Sensitive and rapid detection of three foodborne pathogens in meat by recombinase polymerase amplification with lateral flow dipstick (RPA-LFD)

被引:0
|
作者
Bai, Wenxia [1 ]
Chen, Jie [1 ]
Chen, Dong [2 ]
Zhu, Yike [1 ]
Hu, Kairui [1 ]
Lin, Xiaoyu [1 ]
Chen, Junlin [1 ]
Song, Dafeng [1 ]
机构
[1] Zhejiang Gongshang Univ, Sch Food Sci & Biotechnol, Key Lab Food Microbial Technol Zhejiang Prov, 18 Xuezheng Str, Hangzhou 310018, Zhejiang, Peoples R China
[2] Assure Tech Hangzhou Co Ltd, Bldg 4,1418-50,Moganshan Rd, Hangzhou 310011, Peoples R China
关键词
Recombinase polymerase amplification; Lateral flow dipstick; Foodborne diseases; Rapid detection; ANTIMICROBIAL RESISTANCE;
D O I
10.1016/j.ijfoodmicro.2024.110822
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Foodborne illnesses, caused by harmful microorganisms in food, are a significant global health issue. Current methods for identifying these pathogens are both labor-intensive and time-consuming. In this research, we devised a swift and precise detection technique using recombinase polymerase amplification combined with a lateral flow dipstick (RPA-LFD) for three foodborne pathogens found in meat. By employing a dedicated detection device, RPA-LFD allows for the rapid analysis of DNA from Escherichia coli O157 (E. coli O157), Salmonella, and Shigella-pathogens that are prohibited in food. The detection thresholds for E. coli O157, Salmonella, and Shigella are 0.168 fg/mu l (1.04 CFU/ml), 0.72 fg/mu l (27.49 CFU/ml), and 1.25 fg/mu l (48.84 CFU/ml), respectively. This method provides a short detection window, operates at low temperatures, follows simple procedures, and exhibits high sensitivity. Our study establishes the RPA-LFD method for simultaneously identifying the nucleic acid of three foodborne pathogens, offering an efficient solution for quickly identifying multiple contaminants.
引用
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页数:8
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