A microfluidic based biosensor for rapid detection of Salmonella in food products

PLoS One. 2019 May 14;14(5):e0216873. doi: 10.1371/journal.pone.0216873. eCollection 2019.

Abstract

An impedance based microfluidic biosensor for simultaneous and rapid detection of Salmonella serotypes B and D in ready-to-eat (RTE) Turkey matrix has been presented. Detection of Salmonella at a concentration as low as 300 cells/ml with a total detection time of 1 hour has been achieved. The sensor has two sensing regions, with each formed from one interdigitated electrode array (IDE array) consisting of 50 finger pairs. First, Salmonella antibody type B and D were prepared and delivered to the sensor to functionalize each sensing region without causing any cross contamination. Then the RTE Turkey samples spiked with Salmonella types B and D were introduced into the biosensor via the antigen inlet. The response signal resulted from the binding between Salmonella and its specific antibody demonstrated the sensor's ability to detect a single type of pathogen, and multiple pathogens simultaneously. In addition, the biosensor's selectivity was tested using non-specific binding of E. coli O157 and E. coli DH5 Alpha while the IDE array was coated with the Salmonella antibody. The results also showed the sensor is capable to differentiate low concentration of live Salmonella cells from high concentration of dead Salmonella cells, and high concentration of E. coli cells. A detailed study on antibody immobilization that includes antibody concentration, antibody coating time (0.5-3 hours) and use of cross-linker has been performed. The study showed that Salmonella antibody to Salmonella antigen is not a factor of antibody concentration after electrodes were saturated with antibody, while the optimal coating time was found to be 1.5 hours, and the use of cross-linker has improved the signal response by 45-60%.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Antibodies, Immobilized / chemistry
  • Biosensing Techniques / economics
  • Biosensing Techniques / instrumentation*
  • Equipment Design
  • Food Analysis / economics
  • Food Analysis / instrumentation*
  • Food Contamination / analysis*
  • Microfluidic Analytical Techniques / economics
  • Microfluidic Analytical Techniques / instrumentation*
  • Salmonella / isolation & purification*
  • Time Factors

Substances

  • Antibodies, Immobilized

Grants and funding

This work and authors (JL, ZS, IJ, SZ, MA) were supported in part by USDA and Coulter Foundation/MU partnership. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.