First report of BVDV circulation in sheep in Argentina

Preventive Veterinary Medicine

Volumn 90, Issue 3-4, 2009, Pages 274-277

  Julia S ^a   Craig, M I ^a   Jimenez L S ^a   Pinto, G B ^a   Weber, E L ^a  

^a INSTITUTO NACIONAL DE TECNOLOGÍA AGROPECUARIA INTA   (Argentina)

Author keywords

Argentina; BVDV; Pestivirus; Reservoir; Sheep

Indexed keywords

ANIMAL; ANIMAL DISEASE; ARTICLE; BLOOD; BOVINE DIARRHEA VIRUS; GENETICS; ISOLATION AND PURIFICATION; PHYLOGENY; POLYMERASE CHAIN REACTION; SEROLOGY; SHEEP; VIROLOGY;

ANIMALS; DIARRHEA VIRUSES, BOVINE VIRAL; PHYLOGENY; POLYMERASE CHAIN REACTION; SEROLOGIC TESTS; SHEEP;

ANIMALIA; BORDER DISEASE VIRUS; BORNA DISEASE VIRUS; BOS; BOVINE VIRAL DIARRHEA VIRUS 1; BOVINE VIRAL DIARRHEA VIRUS 2; BUBALUS; CLASSICAL SWINE FEVER VIRUS; LAMA GLAMA; OVIS ARIES; PESTIVIRUS; SUS SCROFA; SUS SCROFA DOMESTICA;

EID: 67349104439     PISSN: 01675877     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.prevetmed.2009.05.015     Document Type: Article

References (32)

