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Hamelet, J., Demluth, K., Paul, J.L., Delabar, J.M. and Janel, N,” Hyperhomo-cysteinemia due to cystathionine beta synthase deficiency induces dysregulation of genes involved in hepatic lipid homeostasis in mice. Journal of Hepatolology, 46 (1): 151-159. 2007.

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Article

Antimicrobial Effects of Camel Milk against Some Bacterial Pathogens

1Department of Medical Microbiology, Faculty of Applied Medical Sciences, Turabah, Taif University, Saudi Arabia

2Reproductive diseases Department, Animal Reproduction Research Institute, Al-Haram, Egypt

3Medical Laboratory Department, Faculty of Applied Medical Sciences, Turabah, Taif University, Saudi Arabia

4Department of Biochemistry, Faculty of Veterinary Medicine, Benha University, Egypt

5Immunopharmacology Unit, Animal Reproduction Research Institute, Al-Haram, Egypt


Journal of Food and Nutrition Research. 2015, Vol. 3 No. 3, 162-168
DOI: 10.12691/jfnr-3-3-6
Copyright © 2015 Science and Education Publishing

Cite this paper:
Magdy Hassan YASSIN, Mahamed Mohamed Soliman, Salama Abd-Elhafez Mostafa, Hussein Abdel-Maksoud Ali. Antimicrobial Effects of Camel Milk against Some Bacterial Pathogens. Journal of Food and Nutrition Research. 2015; 3(3):162-168. doi: 10.12691/jfnr-3-3-6.

Correspondence to: Magdy  Hassan YASSIN, Department of Medical Microbiology, Faculty of Applied Medical Sciences, Turabah, Taif University, Saudi Arabia. Email: magdymyh@gmail.com

Abstract

The present study was aimed to investigate the protective effects of camel milk against pathogenicity induced by Staphylococcus aureus (S. aureus) and E. coli in Wistar rats. Sixty healthy adult male Wistar rats were divided into six groups (10 per group). Group 1 served as a control without any treatment. Group 2 received camel milk for two consecutive weeks. Group 3 injected intraperitoneally (IP) by S. aureus in a doses of 2x109 CFU/ml per rat. Group 4 injected IP by E.coli in a dose of 5x1010 CFU/ml per rat. Group 5 supplemented with camel milk for two consecutive weeks and then injected IP by S.aureus (2x109 CFU/ml per rat). Group 6 supplemented with camel milk for two consecutive weeks and then injected IP by E.coli (5x1010 CFU/ml per rat). All animals were decapitated after 3 weeks, serum was extracted and liver, kidney and lung tissues were taken for pathogen isolation. The isolation rate and pathogenicity of S. aureus and E. coli was high in rats injected pathogens alone (group 3 and 4) compared to camel milk and pathogens administered rats (group 5 and 6). The isolation of S. aureus and E. coli was high in intestine, then lung, kidney and liver. Prior camel milk supplementation ameliorated the degree of pathogenicity induced by pathogens. Camel milk had synergistic action with ciprofloxacin against S. aureus and E. coli to reduce bacterial resistance and decrease the dose of antibiotics. Pathogens injection alone induced significant amelioration in liver and kidney functions and prior camel milk administration inhibited such changes. Moreover, oxidative stress represented by the increase in malondialdehyde levels in serum of pathogens injected rats was decreased by prior camel milk administration. In conclusion, camel milk has beneficial role as antibacterial food supplement against S.aureus and E.coli pathogenicity in Wistar rats.

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