Development of a fluorescence aptasensor for rapid and sensitive detection of Listeria monocytogenes in food

被引:69
作者
Liu, Rui [1 ]
Zhang, Yunlian [1 ]
Ali, Shujat [1 ]
Haruna, Suleiman A. [1 ]
He, Peihuan [1 ]
Li, Huanhuan [1 ]
Ouyang, Qin [1 ,2 ]
Chen, Quansheng [1 ,2 ]
机构
[1] Jiangsu Univ, Sch Food & Biol Engn, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Jiangsu Univ, Inst Agr Engn, Zhenjiang 212013, Jiangsu, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Fluorescence aptasensor; Real-time PCR; L; monocytogenes; Food; PATHOGENIC BACTERIA; NANOPARTICLES; APTAMER; IDENTIFICATION; SEPARATION; OUTBREAKS; SELECTION; SYSTEM; GENE;
D O I
10.1016/j.foodcont.2020.107808
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
In this study, a simple fluorescence aptasensor was developed for rapid and sensitive detection of Listeria monocytogenes in food. The aptasensor was comprised of two parts. Aptamer-functionalized upconversion nanoparticles (UCNPs) recognized and adhered to the L. monocytogenes cells and provided strong fluorescent signals. Aptamer-functionalized magnetic nanoparticles (MNPs), which also recognized and adhered to the cells, were used to concentrate the aptamer-UCNP/L. monocytogenes/aptamer-MNP complex. The fluorescence intensity was measured and calibrated to a concentration series of L. monocytogenes. A low limit of detection of 8 cfu mL(-1) was estimated from the range of 68 to 68 x 10(6) cfu mL(-1). Compared with other methods currently available, the proposed method had wider detection range and higher sensitivity. Furthermore, the selectivity and functionality when used to detect L. monocytogenes in real food samples suggest it may be useful for practical applications.
引用
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页数:8
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