In vitro activities of linezolid against important gram-positive bacterial pathogens including vancomycin-resistant enterococci

被引:115
作者
Noskin, GA
Siddiqui, F
Stosor, V
Hacek, D
Peterson, LR
机构
[1] Northwestern Univ, Sch Med, Dept Med, Div Infect Dis, Chicago, IL 60611 USA
[2] Northwestern Univ, Sch Med, Dept Pathol, Clin Microbiol Div, Chicago, IL 60611 USA
[3] NW Mem Hosp, Dept Infect Control, Chicago, IL 60611 USA
[4] NW Mem Hosp, Dept Prevent & Clin Microbiol, Chicago, IL 60611 USA
关键词
D O I
10.1128/AAC.43.8.2059
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The emergence of resistance in gram-positive bacteria has necessitated a search for new antimicrobial agents. Linezolid is an oxazolidinone, a new class of antibacterial agents with enhanced activity against pathogens. We compared the activity of linezolid to those of other antimicrobial agents against 3,945 clinical isolates. Linezolid demonstrated potent activity against all isolates tested. For all vancomycin-susceptible enterococci, staphylococci, and streptococci, the activity of linezolid was comparable to that of vancomycin. Against oxacillin-resistant staphylococci and vancomycin-resistant enterococci, linezolid was the most active agent tested. In summary, linezolid appears to be a promising new antimicrobial agent for the treatment of gram-positive infections.
引用
收藏
页码:2059 / 2062
页数:4
相关论文
共 14 条
[1]   Stability of vancomycin-resistant enterococcal genotypes isolated from long-term-colonized patients [J].
Bonten, MJM ;
Hayden, MK ;
Nathan, C ;
Rice, TW ;
Weinstein, RA .
JOURNAL OF INFECTIOUS DISEASES, 1998, 177 (02) :378-382
[2]   Comparative in vitro and bactericidal activity of oxazolidinone antibiotics against multidrug-resistant enterococci [J].
Bostic, GD ;
Perri, MB ;
Thal, LA ;
Zervos, MJ .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1998, 30 (02) :109-112
[3]   MECHANISM OF ACTION AND INVITRO AND INVIVO ACTIVITIES OF S-6123, A NEW OXAZOLIDINONE COMPOUND [J].
DALY, JS ;
ELIOPOULOS, GM ;
WILLEY, S ;
MOELLERING, RC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (09) :1341-1346
[4]   ACTIVITY AND MECHANISM OF ACTION OF DUP-105 AND DUP-721, NEW OXAZOLIDINONE COMPOUNDS [J].
DALY, JS ;
ELIOPOULOS, GM ;
REISZNER, E ;
MOELLERING, RC .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1988, 21 (06) :721-730
[5]   Control of endemic glycopeptide-resistant enterococci [J].
Dembry, LM ;
Uzokwe, K ;
Zervos, MJ .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 1996, 17 (05) :286-292
[6]  
Dresser LD, 1998, PHARMACOTHERAPY, V18, P456
[7]   The oxazolidinone eperezolid binds to the 50S ribosomal subunit and competes with binding of chloramphenicol and lincomycin [J].
Lin, AH ;
Murray, RW ;
Vidmar, TJ ;
Marotti, KR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (10) :2127-2131
[8]  
*NATL COMM CLIN LA, 1997, M7A4 NATL COMM CLIN
[9]   Successful treatment of persistent vancomycin-resistant Enterococcus faecium bacteremia with linezolid and gentamicin [J].
Noskin, GA ;
Siddiqui, F ;
Stosor, V ;
Kruzynski, J ;
Peterson, LR .
CLINICAL INFECTIOUS DISEASES, 1999, 28 (03) :689-690
[10]   TESTS FOR BACTERICIDAL EFFECTS OF ANTIMICROBIAL AGENTS - TECHNICAL PERFORMANCE AND CLINICAL RELEVANCE [J].
PETERSON, LR ;
SHANHOLTZER, CJ .
CLINICAL MICROBIOLOGY REVIEWS, 1992, 5 (04) :420-432