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A gold nanoparticles-assisted multiplex PCR assay for simultaneous detection of Salmonella typhimurium, Listeria monocytogenes and Escherichia coli O157:H7

机译:用于同时检测沙门氏菌,李斯特菌单核细胞元和大肠杆菌O157:H7的金纳米粒子辅助多重PCR测定

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Foodborne pathogens are a major cause of foodborne illness, leading to a growing food safety problem in public health. This work aims to develop a novel gold nanoparticles (AuNPs)-assisted multiplex PCR assay for rapid, simple and simultaneous detection of Salmonella typhimurium (S. typhimurium), Listeria monocytogenes (L. monocytogenes) and Escherichia coli O157:H7 (E. coli O157:H7), which are the top three foodborne pathogenic bacteria. Flower-shaped AuNPs (F-AuNPs) were used as a colorimetric sensor in this assay, based on PCR product that can help improve stability of the F-AuNPs in a certain concentration of salt solution. Detection of PCR product can be directly achieved by mixing it with F-AuNPs and NaCl, and the result is visible to the naked eye. Results showed that the optimal annealing temperature was 53.1 degrees C to amplify the three target pathogenic strains in multiplex PCR assay, and the optimal concentrations of the primer pairs were 0.4 mu M for each of L. monocytogenes and E. coli O157:H7, and 0.2 mu M for S. typhimurium. The colorimetric detection limit of PCR products by F-AuNPs was 3.125 ng mu L-1, and the detection time was approximately 10 min. Simultaneous detection limit of the multiplex PCR method was 10 pg mu L-1 for L. monocytogenes and S. typhimurium, and 50 pg mu L-1 for E. coli O157:H7. Compared with conventional multiplex PCR assay, the F-AuNPs-assisted assay is a convenient, rapid and simple visual detection method. The excellent performance of the colorimetric sensor shows potential application in on-site detection of foodborne pathogenic strains in food samples.
机译:食源性病原体是食源性疾病的主要原因,导致公共卫生的不断增长的食品安全问题。这项工作旨在开发一种新的金纳米颗粒(AUNP) - 拟型多重PCR测定,用于快速,同时检测沙门氏菌毒蕈氏菌(S. Typhimurium),Histeria单核细胞增生(L.单核细胞元)和大肠杆菌O157:H7(大肠杆菌O157:H7),这是前三种食源性致病细菌。在该测定中,在该测定中使用花形AUNPS(F-AUNPS),基于PCR产物,可以有助于提高在一定浓度的盐溶液中的F-AUNP的稳定性。通过将其与F-AUNP和NaCl混合,可以直接达到PCR产物的检测,并且结果对肉眼可见。结果表明,最佳退火温度为53.1摄氏度,以扩增多重PCR测定中的三个靶致病菌菌株,底漆对的最佳浓度为L.单核细胞元和大肠杆菌O157:H7,以及对于触风丘疹0.2亩。 F-AUNP的PCR产物的比色检测限为3.125 ng mu L-1,检测时间约为10分钟。多重PCR方法的同时检测极限为L.单核细胞元和培氏毒蕈生成的10 pg mu L-1,以及50pg mu L-1的大肠杆菌O157:H7。与常规多重PCR测定相比,F-AUNPS辅助测定是一种方便,快速和简单的视觉检测方法。比色传感器的优异性能显示出在食品样品中的食源性致病菌株的现场检测中的潜在应用。

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