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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Tehran University of Medical Sciences,
2007-09-01T00:00:00Z.
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001 | doaj_2a0bed914e4f4cc7adf9a43313aeab0f | ||
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. |