Recombinase Polymerase Amplification Combined with Unmodified Gold Nanoparticles for Salmonella Detection in Milk

被引:21
作者
Chen, Zhi-guang [1 ,2 ]
Zhong, Hai-xia [2 ]
Luo, Huan [2 ]
Zhang, Ren-yu [2 ]
Huang, Jun-rong [1 ]
机构
[1] Shaanxi Univ Sci & Technol, Sch Food & Biol Engn, Xian 710016, Shaanxi, Peoples R China
[2] Neijiang Vocat & Tech Coll, Dept Agr Technol, Neijiang 641000, Peoples R China
关键词
RPA; AuNPs; Food detection; Salmonella; REAL-TIME PCR; STAPHYLOCOCCUS-AUREUS; RAPID DETECTION; QUANTIFICATION; ENTERICA; ASSAY;
D O I
10.1007/s12161-018-1351-6
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Salmonella is one of the most common pathogenic bacterium, which causes food spoilage and human diseases. The national standard detection method (GB4789.4) and other fast detection methods for Salmonella cannot satisfy the requirements in the present climate because of their inefficiency, low accuracy, high equipment requirements, or high cost. In this study, we combine isothermal recombinase polymerase amplification (RPA) with unmodified gold nanoparticles (AuNPs) to detect Salmonella in milk. A rapid, effective, visualized, and low-cost RPA-AuNP assay was developed, with a detection limit of 50CFU for milk samples after enrichment for 6h or 1pg for DNA within 15min at 37 degrees C using simple water bath equipment. Furthermore, it exhibited no cross-reactions with other pathogens by using highly specific region of invA of Salmonella as the target detection gene. And it may apply to the local food inspection and detection center whose equipment conditions are poor.
引用
收藏
页码:190 / 197
页数:8
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