ISSN: 0973-7510

E-ISSN: 2581-690X

Moussa I. Mohamed1 , Ashgan M. Hessain2,3, Dalia K.Ismail4, Abdullah A. Al-Arfaj5 and Hemeg H.A.6
1Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
2Department of Health Science, College of Applied Studies and Community Service, King Saud University, P. O. Box 22459 Riyadh11495, Saudi Arabia.
3Department of Microbiology, Faculty of Vet. Medicine, Cairo University, Giza, Egypt.
4Department of Clinical Pathology, Kasr Eleini Hospital, Cairo University, P.O. Box 109, Cairo 11559,Egypt.
5Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
6Department of Medical Technology/Microbiology, College of Applied Sciences, Taibah University, Madinah, Saudi Arabia.
J Pure Appl Microbiol. 2013;7(Spl. Edn.: November):441-445
© The Author(s). 2013
Received: 23/08/2013 | Accepted: 20/10/2013 | Published: 30/11/2013
Abstract

Raw, unpasteurized milk can carry dangerous bacteria such as Salmonella,
E. coli
, and Listeria, which are responsible for causing numerous foodborne illnesses. The objective of this study was molecular characterization of shiga toxogenic E. coli in raw milk collected from different Egyptian governorates by multiplex PCR. During the period of 25th May to 25th October 2012, a total of 320 bulk-tank milk samples were collected from 10 cow farms located in different Egyptian governorates. Bacteriological examination of milk samples revealed the presence of E. coli organisms in 65 samples (20.3%), serotyping of the E. coli isolates revealed, 35 strains (10.94%) O111, 15 strains (4.69%) O157: H7, 10 strains (3.13%) O128 and 5 strains (1.56%) O119. Multiplex PCR for detection of shiga toxin type 2 and intimin genes revealed positive amplification of 255 bp fragment of shiga toxin type 2 gene and 384 bp fragment of intimin gene from all E. coli serovar O157: H7, while from serovar O111 were 25 (71.43%), 20 (57.14%) and from serovar O128 were 6 (60%), 8 (80%), respectively. The results of multiplex PCR as­say are useful for identification of STEC possessing the eaeA and stx2 genes.

Keywords

Raw milk, E. coli, multiplex PCR, Shiga toxin type 2, intimin gene

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