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基于微阵列的革兰氏阳性菌90种抗生素抗性基因检测

Microarray-based detection of 90 antibiotic resistance genes of gram-positive bacteria.

作者信息

Perreten Vincent, Vorlet-Fawer Lorianne, Slickers Peter, Ehricht Ralf, Kuhnert Peter, Frey Joachim

机构信息

Institute of Veterinary Bacteriology, University of Berne, Längass-Strasse 122, Postfach, CH-3001 Bern, Switzerland.

出版信息

J Clin Microbiol. 2005 May;43(5):2291-302. doi: 10.1128/JCM.43.5.2291-2302.2005.

Abstract

A disposable microarray was developed for detection of up to 90 antibiotic resistance genes in gram-positive bacteria by hybridization. Each antibiotic resistance gene is represented by two specific oligonucleotides chosen from consensus sequences of gene families, except for nine genes for which only one specific oligonucleotide could be developed. A total of 137 oligonucleotides (26 to 33 nucleotides in length with similar physicochemical parameters) were spotted onto the microarray. The microarrays (ArrayTubes) were hybridized with 36 strains carrying specific antibiotic resistance genes that allowed testing of the sensitivity and specificity of 125 oligonucleotides. Among these were well-characterized multidrug-resistant strains of Enterococcus faecalis, Enterococcus faecium, and Lactococcus lactis and an avirulent strain of Bacillus anthracis harboring the broad-host-range resistance plasmid pRE25. Analysis of two multidrug-resistant field strains allowed the detection of 12 different antibiotic resistance genes in a Staphylococcus haemolyticus strain isolated from mastitis milk and 6 resistance genes in a Clostridium perfringens strain isolated from a calf. In both cases, the microarray genotyping corresponded to the phenotype of the strains. The ArrayTube platform presents the advantage of rapidly screening bacteria for the presence of antibiotic resistance genes known in gram-positive bacteria. This technology has a large potential for applications in basic research, food safety, and surveillance programs for antimicrobial resistance.

摘要

开发了一种一次性微阵列,用于通过杂交检测革兰氏阳性菌中多达90种抗生素抗性基因。除了9个只能开发一种特异性寡核苷酸的基因外,每个抗生素抗性基因由从基因家族的共有序列中选择的两种特异性寡核苷酸代表。总共137种寡核苷酸(长度为26至33个核苷酸,具有相似的物理化学参数)被点样到微阵列上。微阵列(ArrayTubes)与36株携带特定抗生素抗性基因的菌株杂交,从而可以测试125种寡核苷酸的敏感性和特异性。其中包括特征明确的粪肠球菌、屎肠球菌和乳酸乳球菌的多重耐药菌株,以及携带广泛宿主范围抗性质粒pRE25的无毒炭疽芽孢杆菌菌株。对两株多重耐药的现场菌株进行分析,使得能够在从乳腺炎乳汁中分离出的溶血葡萄球菌菌株中检测到12种不同的抗生素抗性基因,在从小牛中分离出的产气荚膜梭菌菌株中检测到6种抗性基因。在这两种情况下,微阵列基因分型都与菌株的表型相符。ArrayTube平台具有快速筛选细菌中革兰氏阳性菌已知抗生素抗性基因的优势。这项技术在基础研究、食品安全和抗菌药物耐药性监测计划中具有很大的应用潜力。

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