Physical characterization of bacteriophages isolated against Salmonella Dublin
231 / 63
Keywords:
Bacteriophage, Physical, pH, Salmonella, SunlightAbstract
In the present study a total of 5 phages were isolated against Salmonella Dublin using agar overlay technique from 25 samples of dairy effluent. These phages were purified, enriched and subjected to various physical (pH, temperature and sun light exposure) to evaluate their survival ability. On physical characterization of the phages it was found that the phages could survive varied pH conditions with reduction in its numbers from the initial concentration. Upon exposure to various temperature conditions it was observed that the phages can withstand a maximum 50°C and above this temperature it was deleterious for almost all the phages. Exposure to direct sunlight indicated that phages can withstand maximum continuous exposure up to 6 days and beyond that it was found to be deleterious for survival of the phage.
Downloads
References
Adams M H. 1959. Bacteriophages. Interscience Publisher, New York.
Brussow H. 2005. Phage therapy: The E. coli experience. Micorbiology 151: 2133–40.
Chandra M, Chachra, D and Saxena H M. 2008. Application of bacteriophages in the diagnosis and therapy of bacterial infection. Punjab Veterinary Journal 6(1–2): 91–9.
Chilamban C, Rawat M and Somvanshi R. 2004. Pre-clinical studies on therapy of Staphylococcus aureus mastitis by bacteriophage in mice model. Indian Journal of Comparative Microbiology Immunology and Infectious Diseases 25(2): 98–103.
Hanlon G W. 2007. Bacteriophages: an appraisal of their role in the treatment of bacterial infections. International Journal of Antimicrobial Agents 30: 118–128.
Lederberg J. 1996. Smaller fleas ad infinitum: Therapeutic bacteriophage redux. Proceeding of National Academy of Science USA 93: 3167–68.
Popoff M Y. 2001. Antigenic formulae of the Salmonella serovars. World Health Organization collaborating centre for reference and research on Salmonella. 8th edn. Pasteur Institute, Paris, France.
Reeves M W, Evins, G M, Heiba, A A, Plikaytis, B D and Farmer J J. 1989. Clonal nature of Salmonella Typhi and its genetic relatedness to other salmonellae as shown by multilocus enzyme electrophoresis and proposal of Salmonella bongori comb. nov. Journal of Clinical Microbiology 27: 313–20.
Rohwer F and Edwards R. 2002. The phage proteomic tree: a genome based taxonomy for phage. Journal of Bacteriology 184: 4529–35.
Salama S, Bolton F J and Hutchinson D N. 1989. Improved method for the isolation of Campylobacter jejuni and Campylobacter coli bacteriophages. Letters in Applied Microbiology 8: 5–7.
Schuch R, Nelson D and Fischetti V A. 2002. A bacteriolytic agent that detects and kills Bacillus anthracis. Nature 418: 884–889.
Sheng H, Knecht H J, Kudva I T and Hovde C J. 2006. Application of bacteriophages to control intestinal Escherichia coli. Applied
Environmental Microbiology 72(8): 5359–66.
Vinodkumar C S, Kalsurmath S and Neelagund Y F. 2008. Utility of lytic bacteriophage in the treatment of multi drug resistant Pseudomonas aeruginosa septicemia. Indian Journal of Pathology and Microbiology 51(3): 360–366.
Wray C and Wray A. 2000. Salmonella in Domestic Animals. pp169. CABI Publishing, New York,
Xie H, Zhuang X, Kong J, Ma G and Zhang H. 2005. Bacteriophage Esc-A is an efficient therapy for Escherichia coli 3–1 caused diarrhea in chickens. Journal of General and Applied Microbiology 51: 159–163.
Downloads
Submitted
Published
Issue
Section
License
Copyright (c) 2014 The Indian Journal of Animal Sciences

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
The copyright of the articles published in The Indian Journal of Animal Sciences is vested with the Indian Council of Agricultural Research, which reserves the right to enter into any agreement with any organization in India or abroad, for reprography, photocopying, storage and dissemination of information. The Council has no objection to using the material, provided the information is not being utilized for commercial purposes and wherever the information is being used, proper credit is given to ICAR.