In vitro and in vivo activities of AM-1155, a new fluoroquinolone, against Chlamydia spp.

被引:53
作者
Miyashita, N [1 ]
Niki, Y [1 ]
Kishimoto, T [1 ]
Nakajima, M [1 ]
Matsushima, T [1 ]
机构
[1] KAWASAKI MED SCH, DEPT MED,DIV RESP DIS, KURASHIKI, OKAYAMA 70101, JAPAN
关键词
D O I
10.1128/AAC.41.6.1331
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The in vitro and in vivo activities of AM-1155, a new quinolone, against Chlamydia spp. were investigated, The MIC of AM-1155 for 10 standard strains of different Chlamydia spp. and 25 wild-type strains of Chlamydia pneumoniae isolated in Japan, which were morphologically different from clinical isolates from the United States, ranged from 0.063 to 0.125 mu g/ml. Its activity was almost the same as those of sparfloxacin and tosufloxacin and was 4 and 16 times superior to those of levofloxacin and ciprofloxacin, respectively, but lower than those of clarithromycin and minocycline (range for each, 0.016 to 0.031 mu g/ml). The minimal chlamydiacidal concentration of AM-1155 ranged from 0.063 to 0.125 mu g/ml, while those of clarithromycin and minocycline ranged from 0.016 to 0.031 mu g/ml and 0.016 to 0.063 mu g/ml, respectively, The therapeutic effect of a 7-day course of AM-1155 at doses of 5 and 10 mg/kg of body weight administered orally twice daily to mice with experimental Chlamydia psittaci pneumonia was excellent, with a 100% survival rate at 21 days after infection, The efficacy was equal to those of clarithromycin and minocycline and higher than those of ciprofloxacin and ofloxacin.
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页码:1331 / 1334
页数:4
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