4.6 Article

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

Journal

ANALYTICAL METHODS
Volume 12, Issue 2, Pages 212-217

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9ay02282a

Keywords

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Funding

  1. National Key Technology R&D Program of China [2016YFD040040304]
  2. Scientific and Technological Project of Henan Province [182102110392]
  3. Doctoral Scientific Research Foundation of Zhengzhou University of Light Industry [13501050060]

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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.

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