Survival of classical swine fever virus at various temperatures in faeces and urine derived from experimentally infected pigs

Veterinary Microbiology

Volumn 132, Issue 3-4, 2008, Pages 249-259

  Weesendorp, Eefke ^a,b   Stegeman, Arjan ^b   Loeffen, Willie L A ^a  

^a WAGENINGEN UNIVERSITY   (Netherlands)

^b UTRECHT UNIVERSITY   (Netherlands)

Author keywords

Classical swine fever virus; Faeces and urine; Indirect transmission; Survival; Virus inactivation

Indexed keywords

VIRUS RNA;

ANIMAL EXPERIMENT; ARTICLE; FECES ANALYSIS; INOCULATION; MALE; NONHUMAN; PESTIVIRUS; REAL TIME POLYMERASE CHAIN REACTION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TEMPERATURE; URINALYSIS; VIRULENCE; VIRUS INACTIVATION; VIRUS STRAIN; VIRUS SURVIVAL; VIRUS TITRATION; VIRUS TRANSMISSION;

ANIMALS; CLASSICAL SWINE FEVER; CLASSICAL SWINE FEVER VIRUS; FECES; MALE; RNA, VIRAL; SWINE; TEMPERATURE; TIME FACTORS;

CLASSICAL SWINE FEVER VIRUS; SUIDAE;

EID: 53549128090     PISSN: 03781135     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.vetmic.2008.05.020     Document Type: Article

References (35)

