resistant to streptogramin A and harbored vga(A) gene (1 isolate) or vga(A)LC gene (19 isolates). MICs for quinupristin/dalfopristin were higher for isolates with combination of streptogramin A resistance and constitutive MLSB resistance (MIC = 3-8 mg/L in 4 isolates) than for streptogramin A-resistant isolates susceptible to streptogramin B (MIC = 0.5-2 mg/L in 16 isolates). In addition to S. haemolyticus, vga(A)LC was newly identified in S. epidermidis and S. warnerii indicating its widespread occurrence in CoNS. Misidentification of low-level resistant isolates by DDM may contribute to dissemination of streptogramin A resistance.
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