Typing of Listeria monocytogenes Strains by Repetitive Element Sequence-Based PCR

Author:

Jeršek B.1,Gilot P.2,Gubina M.3,Klun N.4,Mehle J.5,Tcherneva E.6,Rijpens N.1,Herman L.1

Affiliation:

1. Centre of Agricultural Research, Department of Animal Product Quality (DVK), B-9090 Melle,1 and

2. National Reference Center for Listeriosis, Institute of Hygiene and Epidemiology, B-1050 Brussels,2 Belgium;

3. Medical Faculty, Institute of Microbiology3 and

4. Department of Sanitary Microbiology, Institute of Public Health of the Republic of Slovenia,4 1000 Ljubljana, Slovenia; and

5. Veterinary Faculty,5 University of Ljubljana, and

6. Central Veterinary Research Institute, 1606 Sofia, Bulgaria6

Abstract

ABSTRACT Listeria monocytogenes strains possess short repetitive extragenic palindromic (REP) elements and enterobacterial repetitive intergenic consensus (ERIC) sequences. We used repetitive element sequence-based PCR (rep-PCR) to evaluate the potential of REP and ERIC elements for typing L. monocytogenes strains isolated from humans, animals, and foods. On the basis of rep-PCR fingerprints, L. monocytogenes strains were divided into four major clusters matching origin of isolation. rep-PCR fingerprints of human and animal isolates were different from those of food isolates. Computer evaluation of rep-PCR fingerprints allowed discrimination among the tested serotypes 1/2a, 1/2b, 1/2c, 3b, and 4b within each major cluster. The index of discrimination calculated for 52 epidemiologically unrelated isolates of L. monocytogenes was 0.98 for REP- and ERIC-PCR. Our results suggest that rep-PCR can provide an alternative method for L. monocytogenes typing.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference37 articles.

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