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Simultaneous quantitative detection of Listeria spp. and Listeria monocytogenes using a duplex real-time PCR-based assay

  • David Rodríguez-Lázaro
  • , Marta Hernández
  • , Maria Pla
  • CSIC - Molecular Biology Institute of Barcelona

Research output: Contribution to journalScientific articlepeer-review

62 Citations (Scopus)

Abstract

We report a duplex real-time PCR-based assay for the simultaneous quantitative detection of Listeria spp. and the food-borne pathogen Listeria monocytogenes. The targets of this single tube reaction were the 23S rDNA and hly genes of Listeria spp. and L. monocytogenes, respectively. Our assay was efficient, 100% selective (i.e., it allowed accurate simultaneous identification of 52 L. monocytogenes and 120 Listeria spp. strains through the FAM-labelled hly and the VIC-labelled 23S rDNA probes, respectively); and had a detection limit of one target molecule in 100% (23S rDNA) and 56% (hly) of the reactions. Simultaneous quantification was possible along a 5-log dynamic range, with an upper limit of 30 target molecules and R2 values >0.995 in both cases. Our results indicate that this assay based on the amplification of the 23S rDNA gene can accurately quantify any mixture of Listeria species and simultaneously unambiguously quantify L. monocytogenes.

Original languageEnglish
Pages (from-to)257-267
Number of pages11
JournalFEMS Microbiology Letters
Volume233
Issue number2
DOIs
Publication statusPublished - 15 Apr 2004

Keywords

  • Food-borne pathogen detection
  • Listeria monocytogenes
  • Listeria spp
  • Multiplex
  • Real-time PCR

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