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

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, i...

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Main Authors: MR Khorramizadeh (Author), MM Soltan-Dallal (Author), F Safavifar (Author), F Saadat (Author), S Rezaie (Author), S Hashemi (Author), M Taremi (Author), S Ar­dalan (Author), MR Zali (Author)
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Published: Tehran University of Medical Sciences, 2007-09-01T00:00:00Z.
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042 |a dc 
100 1 0 |a MR Khorramizadeh  |e author 
700 1 0 |a MM Soltan-Dallal  |e author 
700 1 0 |a F Safavifar  |e author 
700 1 0 |a F Saadat  |e author 
700 1 0 |a S Rezaie  |e author 
700 1 0 |a S Hashemi  |e author 
700 1 0 |a M Taremi  |e author 
700 1 0 |a S Ar­dalan  |e author 
700 1 0 |a MR Zali  |e author 
245 0 0 |a Assessment of Ail Gene Marker Amplicon for Mo­lecular Characterization of Pathogenic Yersinia enterocolitica in Food Samples Collected in Iran 
260 |b Tehran University of Medical Sciences,   |c 2007-09-01T00:00:00Z. 
500 |a 2251-6085 
520 |a 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. 
546 |a EN 
690 |a Ggenetic markers 
690 |a Real- time systems 
690 |a Molecular sequencing data 
690 |a Public aspects of medicine 
690 |a RA1-1270 
655 7 |a article  |2 local 
786 0 |n Iranian Journal of Public Health, Vol 36, Iss 3, Pp 8-15 (2007) 
787 0 |n http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/3809.pdf&manuscript_id=3809 
787 0 |n https://doaj.org/toc/2251-6085 
856 4 1 |u https://doaj.org/article/2a0bed914e4f4cc7adf9a43313aeab0f  |z Connect to this object online.