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. 2007 Nov 19;151(6):615–642. doi: 10.1016/S0007-1935(95)80145-6

Ruminant pestiviruses

PF Nettleton 1, G Entrican 1
PMCID: PMC7130397  PMID: 8605577

Abstract

The ruminant pestiviruses, bovine virus diarrhoea virus (BVDV) and border disease virus (BDV) are highly successful and important pathogens which infect ruminant species worldwide. Although the serological relationships among ruminant pestiviruses require further clarification, there is growing evidence for two antigenic groups, one of which predominates in cattle and one in sheep. The success of pestiviruses stems from the ability of the non-cytopathic (NCP) biotype of the virus to cross the placenta and establish a persistent infection (PI) in the developing foetus. This biotype should be regarded as the ‘normal’ biotype with the cytopathic (CP) biotype being an abnormal virus that is usually isolated only from PI animals dying from mucosal disease. Recent molecular evidence points to CP viruses arising from their NCP counterparts by recombination events that include the insertion of host RNA and/or the duplication of viral RNA sequences. However, the biological mechanism through which CP viruses kill cells remains unknown. Virtually all CP and NCP viruses cause only mild, transient clinical symptoms in healthy adult animals and stimulate a protective immune response. Despite the urgent requirement for a safe, effective vaccine, there is still no commercial vaccine that has been shown to immunize dams so that foetal infection is prevented. In the absence of an effective vaccine, reliable diagnostic techniques are essential to implement effective control measures. There is now a range of monoclonal antibody-based enzyme-linked immunosorbent assays for identifying PI or convalescent animals. These tests are specific, rapid, sensitive and reliable but may themselves become redundant as they are superceded by ever-increasing molecular biology-based techniques.

Keywords: Bovine virus diarrhoea, border disease, pestivirus, virus persistence, congenital infection

References

  1. Barber D.M.L., Nettleton P.F. Investigations into bovine viral diarrhoea virus in a dairy herd. Veterinary Record. 1993;133:549–550. doi: 10.1136/vr.133.22.549. [DOI] [PubMed] [Google Scholar]
  2. Barber D.M.L., Nettleton P.F., Herring J.A. Disease in a dairy herd associated with the introduction and spread of bovine virus diarrhoea virus. Veterinary Record. 1985;117:459–464. doi: 10.1136/vr.117.18.459. [DOI] [PubMed] [Google Scholar]
  3. Barlow R.M., Patterson D.S.P. Border disease of sheep: a virus-induced teratogenic disorder. Advances in Veterinary Medicine. 1982;36:1–90. [Google Scholar]
  4. Becher P., Shannon A.D., Tautz N., Thiel H.-J. Molecular characterisation of border disease virus, a pestivirus from sheep. Virology. 1994;198:542–551. doi: 10.1006/viro.1994.1065. [DOI] [PubMed] [Google Scholar]
  5. Berry E.S., Lewis T.L., Ridpath J.F., Evermann J.F., Rupnow B.A., Qi F. Proceedings of the 2nd Symposium on Pestiviruses. Fondation Marcel Merieux, for ESVV; Lyon, France: 1993. Genomic comparison of ruminant pestiviruses; pp. 53–59. [Google Scholar]
  6. Bielefeldt Ohmann H., Ronsholt L., Bloch B. Demonstration of bovine viral diarrhea virus in peripheral blood mononuclear cells of persistently infected, clinically normal cattle. Journal of General Virology. 1987;68:1971–1982. doi: 10.1099/0022-1317-68-7-1971. [DOI] [PubMed] [Google Scholar]
