Hector Richard F, Davidson Autumn P, Johnson Suzanne M
Department of Epidemiology and Biostatistics, University of California, San Francisco, CA 94143, USA.
Am J Vet Res. 2005 Jun;66(6):1090-3. doi: 10.2460/ajvr.2005.66.1090.
To evaluate and compare the in vitro antifungal properties of lufenuron and nikkomycin Z against isolates of Coccidioides immitis and Aspergillus fumigatus when used singly and in combination with the azole antifungal agent itraconazole.
3 clinical isolates of A fumigatus and the Silveira strain of C immitis.
The fungal isolates were tested in vitro for susceptibility to the single and combination of compounds by use of microtiter-format susceptibility methods. Minimum inhibitory concentration end points were determined visually, and the contents of representative wells were examined microscopically for evidence of morphologic effects on fungi.
No evidence of inhibition, either by susceptibility testing or direct microscopic examination of treated cells, was obtained with lufenuron under experimental conditions. In contrast, nikkomycin Z, a known inhibitor of fungal chitin synthesis, had potent activity against C immitis when used singly. A synergistic interaction between nikkomycin Z and itraconazole was found against isolates of both species tested.
On the basis of our in vitro data, lufenuron does not appear to possess antifungal properties.
评估并比较虱螨脲和多氧霉素Z单独使用以及与唑类抗真菌药伊曲康唑联合使用时,对粗球孢子菌和烟曲霉分离株的体外抗真菌特性。
3株烟曲霉临床分离株和粗球孢子菌的西尔韦拉菌株。
采用微量滴定板药敏试验方法,对真菌分离株进行体外单一化合物及联合用药的敏感性测试。通过肉眼观察确定最低抑菌浓度终点,并对代表性孔中的内容物进行显微镜检查,以寻找真菌形态学效应的证据。
在实验条件下,通过药敏试验或对处理细胞的直接显微镜检查,均未发现虱螨脲有抑制作用的证据。相比之下,已知的真菌几丁质合成抑制剂多氧霉素Z单独使用时,对粗球孢子菌有强效活性。发现多氧霉素Z与伊曲康唑对两种受试菌的分离株均有协同相互作用。
根据我们的体外数据,虱螨脲似乎不具有抗真菌特性。