Multi-laboratory assessment of the linezolid spectrum of activity using the Kirby-Bauer disk diffusion method:: Report of the Zyvox® Antimicrobial Potency Study (ZAPS) in the United States

被引:81
作者
Jones, RN [1 ]
Ballow, CH
Biedenbach, DJ
机构
[1] Jones Grp, JMI Labs, N Liberty, IA 52317 USA
[2] Buffalo Clin Res Ctr, Buffalo, NY USA
关键词
D O I
10.1016/S0732-8893(01)00235-8
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The in vitro activity of linezolid against common Gram-positive pathogens was compared to that of penicillin or ampicillin or oxacillin (depending upon genus), cefazolin, erythromycin, clindamycin, quinupristin/dalfopristin, levofloxacin, nitrofurantoin and vancomycin by disk diffusion methods. One hundred and six centers (31 states in US) tested recent clinical isolates of Staphylococcus aureus coagulase-negative staphylococci, Enterococcus faecium, E. faecalis, Streptococcus pneumoniae, and other streptococci. Testing was conducted using the standardized disk diffusion method and concurrent quality control testing was performed. Strains with linezolid zone diameters of less than or equal to 20 mm were requested for referral to the microbiology monitor for confirmation. A total of 3,100 isolates (97% compliance) were tested. Susceptibility (zone diameters, greater than or equal to 21 mm) of staphylococci and streptococci to linezolid was reported in 100% and 99.4% of staphylococci and streptococci, respectively. Susceptibility (zone diameters, greater than or equal to 23 mm) of enterococci to linezolid was 96.0% with only three isolates (0.4%) reported as resistant (zone diameters, less than or equal to 20 mm; unconfirmed). Among a total of nine isolates (0.3%) reported to have zone diameters 20 mm, six were not submitted for further testing, two were contaminated with Gram-negative bacilli and one was determined to be linezolid-susceptible. There were no differences in linezolid susceptibility in the vancomycin- or oxacillin- or penicillin-resistant subsets of strains. This susceptibility pattern for US medical centers is indicative of the excellent and nearly complete in vitro activity against the key Gram-positive pathogens for which linezolid has received US Food and Drug Administration indications for clinical use. (C) 2001 Elsevier Science Inc. All rights reserved.
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页码:59 / 66
页数:8
相关论文
共 31 条
[1]   Association between decreased susceptibility to a new antibiotic for treatment of human diseases, everninomicin (SCH 27899), and resistance to an antibiotic used for growth promotion in animals, avilamycin [J].
Aarestrup, FM .
MICROBIAL DRUG RESISTANCE, 1998, 4 (02) :137-141
[2]  
[Anonymous], M100S11 NCCLS
[3]  
[Anonymous], 2000, M2A7 NCCLS
[4]   Gram-positive resistance: challenge for the development of new antibiotics [J].
Baquero, F .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 39 :1-6
[5]   Disk diffusion test interpretive criteria and quality control recommendations for testing linezolid (U-100766) and eperezolid (U-100592) with commercially prepared reagents [J].
Biedenbach, DJ ;
Jones, RN .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (12) :3198-3202
[6]  
Brickner SJ, 1996, CURR PHARM DESIGN, V2, P175
[7]   Synthesis and antibacterial activity of U-100592 and U-100766, two oxazolidinone antibacterial agents for the potential treatment of multidrug-resistant Gram-positive bacterial infections [J].
Brickner, SJ ;
Hutchinson, DK ;
Barbachyn, MR ;
Manninen, PR ;
Ulanowicz, DA ;
Garmon, SA ;
Grega, KC ;
Hendges, SK ;
Toops, DS ;
Ford, CW ;
Zurenko, GE .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (03) :673-679
[8]   Decreased susceptibility of Streptococcus pneumoniae to fluoroquinolones in Canada [J].
Chen, DK ;
McGeer, A ;
de Azavedo, JC ;
Low, DE .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (04) :233-239
[9]   Emergence of increased resistance to quinupristin/dalfopristin during therapy for Enterococcus faecium bacteremia [J].
Chow, JW ;
Donabedian, SM ;
Zervos, MJ .
CLINICAL INFECTIOUS DISEASES, 1997, 24 (01) :90-91
[10]   Emerging resistance to antimicrobial agents in gram-positive bacteria - Enterococci, staphylococci and nonpneumococcal streptococci [J].
Cormican, MG ;
Jones, RN .
DRUGS, 1996, 51 :6-12