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用于检测临床分离株中喹诺酮耐药性大肠杆菌的诊断性DNA微阵列的开发与验证

Development and validation of a diagnostic DNA microarray to detect quinolone-resistant Escherichia coli among clinical isolates.

作者信息

Yu Xiaolei, Susa Milorad, Knabbe Cornelius, Schmid Rolf D, Bachmann Till T

机构信息

Institute of Technical Biochemistry, University of Stuttgart, Allmandring 31, D-70569 Stuttgart, Germany.

出版信息

J Clin Microbiol. 2004 Sep;42(9):4083-91. doi: 10.1128/JCM.42.9.4083-4091.2004.

Abstract

The incidence of resistance against fluoroquinolones among pathogenic bacteria has been increasing in accordance with the worldwide use of this drug. Escherichia coli is one of the most relevant species for quinolone resistance. In this study, a diagnostic microarray for single-base-mutation detection was developed, which can readily identify the most prevalent E. coli genotypes leading to quinolone resistance. Based on genomic sequence analysis using public databases and our own DNA sequencing results, two amino acid positions (83 and 87) on the A subunit of the DNA gyrase, encoded by the gyrA gene, have been identified as mutation hot spots and were selected for DNA microarray detection. Oligonucleotide probes directed against these two positions were designed so that they could cover the most important resistance-causing and silent mutations. The performance of the array was validated with 30 clinical isolates of E. coli from four different hospitals in Germany. The microarray results were confirmed by standard DNA sequencing and were in full agreement with phenotypic antimicrobial susceptibility testing.

摘要

随着氟喹诺酮类药物在全球范围内的使用,病原菌对其耐药性的发生率一直在上升。大肠杆菌是对喹诺酮类耐药最相关的菌种之一。在本研究中,开发了一种用于单碱基突变检测的诊断微阵列,它可以很容易地识别导致喹诺酮耐药的最常见大肠杆菌基因型。基于使用公共数据库的基因组序列分析和我们自己的DNA测序结果,由gyrA基因编码的DNA回旋酶A亚基上的两个氨基酸位置(83和87)已被确定为突变热点,并被选择用于DNA微阵列检测。针对这两个位置设计了寡核苷酸探针,以便它们能够覆盖最重要的耐药性导致突变和沉默突变。用来自德国四家不同医院的30株临床分离大肠杆菌对该阵列的性能进行了验证。微阵列结果通过标准DNA测序得到证实,并且与表型抗菌药物敏感性测试完全一致。

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