  7. Bolin S.R. Viral and viral protein specificity of antibodies induced in cows persistently infected with noncytopathic bovine viral diarrhea virus after vaccination with cytopathic bovine viral diarrhea virus. American Journal of Veterinary Research. 1988;49:1040–1044. [PubMed] [Google Scholar]
  8. Bolin S.R. Control of bovine virus diarrhoea virus. Revue Scientifique et Technique Office International des Epizooties. 1990;9:163–171. doi: 10.20506/rst.9.1.483. [DOI] [PubMed] [Google Scholar]
  9. Bolin S.R., Moennig V., Kelso Gourley N.E., Ridpath J. Monoclonal antibodies with neutralizing activity segregate isolates of bovine viral diarrhea virus into groups. Archives of Virology. 1988;99:117–123. doi: 10.1007/BF01311029. [DOI] [PubMed] [Google Scholar]
  10. Bonniwell M.A., Nettleton P.F., Gardiner A.C., Barlow R.M., Gilmour J.S. Border disease without nervous signs or fleece changes. Veterinary Record. 1987;120:246–249. doi: 10.1136/vr.120.11.246. [DOI] [PubMed] [Google Scholar]
  11. Bootman J.S., Kitchin P.A. An international collaborative study to assess a set of reference reagents for HIV-1 PCR. Journal of Virological Methods. 1992;37:23–42. doi: 10.1016/0166-0934(92)90018-9. [DOI] [PubMed] [Google Scholar]
  12. Brock K.V., Potgieter L.N.D. Detection of bovine viral diarrhea virus in serum from cattle by dot blot hybridization assay. Veterinary Microbiology. 1990;24:297–306. doi: 10.1016/0378-1135(90)90179-Y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Brock K.V. Detection of persistent bovine viral diarrhea virus infections by DNA hybridization and polymerase chain reaction assay. Archives of Virology. 1991;(Suppl. 3):199–208. doi: 10.1007/978-3-7091-9153-8_24. [DOI] [PubMed] [Google Scholar]
  14. Brown G.B., Bolin S.R., Frank D.E., Roth J.A. Defective function of leukocytes from cattle persistently infected with bovine viral diarrhea virus, and the influence of recombinant cytokines. American Journal of Veterinary Reseach. 1991;52:381–387. [PubMed] [Google Scholar]
  15. Brownlie J. The pathways for bovine virus diarrhoea virus biotypes in the pathogenesis of disease. Archives of Virology. 1991;(Suppl. 3):79–96. doi: 10.1007/978-3-7091-9153-8_10. [DOI] [PubMed] [Google Scholar]
  16. Burrells C., Nettleton P.F., Reid H.W. Lymphocytes subpopulations in the blood of sheep persistently infected with border disease virus. Clinical and Experimental Immunology. 1989;76:446–451. [PMC free article] [PubMed] [Google Scholar]
  17. Carllson U. Border disease in sheep caused by transmission of virus from cattle persistently infected with bovine virus diarrhoea virus. Veterinary Record. 1991;128:145–147. doi: 10.1136/vr.128.7.145. [DOI] [PubMed] [Google Scholar]
  18. Carllson U., Alenius S., Sunquist B. Protective effect of an ISCOM bovine virus diarrhoea virus (BVDV) vaccine against an experimental BVDV infection in vaccinated and non-vaccinatedpregnant ewes. Vaccine. 1991;9:557–580. doi: 10.1016/0264-410x(91)90245-2. [DOI] [PubMed] [Google Scholar]
  19. Chappuis G., Brun A., Kato F., Dauvergne M., Reynaud G., Duret C. Etudes serologiques et immunologiques realisée à la suite de l'isolement d'un pestivirus dans un foyer ovina chez des moutons de l'Aveyron. In: Espinasse J., Savey M., editors. Pestiviroses des ovins et des bovins: nouvelles connaissances utilisation pour une strategie de controle. Societe Francaise de Buiatrie; 1986. pp. 55–66. [Google Scholar]
  20. Cho H.J., Masri S.A., Deregt D., Yeo S.-G., Golsteyn Thomas E.J. Sensitivity and specificity of an enzyme-linked immuno-sorbent assay for the detection of bovine viral diarrhea virus antibody in cattle. Canadian Journal of Veterinary Research. 1991;55:56–59. [PMC free article] [PubMed] [Google Scholar]
