Detection and Differentiation of Listeria spp. by a Single Reaction Based on Multiplex PCR

Author:

Bubert Andreas12,Hein Inge3,Rauch Marcus1,Lehner Angelika3,Yoon ByoungSu4,Goebel Werner1,Wagner Martin3

Affiliation:

1. Lehrstuhl für Mikrobiologie, Theodor-Boveri-Institut für Biowissenschaften, Universität Würzburg, 97074 Würzburg,1 and

2. Microbiological Analytics, Merck KGaA, 64271 Darmstadt,2 Germany;

3. Institut für Milchhygiene und Milchtechnologie, Veterinärmedizinische Universität Wien, Vienna, Austria3; and

4. Department of Biology, Kyonggi University, Suwon, Kyonggi-Do 442-760, Korea4

Abstract

ABSTRACT The iap gene encodes the protein p60, which is common to all Listeria species. A previous comparison of the DNA sequences indicated conserved and species-specific gene portions. Based on these comparisons, a combination consisting of only five different primers that allows the specific detection and differentiation of Listeria species with a single multiplex PCR and subsequent gel analysis was selected. One primer was derived from the conserved 3′ end and is specific for all Listeria species; the other four primers are specific for Listeria monocytogenes , L. innocua , L. grayi , or the three grouped species L. ivanovii , L. seeligeri , and L. welshimeri , respectively. The PCR method, which also enables the simultaneous detection of L. monocytogenes and L. innocua , was evaluated against conventional biotyping with 200 food hygiene-relevant Listeria strains. The results indicated the superiority of this technique. Thus, this novel type of multiplex PCR may be useful for rapid Listeria species confirmation and for identification of Listeria species for strains isolated from different sources.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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