1. Anderson E.C., and Rowe L.W. The prevalence of antibody to the viruses of bovine virus diarrhoea, bovine herpes virus 1, rift valley fever, ephemeral fever and bluetongue and to Leptospira sp in free-ranging wildlife in Zimbawe. Epidemiol. Infect. 121 (1998) 441-449
2. Becher P., Orlich M., Shannon A.D., Horner G., König M., and Thiel H.-J. Phylogenetic analysis of pestiviruses from domestic and wild ruminants. J. Gen. Virol. 78 (1997) 1357-1366
3. Becher P., Orlich M., Kosmidou A., König M., Baroth M., and Thiel H.-J. Genetic diversity of pestiviruses: identification of novel groups and implications for classification. Virology 262 (1999) 64-71
4. Becher P., Avalos Ramirez R., Orlich M., Cedillo Rosales S., Konig M., Schweizer M., Stalder H., Schirrmeier H., and Thiel H.-J. Genetic and antigenic characterization of novel pestivirus genotypes: implications for classification. Virology 311 (2003) 96-104
5. Carlsson U. Border disease in sheep caused by transmission of virus from cattle persistently infected with bovine virus diarrhoea virus. Vet. Rec. 128 (1991) 145-147
6. Carlsson U., and Belák K. Border disease virus transmitted to sheep and cattle by a persistently infected ewe: epidemiology and control. Acta Vet. Scand. 35 (1994) 79-88
7. Craig M.I., Venzano A., König G., Morris W.E., Jiménez L., Juliá S., Capellino F., Blanco Viera J., and Weber E.L. Detection of bovine viral diarrhoea virus (BVDV) nucleic acid and antigen in different organs of water buffaloes (Bubalus bubalis). Res. Vet. Sci. 85 (2008) 194-196
8. Duffell S.J., and Harkness J.W. Bovine virus diarrhoea-mucosal disease infection in cattle. Vet. Rec. 117 (1985) 240-245
9. Felsenstein, J. 1989. PHYLIP - Phylogeny Inference Package (Version 3.2). Cladistics 5: 164-166.
10. Hamblin C., and Hedger R.S. The prevalence of antibodies to bovine viral diarrhoea/mucosal disease virus in African wildlife. Comp. Immunol. Microbiol. Infect. Dis. 2 (1979) 295-303
11. Jones L.R., Zandomeni R., and Weber E.L. Genetic typing of bovine viral diarrhea virus isolates from Argentina. Vet. Microbiol. 81 (2001) 367-375
12. Løken T., Krogsrud J., and Bjerkás I. Outbreaks of border disease in goats induced by a pestivirus-contaminated orf vaccine, with virus transmission to sheep and cattle. J. Comp. Pathol. 104 (1991) 195-209
13. Meyer H., Liess B., Frey H.R., Hermanns W., and Trautwein G. Experimental transplacental transmission of hog colera virus in pigs. IV. Virological and serological studies in newborn piglets. Zentrlbl. Veterinarmed. B 28 (1981) 659-668
14. Nettleton P.F., and Entrican G. Ruminant pestiviruses. Br. Vet. J. 151 (1995) 615-642
15. Nettleton P.F., Gilmour J.S., Herring J.A., and Sinclair J.A. The production and survival of lambs persistently infected with border disease virus. Comp. Immunol. Microbiol. Infect. Dis. 15 (1992) 179-188
16. Pacheco J.M., and Lager I. Indirect method ELISA for the detection of antibodies against bovine diarrhea virus in bovine serum. Rev. Argent. Microbiol. 35 (2003) 19-23
17. Paton D.J., Simpson V., and Done S.H. Infection of pigs and cattle with bovine viral diarrhoea virus on a farm in England. Vet. Rec. 131 (1992) 185-188
18. Paton D.J., Carlsson U., Lowings J.P., Sands J.J., Vilcek S., and Alenius S. Identification of herd-specific bovine viral diarrhoea virus isolates from infected cattle and sheep. Vet. Microbiol. 43 (1995) 283-294
19. Puntel M., Fondevila N.A., Blanco Viera J., ÓDonnell V.K., Marcovecchio J.F., Carrillo B.J., and Schudel A.A. Serological survey of viral antibodies in llamas (Lama glama) in Argentina. Zentralbl. Veterinarmed. B 46 (1999) 157-161
20. Rweyemamu M.M., Fernandez A.A., Espinosa A.M., Schudel A.A., Lager I.A., and Mueller S.B. Incidence, epidemiology and control of bovine virus diarrhoea virus in South America. Rev. Sci. Tech. 9 (1990) 207-221
21. Saliki J.T., and Dubovi E.J. Laboratory diagnosis of bovine viral diarrhea virus infections. Vet. Clin. North Am. Food Anim. Pract. 20 (2004) 69-83
22. Scherer C.F., Flores E.F., Weiblen R., Caron L., Irigoyen L.F., Neves J.P., and Maciel M.N. Experimental infection of pregnant ewes with bovine viral diarrhea virus type-2 (BVDV-2): effects on the pregnancy and fetus. Vet. Microbiol. 79 (2001) 285-299
23. Snowdon W.A., and French E.L. The bovine mucosal disease-swine fever virus complex in pigs. Aust. Vet. J. 44 (1968) 179-184
24. Sullivan D.G., and Akkina R.K. A nested polymerase chain reaction assay to differentiate pestiviruses. Virus Res. 38 (1995) 231-239
25. Terpstra C., and Wensvoort G. Natural infections of pigs with bovine viral diarrhea virus associated with signs resembling swine fever. Res. Vet. Sci. 45 (1988) 137-142
26. Toplak I., Sandvik T., Barlic-Maganja D., Grom J., and Paton D.J. Genetic typing of bovine viral diarrhoea virus: most Slovenian isolates are of genotypes 1d and 1f. Vet. Microbiol. 99 (2004) 175-185
27. van Oirschot J.T., and Terpstra C. A congenital persistent swine fever infection. I. Clinical and virological observations. Vet. Microbiol. 2 (1977) 121-132
28. Vilcek S., Herring A.J., Herring J.A., Nettleton P.F., Lowings J.P., and Paton D.J. Pestiviruses isolated from pigs, cattle and sheep can be allocated into at least three genogroups using polymerase chain reaction and restriction endonuclease analysis. Arch. Virol. 136 (1994) 309-323
29. Vilcek S., and Belák S. Genetic identification of pestivirus strain Frijters as a border disease virus from pigs. J. Virol. Methods 60 (1996) 103-108
30. Vilcek S., Nettleton P.F., Paton D.J., and Belák S. Molecular characterization of ovine pestiviruses. J. Gen. Virol. 78 (1997) 725-735
31. Vilcek S., Durkovic B., Kolesárová M., Greiser-Wilke I., and Paton D. Genetic diversity of international bovine viral diarrhoea virus (BVDV) isolates: identification of a new BVDV-1 genetic group. Vet. Res. 35 (2004) 609-615
32. Vilcek S., and Nettleton P.F. Pestiviruses in wild animals. Vet. Microbiol. 116 (2006) 1-12