A duplex qPCR for the simultaneous detection of Escherichia coli O157: H7 and Listeria monocytogenes using LNA probes

S. S. Nitecki, N. Teape, B. F. Carney, J. W. Slater, W. M. Brück

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)

Abstract

In this study, a duplex qPCR assay was developed for the needs of the Irish fish industry to screen for the two major food-borne pathogens of fish, Listeria monocytogenes and Escherichia coli O157:H7. The assay can claim positive or negative results for two pathogens in one go in only 20 h including 16 h universal pre-enrichment and compared to traditional ISO approved plate culture methods the labour and the cost involved in testing of one sample is reduced to minimum. The highly specific genomic areas targeted for PCR amplification in the assay are the hly gene for listeriolysin O (LLO) of L. monocytogenes and the stx gene for Shiga-like toxin expressed by E. coli O157:H7. The detection limit of the assay is consistent with the consumer protection limits of 1 pg genomic DNA or 1 CFU 25 g-1 fish meat (with enrichment) allowing the test to be considered as a substitute to standard plate culture methods.

Original languageEnglish
Pages (from-to)20-27
Number of pages8
JournalLetters in Applied Microbiology
Volume61
Issue number1
DOIs
Publication statusPublished - 1 Jul 2015

Keywords

  • Diseases
  • Escherichia coli (all potentially pathogenic types)
  • Fish (as food)
  • Listeria
  • PCR (polymerase chain reaction)

Fingerprint

Dive into the research topics of 'A duplex qPCR for the simultaneous detection of Escherichia coli O157: H7 and Listeria monocytogenes using LNA probes'. Together they form a unique fingerprint.

Cite this