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Acta Veterinaria Scandinavica logoLink to Acta Veterinaria Scandinavica
. 1988 Mar 1;29(1):77–84. doi: 10.1186/BF03548395

BVD Virus Antigens in Tissues of Persistently Viraemic, Clinically Normal Cattle: Implications for the Pathogenesis of Clinically Fatal Disease

H Bielefeldt Ohmann 111,211,
PMCID: PMC8152537  PMID: 2849295

Abstract

The cellular events involved in precipitation of the clinically fatal outcome of an infection with bovine viral diarrhoea virus (BVDV) remain unresolved, though it is now known that this course of the infection, Mucosal Disease (MD), only occurs in calves persistently infected with non-cytopathic BVDV. In studies aimed at elucidating the pathogenesis of MD, the distribution of BVDV antigens and infectious virus in tissues of persistently infected, clinically normal calves was investigated. Virus antigen was detected in most tissues, in epithelial and immune cells. No signs of an inflammatory response were detected and cytopathological changes were subtle or absent. The infection may nevertheless create a cell-environment which will enhance replication of cytopathic virus. Variations in the clinical, pathomorphologies and virological appearance of MD-cases may depend on both the host-reactions, including virus-induced immunopathology, and the virus-strain combinations in a putative mixed infection.

Keywords: bovine viral diarrhoea virus; persistent infection; tissue distribution; immunocytochemistry, viral pathogenesis.

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Acknowledgements

This work was supported by the Danish Agricultural and Veterinary Research Council (grant nos. SJVF 13-3681 and 13-3857) and »Landbrugets Hudefond«, Copenhagen, DK. H. Bielefeldt Ohmann is a senior fellow of the Royal Veterinary and Agricultural University of Copenhagen. Thanks are due to Irene Kosokowsky for typing the manuscript.

