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利用新型种特异性聚合酶链反应引物靶向 DNA 拓扑异构酶亚单位 B(gyrB)基因鉴定阪崎克罗诺杆菌和都柏林克罗诺杆菌。

Use of novel species-specific PCR primers targeted to DNA gyrase subunit B (gyrB) gene for species identification of the Cronobacter sakazakii and Cronobacter dublinensis.

机构信息

Bioresource Collection and Research Center, Food Industry Research and Development Institute, 331 Shih-Pin Road, Hsinchu 30062, Taiwan, ROC.

出版信息

Mol Cell Probes. 2013 Feb;27(1):15-8. doi: 10.1016/j.mcp.2012.08.004. Epub 2012 Aug 23.

Abstract

Cronobacter sakazakii and its phylogenetically closest species are considered to be an opportunistic pathogens associated with food-borne disease in neonates and infants. Neither phenotypic nor genotypic (16S ribosomal DNA sequence analysis) techniques can provide sufficient resolutions for accurately and rapidly identification of these species. The objective of this study was to develop species-specific PCR based on the gyrB gene sequence for direct species identification of the C. sakazakii and Cronobacter dublinensis within the C. sakazakii group. Two pair of species-specific primers were designed and used to specifically identify C. sakazakii and C. dublinensis, but none of the other C. sakazakii group strains. Our data indicate that the novel species-specific primers could be used to rapidly and accurately identify the species of C. sakazakii and C. dublinensis from C. sakazakii group by the PCR based assays.

摘要

阪崎克罗诺杆菌及其亲缘关系最密切的种被认为是与新生儿和婴儿食源性疾病相关的机会致病菌。表型和基因型(16S 核糖体 DNA 序列分析)技术均无法提供足够的分辨率,无法准确快速地鉴定这些种。本研究旨在基于 gyrB 基因序列开发种特异性 PCR,用于直接鉴定阪崎克罗诺杆菌组内的阪崎克罗诺杆菌和都柏林克罗诺杆菌。设计了两对种特异性引物,用于特异性鉴定阪崎克罗诺杆菌和都柏林克罗诺杆菌,但不能鉴定其他阪崎克罗诺杆菌组菌株。我们的数据表明,新型种特异性引物可通过基于 PCR 的检测方法快速准确地鉴定阪崎克罗诺杆菌组中的阪崎克罗诺杆菌和都柏林克罗诺杆菌的种。

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