  21. Collett M.S. Molecular genetics of pestiviruses. Comparative Immunology, Microbiology and Infectious Diseases. 1992;15:145–154. doi: 10.1016/0147-9571(92)90087-8. [DOI] [PubMed] [Google Scholar]
  22. Collett M.S., Larson R., Gold C., Strick D., Anderson D.K., Purchio A.F. Molecular cloning and nucleotide sequence of the pestivirus bovine viral diarrhea virus. Virology. 1988;165:191–199. doi: 10.1016/0042-6822(88)90672-1. [DOI] [PubMed] [Google Scholar]
  23. Collett M.S., Tamura J.K., Warrener P., Poole T., Potgieter L.N.D., Wiskerchen M.A. Proceedings of the 2nd Symposium on Pestiviroses. Fondation Marcel Merieux, for ESW; Lyon, France: 1993. Pestivirus protein biogenesis and enzymatic activities associated with viral proteins; pp. 7–15. [Google Scholar]
  24. Corapi W.V., Donis R.O., Dubovi E.J. Characterisation of a panel of monoclonal antibodies and their use in the study of the antigenic diversity of bovine viral diarrhea virus. American Journal of Veterinary Research. 1989;51:1388–1394. [PubMed] [Google Scholar]
  25. Darbyshire J.H. A serological relationship between swine fever and mucosal disease of cattle. Veterinary Record. 1960;72:331. [Google Scholar]
  26. David G.P., Crawshaw T.R., Gunning R.F., Hibberd R.C., Lloyd G.M., Marsh P.R. Severe disease in adult daily cattle in three UK dairy herds associated with BVD virus infection. Veterinary Record. 1994;134:468–472. doi: 10.1136/vr.134.18.468. [DOI] [PubMed] [Google Scholar]
  27. De Moerlooze L., Desport M., Renard A., Lecomte C., Brownlie J., Martial J.A. The coding region for the 54 kDa protein of several pestiviruses lacks host insertions but reveals a ‘zinc finger-like’ domain. Virology. 1990;177:812–815. doi: 10.1016/0042-6822(90)90555-6. [DOI] [PubMed] [Google Scholar]
  28. De Moerlooze L., Renard A., Lecomte C., Martial J.A. A “zinc finger-like” domain in the 54 kDa protein of several pestiviruses. Archives of Virology. 1991;(Suppl. 3):41–46. [PubMed] [Google Scholar]
  29. Deng R., Brock K.W. Molecular cloning and nucleotide sequence of a pestivirus genome, noncytopathic bovine viral diarrhoea virus strain SD-1. Virology. 1992;191:867–879. doi: 10.1016/0042-6822(92)90262-n. [DOI] [PubMed] [Google Scholar]
  30. Depner K., Hubschle O.J.B., Liess B. BVD-virus infections in goats—experimental studies on transmissibility of the virus and its effect on reproduction. Archives of Virology. 1991;(Suppl. 3):253–256. doi: 10.1007/978-3-7091-9153-8_31. [DOI] [PubMed] [Google Scholar]
  31. Depner K., Bauer Th., Liess B. Thermal and pH stability of pestiviruses. Revue Scientifique et Technique Office International des Epizooties. 1992;11:885–893. doi: 10.20506/rst.11.3.638. [DOI] [PubMed] [Google Scholar]
  32. Deregt D., Masri S.A., Cho H.J., Bielefeldt Ohmann H. Monoclonal antibodies to the p80/125 and gp53 proteins of bovine viral diarrhea virus: their potential use as diagnostic reagents. Canadian Journal of Veterinary Research. 1990;54:343–348. [PMC free article] [PubMed] [Google Scholar]
  33. Donis R.O., Corapi W., Dubovi E.J. Neutralizing monoclonal antibodies to bovine viral diarrhoea virus bind to the 56 K to 58 K glycoprotein. Journal of General Virology. 1988;69:77–86. doi: 10.1099/0022-1317-69-1-77. [DOI] [PubMed] [Google Scholar]
  34. Durham P.J.K., Hassard L.E. An enzyme-linked immunosorbent assay (ELISA) for antibodies to bovine viral diarrhea virus. Veterinary Microbiology. 1990;22:1–10. doi: 10.1016/0378-1135(90)90118-f. [DOI] [PubMed] [Google Scholar]
