Phelouzat M A, Lawrence F, Robert-Gero M
Institut de Chimie des Substances Naturelles, CNRS, Gif sur Yvette, France.
Parasitol Res. 1993;79(8):683-9. doi: 10.1007/BF00932511.
Promastigotes resistant to sinefungin (SF), a nucleoside antibiotic that is structurally related to S-adenosylmethionine (AdoMet), were obtained starting from two cloned strains of Leishmania donovani. The resistance was induced by increasing the drug pressure gradually until promastigotes capable of growing in the presence of concentrations 10,000 times higher than the 50% growth-inhibitory (IC50) values for the control cells were obtained. The resistance to SF of both clones was specific and stable in the absence of drug pressure. High-performance liquid chromatographic (HPLC) analyses indicated highly reduced levels of SF in the two resistant clones. However, the intracellular SF concentration in these resistant cells was much higher than the IC50 values for wild-type cells. In one clone, the decreased drug uptake was coupled to a decrease in the affinity of two protein methylases for SF, whereas in the other clone the biosynthesis of polyamine precursors was modified. This study demonstrates that resistance to a drug molecule with pleiotropic targets can be developed through various mechanisms by different strains.
从杜氏利什曼原虫的两个克隆菌株出发,获得了对辛二胍(SF)具有抗性的前鞭毛体。辛二胍是一种核苷抗生素,其结构与S-腺苷甲硫氨酸(AdoMet)相关。通过逐渐增加药物压力来诱导抗性,直到获得能够在比对照细胞的50%生长抑制(IC50)值高10000倍的浓度下生长的前鞭毛体。在没有药物压力的情况下,两个克隆对SF的抗性都是特异性且稳定的。高效液相色谱(HPLC)分析表明,两个抗性克隆中SF的水平大幅降低。然而,这些抗性细胞中的细胞内SF浓度远高于野生型细胞的IC50值。在一个克隆中,药物摄取的减少与两种蛋白质甲基化酶对SF的亲和力降低有关,而在另一个克隆中,多胺前体的生物合成发生了改变。这项研究表明,不同菌株可以通过多种机制对具有多效性靶点的药物分子产生抗性。