Susceptibilities of Legionella spp. to newer antimicrobials in vitro

被引:94
作者
Schülin, T
Wennersten, CB
Ferraro, MJ
Moellering, RC
Eliopoulos, GM
机构
[1] Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] Massachusetts Gen Hosp, Boston, MA 02114 USA
关键词
D O I
10.1128/AAC.42.6.1520
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The in vitro activities of 13 antimicrobial agents against 30 strains of legionella spp. were determined. Rifapentine, rifampin, and clarithromycin were the most potent agents (MICs at which 90% of isolates are inhibited [MIC(90)s], less than or equal to 0.008 mu g/ml). The ketolide HMR 3647 and the fluoroquinolones levofloxacin and BAY 12-8039 (MIC(90)s, 0.03 to 0.06 mu g/ml) were more active than erythromycin A or roxithromycin. The MIC(90)s of dalfopristin-quinupristin and linezolid were 0.5 and 8 mu g/ml, respectively. Based on class characteristics and in vitro activities, several of these agents may have potential roles in the treatment of Legionella infections.
引用
收藏
页码:1520 / 1523
页数:4
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