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Jami, S., Jamshidi, A., Khanzadi, S.. (1389). The presence of Listeria monocytogenesin raw milk samples in Mashhad, Iran. , 11(4), 363-367. doi: 10.22099/ijvr.2010.108
S. Jami; A. Jamshidi; S. Khanzadi. "The presence of Listeria monocytogenesin raw milk samples in Mashhad, Iran". , 11, 4, 1389, 363-367. doi: 10.22099/ijvr.2010.108
Jami, S., Jamshidi, A., Khanzadi, S.. (1389). 'The presence of Listeria monocytogenesin raw milk samples in Mashhad, Iran', , 11(4), pp. 363-367. doi: 10.22099/ijvr.2010.108
Jami, S., Jamshidi, A., Khanzadi, S.. The presence of Listeria monocytogenesin raw milk samples in Mashhad, Iran. , 1389; 11(4): 363-367. doi: 10.22099/ijvr.2010.108

The presence of Listeria monocytogenesin raw milk samples in Mashhad, Iran

Iranian Journal of Veterinary Research
مقاله 10، دوره 11، شماره 4 - شماره پیاپی 33، 2010، صفحه 363-367    اصل مقاله (125.13 K)
نوع مقاله: Short paper
شناسه دیجیتال (DOI): 10.22099/ijvr.2010.108
نویسندگان
S. Jami1؛ A. Jamshidi* 2؛ S. Khanzadi2
1Graduated from Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran
2Department of Food Hygiene and Public Health, Facultyof Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran
چکیده
The purpose of this preliminary study was to determine the prevalence of raw milk contamination with
Listeria monocytogenes. In this study, 100 bulk tank milk samples were collected randomly and delivered to
Pegah Pasteurization Factory in Mashhad.For isolation and identification of L. monocytogenes, the samples
were first enriched using cold enrichment method in Listeriaenrichment broth, followed by plating onto
supplemented Oxford agar. For final identification of suspected colonies a multiplex-PCR assay, using two
pair of primers was employed. The prsprimers are specific for putative phophoribosyl pyrophosphate
synthetase (prs) gene of  Listeriaspp. and the LM lip1primers are specific for prfA gene of its monocytogenesserovar. Using this method, the contamination of raw milk with L. monocytogeneswas
determined to be 4% and the sensitivity of the primers was 3.5 × 103 cfu ml -1, and the specificity was
determined to be 100%. Considering the high specificity and sensitivityof the employed multiplex-PCR
assay, it is recommended to use this method for the identification of suspected colonies of Listeriaspp. and
L. monocytogenes.
کلیدواژه‌ها
Listeria spp؛ Listeria monocytogenes؛ Bulk tank milk؛ Multiplex PCR
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