Assessment of Ail Gene Marker Amplicon for Mo­lecular Characterization of Pathogenic Yersinia enterocolitica in Food Samples Collected in Iran

Autor: MR Khorramizadeh, MM Soltan-Dallal, F Safavifar, F Saadat, S Rezaie, S Hashemi, M Taremi, S Ar­dalan, MR Zali
Jazyk: angličtina
Rok vydání: 2007
Předmět:
Zdroj: Iranian Journal of Public Health, Vol 36, Iss 3 (2007)
Druh dokumentu: article
ISSN: 2251-6085
2251-6093
Popis: Background: To assess the utility of the chromosomal ail virulence gene sequence for detection of pathogenic Yersinia en­terocolitica in raw meet food products (beef, lamb, and chicken). Methods: This study included 39 Yersinia enterocolitica positive cultures from suspicious food samples, in a working pe­riod of six months. These samples were referred to the "Food-Borne Diseases and Chronic Diarrhea Lab at Research Cen­tre for Gastric and Liver Diseases" of the Taleghani Hospital at Shahid Beheshti University of Medical Sciences, Te­hran, Iran. Isolates from 8 cultured Y. intermedia, Y. aldovi, Y. intermedia type O:45, Y. kristensenii, Y. enterocolitica type O:12/26, Y. enterocolitica type1/7/8, Y. frederiksenii type O:39, and Y. enterocolitica type O:8 samples were in­cluded in the study. Four non-Yersinia species Salmonella typhi, Shigella dysenteriae, Shigella flexeneri, and Proteus mirabi­lis were used for specificity testing. An established Yersinia type O:9 was used as positive control and for sensitiv­ity testing. An in-house real-time PCR assay was designed in order to rapidly and specifically identifies the pres­ence of specific Yersinia species. Results: Out of 39 tested Y. enterocolitica samples, 6(2.3%) showed positive results for the ail gene PCR prod­uct, typed as O:8, and O:9, respectively. PCR products were sent for sequencing. Two sequences were registered with the Na­tional Center for Biotechnology Information (NCBI Genbank) as polymorphic ail gene sequences under the acces­sion numbers of DQ157767 and DQ003329. Conclusions: Collectively, this test is well adapted for definite confirmation of pathogenic Y. en­terocolitica in food sam­ples.
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