Comparative detection of classical swine fever virus in striated muscles from experimentally infected pigs by reverse transcription polymerase chain reaction, cell culture isolation and immunohistochemistry

Journal of Virological Methods

Volumn 74, Issue 1, 1998, Pages 47-56

  Thur B ^a   Hofmann, M A ^a  

^a INSTITUTE OF VIROLOGY AND IMMUNOLOGY   (Switzerland)

Author keywords

Classical swine fever virus; Meat; Pestivirus; RT PCR; Striated muscle

Indexed keywords

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; IMMUNOHISTOCHEMISTRY; NONHUMAN; PESTIVIRUS; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SKELETAL MUSCLE; SWINE; VIRUS DETECTION; VIRUS INFECTION; VIRUS ISOLATION; VIRUS REPLICATION;

ANIMALS; CELLS, CULTURED; CLASSICAL SWINE FEVER; CLASSICAL SWINE FEVER VIRUS; IMMUNOENZYME TECHNIQUES; MUSCLE, SKELETAL; POLYMERASE CHAIN REACTION; SWINE; TIME FACTORS; TRANSCRIPTION, GENETIC;

EID: 0344589339     PISSN: 01660934     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0166-0934(98)00069-X     Document Type: Article

References (33)

1. Bielefeldt-Ohmann, H., 1988. BVD virus antigens in tissues of persistently viraemic, clinically normal cattle: implications for the pathogenesis of clinically fatal disease. Acta Vet. Scand. 29, 77-84.
2. Bobrow, M.N., Harris, T.D., Shaughnessy, K.J., Litt, G.J., 1989. Catalyzed reporter deposition, a novel method of signal amplification. J. Immunol. Methods 125, 279-285.
3. Dahle, J., Liess, B., 1992. A review on classical swine fever infections in pigs: epizootiology, clinical disease and pathology. Comp. Immunol. Microbiol. Infect. Dis. 15, 203-211.
4. Dahle, J., Schlagemann, G., Moennig, V., Liess, B., 1993. Clinical, virological and serological findings after intranasal inoculation of pigs with bovine viral diarrhoea virus and subsequent intranasal challenge with hog cholera virus. J. Vet. Med. B 40, 46-54.
5. de las Mulas, J.M., Ruiz-Villamor, E., Donoso, S., Quezada, M., Lecocq, C., Sierra, M.A., 1997. Immunohistochemical detection of hog cholera viral glycoprotein 55 in paraffin-embedded tissues. J. Vet. Diagn. Invest. 9, 10-16.
6. Depner, K.R., Müller, A., Gruber, A., Rodriguez, A., Bickhardt, K., Liess, B., 1995. Classical swine fever in wild boar (Sus scorfa)-experimental infections and viral persistence. Deut. Tierarztl. Wochenschr. 102, 381-384.
7. Desenclos, J.-C.A., Klontz, K.C., Wilder, M.H., Nainan, O.V., Margolis, H.S., Gunn, R.A., 1991. A multistate outbreak of hepatits A caused by the consumption of raw oysters. Am. J. Public Health 81, 1268-1272.
8. Farez, S., Morley, R.S., 1997. Potential animal health hazards of pork and pork products. Rev. Sci. Tech. Off. Int. Epiz. 16, 65-78.
9. Greiser-Wilke, I., Moennig, V., Coulibaly, C.O.Z., Dahle, J., Leder, L., Liess, B., 1990. Identification of conserved epitopes on a hog cholera virus protein. Arch. Virol. 111, 213-225.
10. Haines, D.M., Clark, E.G., Dubovi, E.J., 1992. Monoclonal antibody-based immunohistochemical detection of bovine viral diarrhea virus in formalin-fixed paraffin-embedded tissues. Vet. Pathol. 29, 27-32.
11. Higuchi, R., 1989. Simple and rapid preparation of samples for PCR. In: Ehrlich, H.A. (Ed.), PCR Technology, Principles and Applications for DNA Amplification. Stockton Press, New York, pp. 31-38.
12. Hofmann, M.A., Bossy, S., 1998. Molecular epidemiological analysis of classical swine fever virus isolates from the 1993 disease outbreaks in Swikerland. Schweiz. Arch. Tierheilkd (in press).
13. Hofmann, M.A., Brechtbuhl, K., Stäuber, N., 1994. Rapid characterization of new pestivirus strains by direct sequencing of PCR-amplified cDNA from the 5′ noncoding region. Arch. Virol. 139, 217-229.
