Fluorescence immunoassay for the targeted determination of trace Listeria monocytogenes based on immunomagnetic

Shan Liang1, Li Ji1, Yingying Zhong1

  • 1Department of Pharmaceutical Engineering, School of Biomedical and Pharmaceutical Sciences, Guangdong University of Technology, Guangzhou 510006, People's Republic of China. qlli19@gdut.edu.cn.

Insights

A new fluorescence immunoassay accurately detects trace Listeria monocytogenes in food. This method uses antibody-functionalized nanoparticles and quantum dots for sensitive and rapid food safety testing.

Area of Science:

  • Food Safety
  • Analytical Chemistry
  • Biotechnology

Background:

  • Invasive Listeria monocytogenes infections pose significant public health risks due to high morbidity and mortality.
  • Sensitive, specific, and rapid detection of L. monocytogenes is crucial for food safety and preventing outbreaks.

Purpose of the Study:

  • To develop a highly sensitive and specific fluorescence immunoassay for detecting trace amounts of L. monocytogenes.
  • To create a rapid detection method for L. monocytogenes in food matrices.

Main Methods:

  • Fabrication of a fluorescence immunoassay using guinea pig antibody-functionalized magnetic nanoparticles (Fe3O4 NPs/pAb1) and rabbit antibody-anchored CdZnTe quantum dots (CdZnTe QDs/pAb2).
  • Utilized antibody-directed magnetic separation and long-wave fluorescent emission from CdZnTe QDs for detection.
  • Tested the immunosensor's performance with spiked tap water and pasteurized milk samples.

Main Results:

  • The immunosensor demonstrated excellent anti-interference performance in biological matrices.
  • Achieved a wide detection range from 1 to 10^9 CFU mL^-1 for L. monocytogenes.
  • Exhibited a low limit of detection (LOD) of 1 CFU mL^-1, indicating exceptional sensitivity.
  • Showcased good specificity and a rapid detection time of 60 minutes.

Conclusions:

  • The developed fluorescence immunoassay offers a sensitive, specific, and rapid method for detecting trace L. monocytogenes.
  • This approach significantly enhances food safety and public health monitoring capabilities.
  • The immunosensor's performance in real-world samples (tap water, pasteurized milk) validates its practical applicability.

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