In Vitro activity of telithromycin and quinupristin/dalfopristin against methicillin-resistant coagulase-negative staphylococci with defined resistance genotypes
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  • 作者:G. Novotná (1)
    J. Spí?ek (1)
    J. Janata (1)
  • 刊名:Folia Microbiologica
  • 出版年:2007
  • 出版时间:November 2007
  • 年:2007
  • 卷:52
  • 期:6
  • 页码:593-599
  • 全文大小:265KB
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  • 作者单位:G. Novotná (1)
    J. Spí?ek (1)
    J. Janata (1)

    1. Institute of Microbiology, Academy of Sciences of the Czech Republic, 142 20, Prague, Czechia
文摘
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 constitutiveerm genes) or demonstrated telithromycin D-shaped zone (60 isolates with induciblemsr(A) and/orerm). However, the level of inducible resistance conferred bymsr(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- mg/L) and two isolates resistant (MIC = 8 mg/L) if tested by E-test. All these isolates were resistant to streptogramin A and harboredvga(A) gene (1 isolate) orvga(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- mg/L in 4 isolates) than for streptogramin A-resistant isolates susceptible to streptogramin B (MIC = 0.5- mg/L in 16 isolates). In addition toS. haemolyticus, vga(A)LC was newly identified inS. epidermidis andS. 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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