14. Katz, J.B., Ridpath, J.F., Bolin, S.R., 1993. Presumptive diagnostic differentiation of hog cholera virus from bovine viral diarrhea and border disease viruses by using a cDNA nested-amplification approach. J. Clin. Microbiol. 3, 565-568.
15. Krassnig, R., Schuller, W., Heinrich, J., Werfring, F., Kalaus, P., Fruhwirth, M., 1995. Isolierung des Erregers der Europäischen Schweinepest (ESP) aus importiertem gefrorenen Wildschweinfleisch. Deut. Tierarztl. Wochenschr. 102, 56.
16. Larochelle, R., Magar, R., 1997. Evaluation of the presence of porcine reproductive and respiratory syndrome virus in packaged pig meat using virus isolation and polymerase chain reaction (PCR) method. Vet. Microbiol. 58, 1-8.
17. Liebler, E.M., Waschbüsch, J., Pohlenz, J.F., Moennig, V., Liess, B., 1991. Distribution of antigen of nonc,vtopathogenic and cytopathogenic bovine virus diarrhea virus biotypes in the intestinal tract of calves following experimental production of mucosal disease. Arch. Virol. Suppl. 3, 109-124.
18. Mahnel, H., Mayr, A., 1974. Schweinepest. Ferdinand Enke Verlag, Stuttgart, pp. 2329.
19. Mayr, A., 1997. Vergleichende Untersuchungen über praxisorientierte Methoden zum Nachweis von Viren in Lebensmitteln am Beispiel Aujeszky-lnfektion beim Schwein. J. Vet. Med. B 44, 565-576.
20. Mittelholzer, C., Moser, C., Tratschin, J.D., Hofmann, M.A., 1997. Generation of cytopathogenic subgenomic RNA of classical swine fever virus in persistently infected porcine cell lines. Virus Res. 51, 125-137.
21. Panaccio, M., Lew, A., 1991. PCR based diagnosis in the presence of 8% (v/v) blood. Nucleic Acids Res. 19, 1151.
22. Panaccio, M., Lew, A., 1994. Direct PCR from whole blood using formamide and low temperatures. In: Griffin, H.G., Griffin, A.M. (Eds.), PCR Technology, Current Innovations. CRC Press, Boca Raton, FL, pp. 151-157.
23. Pearson, J.E., 1992. Hog cholera diagnostic techniques. Comp. Immunol. Microbiol. Infect. Dis. 15, 213-219.
24. Peters, W., Greiser-Wilke, I., Moennig, V., Liess, B., 1986. Preliminary serological characterization of bovine viral diarrhoea virus strains using monoclonal antibodies. Vet. Microbiol. 12, 195-200.
25. Ressang, A.A., 1973. Studies on the pathogenesis of hog cholera. Zbl. Vet. Med. B. 20, 272-288.
26. Ruggli, N., Tratschin, J.-D., Mittelholzer, C., Hofmann, M.A., 1996. Nucleotide sequence of classical swine fever virus strain Alfort/187 and transcription of infectious RNA from stably cloned full-length cDNA. J. Virol. 70, 3478-3487.
27. Sandvik, T., Paton, D.J., Lowings, P.J., 1997. Detection and identification of ruminant and porcine pestiviruses by nested amplification of 5′ untranslated cDNA regions. J. Virol. Methods 64, 43-56.
28. Stewart, W.C., Downing, D.R., Carbrey, E.A., Kresse, J.I., Snyder, M.L., 1979. Thermal inactivation of hog cholera virus in ham. Am. J. Vet. Res. 40, 739-741.
29. Summerfield, A., Hofmann, M., McCullough, K.C., 1998. Low density granulocytic cells induced during classical swine fever are targets for virus infection. Vet. Immunol. Immunpathol. (in press).
30. Thür, B., Zlinszky, K., Ehrensperger, F., 1996. Immunhistologie als zuverlässige und effiziente Methode für die Diagnose von BVDV-lnfektionen. Schweiz. Arch. Tierheilkd. 138, 476-482.
31. Voet, D., Voet, J.G., 1990. Biochemistry, Wiley, New York, pp. 210-244.
32. Waldvogel, A.S., Ehrensperger, F., Staub, O.C., 1995. An immunohistochemical study of the distribution of border disease virus in persistently infected sheep. J. Comp. Pathol. 113, 191-200.
33. Wirz, B., Tratschin, J.-D., Müller, H.K., Mitchell, D.B., 1993. Detection of hog cholera virus and differentiation from other pestiviruses by polymerase chain reaction. J. Clin. Microbiol. 31, 1148-1158.