References

  1. Barber D M, Nettleton P F, Herring JA. Disease in a dairy herd associated with the introduction and spread of bovine virus diarrhoea virus. Vet. Ree. 1985;117:459–464. doi: 10.1136/vr.117.18.459. [DOI] [PubMed] [Google Scholar]
  2. Barlow RM, Nettleton PF, Gardiner A C, Campbell JR, Bonn JM. Persistent bovine virus diarrhoea virus infection in a bull. Vet. Ree. 1986;118:321–324. doi: 10.1136/vr.118.12.321. [DOI] [PubMed] [Google Scholar]
  3. Bielefeldt O H. Bovine viral diarrhoea virus infections. II. Pathogenic studies of spontaneous and experimental cases. Pathomorphologies im-munocytochemical and serological investigations. Copenhagen: Royal Veterinary and Agricultural University; 1981. [Google Scholar]
  4. Bielefeldt O H. Pathogenesis of bovine viral diarrhoea - mucosal disease: distribution and significance of BVDV antigen in diseased calves. Res. Vet. Sci. 1983;34:5–10. doi: 10.1016/S0034-5288(18)32272-0. [DOI] [PubMed] [Google Scholar]
  5. Bielefeldt O H. Double-immuno-labelling systems for phenotyping of immune cells harboring bovine viral diarrhea virus. J. Histochem. Cyto-chem. 1987;35:627–633. doi: 10.1177/35.6.3033062. [DOI] [PubMed] [Google Scholar]
  6. Bielefeldt O H, Bloch H B. Electron microscopic studies of bovine viral diarrhoea virus in tissues on diseases calves and in cell cultures. Arch. Virol. 1982;71:57–74. doi: 10.1007/BF01315175. [DOI] [PubMed] [Google Scholar]
  7. Bielefeldt O, Rønsholt L, Bloch B. Demonstration of bovine viral diarrhoea virus in peripheral blood mononuclear cells of persistently infected, clinically normal cattle. J. Gen. Virol. 1987;68:1971–1982. doi: 10.1099/0022-1317-68-7-1971. [DOI] [PubMed] [Google Scholar]
  8. Bolin S R, McClurkin A W, Cutlip R C, Coria MF. Severe clinical disease induced in cattle persistently infected with non-cytopathic bovine viral diarrhea virus by superinfection with cytopathic bovine viral diarrhea virus. Amer. J. Vet. Res. 1985;46:573–576. [PubMed] [Google Scholar]
  9. Bolin SR, McClurkin A W, CutlipR C, Coria MF. Response of cattle persistently infected with non-cytopathic bovine viral diarrhea virus 1. vaccination for viral diarrhea and to subseqeuent challenge exposure with cytopathic bovine viral diarrhea virus. Amer. J. Vet. Res. 1985;46:2467–2470. [PubMed] [Google Scholar]
  10. Brownlie J, Clarke M C, Howard C J. Experimental production of fatal mucosal disease in cattle. Vet. Ree. 1984;114:535–536. doi: 10.1136/vr.114.22.535. [DOI] [PubMed] [Google Scholar]
  11. Brownlie J, Clarke MC, Howard CJ, Pockock DH. Mucosal disease - a combination of precise immunotolerance and viral superinfection. Ontario: Proc 1st Int. Vet. Immunol Symp. Guelph; 1986. p. 105. [Google Scholar]
  12. Candurra N A, Damonte E B. Influence of cellular functions on the evolution of persistent infections with Junin virus. Arch. Virol. 1985;86:275–282. doi: 10.1007/BF01309831. [DOI] [PubMed] [Google Scholar]
  13. Coria MF, McClurkin A W. Specific immune tolerance in an apparantly healthy bull persistently infected with bovine viral diarrhea virus. J. Amer. Vet. Med. Assoc. 1978;172:449–451. [PubMed] [Google Scholar]
  14. Cutlip R C, McClurkin A W, Coria MF. Lesions in clinically healthy cattle persistently infected with the virus of bovine viral diarrhea - glomerulonephritis and encephalitis. Amer. J. Vet. Res. 1980;47:1938–1941. [PubMed] [Google Scholar]
  15. Diderholm H, Dinter Z: Interference between strains of bovine virus diarroea virus and their capacity to suppress interferon of a heterologous virus. Proc. Soc. Exp. Biol. Med. 1966, 121, 976–980. [DOI] [PubMed]
  16. Done J T, Terlecki S, Richardson C, Harkness J W, Sands J J, Patterson DSP, Sweasey D, Shaw I G, Winkler C E, Duff e S J. Bovine virus diarr-hoea-mucosal disease virus: pathogenicity for the fetal calf following maternal infection. Vet. Ree. 1980;705:473–479. doi: 10.1136/vr.106.23.473. [DOI] [PubMed] [Google Scholar]
  17. Duffell S J, Harkness J W. Bovine virus diarrhoea-mucosal disease infection in cattle. Vet. Ree. 1985;777:240–245. doi: 10.1136/vr.117.10.240. [DOI] [PubMed] [Google Scholar]
  18. Hewicker M, Trautwein G, Stahl C, Liess B. Kidney lesions in cattle persistently infected with bovine viral diarrhoea virus. J. Vet. Med. B. 1987;34:1–12. doi: 10.1111/j.1439-0450.1987.tb00364.x. [DOI] [PubMed] [Google Scholar]
  19. Holland J, Spindler K, Horodyski F, Graban E, Nichol S, VandePol S. Rapid evolution of RNA genomes. Science. 1982;215:1577–1585. doi: 10.1126/science.7041255. [DOI] [PubMed] [Google Scholar]
  20. Laemmli U K. Cleavage of structural proteins during the assambly of the head of bacteriophage T4. Nature (London) 1970;227:680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  21. Littlejohns IR, Walker K H. Aetiology and pathogenesis of mucosal disease of cattle: current concepts, observations and speculation. Aust. Vet. J. 1985;62:101–103. doi: 10.1111/j.1751-0813.1985.tb14150.x. [DOI] [PubMed] [Google Scholar]
  22. McClurkin A W, Littledike E T, Cutlip R C, Frank G H, Coria M R, Bolin S R. Production of cattle immunotolerant to bovine viral diarrhea virus. Can. J. Comp. Med. 1984;48:156–161. [PMC free article] [PubMed] [Google Scholar]
  23. Mills JML, Luginbuhl R E, Nielsen S W. Transmission of bovine mucosal disease using virus recovered from urine. Res. Vet. Sci. 1968;9:500–505. doi: 10.1016/S0034-5288(18)34502-8. [DOI] [PubMed] [Google Scholar]
  24. Oldstone M B A, Shinha Y N, Blout P, Tishou A, Redriguez M, Wedel R v, Lantpert P W. Virus-induced alterations in homeostasis: alterations in differentiated functions of infected cells in vivo. Science. 1982;218:1125–1127. doi: 10.1126/science.7146898. [DOI] [PubMed] [Google Scholar]
  25. Rager-Zisman B, Egan JE, Dress Y, Bloom B R. Isolation of cold-sensitive mutants of measles virus from persistently infected murine neuroblastoma cells. J. Virol. 1984;57:845–855. doi: 10.1128/JVI.51.3.845-855.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Roeder P L, Drew T W. Mucosal disease of cattle a late sequal to fetal infection. Vet. Ree. 1984;114:309–313. doi: 10.1136/vr.114.13.309. [DOI] [PubMed] [Google Scholar]
  27. Scott D W. Mechanisms in immune tolerance. CRC Crit Rev. Immunol. 1984;5:1–25. [PubMed] [Google Scholar]
  28. SharpeA H, Fields BN. Pathogenesis of viral infections. Basic concepts derived from the reovirus model. New Engl. J. Med. 1985;312:486–497. doi: 10.1056/NEJM198502213120806. [DOI] [PubMed] [Google Scholar]
  29. Shirai J, Tanaka Y, Horiuchi T. Interference patterns between strains of bovine viral diarrhea-mucosal disease (BVD-MD) virus. Jpn. J. Vet. Sci. 1984;46:901–904. doi: 10.1292/jvms1939.46.901. [DOI] [PubMed] [Google Scholar]
  30. Taguchi F, Siddel S G, Wege H, terMeulen V. Characterization of a variant virus selected in rat brains after infection by Coronavirus mouse hepatitis virus HMN. J. Virol. 1985;54:429–435. doi: 10.1128/JVI.54.2.429-435.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Towbin H, Stachelin T, Gordon T. Electrophoretic transfer of proteins from polyacrylamine gels to nitrocellulose sheets. Procedure and some applications. Proc. Nat. Acad Sci. USA. 1979;76:4350–4354. doi: 10.1073/pnas.76.9.4350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Ward PA, Cohen S, Flanagan M D. Leukotactic factors elaborated by virus-infected tissues. J. Exp. Med. 1972;755:1095–1103. doi: 10.1084/jem.135.5.1095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Whitaker-Dowling P, Youngner J S. Viral interference dominance of mutant viruses over wild-ty-pe virus in mixed infections. Microbiol Rev. 1987;57:179–191. doi: 10.1128/MR.51.2.179-191.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Yoneda T, Urade M, Sakuda M, Miyazaki T. Altered growth, differentiation, and responsiveness to epidermal growth factor by persistent rubella virus infection. J. Clin. Invest. 1986;77:1613–1621. doi: 10.1172/JCI112477. [DOI] [PMC free article] [PubMed] [Google Scholar]

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