1. Anonymous. EU Council directive 2001/89/EC of 23 October 2001 on Community measures for the control of classical swine fever. Off. J. Eur. Communities L316 (2001) 5-35
2. Artois M., Depner K.R., Guberti V., Hars J., Rossi S., and Rutili D. Classical swine fever (hog cholera) in wild boar in Europe. Rev. Sci. Tech. Off. Int. Epiz. 21 (2002) 287-303
3. Bøtner. Survival of Aujeszky's disease virus in slurry at various temperatures. Vet. Microbiol. 29 (1991) 225-235
4. Cox D.R., and Hinkley D.V. Theoretical Statistics (1974), Chapman and Hall, London
5. Depner K., Bauer T., and Liess B. Thermal and pH stability of pestiviruses. Rev. Sci. Tech. Off. Int. Epiz. 11 (1992) 885-893
6. De Smit A.J., Bouma A., Terpstra C., and van Oirschot J.T. Transmission of classical swine fever virus by artificial insemination. Vet. Microbiol. 67 (1999) 239-249
7. De Vos C.J., Saatkamp H.W., Nielen M., and Huirne R.B.M. Scenario tree modeling to analyze the probability of classical swine fever virus introduction into member states of the European Union. Risk Anal. 24 (2004) 237-253
8. De Vos C.J., Saatkamp H.W., Nielen M., and Huirne R.B.M. Sensitivity analysis to evaluate the impact of uncertain factors in a scenario tree model for classical swine fever introduction. Risk Anal. 26 (2006) 1311-1322
9. Edwards S. Survival and inactivation of classical swine fever virus. Vet. Microbiol. 73 (2000) 175-181
10. Elbers A.R.W., Stegeman J.A., Moser H., Ekker H.M., Smak J.A., and Pluimers F.H. The classical swine fever epidemic 1997-1998 in the Netherlands: descriptive epidemiology. Prev. Vet. Med. 42 (1999) 157-184
11. Finney D.J. Statistical Methods in Biological Assay (1978), Charles Griffin & Company Ltd., London pp. 394-401
12. Fritzemeier J., Teuffert J., Greiser-Wilke I., Staubach C., Schlüter H., and Moennig V. Epidemiology of classical swine fever in Germany in the 1990s. Vet. Microbiol. 77 (2000) 29-41
13. ® Release 10 (2007), VSN International, Hemel Hempstead, UK
14. Greiser-Wilke I., Fritzemeier J., Koenen F., Vanderhallen H., Rutili D., De Mia G.M., Romero L., Rosell R., Sanchez-Vizcaino J.M., and San Gabriel A. Molecular epidemiology of a large classical swine fever epidemic in the European Union in 1997-1998. Vet. Microbiol. 77 (2000) 17-27
15. Haas B., Ahl R., Böhm R., and Strauch D. Inactivation of viruses in liquid manure. Rev. Sci. Tech. Off. Int. Epiz. 14 (1995) 435-445
16. Harkness J.W. Classical swine fever and its diagnosis: a current view. Vet. Rec. 116 (1985) 288-293
17. Koenen F., Van Caenegem G., Vermeersch J.P., Vandenheede J., and Deluyker H. Epidemiological characteristics of an outbreak of classical swine fever in an area of high pig density. Vet. Rec. 139 (1996) 367-371
18. Liess B. Pathogenesis and epidemiology of hog cholera. Ann. Rech. Vet. 18 (1987) 139-145
19. McKercher P.D., Yedloutschnig R.J., Callis J.J., Murphy R., Panina G.F., Civardi A., Bugnetti M., Foni E., Laddomada A., Scarano C., and Scatozza F. Survival of viruses in 'Prosciutto di Parma' (Parma ham). Can. Inst. Food Sci. Technol. J. 20 (1987) 267-272
20. Panina G.F., Civardi A., Cordioli P., Massirio I., Scatozza F., Baldini P., and Palmia F. Survival of hog cholera virus (HCV) in sausage meat products (Italian salami). Int. J. Food Microbiol. 17 (1992) 19-25
21. Ressang A.A. Studies on the pathogenesis of hog cholera. I. Demonstration of hog cholera virus subsequent to oral exposure. Zbl. Vet. Med. B 20 (1973) 256-271
22. Ribbens S., Dewulf J., Koenen F., Laevens H., Mintiens K., and De Kruif A. An experimental infection (II) to investigate the importance of indirect classical swine fever virus transmission by excretions and secretions of infected weaner pigs. J. Vet. Med. B 51 (2004) 438-442
23. Ribbens S., Dewulf J., Koenen F., Maes D., and De Kruif A. Evidence of indirect transmission of classical swine fever virus through contacts with people. Vet. Rec. 160 (2007) 687-690
24. Searle S.R., Casella G., and McCulloch C.E. Variance Components (1992), John Wiley, New York
25. Sharpe K., Gibbens J., Morris H., and Drew T. Epidemiology of the 2000 CSF outbreak in East Anglia: preliminary findings. Vet. Rec. 148 (2001) 91
26. Stegeman J.A., Elbers A.R.W., Bouma A., and de Jong M.C.M. Rate of inter-herd transmission of classical swine fever virus by different types of contact during the 1997-8 epidemic in The Netherlands. Epidemiol. Infect. 128 (2002) 285-291
27. Stewart W.C., Downing D.R., Carbrey E.A., Kresse J.I., and Snyder M.L. Thermal inactivation of hog cholera virus in ham. Am. J. Vet. Res. 40 (1979) 739-741
28. Terpstra C., and Wensvoort G. The protective value of vaccine-induced neutralising antibody titres in swine fever. Vet. Microbiol. 16 (1988) 123-128
29. Terpstra C., and de Smit A.J. The 1997/1998 epizootic of swine fever in the Netherlands: control strategies under a non-vaccination regimen. Vet. Microbiol. 77 (2000) 3-15
30. Turner C., Williams S.M., and Cumby T.R. The inactivation of foot and mouth disease, Aujeszky's disease and classical swine fever viruses in pig slurry. J. Appl. Microbiol. 89 (2000) 760-767
31. Van Rijn P.A., Wellenberg G.J., Hakze-van der Honing R., Jacobs L., Moonen P.L., and Feitsma H. Detection of economically important viruses in boar semen by quantitative real time PCR technology. J. Virol. Meth. 120 (2004) 151-160
32. Weesendorp E., Landman W.J.M., Stegeman A., and Loeffen W.L.A. Detection and quantification of classical swine fever virus in air samples originating from infected pigs and experimentally produced aerosols. Vet. Microbiol. 127 (2008) 50-62
33. Weesendorp, E., Stegeman, A., Loeffen, W.L.A., in press. Dynamics of virus excretion via different routes in pigs experimentally infected with classical swine fever virus strains of high, moderate or low virulence. Vet. Microbiol., doi:10.1016/j.vetmic.2008.06.008.
34. Wensvoort G., Terpstra C., Boonstra J., Bloemraad M., and Van Zaane D. Production of monoclonal antibodies against swine fever virus and their use in laboratory diagnosis. Vet. Microbiol. 12 (1986) 101-108
35. Wensvoort, G., Terpstra, C., De Kluyver, E.P., Kragten, C., Warnaar, J.C., 1989. Characterization of pestivirus strains with monoclonal antibodies against hog cholera virus. Epitopes on structural proteins of hog cholera (swine fever) virus. Ph.D. Thesis. University of Utrecht, The Netherlands, pp. 41-51.