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用于沙门氏菌菌株分子特征分析和基因分型的寡核苷酸微阵列

Oligonucleotide microarray for molecular characterization and genotyping of Salmonella spp. strains.

作者信息

Majtan T, Majtanova L, Timko J, Majtan V

机构信息

Department of Genomics and Biotechnology, Institute of Molecular Biology SAS, Dubravska cesta 21, 84551 Bratislava 45, Slovakia.

出版信息

J Antimicrob Chemother. 2007 Nov;60(5):937-46. doi: 10.1093/jac/dkm326. Epub 2007 Sep 25.

Abstract

OBJECTIVES

To characterize and subtype multidrug-resistant Salmonella isolates by determining the virulence factors, prophage sequences and antimicrobial resistance genes using a novel Salmonella-specific oligonucleotide microarray.

METHODS

Preliminary screening of 24 Salmonella clinical isolates was carried out by using susceptibility testing, plasmid profiling and class 1 integron PCR. Subsequently, oligonucleotide microarray was involved in genotypic characterization and localization of monitored genetic markers. The presence of antimicrobial resistance genes was also detected and confirmed by PCR and subsequent sequencing. The potential spread of emerging bla(SHV-2) was investigated by bacterial conjugation.

RESULTS

All Salmonella strains revealed resistance to two or more (up to nine) antibiotics. Nineteen of them carried class 1 integrons including dfrA1, dfrA12, aadA1, aadA2, bla(PSE-1) and bla(TEM-1) gene cassettes, respectively. Twenty-three out of 24 Salmonella isolates possessed one or more plasmids. Oligonucleotide microarray characterization and typing revealed the conserved character of Salmonella pathogenicity island virulence factors among three Salmonella enterica serovars, significant variability in prophage sequences and many different antimicrobial resistance gene patterns. Differential labelling of genomic and plasmid DNA, respectively, and hybridization to the microarray made it possible to localize important resistance determinants. Microarray results were successfully confirmed and verified by using PCR. The emerging bla(SHV-2) gene from Salmonella Kentucky SK10944 conferring resistance to ceftriaxone and cefotaxime was transferred via bacterial conjugation to Escherichia coli K-12 3110.

CONCLUSIONS

Salmonella isolates were quickly and thoroughly characterized by a novel oligonucleotide microarray, which could become a useful tool for detection of virulence and resistance genes and monitoring of their dissemination among salmonellae and closely related bacteria.

摘要

目的

通过使用一种新型沙门氏菌特异性寡核苷酸微阵列来确定毒力因子、前噬菌体序列和抗菌抗性基因,从而对多重耐药沙门氏菌分离株进行特征描述和分型。

方法

通过药敏试验、质粒图谱分析和1类整合子PCR对24株沙门氏菌临床分离株进行初步筛选。随后,利用寡核苷酸微阵列进行监测遗传标记的基因分型和定位。抗菌抗性基因的存在也通过PCR及后续测序进行检测和确认。通过细菌接合研究新兴bla(SHV - 2)的潜在传播。

结果

所有沙门氏菌菌株均显示对两种或更多种(多达九种)抗生素耐药。其中19株携带1类整合子,分别包含dfrA1、dfrA12、aadA1、aadA2、bla(PSE - 1)和bla(TEM - 1)基因盒。24株沙门氏菌分离株中有23株拥有一个或多个质粒。寡核苷酸微阵列特征描述和分型显示,三种肠炎沙门氏菌血清型中沙门氏菌致病岛毒力因子具有保守性,前噬菌体序列存在显著变异性,且有许多不同的抗菌抗性基因模式。分别对基因组DNA和质粒DNA进行差异标记,并与微阵列杂交,使得定位重要的抗性决定因素成为可能。微阵列结果通过PCR成功得到确认和验证。来自肯塔基沙门氏菌SK10944的新兴bla(SHV - 2)基因赋予对头孢曲松和头孢噻肟的抗性,通过细菌接合转移至大肠杆菌K - 12 3110。

结论

一种新型寡核苷酸微阵列能够快速且全面地对沙门氏菌分离株进行特征描述,它可能成为检测毒力和抗性基因以及监测它们在沙门氏菌和密切相关细菌中传播的有用工具。

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