微生物学
卡斯波芬金
两性霉素B
粘菌素
伏立康唑
最小抑制浓度
囊性纤维化
生物
药理学
抗生素
抗真菌
遗传学
作者
Haemi P. Schemuth,S. Dittmer,Michaela Lackner,Ludwig Sedlacek,Axel Hamprecht,Eike Steinmann,Jan Buer,P.‐M. Rath,Joerg Steinmann
出处
期刊:Mycoses
[Wiley]
日期:2012-11-22
卷期号:56 (3): 297-303
被引量:29
摘要
Summary Because published reports indicate that the antibiotic colistin (COL) has antifungal properties, this study investigated the antifungal in vitro activity of COL as single agent and in combination with the antifungal compounds voriconazole (VRC), caspofungin (CAS) and amphotericin B (AMB) against Scedosporium/Pseudallescheria spp., Exophiala dermatitidis and Geosmithia argillacea . In total, susceptibility was determined for 77 Scedosporium/Pseudallescheria spp., 82 E. dermatitidis and 17 G. argillacea isolates. The minimal inhibitory concentrations (MICs) of COL and the antifungals as single compound and in combination were determined with MIC test strips. Drug interactions were detected by crossing the MIC test strips at a 90º angle. The fractional inhibitory concentration index was used to categorise the drugs’ interaction. The MIC 50 value of COL was 12 μg ml −1 for S. prolificans , 16 μg ml −1 for P. apiosperma , 16 μg ml −1 for P. boydii , 12 μg ml −1 for E. dermatiditis and 6 μg ml −1 for G. argillacea . VRC was the most active drug in combination without any antagonism with the exception of few P. boydii isolates. COL as single agent and in most combinations with antifungals exhibits in vitro antifungal activity against filamentous ascomycetes occurring in cystic fibrosis patients and may offer a novel therapeutic option, especially for multidrug‐resistant S. prolificans .
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