In vitro activity of telithromycin and quinupristin/dalfopristin against methicillin-resistant coagulase-negative staphylococci with defined resistance genotypes

被引:7
作者
Novotna, G. [1 ]
Spizek, J. [1 ]
Janata, J. [1 ]
机构
[1] Acad Sci Czech Republic, Inst Microbiol, CR-14220 Prague, Czech Republic
关键词
D O I
10.1007/BF02932188
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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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页码:593 / 599
页数:7
相关论文
共 29 条
[1]   Distribution of genes encoding resistance to streptogramin A and related compounds among staphylococci resistant to these antibiotics [J].
Allignet, J ;
Aubert, S ;
Morvan, A ;
ElSolh, N .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (11) :2523-2528
[2]   Selection of ketolide resistance in Staphylococcus aureus [J].
Besier, S ;
Hunfeld, KP ;
Giesser, I ;
Schäfer, V ;
Brade, V ;
Wichelhaus, TA .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2003, 22 (01) :87-88
[3]   Ketolides lack inducibility properties of MLSB resistance phenotype [J].
Bonnefoy, A ;
Girard, AM ;
Agouridas, C ;
Chantot, JF .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 40 (01) :85-90
[4]   Effects of genes encoding resistance to streptogramins A and B on the activity of quinupristin-dalfopristin against Enterococcus faecium [J].
Bozdogan, B ;
Leclercq, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (11) :2720-2725
[5]  
Clinical and Laboratory Standards Institute (CLSI), 2007, PERF STAND ANT SUS S, P1987
[6]   Induction of telithromycin resistance by erythromycin in isolates of macrolide-resistant Staphylococcus spp. [J].
Davis, KA ;
Crawford, SA ;
Fiebelkorn, KR ;
Jorgensen, JH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (07) :3059-3061
[7]   Activity of a new oral streptogramin, XRP2868, against gram-positive cocci harboring various mechanisms of resistance to streptogramins [J].
Dupuis, M ;
Leclercq, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (01) :237-242
[8]   Patterns of phenotypic resistance to the macrolide-lincosamide-ketolide-streptogramin group of antibiotics in staphylococci [J].
Hamilton-Miller, JMT ;
Shah, S .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2000, 46 (06) :941-949
[9]   Clonal diversity among streptogramin A-resistant Staphylococcus aureus isolates collected in French hospitals [J].
Haroche, J ;
Morvan, A ;
Davi, M ;
Allignet, J ;
Bimet, F ;
El Solh, N .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (02) :586-591
[10]   PLASMID-MEDIATED RESISTANCE TO LINCOMYCIN BY INACTIVATION IN STAPHYLOCOCCUS-HAEMOLYTICUS [J].
LECLERCQ, R ;
CARLIER, C ;
DUVAL, J ;
COURVALIN, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1985, 28 (03) :421-424