Hawser S, Francolini M, Islam K
Lepetit Research Center, Marion Merrell Dow Research Institute, Varese, Italy.
J Antimicrob Chemother. 1996 Oct;38(4):579-87. doi: 10.1093/jac/38.4.579.
The effects of antifungal agents, with different mechanisms of action, on the morphogenetic transformation by synchronised yeast-phase Candida albicans cells in vitro and their respective anti-Candida activities are described. MIC data demonstrated that the azoles, amphotericin B and echinocandin were the most active agents against four C. albicans strains. Morphogenetic transformation experiments demonstrated that amphotericin B was significantly better at preventing the transformation, under a variety of test conditions, than the azoles and flucytosine: amphotericin B abolished the transformation at low concentrations while the azoles only prevented the morphogenetic transformation at much higher concentrations (> 100 x MIC).
描述了具有不同作用机制的抗真菌剂对体外同步酵母相白色念珠菌细胞形态发生转化的影响及其各自的抗念珠菌活性。最低抑菌浓度(MIC)数据表明,唑类、两性霉素B和棘白菌素是对四种白色念珠菌菌株最具活性的药物。形态发生转化实验表明,在各种测试条件下,两性霉素B在预防转化方面明显优于唑类和氟胞嘧啶:两性霉素B在低浓度时就能消除转化,而唑类只有在高得多的浓度(>100×MIC)时才能预防形态发生转化。