Clinicopathological studies on experimentally infected rabbits with bovine herpesvirus -1

Forty-eight pathogen free New Zealand rabbits were divided into two groups, the first group contained eighteen rabbits served as normal control and the second group of thirty rabbits were received 1 ml bovine herpesvirus-1 (BHV-1) virus suspension (107 TCID 50) by intraperitoneal route. Rabbits both...

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Veröffentlicht in:Journal of veterinary medical research 2005-12, Vol.15 (2), p.25-33
Hauptverfasser: Sayed, Walaa M., Kamel, H. H., Abd-El-Rahman, Azza H., El-Nesr, K. A., Madbouly, H. M., Mohamed, Amira H.
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Sprache:eng
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Zusammenfassung:Forty-eight pathogen free New Zealand rabbits were divided into two groups, the first group contained eighteen rabbits served as normal control and the second group of thirty rabbits were received 1 ml bovine herpesvirus-1 (BHV-1) virus suspension (107 TCID 50) by intraperitoneal route. Rabbits both groups were subjected to hematological, serum biochemical, different serological and histopathological examination 3,7,10,14,21 and 28 days post infection. Clinical observation of infected rabbits showed febrile response and mild conjunctivitis after 24 and 48h. of inoculation, respectively. The hemogram revealed no significant alteration in the erythrogram while leucogram showed leucocytosis accompanied with heterophilia, lymphopenia and monocytopenia at the 3rd and 7th days post infection. Serum biochemical analysis showed significant elevation in the activity of AST, ALT and AP and in blood urea nitrogen and creatinine concentration along the experimental period. Serum total proteins, albumin, :, ; and < globulin significantly increased at different periods of the experiment. BHV-1 antibodies were detected in the sera of infected rabbits by Dot ELISA and ELISA from the first week until the forth week post infection. Histopathological examination revealed that the most affected organs were the trachea, lungs and liver while adrenals, kidneys, and spleen showed mild pathological alterations.
ISSN:2357-0520
2357-0512
2357-0520
DOI:10.21608/jvmr.2005.77927