1Zoonoses Department, Faculty of Veterinary Medicine, Benha University, Toukh, 13736, Egypt
2Bacteriology, Immunologyand Mycology Department, Faculty of Veterinary Medicine, Benha University, Toukh 13736, Egypt
3Biotechnology Department, Animal Health Research Institute (AHRI), Giza 11331, Egypt
4Zoonoses Department, National Research Center, Dokki, 12622, Giza, Egypt
American Journal of Infectious Diseases and Microbiology.
2015,
Vol. 3 No. 1, 32-37
DOI: 10.12691/ajidm-3-1-5
Copyright © 2015 Science and Education PublishingCite this paper: Nashwa O. Khalifa, Fatma I. Elhofy, Hanan A. Fahmy, A. M. A. Barakat. Epidemiologicl and Genetic Studies of Enterotoxigenic
Staphylococcus aureus Isolated from Goat and Human.
American Journal of Infectious Diseases and Microbiology. 2015; 3(1):32-37. doi: 10.12691/ajidm-3-1-5.
Correspondence to: Nashwa O. Khalifa, Zoonoses Department, Faculty of Veterinary Medicine, Benha University, Toukh, 13736, Egypt. Email:
fatmaelhofy@yahoo.comAbstract
The objective of the present study was to investigate the epidemiological and genetic relationships of classical enterotoxins of S. aureus in goat’s raw milk, meat and food handlers in Toukh city in Qaluobia governorate, Egypt. A total of 100 goat, s raw milk and meat samples (50 of each) were collected from randomly distributed herds in streets for buying milk and in public markets for peddler meat. Hand and nasal swabs were collected from milkers and butchers (30 of ech). All samples were subjected for bacteriological examination for isolation and identification of S. aureus. Isolates were underwent reversed passive latex agglutination technique for detection of enterotoxigenic S. aureus. A multiplex PCR assay could successfully amplify the diagnostic DNA bands of 270bp, 165bp, 69bp and 306bp of genes for staphylococcal enterotoxins A, B, C, and D respectively. PCR was applied on the serologically identified 16 (20.25%) isolates out of 79 S. aureus which isolated from the examined goat’s food samples and human handlers by using one universal forward and reverse primers, specific for each individual toxin gene. None of the samples was positive for SEE indicating the zoonotic and genetic relationships.
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