alexa Distribution of Pasteurella multocida B:2 in the Respir
ISSN: 2157-7579

Journal of Veterinary Science & Technology
Open Access

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Research Article

Distribution of Pasteurella multocida B:2 in the Respiratory, Gastrointestinal and Urinary Tracts of Buffaloes Following Experimental Subcutaneous Inoculation

Annas S, Zamri-Saad M*, Abubakar MS, Jesse FFA and Zunita Z

Research Centre for Ruminant Diseases, Faculty of Veterinary Medicine, Universiti Putra Malaysia, Malaysia

*Corresponding Author:
Zamri-Saad M
Research Centre for Ruminant Diseases
Faculty of Veterinary Medicine
Universiti Putra Malaysia, Malaysia
Tel: +603 86093453
E-mail: [email protected]

Received date: April 17, 2014; Accepted date: June 27, 2014; Published date: June 30, 2014

Citation: Annas S, Zamri-Saad M, Abubakar MS, Jesse FFA, Zunita Z (2014) Distribution of Pasteurella multocida B:2 in the Respiratory, Gastrointestinal and Urinary Tracts of Buffaloes Following Experimental Subcutaneous Inoculation. J Veterinar Sci Technol 5:177. doi:10.4172/2157-7579.1000177

Copyright: © 2014 Annas S, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.



Pasteurella multocida B:2 causes haemorrhagic septicaemia (HS) in cattle and buffalo, leading to acute death of many animals, usually in the form of outbreaks. HS occurs especially in Asia and Africa, leading to devastating loss of animals and economics. The involvement of respiratory tract as the route of infection and transmission has been well established. The present study describes the distribution of P. multocida B:2 using bacteriological isolations in the respiratory, gastrointestinal and urinary tracts of buffalo calves following different dosages of subcutaneous exposure to live wild-type P. multocida B:2. Nine buffalo calves were divided into 3 groups before calves of Group 1 were inoculated subcutaneously with 109 cfu/ml of live wild-type P. multocida B:2. Calves of Group 2 were similarly inoculated with 105 cfu/ml while calves of Group 3 were exposed to PBS. All calves of Group 1 were euthanised between 6 and 12 h post-infection, while calves Group 2 were euthanized between 24 and 48 h post-infection. P. multocida B:2 was isolated from the lungs, liver, deodenum, rectum, urinary bladder swabs and the urine of all infected calves of Groups 1 and 2. Bacterial concentration varied between the organs with the lungs showed significantly (p<0.05) higher concentration than other tracts. Nevertheless, duodenum, colon, liver and urinary bladder of infected calves showed considerably high concentrations of P. multocida B: 2. Both infected groups showed similar concentrations of P. multocida B:2 in the respiratory, gastrointestinal and urinary tracts. Isolation and detection of P. multocida B:2 in the gastrointestinal and urinary tracts of infected calves re-emphasize the role of these tracts in transmission of haemorrhagic septicaemia and aid in understanding the terminal stage of bacteraemia in HS.


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