Susceptibility of a variety of clinical isolates to linezolid: a European inter-country comparison

被引:49
作者
Gemmell, CG [1 ]
机构
[1] Glasgow Royal Infirm, Dept Bacteriol, Glasgow G4 0SF, Lanark, Scotland
关键词
D O I
10.1093/jac/48.1.47
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Using standardized in vitro susceptibility tests, 3382 bacteria recently isolated from skin, blood or respiratory tract infections were analysed for their susceptibility to linezolid, a new oxazolidinone, and a number of comparator antibacterial agents. Isolates originated in France, Italy, Germany, Spain, Sweden, The Netherlands and the UK. Laboratories in each country independently conducted broth microdilution susceptibility tests using NCCLS methods and epsilonometry (Etest). Isolates of Gram-positive cocci tested in each laboratory included methicillin-susceptible and -resistant Staphylococcus aureus, methicillin-susceptible and -resistant Staphylococcus epidermidis, Streptococcus pyogenes, Streptococcus agalactiae, Streptococcus pneumoniae and Enterococcus spp. Isolates of Moraxella catarrhalis and Haemophilus influenzae were also included. Where appropriate, comparator drugs (oxacillin, vancomycin, gentamicin, co-amoxiclav, ciprofloxacin, erythromycin, penicillin G, clindamycin and ampicillin) were also tested. Linezolid demonstrated excellent activity against all of the Gram-positive cocci with MIC(50)s ranging from 0.5 to 4 mg/L. The drug demonstrated only modest activity against M. catarrhalis and H. influenzae with MIC(50)s ranging from 4 to 16 mg/L.
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页码:47 / 52
页数:6
相关论文
共 12 条
[1]  
FORD CW, 1996, ANTIMICROBIAL AGENTS, V40, P1608
[2]  
GEMMELL CG, 1997, 8 EUR C CLIN MICR IN, P289
[3]   In vitro antimicrobial activities and spectra of U-100592 and U-100766, two novel fluorinated oxazolidinones [J].
Jones, RN ;
Johnson, DM ;
Erwin, ME .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (03) :720-726
[4]  
JONES RN, 1999, 37 ANN M INF DIS SOC
[5]   In vitro activities of oxazolidinones U-100592 and U-100766 against penicillin-resistant and cephalosporin-resistant strains of Streptococcus pneumoniae [J].
Mason, EO ;
Lamberth, LB ;
Kaplan, SL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (04) :1039-1040
[6]   In vitro activities of two novel oxazolidinones (U100592 and U100766), a new fluoroquinolone (trovafloxacin), and dalfopristin-quinupristin against Staphylococcus aureus and Staphylococcus epidermidis [J].
Mulazimoglu, L ;
Drenning, SD ;
Yu, VL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (10) :2428-2430
[7]  
National Committee for Clinical Laboratory Standards, 1997, METH DIL ANT SUSC TE
[8]   In vitro activities of linezolid against important gram-positive bacterial pathogens including vancomycin-resistant enterococci [J].
Noskin, GA ;
Siddiqui, F ;
Stosor, V ;
Hacek, D ;
Peterson, LR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (08) :2059-2062
[9]   Mechanism of action of oxazolidinones: Effects of linezolid and eperezolid on translation reactions [J].
Shinabarger, DL ;
Marotti, KR ;
Murray, RW ;
Lin, AH ;
Melchior, EP ;
Swaney, SM ;
Dunyak, DS ;
Demyan, WF ;
Buysse, JM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (10) :2132-2136
[10]   OXAZOLIDINONES, A NEW CLASS OF SYNTHETIC ANTIBACTERIAL AGENTS - INVITRO AND INVIVO ACTIVITIES OF DUP-105 AND DUP-721 [J].
SLEE, AM ;
WUONOLA, MA ;
MCRIPLEY, RJ ;
ZAJAC, I ;
ZAWADA, MJ ;
BARTHOLOMEW, PT ;
GREGORY, WA ;
FORBES, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1987, 31 (11) :1791-1797