Division of Infectious Diseases and Center for Microbial Interface Biology, The Ohio State University, Columbus, OH 43210, USA.
Parasitol Res. 2013 May;112(5):2095-9. doi: 10.1007/s00436-013-3274-x. Epub 2013 Feb 8.
The digenetic protozoan Leishmania is dependent on ergosterol synthesis for growth and viability. We compared the in vitro activity of ergosterol synthesis inhibitor voriconazole with fluconazole and ketoconazole against cutaneous and visceral Leishmania species. We found the IC50 of voriconazole was comparable to ketoconazole and both were superior to fluconazole. Both ketoconazole and voriconazole were active against insect and mammalian stage parasites. This is the first report of the in vitro activity of voriconazole against leishmanial species.
双生原生动物利什曼原虫的生长和存活依赖于麦角固醇合成。我们比较了体外麦角固醇合成抑制剂伏立康唑与氟康唑和酮康唑对皮肤利什曼原虫和内脏利什曼原虫的活性。我们发现伏立康唑的 IC50 与酮康唑相当,两者均优于氟康唑。酮康唑和伏立康唑对昆虫和哺乳动物阶段的寄生虫均具有活性。这是首次报道伏立康唑对利什曼原虫的体外活性。