Daptomycin activity and spectrum: a worldwide sample of 6737 clinical Gram-positive organisms

被引:106
作者
Streit, JM
Jones, RN
Sader, HS
机构
[1] JONES Grp JMI Labs Inc, N Liberty, IA 52317 USA
[2] Tufts Univ, Sch Med, Boston, MA 02111 USA
关键词
resistance; glycopeptides; multidrug-resistant;
D O I
10.1093/jac/dkh143
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Increasing antimicrobial resistance among bacterial pathogens has prompted attempts to develop new antimicrobial agents active against multidrug-resistant Gram-positive pathogens. Objectives: To evaluate the in vitro activity of daptomycin against a worldwide collection of clinical bacterial isolates. Methods: Daptomycin is a novel cyclic lipopeptide recently approved by the United States Food and Drug Administration. Daptomycin and selected comparators were tested against 6737 clinical Gram-positive strains from more than 70 centres located in Europe, North America and South America. Results: The overall distribution of daptomycin MIC values were in the range less than or equal to0.12-8 mg/L and 99.4% of all strains were inhibited at less than or equal to2 mg/L. Despite resistances to other antimicrobial agents, >99.9% of staphylococcal isolates were inhibited at less than or equal to1 mg/L of daptomycin (MIC90 0.5 mg/L for staphylococci). Streptococcal isolates were very susceptible to daptomycin independent of their susceptibility to penicillin. MIC50/90 values were less than or equal to0.12 and 0.25 mg/L, respectively. Enterococci showed the highest daptomycin MIC values, but all isolates tested were inhibited at less than or equal to4 mg/L (except for one Enterococcus faecium isolate which showed a daptomycin MIC of 8 mg/L). Conclusions: Daptomycin exhibited excellent in vitro activity against a wide spectrum of Gram-positive organisms and may represent a therapeutic option for infections caused by multidrug-resistant pathogens worldwide.
引用
收藏
页码:669 / 674
页数:6
相关论文
共 10 条
[1]   Baseline study to determine in vitro activities of daptomycin against gram-positive pathogens isolated in the United States in 2000-2001 [J].
Critchley, IA ;
Blosser-Middleton, RS ;
Jones, ME ;
Thornsberry, C ;
Sahm, DF ;
Karlowsky, JA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (05) :1689-1693
[2]  
*CUB PHARM INC, 2003, CUB DAPT INJ
[3]   Pharmacodynamic profile of daptomycin against Enterococcus species and methicillin-resistant Staphylococcus aureus in a murine thigh infection model [J].
Dandekar, PK ;
Tessier, PR ;
Williams, P ;
Nightingale, CH ;
Nicolau, DP .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 52 (03) :405-411
[4]   Daptomycin pharmacokinetics and safety following administration of escalating doses once daily to healthy subjects [J].
Dvorchik, BH ;
Brazier, D ;
DeBruin, MF ;
Arbeit, RD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (04) :1318-1323
[5]   Daptomycin susceptibility tests: interpretive criteria, quality control, and effect of calcium on in vitro tests [J].
Fuchs, PC ;
Barry, AL ;
Brown, SD .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2000, 38 (01) :51-58
[7]  
*NCCLS, 2003, M100S13 NCCLS
[8]  
NCCLS, 2003, M7A6 NCCLS
[9]   Correlation of daptomycin bactericidal activity and membrane depolarization in Staphylococcus aureus [J].
Silverman, JA ;
Perlmutter, NG ;
Shapiro, HM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (08) :2538-2544
[10]  
Thorne Grace M., 2002, Clinical Microbiology Newsletter, V24, P33, DOI 10.1016/S0196-4399(02)80007-1