  35. Dutia B.M., Entrican G., Nettleton P.F. Cytopathic and noncytopathic biotypes of Border disease virus induce polypeptides of different molecular weight with common antigenic determinants. Journal of General Virology. 1990;71:1227–1232. doi: 10.1099/0022-1317-71-5-1227. [DOI] [PubMed] [Google Scholar]
  36. Edwards S., Sands J.J., Harkness J.W. The application of monoclonal antibody panels to characterise pestivirus isolates from ruminants in Great Britain. Archives of Virology. 1988;102:197–206. doi: 10.1007/BF01310825. [DOI] [PubMed] [Google Scholar]
  37. Edwards S., Moennig V., Wensvoort G. The development of an international reference panel of monoclonal antibodies for the differentiation of hog cholera virus from other pestiviruses. Veterinary Microbiology. 1991;29:101–108. doi: 10.1016/0378-1135(91)90118-y. [DOI] [PubMed] [Google Scholar]
  38. Ellis J.A., Davis W.C., Belden E.I., Pratt D.L. Flow cytofluorimetric analysis of lymphocyte subset alterations in cattle infected with bovine viral diarrhea virus. Veterinary Pathology. 1988;25:231–236. doi: 10.1177/030098588802500308. [DOI] [PubMed] [Google Scholar]
  39. Entrican G., Flack A., Hopkins J., MacLean M., Nettleton P.F. Detection of border disease virus in sheep efferent lymphocytes by immunocytochemical and in situ hybridisation techniques. Archives of Virology. 1991;(Suppl. 3):175–180. doi: 10.1007/978-3-7091-9153-8_21. [DOI] [PubMed] [Google Scholar]
  40. Entrican G., Hopkins J., MacLean M., McConnell I., Nettleton P.F. Cell phenotypes in the efferent lymph of sheep persistently infected with border disease virus. Clinical and Experimental Immunology. 1992;87:393–398. doi: 10.1111/j.1365-2249.1992.tb03008.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Entrican G., Dand A., Nettleton P.F. Evaluation of anti-pestivirus monoclonal antibodies for the development of an ELISA to detect viraemic cattle and sheep. Veterinary Microbiology. 1995;43:65–74. doi: 10.1016/0378-1135(94)00081-7. [DOI] [PubMed] [Google Scholar]
  42. Fenton A., Entrican G., Herring J.A., Nettleton P.F. An ELISA for detecting pestivirus antigen in the blood of sheep persistently infected with border disease virus. Journal of Virological Methods. 1990;27:253–260. doi: 10.1016/0166-0934(90)90093-u. [DOI] [PubMed] [Google Scholar]
  43. Fenton A., Nettleton P.F., Entrican G., Herring J.A., Malloy C., Greig A., Low J.C. Identification of cattle infected with bovine virus diarrhoea virus using a monoclonal antibody capture ELISA. Archives of Virology. 1991;(Suppl. 3):169–174. doi: 10.1007/978-3-7091-9153-8_20. [DOI] [PubMed] [Google Scholar]
  44. Fenton A., Sinclair J.A., Entrican G., Herring J.A., Malloy C., Nettleton P.F. A monoclonal antibody capture ELISA to detect antibody to border disease virus in sheep serum. Veterinary Microbiology. 1991;28:327–333. doi: 10.1016/0378-1135(91)90067-p. [DOI] [PubMed] [Google Scholar]
  45. Fernelius A.L., Lambert G., Packer R.A. Bovine viral diarrhea virus-host cell interactions: adaptation, propagation, modification and detection of virus in rabbits. American Journal of Veterinary Research. 1969;30:1541–1550. [PubMed] [Google Scholar]
  46. Giangaspero M., Vacirca G., Buettner M., Wolf G., Vanopdenbosch E., Muyldermans G. Serological and antigenical findings indicating pestivirus in man. Archives of Virology. 1993;(Suppl. 7):53–62. doi: 10.1007/978-3-7091-9300-6_5. [DOI] [PubMed] [Google Scholar]
