Rapid Detection of Cronobacter sakazakii Using Recombinase Polymerase Amplification Combined with Lateral Flow Strip

被引:0
|
作者
Chen, Chunyang [1 ]
Zhang, Chenning [1 ]
Shi, Aiying [1 ]
Du, Xinjun [1 ]
Wang, Shuo [1 ]
机构
[1] State Key Laboratory of Food Nutrition and Safety, College of Food Science and Engineering, Tianjin University of Science and Technology, Tianjin,300457, China
来源
Shipin Kexue/Food Science | 2019年 / 40卷 / 24期
关键词
Cronobacter sakazakii - Cross reactivity - Double stranded DNA - Isothermal amplifications - Limit of detection - National standard - Rapid detection - Test strips;
D O I
10.7506/spkx1002-6630-20190411-152
中图分类号
学科分类号
摘要
In this study, recombinase polymerase isothermal amplification (RPA) combined with lateral fl ow test strips (LF)was developed to quickly and reliably detect Cronobacter sakazakii. RPA using the primers modified with biotin and digoxin produced large amounts of double-stranded DNA products labeled with biotin and digoxin at each end. The products could interact with gold-labeled anti-digoxin antibody and streptavidin fixed on the LF, giving visible results on the strip. The RPA-LF method showed a limit of detection (LOD) of 1.7 × 102 CFU/mL for C. sakazakii in pure culture with no cross-reactivity with other common pathogens. The LOD of the RPA-LF was 1.7 × 100 CFU/g after 4 or 6 h enrichment for different types of atrifically contaminated food samples. In order to further evaluate its performance, 20 real food samples were detected by the RPA-LF in comparison with the national standard method. The results obtained were consistent with each other. © 2019, China Food Publishing Company. All right reserved.
引用
收藏
页码:306 / 312
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