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首页> 外文期刊>Journal of bacteriology >Specific Chromosome Alterations in Fluconazole-Resistant Mutants of Candida albicans
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Specific Chromosome Alterations in Fluconazole-Resistant Mutants of Candida albicans

机译:白念珠菌耐氟康唑的突变体中的特定染色体改变

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摘要

The exposure of Candida albicans to fluconazole resulted in the nondisjunction of two specific chromosomes in 17 drug-resistant mutants, each obtained by an independent mutational event. The chromosomal changes occurred at high frequencies and were related to the duration of the drug exposure. The loss of one homologue of chromosome 4 occurred after incubation on a fluconazole medium for 7 days. A second change, the gain of one copy of chromosome 3, was observed after exposure for 35 or 40 days. We found that the mRNA levels of ERG11, CDR1, CDR2, andMDR1, the candidate fluconazole resistance genes, remained either the same or were diminished. The lack of overexpression of putative drug pumps or the drug target indicated that some other mechanism(s) may be operating. The fluconazole resistance phenotype, electrophoretic karyotypes, and transcript levels of mutants were stable after growth for 112 generations in the absence of fluconazole. This is the first report to demonstrate that resistance to fluconazole can be dependent on chromosomal nondisjunction. Furthermore, we suggest that a low-level resistance to fluconazole arising during the early stages of clinical treatment may occur by this mechanism. These results support our earlier hypothesis that changes in C. albicanschromosome number is a common means to control a resource of potentially beneficial genes that are related to important cellular functions.
机译:白色念珠菌暴露于氟康唑导致17个耐药突变体中的两个特定染色体不分离,每个突变体都是通过独立的突变事件获得的。染色体变化以高频发生,并且与药物暴露时间有关。在氟康唑培养基上孵育7天后,发生了第4号染色体一个同源物的丢失。暴露35或40天后观察到第二个变化,即3号染色体一个拷贝的获得。我们发现氟康唑抗性候选基因 ERG11 CDR1 CDR2 MDR1 的mRNA水平,保持不变或减少。缺乏假定药物泵的过度表达或药物靶标表明某些其他机制可能正在发挥作用。在不存在氟康唑的情况下生长112代后,突变体的氟康唑抗性表型,电泳核型和转录水平稳定。这是第一个证明对氟康唑的耐药性可能依赖于染色体非分离的报告。此外,我们建议通过这种机制可以在临床治疗的早期阶段对氟康唑产生低水平的耐药性。这些结果支持了我们先前关于 C发生变化的假设。白色念珠菌染色体数目是控制与重要细胞功能相关的潜在有益基因资源的常用手段。

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