  47. Greiser-Wilke I., Haas L., Dittmar K., Liess B., Moennig V. RNA insertions and gene duplications in the nonstructural protein p125 region of pestivirus strains and isolates in vitro and in vivo. Virology. 1993;193:977–980. doi: 10.1006/viro.1993.1209. [DOI] [PubMed] [Google Scholar]
  48. Gunn H.M. Role of fomites and flies in the transmission of bovine viral diarrhoea virus. Veterinary Record. 1993;132:584–585. doi: 10.1136/vr.132.23.584. [DOI] [PubMed] [Google Scholar]
  49. Harkness J.W., Roeder P.L. The comparative biology of classical swine fever. In: Liess B., editor. Classical Swine Fever and Related Viral Infections. Martinus Nijhoff Publishing; Amsterdam: 1988. pp. 233–288. [Google Scholar]
  50. Houe H., Heron I. Immune response to other agents of calves persistently infected with bovine virus diarrhoea virus (BVDV) Acta Veterinaria Scandinavica. 1993;34:305–310. doi: 10.1186/BF03548195. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Houe H., Meyling A. Prevalence of bovine virus diarrhoea (BVD) in 19 Danish dairy herds and estimation of incidence of infection in early pregnancy. Preventative Veterinary Medicine. 1991;11:9–16. [Google Scholar]
  52. Howard C.J. Immunological responses to bovine viral diarrhoea virus infections. Revue Scientifique et Technique Office International des Epizooties. 1990;9:95–103. doi: 10.20506/rst.9.1.488. [DOI] [PubMed] [Google Scholar]
  53. Howard C.J., Brownlie J., Clarke M.C. Comparison by the neutralisation assay of pairs of non-cytopathogenic and cytopathogenic strains of bovine virus diarrhoea virus isolated from cases of mucosal disease. Veterinary Microbiology. 1987;13:361–369. doi: 10.1016/0378-1135(87)90067-8. [DOI] [PubMed] [Google Scholar]
  54. Howard C.J., Clarke M.C., Sopp P., Brownlie J. Immunity to bovine virus diarrhoea virus in calves: the role of different T cell subpopulations analysed by specific depletion in vivo withmonoclonal antibodies. Veterinary Immunology and Immunopathology. 1992;32:303–314. doi: 10.1016/0165-2427(92)90052-r. [DOI] [PubMed] [Google Scholar]
  55. Jensen J., Schultz R.D. Effect of infection by bovine viral diarrhea virus (BVDV) in vitro on interleukin-1 activity of bovine monocytes. Veterinary Immunology and Immunopathology. 1991;29:251–265. doi: 10.1016/0165-2427(91)90018-8. [DOI] [PubMed] [Google Scholar]
  56. Katz J.B., Ridpath J.F., Bolin S.R. Presumptive diagnostic differentiation of hog cholera virus from bovine viral diarrhea and border disease viruses by using a cDNAnested-amplification approach. Journal of Clinical Microbiology. 1993;31:565–568. doi: 10.1128/jcm.31.3.565-568.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. Kirkland P.D., Hart K.G., Moyle A., Rogan E. The impact of pestivirus on an artifical breeding program for cattle. Australian Veterinary Journal. 1990;67:261–263. doi: 10.1111/j.1751-0813.1990.tb07782.x. [DOI] [PubMed] [Google Scholar]
  58. Kirkland P.D., Richards S.G., Rothwell S.G., Stanley J.F. Replication of bovine viral diarrhoea virus in the reproductive tract and excretion of virus in semen during acute and chronic infections. Veterinary Record. 1991;128:587–590. doi: 10.1136/vr.128.25.587. [DOI] [PubMed] [Google Scholar]
  59. Kreeft H.A.J.G., Greiser-Wilke I., Moennig V., Horzinek M.C. Attempts to characterise bovine viral diarrhea virus isolated from cattle after immunization with a contaminated vaccine. Deutsche Tierarztliche Wochenzeitschrift. 1990;97:63–65. [PubMed] [Google Scholar]
