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首页> 外文期刊>International journal of antimicrobial agents >Deciphering azole resistance mechanisms with a focus on transcription factor-encoding genes TAC1, MRR1 and UPC2 in a set of fluconazole-resistant clinical isolates of Candida albicans
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Deciphering azole resistance mechanisms with a focus on transcription factor-encoding genes TAC1, MRR1 and UPC2 in a set of fluconazole-resistant clinical isolates of Candida albicans

机译:在白色念珠菌耐氟康唑的临床分离物中,重点研究转录因子编码基因TAC1,MRR1和UPC2的吡咯抗性机制

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摘要

Several and often combined mechanisms can lead to acquired azole resistance in Candida albicans and subsequent therapeutic failure. The aim of this study was to provide a complete overview of the molecular basis of azole resistance in a set of six C. albicans clinical isolates recovered from patients who failed azole therapy. For this purpose, expression levels of CDR1, MDR1 and ERG11 were investigated by reverse transcription PCR (RT-PCR) together with amplification and sequencing of the genes encoding their transcription factors TAC1, MRR1 and UPC2. In all, the data underline that azole resistance in this set of clinical isolates results from distinct, often combined, mechanisms, being mostly driven by CDR1 and/or MDR1 active efflux. We show that gain-of-function (GOF) mutations in the transcription-factor-encoding genes TAC1, MRR1 and UPC2 are a common event in azole-resistant C. albicans clinical isolates. In addition, together with the finding that these genes are highly permissive to nucleotide changes, we describe several novel mutations that could act as putative GOF mutations involved in fluconazole resistance.
机译:几种通常结合的机制可能导致白色念珠菌获得性唑耐药,并随后导致治疗失败。这项研究的目的是提供从唑治疗失败的患者中回收的六种白色念珠菌临床分离株中对唑耐药性分子基础的完整概述。为此,通过逆转录PCR(RT-PCR)以及编码其转录因子TAC1,MRR1和UPC2的基因的扩增和测序研究了CDR1,MDR1和ERG11的表达水平。总之,数据强调了这组临床分离株中的唑耐药性来自不同的,通常是组合的机制,主要由CDR1和/或MDR1活性外排驱动。我们显示在转录因子编码基因TAC1,MRR1和UPC2中的功能获得(GOF)突变是在耐唑的白色念珠菌临床分离株中的常见事件。此外,连同发现这些基因高度允许核苷酸变化的发现,我们描述了一些新的突变,这些突变可能充当与氟康唑耐药有关的推定GOF突变。

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