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用于检测大环内酯类耐药基因的DNA微阵列

DNA microarray for detection of macrolide resistance genes.

作者信息

Cassone Marco, D'Andrea Marco M, Iannelli Francesco, Oggioni Marco R, Rossolini Gian Maria, Pozzi Gianni

机构信息

LAMMB, Università di Siena, Policlinico Le Scotte/V Lotto, Italy.

出版信息

Antimicrob Agents Chemother. 2006 Jun;50(6):2038-41. doi: 10.1128/AAC.01574-05.

Abstract

A DNA microarray was developed to detect bacterial genes conferring resistance to macrolides and related antibiotics. A database containing 65 nonredundant genes selected from publicly available DNA sequences was constructed and used to design 100 oligonucleotide probes that could specifically detect and discriminate all 65 genes. Probes were spotted on a glass slide, and the array was reacted with DNA templates extracted from 20 reference strains of eight different bacterial species (Streptococcus pneumoniae, Streptococcus pyogenes, Enterococcus faecalis, Enterococcus faecium, Staphylococcus aureus, Staphylococcus haemolyticus, Escherichia coli, and Bacteroides fragilis) known to harbor 29 different macrolide resistance genes. Hybridization results showed that probes reacted with, and only with, the expected DNA templates and allowed discovery of three unexpected genes, including msr(SA) in B. fragilis, an efflux gene that has not yet been described for gram-negative bacteria.

摘要

开发了一种DNA微阵列来检测赋予对大环内酯类及相关抗生素耐药性的细菌基因。构建了一个包含从公开可用DNA序列中选择的65个非冗余基因的数据库,并用于设计100个寡核苷酸探针,这些探针可以特异性检测和区分所有65个基因。将探针点样在载玻片上,该阵列与从8种不同细菌物种(肺炎链球菌、化脓性链球菌、粪肠球菌、屎肠球菌、金黄色葡萄球菌、溶血葡萄球菌、大肠杆菌和脆弱拟杆菌)的20个参考菌株中提取的DNA模板进行反应,已知这些菌株含有29种不同的大环内酯耐药基因。杂交结果表明,探针与预期的DNA模板发生反应,且仅与预期的DNA模板发生反应,并发现了三个意外基因,包括脆弱拟杆菌中的msr(SA),这是一种革兰氏阴性菌中尚未描述的外排基因。

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