1Division of Veterinary Pathology, Faculty of Veterinary Sciences & Animal Husbandry, Sher-e-Kashmir University of Agricultural Sciences & Technology-Jammu, RS Pura-181102, Jammu & Kashmir, India
2Department of Veterinary Pathology, College of Veterinary Science, Assam Agricultural University, Guwahati, 781022, Assam, India
3Department of Microbiology, College of Veterinary Science, Assam Agricultural University, Guwahati, 781022, Assam, India
4Division of Veterinary Physiology and Biochemistry, Faculty of Veterinary Sciences & Animal Husbandry, Sher-e-Kashmir University of Agricultural Sciences & Technology-Jammu, RS Pura-181102, Jammu & Kashmir, India
5Department of Veterinary Medicine, College of Veterinary Science, Assam Agricultural University, Guwahati, 781022, Assam, India
Department of Veterinary Pathology, College of Veterinary Science, Assam Agricultural University, Guwahati-781 022, Assam, India
*Corresponding author's e-mail: nawabn1@rediffmail.com
Online published on 19 December, 2016.
Continuous foetal lamb testis cells OA3. Ts was used to compare the isolation of a vaccine orf virus (ORFV) strain that had been adapted to primary lamb testes cells, with scab derived wild-type/field ORFV isolates. The wild type virus showed an accelerated and exaggerated cyto-pathic effect (CPE) than the vaccine virus as has been demonstrated by immunofluorescent detection of viral antigen using ORFV monoclonal antibodies. ORFV could be successfully isolated in OA3. Ts foetal lamb testes cells and can be used for direct isolation of the virus from clinical samples. Two different methods of cell culture infection were also compared during sub-culture, one using infected supernatant as the inoculum and the other using infected cells as a modified method for infecting healthy culture cells. The present study also indicates that a higher infection can probably be achieved with inoculating infected cells together with healthy ones as a co-culture method during propagation of ORFV. This has been revealed as visibly pronounced CPE and presence of larger and multiple aggregates of cytoplasmic inclusions than cells infected with infected supernatant alone.
Antigen, Cell culture, CPE, Immune-detection, Orf virus (ORFV)