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In vitro susceptibility of chromoblastomycosis and phaeohyphomycosis agents to antifungal drugs
被引:21
|作者:
Caligiorne, RB
Resende, MA
Melillo, PHC
Peluso, CP
Carmo, FHS
Azevedo, V
机构:
[1] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Microbiol, BR-31270901 Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Biol Geral, Belo Horizonte, MG, Brazil
关键词:
antifungal drugs;
chromoblastomycosis;
dematiaceous fungi;
phaeohyphomycosis;
D O I:
10.1046/j.1365-280X.1999.00245.x
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
The in vitro susceptibility of chromoblastomycosis and phaeohyphomycosis agents to antifungal drugs was appraised using the reference macrodilution method proposed by the National Committee for Clinical Laboratory Standards (NCCLS) for yeasts modified for filamentous fungi. The antifungal drugs amphotericin B, 5-fluorocytosine, itraconazole and fluconazole were tested against one environmental and 18 clinical isolates. This work amended the macrodilution methods proposed by NCCLS and suggests that a conidial suspension free of hyphae leads to a more reliable assay and provides for better reproducibility. The macrodilution method was performed with 10(4) conidia ml(-1). The MIC values ranged from 1.0 to 16.0 mu g ml(-1) for amphotericin B and 3.12 to 25.0 mu g ml(-1) for 5-fluorocytosine. A MIC range of 0.06 to 1.95 mu g ml(-1) was determined for itraconazole while 2.0 to 64.0 mu g ml(-1) was detected for fluconazole.
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页码:405 / 409
页数:5
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