Detection of Yersinia enterocolitica in the Shami goat’s milk in the North Sinai Governorate

Considerable difficulties are associated with the isolation of Yersinia enterocolitica from food particularly milk and milk products. Most methods are time consuming require enrichment steps and are unable to differentiate pathogenic isolates from non pathogenic ones. The purpose of this study was t...

Full description

Bibliographic Details
Main Authors: Y. M. Kamel, A. L. El-Naggar, H. M. El-Shaer
Format: Article
Language:English
Published: Beni-Suef University 2005-12-01
Series:Journal of Veterinary Medical Research
Subjects:
Online Access:https://jvmr.journals.ekb.eg/article_77966.html
id doaj-4c6c56f0ae0d4342996f88b6975f9ee4
record_format Article
spelling doaj-4c6c56f0ae0d4342996f88b6975f9ee42020-11-25T01:43:18ZengBeni-Suef University Journal of Veterinary Medical Research 2357-05122357-05202005-12-01152180183 Detection of Yersinia enterocolitica in the Shami goat’s milk in the North Sinai GovernorateY. M. Kamel0 A. L. El-Naggar1 H. M. El-Shaer2Animal and Poultry Production Division, Desert Research Center, El- Mataria, Cairo, EgyptAnimal and Poultry Production Division, Desert Research Center, El- Mataria, Cairo, EgyptAnimal and Poultry Production Division, Desert Research Center, El- Mataria, Cairo, EgyptConsiderable difficulties are associated with the isolation of Yersinia enterocolitica from food particularly milk and milk products. Most methods are time consuming require enrichment steps and are unable to differentiate pathogenic isolates from non pathogenic ones. The purpose of this study was to evaluate the detection of Yersinia enterocolitica in milk by both polymerase chain reaction (PCR) and conventional culturing methods. Fifty milk samples were collected from Shami goats in North Sinai governorate. Two primers (DG26 and DG63) were used in PCR and the size of the PCR-product was 440bp. The results obtained by PCR technique were in good agreement with that obtained by conventional culturing method. Five samples (10%) were positive by PCR while 4 samples were positive by conventional culturing method. Interestingly, PCR results are obtained within few hours. Moreover, it solved the problem of interpretation of classical biochemical and serological typing in one step without necessity of using additional examinations. This makes diagnosis in food control laboratories much faster and more efficient. https://jvmr.journals.ekb.eg/article_77966.htmlyersinia enterocolitica; the shami goat’s; milk
collection DOAJ
language English
format Article
sources DOAJ
author Y. M. Kamel
A. L. El-Naggar
H. M. El-Shaer
spellingShingle Y. M. Kamel
A. L. El-Naggar
H. M. El-Shaer
Detection of Yersinia enterocolitica in the Shami goat’s milk in the North Sinai Governorate
Journal of Veterinary Medical Research
yersinia enterocolitica; the shami goat’s; milk
author_facet Y. M. Kamel
A. L. El-Naggar
H. M. El-Shaer
author_sort Y. M. Kamel
title Detection of Yersinia enterocolitica in the Shami goat’s milk in the North Sinai Governorate
title_short Detection of Yersinia enterocolitica in the Shami goat’s milk in the North Sinai Governorate
title_full Detection of Yersinia enterocolitica in the Shami goat’s milk in the North Sinai Governorate
title_fullStr Detection of Yersinia enterocolitica in the Shami goat’s milk in the North Sinai Governorate
title_full_unstemmed Detection of Yersinia enterocolitica in the Shami goat’s milk in the North Sinai Governorate
title_sort detection of yersinia enterocolitica in the shami goat’s milk in the north sinai governorate
publisher Beni-Suef University
series Journal of Veterinary Medical Research
issn 2357-0512
2357-0520
publishDate 2005-12-01
description Considerable difficulties are associated with the isolation of Yersinia enterocolitica from food particularly milk and milk products. Most methods are time consuming require enrichment steps and are unable to differentiate pathogenic isolates from non pathogenic ones. The purpose of this study was to evaluate the detection of Yersinia enterocolitica in milk by both polymerase chain reaction (PCR) and conventional culturing methods. Fifty milk samples were collected from Shami goats in North Sinai governorate. Two primers (DG26 and DG63) were used in PCR and the size of the PCR-product was 440bp. The results obtained by PCR technique were in good agreement with that obtained by conventional culturing method. Five samples (10%) were positive by PCR while 4 samples were positive by conventional culturing method. Interestingly, PCR results are obtained within few hours. Moreover, it solved the problem of interpretation of classical biochemical and serological typing in one step without necessity of using additional examinations. This makes diagnosis in food control laboratories much faster and more efficient.
topic yersinia enterocolitica; the shami goat’s; milk
url https://jvmr.journals.ekb.eg/article_77966.html
work_keys_str_mv AT ymkamel detectionofyersiniaenterocoliticaintheshamigoatsmilkinthenorthsinaigovernorate
AT alelnaggar detectionofyersiniaenterocoliticaintheshamigoatsmilkinthenorthsinaigovernorate
AT hmelshaer detectionofyersiniaenterocoliticaintheshamigoatsmilkinthenorthsinaigovernorate
_version_ 1725032185016090624