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首页> 外文期刊>Journal of Microbiological Methods >A novel universal DNA labeling and amplification system for rapid microarray-based detection of 117 antibiotic resistance genes in Gram-positive bacteria
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A novel universal DNA labeling and amplification system for rapid microarray-based detection of 117 antibiotic resistance genes in Gram-positive bacteria

机译:一种新型通用DNA标记和扩增系统,用于基于微阵列的革兰氏阳性细菌中117种抗生素抗性基因的快速检测

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摘要

A rapid and simple DNA labeling system has been developed for disposable microarrays and has been validated for the detection of 117 antibiotic resistance genes abundant in Gram-positive bacteria. The DNA was fragmented and amplified using phi-29 polymerase and random primers with linkers. Labeling and further amplification were then performed by classic PCR amplification using biotinylated primers specific for the linkers. The microarray developed by Perreten et al. (Perreten, V., Vorlet-Fawer, L, Slickers, P., Ehricht, R., Kuhnert, P., Frey, J., 2005. Microarray-based detection of 90 antibiotic resistance genes of gram-positive bacteria. J.Clin.Microbiol. 43, 2291-2302.) was improved by additional oligonucleotides. A total of 244 oligonucleotides (26 to 37 nucleotide length and with similar melting temperatures) were spotted on the microarray, including genes conferring resistance to clinically important antibiotic classes like beta-lactams, macrolides, aminoglycosides, glycopeptides and tetracyclines. Each antibiotic resistance gene is represented by at least 2 oligonucleotides designed from consensus sequences of gene families. The specificity of the oligonucleotides and the quality of the amplification and labeling were verified by analysis of a collection of 65 strains belonging to 24 species. Association between genotype and phenotype was verified for 6 antibiotics using 77 Staphylococcus strains belonging to different species and revealed 95% test specificity and a 93% predictive value of a positive test. The DNA labeling and amplification is independent of the species and of the target genes and could be used for different types of microarrays. This system has also the advantage to detect several genes within one bacterium at once, like in Staphylococcus aureus strain BM3318, in which up to 15 genes were detected. This new microarray-based detection system offers a large potential for applications in clinical diagnostic, basic research, food safety and surveillance programs for antimicrobial resistance. (C) 2014 Elsevier B.V. All rights reserved.
机译:已开发出一种用于一次性微阵列的快速,简单的DNA标记系统,并已通过验证,可检测出革兰氏阳性细菌中丰富的117种抗生素抗性基因。使用phi-29聚合酶和带有接头的随机引物将DNA片段化和扩增。然后使用对接头具有特异性的生物素化引物,通过经典PCR扩增进行标记和进一步扩增。 Perreten等人开发的微阵列。 (Perreten,V.,Vorlet-Fawer,L,Slickers,P.,Ehricht,R.,Kuhnert,P.,Frey,J.,2005。基于微阵列的革兰氏阳性细菌90种抗生素抗性基因的检测。 (Clin.Microbiol.43,2291-2302。)通过另外的寡核苷酸改进。在微阵列上总共发现了244个寡核苷酸(26至37个核苷酸长度,具有相似的解链温度),包括赋予对临床上重要的抗生素类(如β-内酰胺类,大环内酯类,氨基糖苷类,糖肽类和四环素类)耐药的基因。每个抗生素抗性基因由从基因家族的共有序列设计的至少2个寡核苷酸代表。通过分析属于24个物种的65个菌株的集合,验证了寡核苷酸的特异性以及扩增和标记的质量。使用77个属于不同物种的葡萄球菌菌株验证了6种抗生素的基因型与表型之间的关联,并显示出95%的测试特异性和93%的阳性测试预测值。 DNA标记和扩增与物种和目标基因无关,可用于不同类型的微阵列。该系统还具有一次检测一个细菌内几个基因的优势,例如在金黄色葡萄球菌BM3318菌株中,可检测到多达15个基因。这种基于微阵列的新型检测系统为临床诊断,基础研究,食品安全性和抗药性监测程序提供了广阔的应用前景。 (C)2014 Elsevier B.V.保留所有权利。

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