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基于 carB 基因的寡核苷酸微阵列对三种致病性沙门氏菌亚种肠亚种血清型的特异性鉴别。

Specific discrimination of three pathogenic Salmonella enterica subsp. enterica serotypes by carB-based oligonucleotide microarray.

机构信息

Department of Chemical Engineering, Pohang University of Science and Technology, Pohang, South Korea.

出版信息

Appl Environ Microbiol. 2014 Jan;80(1):366-73. doi: 10.1128/AEM.02978-13. Epub 2013 Nov 1.

Abstract

It is important to rapidly and selectively detect and analyze pathogenic Salmonella enterica subsp. enterica in contaminated food to reduce the morbidity and mortality of Salmonella infection and to guarantee food safety. In the present work, we developed an oligonucleotide microarray containing duplicate specific capture probes based on the carB gene, which encodes the carbamoyl phosphate synthetase large subunit, as a competent biomarker evaluated by genetic analysis to selectively and efficiently detect and discriminate three S. enterica subsp. enterica serotypes: Choleraesuis, Enteritidis, and Typhimurium. Using the developed microarray system, three serotype targets were successfully analyzed in a range as low as 1.6 to 3.1 nM and were specifically discriminated from each other without nonspecific signals. In addition, the constructed microarray did not have cross-reactivity with other common pathogenic bacteria and even enabled the clear discrimination of the target Salmonella serotype from a bacterial mixture. Therefore, these results demonstrated that our novel carB-based oligonucleotide microarray can be used as an effective and specific detection system for S. enterica subsp. enterica serotypes.

摘要

快速而有选择性地检测和分析污染食物中的致病性沙门氏菌亚种。肠炎亚种对于降低沙门氏菌感染的发病率和死亡率以及保证食品安全非常重要。在本工作中,我们开发了一种基于 carB 基因的寡核苷酸微阵列,该基因编码氨甲酰磷酸合成酶大亚基,作为一种经过遗传分析评估的有能力的生物标志物,可选择性和有效地检测和区分三种沙门氏菌亚种。肠炎:肠炎、肠炎和肠炎。使用开发的微阵列系统,在低至 1.6 至 3.1 nM 的范围内成功分析了三种血清型靶标,并且彼此之间没有特异性信号的特异性区分。此外,构建的微阵列与其他常见的致病性细菌没有交叉反应,甚至能够从细菌混合物中清晰地区分目标沙门氏菌血清型。因此,这些结果表明,我们基于新型 carB 的寡核苷酸微阵列可以用作沙门氏菌亚种的有效和特异性检测系统。肠炎。

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本文引用的文献

1
Molecular serotyping of Salmonella enterica by complete rpoB gene sequencing.
J Microbiol. 2012 Dec;50(6):962-9. doi: 10.1007/s12275-012-2547-x. Epub 2012 Dec 30.
2
Specific multiplex analysis of pathogens using a direct 16S rRNA hybridization in microarray system.
Anal Chem. 2012 Jun 5;84(11):4873-9. doi: 10.1021/ac300476k. Epub 2012 May 11.
3
Comparative genomics of 28 Salmonella enterica isolates: evidence for CRISPR-mediated adaptive sublineage evolution.
J Bacteriol. 2011 Jul;193(14):3556-68. doi: 10.1128/JB.00297-11. Epub 2011 May 20.
4
High-throughput Universal Probe Salmonella Serotyping (UPSS) by nanoPCR.
J Microbiol Methods. 2010 Nov;83(2):217-23. doi: 10.1016/j.mimet.2010.09.005. Epub 2010 Sep 24.
6
Sensitivity enhancement in DNA hybridization assay using gold nanoparticle-labeled two reporting probes.
Biosens Bioelectron. 2009 Oct 15;25(2):435-41. doi: 10.1016/j.bios.2009.07.031. Epub 2009 Aug 4.
7
Quantitative oligonucleotide microarray data analysis with an artificial standard probe strategy.
Biosens Bioelectron. 2008 Jun 15;23(11):1738-44. doi: 10.1016/j.bios.2008.01.024. Epub 2008 Feb 7.
8
Pathogenesis of enteric Salmonella infections.
Curr Opin Gastroenterol. 2008 Jan;24(1):22-6. doi: 10.1097/MOG.0b013e3282f21388.
9
Salmonella-induced enteritis: molecular pathogenesis and therapeutic implications.
Expert Rev Mol Med. 2007 Jul 2;9(18):1-17. doi: 10.1017/S1462399407000373.

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