Development of a real-time multiplex PCR assay for the detection of multiple Salmonella serotypes in chicken samples
2008

Real-time PCR for Detecting Salmonella in Chicken

Sample size: 63 publication Evidence: high

Author Information

Author(s): O'Regan Edel, McCabe Evonne, Burgess Catherine, McGuinness Sheila, Barry Thomas, Duffy Geraldine, Whyte Paul, Fanning Séamus

Primary Institution: University College Dublin

Hypothesis

Can a real-time multiplex PCR assay effectively detect multiple Salmonella serotypes in chicken samples?

Conclusion

The real-time PCR method is as effective as traditional methods for detecting Salmonella in chicken samples.

Supporting Evidence

  • The real-time PCR assay showed 100% inclusivity and exclusivity on all strains tested.
  • Relative accuracy, sensitivity, and specificity of the real-time PCR method were determined to be 89%, 94%, and 87%, respectively.
  • Both methods detected Salmonella in artificially contaminated chicken samples at levels as low as 1–10 CFU per 25 g.

Takeaway

Scientists created a new test to quickly find bad germs in chicken, and it works just as well as the old way.

Methodology

The study used a real-time multiplex PCR assay with a pre-enrichment step followed by selective enrichment and DNA extraction.

Limitations

The study may not account for all possible food matrices and their effects on PCR results.

Digital Object Identifier (DOI)

10.1186/1471-2180-8-156

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