In vitro activities of six new fluoroquinolones against Brucella melitensis

被引:35
作者
Trujillano-Martín, I
García-Sánchez, E
Martínez, IM
Fresnadillo, MJ
García-Sánchez, JE
García-Rodríguez, JA
机构
[1] Univ Hosp, Dept Microbiol & Parasitol, Salamanca, Spain
[2] Hosp Virgen Puerto, Unidad Microbiol, Plasencia, Caceres, Spain
关键词
D O I
10.1128/AAC.43.1.194
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have tested the in vitro activities of eight fluoroquinolones against 160 Brucella melitensis strains. The most active was sitafloxacin (MIC at which 90% of the isolates are inhibited [MIC90], 0.12 mu g/ml). In decreasing order, the activities (MIC(90)s) of the rest of the tested fluoroquinolones were as follows: levofloxacin, 0.5 mu g/ml; ciprofloxacin, trovafloxacin, and moxifloxacin, 1 mu g/ml; and ofloxacin, grepafloxacin. and gatifloxacin, 2 mu g/ml.
引用
收藏
页码:194 / 195
页数:2
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