  60. Kwang J., Littledike E.T., Bolin S., Collett M.S. Efficiency of various cloned DNA probes for detection of bovine viral diarrhea viruses. Veterinary Microbiology. 1991;28:279–288. doi: 10.1016/0378-1135(91)90082-Q. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Larsson B., Fossum C. Bovine virus diarrhoea virus induces in vitro a proliferative response of peripheral blood mononuclear cells from cattle immunized by infection. Veterinary Microbiology. 1992;311:317–325. doi: 10.1016/0378-1135(92)90124-c. [DOI] [PubMed] [Google Scholar]
  62. Laude H., Gelfi J. Properties of border disease virus as studied in a sheep cell line. Archives of Virology. 1979;62:341–346. doi: 10.1007/BF01318108. [DOI] [PubMed] [Google Scholar]
  63. Lecomte C., Pin J.J., DeMoerlooze L., Vanderbergh D., Lambert A.F., Pastoret P.P., Chappuis G. ELISA detection of bovine viral diarrhoea virus specific antibodies using recombinant antigen and monoclonal antibodies. Veterinary Microbiology. 1990;23:193–201. doi: 10.1016/0378-1135(90)90149-p. [DOI] [PubMed] [Google Scholar]
  64. Lewis T.L., Ridpath J.F., Bolin S.R., Berry E.S. Detection of BVD viruses using synthetic oligonucleotides. Archives of Virology. 1991;117:269–278. doi: 10.1007/BF01310770. [DOI] [PubMed] [Google Scholar]
  65. Liess B., Blindow H., Orban S., Sasse-Patzer B., Frey H.R., Timm D. Aborte, Totgeburten, Kummernb, Lammersteben in Zwei Schafherden nordwest-Deutschlands—“Border disease” in der Bundersrepublik? Deutsche Tierarztliche Wochenzeitschrift. 1982;89:6–11. [PubMed] [Google Scholar]
  66. Loken T., Bjerkas I., Hyllseth B. Border disease in goats in Norway. Research in Veterinary Science. 1982;33:130–131. [PubMed] [Google Scholar]
  67. Loken T., Krogsrud J., Bjerkas I. Outbreaks of border disease in goats induced by a pestivirus-contaminated orf vaccine with virus transmission to sheep and cattle. Journal of Comparative Pathology. 1991;104:195–209. doi: 10.1016/s0021-9975(08)80103-x. [DOI] [PubMed] [Google Scholar]
  68. Lohr C.H., Evermann J.F., Ward A.C. Investigations of dams and their off-spring inoculated with a vaccine contaminated by bovine viral diarrhea virus. Veterinary Medicine Small Animal Clinician. 1983:1263–1266. August. [Google Scholar]
  69. Markham A.J.F., Ramnaraine M.L. Release of Immunosuppressive substances from tissue culture cells infected with bovine viral diarrhea virus. American Journal of Veterinary Research. 1985;46:879–883. [PubMed] [Google Scholar]
  70. Meyers G., Rumenapf T., Thiel H.J., Dubovi E.J. Vol. 90. Cold Spring Harbor Laboratory Press; 1990. Insertion of cellular sequences in the genorne of a togavirus; pp. 47–51. (Vaccines). [Google Scholar]
  71. Meyers G., Tautz N., Dubovi E.J., Thiel H.-J. Viral cytopathogenicity correlated with integration of ubiquitin-coding sequences. Virology. 1991;180:602–616. doi: 10.1016/0042-6822(91)90074-L. [DOI] [PMC free article] [PubMed] [Google Scholar]
  72. Meyers G., Tautz N., Stark R. Rearrangement of viral sequences in cytopathogenic pestiviruses. Virology. 1992;191:368–386. doi: 10.1016/0042-6822(92)90199-Y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  73. Meyling A. Detection of BVD virus in viraemic cattle by an indirect irnrnunoperoxidase technique. In: McNulty M.S., McFerran J.B., editors. Recent Advances in Virus Diagnosis. Martinus Nijhoff for the CEC; Amsterdam: 1984. pp. 37–46. [Google Scholar]
  74. Mignon, B., Dubuisson, J., Bararowski, E. et al. A monoclonal ELISA for bovine viral diarrhoea pestivirus antigen detection in persistently infected cattle. Journal of Virological Methods35, 177–188. [DOI] [PubMed]
