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Journal of Clinical Microbiology, December 2001, p. 4483-4486, Vol. 39, No. 12
National Institute of Public Health and the
Environment, Bilthoven, The Netherlands
Received 19 June 2001/Returned for modification 23 July
2001/Accepted 17 September 2001
A duplex PCR assay targeting the ail and 16S rRNA
genes of Yersinia enterocolitica was developed to
specifically identify pathogenic Y. enterocolitica from
pure culture. Validation of the assay was performed with 215 clinical
Yersinia strains and 40 strains of other bacterial
species. Within an assay time of 4 h, this assay offers a very
specific, reliable, and inexpensive alternative to the conventional
phenotypic assays used in clinical laboratories to identify pathogenic
Y. enterocolitica.
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.12.4483-4486.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Detection of Pathogenic Yersinia
enterocolitica by a Rapid and Sensitive Duplex PCR
Assay
*
Corresponding author. Mailing address: National
Institute of Public Health and the Environment (RIVM), P.O. Box 1, 3720 BA, Bilthoven, The Netherlands. Phone: (31) 30 274 2105. Fax: (31) 30 274 4418. E-mail: wim.wannet{at}rivm.nl.
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