Institut für Molekulare Infektionsbiologie, Universität Würzburg, Würzburg, Germany.
Mol Microbiol. 2012 Nov;86(3):539-56. doi: 10.1111/j.1365-2958.2012.08210.x. Epub 2012 Aug 28.
The pathogenic yeast Candida albicans can develop resistance to the widely used antifungal agent fluconazole, which inhibits ergosterol biosynthesis. Resistance is often caused by gain-of-function mutations in the transcription factors Mrr1, Tac1 and Upc2, which result in constitutive overexpression of multidrug efflux pumps and ergosterol biosynthesis genes respectively. It is not known how the permanently changed gene expression program in resistant strains affects their fitness in the absence of drug selection pressure. We have systematically investigated the effects of activating mutations in Mrr1, Tac1 and Upc2, individually and in all possible combinations, on the degree of fluconazole resistance and on the fitness of C. albicans in an isogenic strain background. All combinations of different resistance mechanisms resulted in a stepwise increase in drug resistance, culminating in 500-fold increased fluconazole resistance in strains possessing mutations in the three transcription factors and an additional resistance mutation in the drug target enzyme Erg11. The acquisition of resistance mutations was associated with reduced fitness under non-selective conditions in vitro as well as in vivo during colonization of a mammalian host. Therefore, without compensatory mutations, the inability to appropriately regulate gene expression results in a loss of competitive fitness of drug-resistant C. albicans strains.
条件致病真菌白色念珠菌可能对广泛使用的抗真菌药物氟康唑产生耐药性,氟康唑可抑制麦角固醇的生物合成。耐药性通常是由转录因子 Mrr1、Tac1 和 Upc2 的功能获得性突变引起的,这些突变分别导致多药外排泵和麦角固醇生物合成基因的组成型过表达。目前尚不清楚耐药菌株中永久性改变的基因表达程序如何影响它们在没有药物选择压力的情况下的适应性。我们系统地研究了 Mrr1、Tac1 和 Upc2 中的激活突变,分别和组合在不同条件下对氟康唑耐药程度和白色念珠菌同系菌株适应性的影响。不同耐药机制的所有组合都导致药物耐药性逐步增加,最终在三个转录因子发生突变且药物靶酶 Erg11 发生额外耐药突变的菌株中,氟康唑耐药性增加了 500 倍。获得耐药性突变与体外非选择性条件下以及哺乳动物宿主定植过程中的适应性降低有关。因此,如果没有补偿性突变,无法适当调节基因表达会导致耐药性白色念珠菌菌株丧失竞争适应性。