重组酶聚合酶扩增
沙门氏菌
化学
色调
清脆的
核酸
基因组DNA
检出限
环介导等温扩增
计算生物学
分子生物学
DNA
人工智能
色谱法
遗传学
基因
生物
细菌
计算机科学
生物化学
作者
Jingrui Yuan,Liu Wang,Liang Huang,Kaiyu He,Hongmei Wang,Xiahong Xu,Bin Su,Jing Wang
标识
DOI:10.1021/acs.analchem.3c03753
摘要
Nucleic acid detection of pathogens in a point-of-need (PON) manner is of great significance yet remains challenging for sensitive and accurate visual discrimination. Here, we report a CRISPR–Cas12a-mediated lateral flow assay for PON detection of Salmonella typhimurium (S.ty) that is a prevailing pathogen disseminated through tainted food. The variation of the fluorescence color of the test line is exploited to interpret the results, enabling the discrimination between positive and negative samples on the basis of a hue-recognition mechanism. By leveraging the cleavage activity of Cas12a and hue-recognition readout, the assay facilitated by recombinase polymerase amplification can yield a visual detection limit of 1 copy μL–1 for S.ty genomic DNA within 1 h. The assay also displays a high specificity toward S.ty in fresh chicken samples, as well as a sensitivity 10-fold better than that of the commercial test strip. Moreover, a semiquantitative detection of S.ty ranging from 0 to 4 × 103 CFU/mL by the naked eye is made possible, thanks to the easily discernible color change of the test line. This approach provides an easy, rapid, accurate, and user-friendly solution for the PON detection of Salmonella and other pathogens.
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