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首页> 外文期刊>Mycopathologia >Clinical Itraconazole-Resistant Strains of Aspergillus fumigatus, Isolated Serially from a Lung Aspergilloma Patient with Pulmonary Tuberculosis, can be Detected with Real-Time PCR Method
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Clinical Itraconazole-Resistant Strains of Aspergillus fumigatus, Isolated Serially from a Lung Aspergilloma Patient with Pulmonary Tuberculosis, can be Detected with Real-Time PCR Method

机译:从肺结核曲霉患者肺结核中串行分离的烟曲霉临床抗伊曲康唑菌株可以通过实时PCR方法检测

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摘要

The invasive aspergillosis, which is commonly caused by Aspergillus fumigatus (A. fumigatus), has increased in recent years. Traditional methods for finding out antifungal resistant strains would take more than 2 weeks, which cannot satisfy the needs of rapid detection. In this study, a real-time PCR method for detection of the serial itraconazole-resistant strains of A. fumigatus isolated from a lung aspergilloma patient was developed. The results showed that the TacMAN-MGB probes, which were covered the loci Gly54, Leu98, Gly138, and Met220 of the enzyme CYP51A coded by the gene cyp51A, as well as the 34-bp tandem repeated sequence in the promoter region (288 and 322 from the start codon) of this gene, could detect the serial itraconazole-resistant strains of A. fumigatus in our study. Besides, this method takes just 6 h to complete the whole detection.
机译:近年来,侵袭性曲霉病通常由烟曲霉(A. fumigatus)引起。寻找抗真菌抗性菌株的传统方法将花费超过2周的时间,无法满足快速检测的需要。在这项研究中,开发了一种实时PCR方法,用于检测从肺曲霉病患者中分离出的烟曲霉系列伊曲康唑耐药菌株。结果显示,TacMAN-MGB探针覆盖了cyp51A基因编码的CYP51A酶CYP51A的基因座Gly54,Leu98,Gly138和Met220,以及启动子区域中的34 bp串联重复序列(288和从该基因的起始密码子开始的第322位),可以在我们的研究中检测到烟曲霉抗伊曲康唑的系列耐药菌株。此外,该方法仅需6小时即可完成整个检测。

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