4.7 Article

Rapid pathogen detection by lateral-flow immunochromatographic assay with gold nanoparticle-assisted enzyme signal amplification

期刊

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ijfoodmicro.2015.04.032

关键词

Lateral-flow immunochromatography; Pathogen detection; Signal enhancement; Rapid detection; Enzyme immunoassay

资金

  1. USDA-ARS project with Center for Food Safety Engineering at Purdue University [1935-42000-049-00D]
  2. National Research Foundation of Korea [31Z20130012916] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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To date most LF-ICA format for pathogen detection is based on generating color signals from gold nanoparticle (AuNP) tracers that are perceivable by naked eye but often these methods exhibit sensitivity lower than those associated with the conventional enzyme-based immunological methods or mandated by the regulatory guidelines. By developing AuNP avidin-biotin constructs in which a number of enzymes can be labeled we report on an enhanced LF-ICA system to detect pathogens at very low levels. With this approach we show that as low as 100 CFU/mL of Escherichia coli O157:H7 can be detected, indicating that the limit of detection can be increased by about 1000-fold due to our signal amplification approach. In addition, extensive cross-reactivity experiments were conducted (19 different organisms were used) to test and successfully validate the specificity of the assay. Semi-quantitative analysis can be performed using signal intensities which were correlated with the target pathogen concentrations for calibration by image processing. (C) 2015 Elsevier B.V. All rights reserved.

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