Clinical Study and Rapid Detection of Feline Parvovirus in Suspected Cats by Polymerase Chain Reaction Method
Venisri Prithivi Raj Prithivi Raj(1*), Aris Haryanto(2)
(1) Acres Wildlife Rescue Center, Jalan Lekar no. 91, Singapore 698917
(2) Department of Biochemistry and Molecular Biology, Faculty of Veterinary Medicine, Universitas Gadjah Mada
(*) Corresponding Author
Abstract
The aim of this research was to detect the presence of Feline Parvovirus (FPV) in blood samples of FPV suspected cats by Polymerase Chain Reaction (PCR) method. This research used eleven fresh blood samples of FPV suspected cats which were obtained from the Internal Medicine Laboratory of Faculty of Veterinary Medicine at UGM, Yogyakarta, Clinic Pet Care in Semarang and Medania Private Clinic in Yogyakarta. The DNA was first extracted from the blood using DNA isolation kit. Then the template of DNA was used for amplification by PCR method using CPV primers to target the Viral Protein-2 (VP-2) encoding gene. The PCR products were then visualized using 1% Agarose Gel electrophoresis and UV-Transilluminator. A positive result was indicated by the appearance of a DNA fragment in size of 518 bp which can be interpreted as the presence of FPV in the obtained blood samples. PCR products were then sent for sequencing to determine the nucleotide sequence of the VP-2 gene. The sequences obtained were aligned using multiple alignment method with three FPV isolates obtained from the database of Genebank using the MEGA6.06 software program. From the eleven cat blood samples obtained, 8 samples indicated positive with FPV infection. These results showed that PCR method can be used to detect FPV in samples derived from blood specimens from FPV suspected cats. Conventional PCR method was also used to confirm the cause of the symptoms shown by the infected cats as some of the symptoms such as gastroenteritis is quite common among many other viral infection.
Key words; Feline Parvovirus (FPV), VP-2 gene, PCR, DNA sequencing,
Full Text:
PDFReferences
Berns K.I., 1990, Parvovirus Replication, Microbiology Review, 54: 316-329. Buonavoglia, C., Martella, V., Pratelli, A., Tempesta, M., Cavalli, A., Buonavoglia, D., Bozzo, G., Elia, G., Decaro, N., Carmichael, L., 2001, Evidence for evolution of canine parvovirus type 2 in Italy. J. Gen. Virol. 82, 3021–3025.
Cassinoti P., Weitz M., and Siegl G., 1993, Parvoviruses, Microbiology and Microbial infections; Volume 1 Virology, Topley & Wilson’s, 14: 261-279.
Decaro, N., Desario, C., Elia, G., Martella, V., Mari, V., Lavazza, A., Nardi, M., and Buonavoglia, C., 2008, Evidence for immunisation failure in vaccinated adult dogs infected with canine parvovirus type 2c. New Microbiol. 31, 125–130
Farr, G.A., Cotmore, S.F, and Tattersall, P. 2006. VP-2 cleavage and the leucine ring at the base of the fivefold cylinder control pHdependent externalization of both the VP1 N terminus and the genome of minute virus of mice. J. Virol. 80 (1):161-71
Goddard A., Leisewitz A.L, and Christopher M.M., 2008, Prognostic usefulness of blood leukocyte changes in canine parvoviral enteritis. J Vet Intern Med. 22: 309–316.
Greene C.E., and Addie D.D., 2013, Feline panleukopenia. In Infectious diseases of the dog and cat, Ed. CE Greene, WB Saunders Company, Philadelphia. pp 78-88
Hueffer K. and Parrish C.R., 2003, Combination of Two Capsid Regions Controlling Canine Host Range Determine Canine Transferrin Receptor Binding by Canine and Feline Parvovirus. Journal of Virology.18: 1009910105.
Kapil S et al. Canine parvovirus types 2c and 2b circulating in North American dogs in 2006 and 2007. J Clin Microbiol 2007; 45:40444047.
Lamm, C.G., and Rezabek, G.B., 2008. Parvovirus infections in domestic companion animals, Veterinary Clinics of North America Small Animal Practice. 38. 837-851.
Laurent S, Vautherot JF, Madelaine MF, Le Gall G, Rasschaert D. 1994. Recombinant rabbit hemorrhagic disease virus capsid protein expressed in baculovirus self-assembles into viruslike particles and induces protection. J. Virol. 68 (10):6794-6798.
Levy J, Crawford C, Hartmann K, HoffmannLehmann R, Little S, Sundahl E, Thayer V; 2008 Feline retrovirus management guidelines.American Association of Feline Practitioners. Compend Contin Educ Vet. 31 (6):E10
Martella, V., Decaro, N., Elia, G., Buonavoglia, C., 2005, Surveillance activity for canine parvovirus in Italy. J. Vet. Med. 52, 312– 315.
Nakamura K, Ikeda Y, Miyazawa T, Tohya Y, Takahashi E, Mochizuki M (2001). Characterisation of cross-reactivity of virus neutralising antibodies induced by feline panleukopenia virus and canine parvoviruses. Res Vet Sci 71:219-222
Parrish, C. R., Aquadro, C. F., Strassheim, M. L., Evermann, J. F., Sgro, J. Y., and Mohammed, H. O., 1991, Rapid antigenic type replacement and DNA sequence evolution of canine parvovirus. J. Virol. 65:6544–6552.
Sonntag F, Bleker S, Leuchs B, Fischer R, Kleinschmidt JA. 2006. Adeno-associated virus type 2 capsids with externalized VP1/ VP2 trafficking domains are generated prior to passage through the cytoplasm and are maintained until uncoating occurs in the nucleus. J Virol. 80 (22):11040-11054.
Steinel A., Parrish C.R., Bloom M.E., and Truyen U., 2001, Review: Parvovirus Infection in Wild Carnivores. Journal of Wildlife Diseases 37 (3): 594-607.
Zhang Q., Xu X.M., Zhai G.Q., Wang Z., Hou S.H., and Zhu H.F., 2010, Molecular Characterisation of Canine Parvovirus Strains Circulating in China. African Journal of Biotechnology 9 (29): 45564560.
DOI: https://doi.org/10.22146/ijvs.v1i1.55186
Article Metrics
Abstract views : 1141 | views : 547Refbacks
- There are currently no refbacks.
Copyright of IJVS (Indonesian Journal of Veterinary Sciences) ISSN 2722-421X (online).
Faculty of Veterinary Medicine, Universitas of Gadjah Mada
Fauna Strat, No.2, Karangmalang, Yogyakarta, Indonesia
Phone: 0274-560862
Fax: 0274-560861
Email: ijvs.fkh@ugm.ac.id
Indonesian Journal of Vaterinary Sciences is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.