Turkish Journal of Veterinary & Animal Sciences




Lungs from 8222 cattle slaughtered at an abattoir in Elazığ were examined macroscopically, and pneumonia was detected in 500 (6.1%) lungs. These samples were inoculated onto blood agar supplemented with 7% sheep blood for isolation of bacterial agents. A polymerase chain reaction (PCR) based upon the use of species-specific primers was carried out on DNA samples extracted from suspected Pasteurella spp. isolates. In addition, a mouse inoculation test was carried out on suspected Pasteurella multocida isolates. A total of 311 (62.2%) bacterial agents were isolated from the lung samples and were identified as 7.2% Staphylococcus aureus, 6% Pasteurella multocida, 6% Corynebacterium spp., 5.8% yeast, 3.8% Streptococcus spp, 3.6% Staphylococcus epidermidis, 2.6% Escherichia coli, 2.2% Bacillus spp., 2% Pseudomonas spp., 1.8% Mannheimia haemolytica, 1.6% Actinobacillus spp., 1.2% Klebsiella spp., 0.2% Moraxella spp., 0.2% Proteus spp., and 18% mixed bacteria.Twenty-four (80%) of the Pasteurella multocida isolates were positive in the mouse inoculation test in cattle. All P. multocida and M. haemolytica strains that were positive by culture were also found to be positive by PCR. However, toxigenic Pasteurella multocida was not detected in any isolates by PCR using primers derived from the toxA gene.


Pneumonia, cattle, Pasteurella multocida, Mannheimia haemolytica, polymerase chain reaction (PCR), culture

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