An integrated flow cytometry-based system for real-time, high sensitivity bacterial detection and identification

PLoS One. 2014 Apr 9;9(4):e94254. doi: 10.1371/journal.pone.0094254. eCollection 2014.

Abstract

Foodborne illnesses occur in both industrialized and developing countries, and may be increasing due to rapidly evolving food production practices. Yet some primary tools used to assess food safety are decades, if not centuries, old. To improve the time to result for food safety assessment a sensitive flow cytometer based system to detect microbial contamination was developed. By eliminating background fluorescence and improving signal to noise the assays accurately measure bacterial load or specifically identify pathogens. These assays provide results in minutes or, if sensitivity to one cell in a complex matrix is required, after several hours enrichment. Conventional assessments of food safety require 48 to 56 hours. The assays described within are linear over 5 orders of magnitude with results identical to culture plates, and report live and dead microorganisms. This system offers a powerful approach to real-time assessment of food safety, useful for industry self-monitoring and regulatory inspection.

Publication types

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

MeSH terms

  • Bacteria / growth & development
  • Bacteria / isolation & purification*
  • Bacterial Load
  • Computer Systems
  • Equipment Design
  • Escherichia coli O157 / growth & development
  • Flow Cytometry / instrumentation
  • Flow Cytometry / methods*
  • Fluorescein-5-isothiocyanate / analysis
  • Fluorescent Dyes / analysis
  • Food Inspection
  • Food Microbiology / instrumentation
  • Food Microbiology / methods*
  • Food Microbiology / standards
  • Industrial Microbiology / instrumentation
  • Industrial Microbiology / methods
  • Paper
  • Ralstonia pickettii / growth & development
  • Sensitivity and Specificity
  • Signal-To-Noise Ratio
  • Species Specificity
  • Time Factors

Substances

  • Fluorescent Dyes
  • Fluorescein-5-isothiocyanate

Grants and funding

This was Federal funded research. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.