Rapid, Visual, and Sequence-Specific Detection of Salmonella in Egg Liquid with vis-NEAA, a CRISPR/Cas12 Empowered New Strategy
文献类型： 外文期刊
作者： Bai, Linlin 1 ; Wang, Liu 2 ; Huang, Shuqin 1 ; Bai, Rong 1 ; Lv, Xucong 1 ; Sun, Liping 2 ; Zhang, Fang 1 ; Xu, Xiahong 2 ;
作者机构： 1.Fuzhou Univ, Coll Biol Sci & Engn, Fuzhou 350108, Peoples R China
2.Zhejiang Acad Agr Sci, Inst Agroprod Safety & Nutr, State Key Lab Managing Biot & Chem Threats Qual &, Key Lab Informat Traceabil Agr Prod,Minist Agr &, Hangzhou 310021, Peoples R China
3.Fujian Key Lab Inspect & Quarantine Technol Res, Fuzhou 350108, Peoples R China
关键词： Salmonella; nicking enzyme-assisted amplification; visual detection; CRISPR/Cas12a; sequence specific
期刊名称：JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY （ 影响因子：5.895； 五年影响因子：6.048 ）
ISSN： 0021-8561
年卷期： 2022 年 70 卷 7 期
页码：
收录情况： SCI
摘要： Salmonella is one of the main pathogenic factors that cause foodborne diseases. Rapid and accurate detection of Salmonella in food is of great importance to ensure food safety. Nicking enzyme-assisted amplification (NEAA) is one of the promising isothermal amplification methods finishing the in vitro amplification in similar to 10 min; however, it suffers from nonspecific amplification a lot (similar to 70% products are noises). In this paper, we introduced CRISPR/Cas12a to specifically recognize the NEAA amplicons and transduce the signals into turned-on fluorescent visual readouts (vis-NEAA). Impressively, with this method, the high efficiency of NEAA has been taken great advantage and the nonspecific products were successfully bypassed at the same time. In comparison to NEAA-gel electrophoresis, vis-NEAA showed complete fidelity toward the presence of specific products, while for real-time PCR, it possesses equivalent sensitivity and specificity but saves similar to 80% of the time. A level of 80 CFU/mL Salmonella in spiked eggs can be detected on-site in similar to 20 min.
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