首页> 外文期刊>Antimicrobial agents and chemotherapy. >Extra copies of the Aspergillus fumigatus squalene epoxidase gene confer resistance to terbinafine: genetic approach to studying gene dose-dependent resistance to antifungals in A. fumigatus.
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Extra copies of the Aspergillus fumigatus squalene epoxidase gene confer resistance to terbinafine: genetic approach to studying gene dose-dependent resistance to antifungals in A. fumigatus.

机译:烟曲霉角鲨烯环氧酶基因的额外拷贝赋予对特比萘芬的抗性:研究烟曲霉抗真菌药的基因剂量依赖性抗性的遗传方法。

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摘要

With the increasing use of antifungals such as amphotericin B, itraconazole, voriconazole, caspofungin, and terbinafine (TRB) in patients at high risk for invasive aspergillosis, resistance of Aspergillus fumigatus to these agents will ultimately emerge. Due to the limited availability of molecular genetics for A. fumigatus, few studies have addressed its mechanisms of resistance to antifungals. We transformed A. fumigatus protoplasts with a pyrG-based A. fumigatus genomic DNA library (constructed in the multicopy nonintegrating vector pRG3-AMA1-NotI, which also has the pyr-4 gene for selection). We obtained one pyrG(+) transformant that grew in medium containing a fungicidal concentration (0.625 microg/ml) of TRB. To determine whether TRB resistance in that transformant was plasmid dependent, we evicted the plasmid and found concomitant loss of uracil prototrophy and TRB resistance. DNA sequence analysis identified the gene responsible for TRB resistance as the A. fumigatus squalene epoxidase gene (ERG1), which encodes the target enzyme of TRB. Authentic A. fumigatus ERG1, amplified from the genome and cloned into pRG3-AMA1-NotI, also conferred TRB-specific resistance. This molecular approach has the potential to enhance our knowledge of the mechanisms of A. fumigatus resistance to modern antifungals.
机译:随着高侵袭性曲霉病高危患者中抗真菌药如两性霉素B,伊曲康唑,伏立康唑,卡泊芬净和特比萘芬(TRB)的使用,最终将出现烟曲霉对这些药物的耐药性。由于烟曲霉的分子遗传学有限,因此很少有研究探讨其对真菌的抗药性。我们用基于pyrG的烟曲霉基因组DNA文库(由多拷贝非整合型载体pRG3-AMA1-NotI构建,它也具有pyr-4基因供选择)转化了烟曲霉原生质体。我们获得了一个pyrG(+)转化子,该转化子在含有TRB杀真菌浓度(0.625微克/毫升)的培养基中生长。为了确定该转化体中的TRB抗性是否是质粒依赖性的,我们逐出了质粒,发现尿嘧啶原营养和TRB抗性同时丧失。 DNA序列分析确定了负责TRB抗性的基因为烟曲霉角鲨烯环氧酶基因(ERG1),该基因编码TRB的目标酶。从基因组扩增并克隆到pRG3-AMA1-NotI中的真实烟曲霉ERG1也具有TRB特异性抗性。这种分子方法有可能增强我们对烟曲霉对现代抗真菌药耐药机制的认识。

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