  75. Nettleton P.F. The epidemiology of bovine virus diarrhoea virus. In: Thrusfield M.V., editor. Proceedings of the Society of Veterinary Epidemiology and Preventative Medicine. 1986. pp. 42–53. [Google Scholar]
  76. Nettleton P.F. Pathogenesis and epidemiology of border disease. Annales de Recherches Veterinaires. 1987;18:147–155. [PubMed] [Google Scholar]
  77. Nettleton P.F. Pestivirus infections in ruminants other than cattle. Revue Scientifique et Technique Office International des Epizoolies. 1990;9:131–150. doi: 10.20506/rst.9.1.485. [DOI] [PubMed] [Google Scholar]
  78. Nettleton P.F., Gilmour J.S., Herring J.A., Sinclair J.A. The production and survival of lambs persistently infected with border disease virus. Comparative Immunology, Microbiology and Infectious Diseases. 1992;15:179–188. doi: 10.1016/0147-9571(92)90091-5. [DOI] [PubMed] [Google Scholar]
  79. Nettleton P.F., Rweyemamu M.M., Sylla D. Pestivirus contamination of veterinary vaccines. Panvac Vaccine Bulletin. 1992;2:24–33. [Google Scholar]
  80. Onions D., Lees G. Human retroviruses and herpesviruses: problems and solutions in safety testing of biologicals. Developments in Biological Standardization. 1991;75:145–158. [PubMed] [Google Scholar]
  81. Onisk D.V., Srikumaran S., Kelling C.L., Frey M.L. Bovine viral diarrhoea virus-specific bovine monoclonal antibody. Archives of Virology. 1991;121:219–225. doi: 10.1007/BF01316756. [DOI] [PubMed] [Google Scholar]
  82. Paton D.J., Ibata G., Edwards S., Wensvoort G. An ELISA detecting antibody to conserved pestivirus epitopes. Journal of Virological Methods. 1991;31:315–324. doi: 10.1016/0166-0934(91)90169-z. [DOI] [PubMed] [Google Scholar]
  83. Paton D.J., Sands J.J., Roehe P.M. BVD monoclonal antibodies: relationship between viral protein specificity and viral strain specificity. Archives of Virology. 1991;(Suppl. 3):47–54. doi: 10.1007/978-3-7091-9153-8_6. [DOI] [PubMed] [Google Scholar]
  84. Paton D.J., Lowings J.R.P., Barrett A.D. Epitope mapping of the gp53 envelope protein of bovine viral diarrhea virus. Virology. 1992;190:763–772. doi: 10.1016/0042-6822(92)90914-b. [DOI] [PubMed] [Google Scholar]
  85. Paton D.J., Simpson V., Done S.H. Infection of pigs and cattle with bovine viral diarrhoea virus on a farm in England. Veterinary Record. 1992;131:185–188. doi: 10.1136/vr.131.9.185. [DOI] [PubMed] [Google Scholar]
  86. Penny C.D., Scott P.R., Watt N.J., Greig A. Necrotic enteritis of unknown aetiology in young beef calves at pasture. Veterinary Record. 1994;134:296–299. doi: 10.1136/vr.134.12.296. [DOI] [PubMed] [Google Scholar]
  87. Pocock D.H., Howard C.J., Clarke M.C., Brownlie J. Variation in the intracellular polypeptide profiles from different isolates of bovine virus diarrhoea virus. Archives of Virology. 1987;94:43–53. doi: 10.1007/BF01313724. [DOI] [PubMed] [Google Scholar]
  88. Potts B.J., Sever J.L., Tzan N.R., Huddleston D., Elder G.A. Possible role of pestiviruses in microcephaly. Lancet. 1987;i:972. doi: 10.1016/s0140-6736(87)90311-4. [DOI] [PubMed] [Google Scholar]
  89. Qi F., Gustad T., Lewis T.L., Berry E.S. The nucleotide sequence of the 5′-untranslated region of bovine viral diarrhoea virus: its use as a probe in rapid detection of bovine viral diarrhoea viruses and border disease viruses. Molernlar and Cellular Probes. 1993;7:349–356. doi: 10.1006/mcpr.1993.1052. [DOI] [PubMed] [Google Scholar]
  90. Qi F., Ridpath J., Lewis T., Bolin S.R., Berry E.S. Analysis of the bovine viral diarrhea virus genome for possible cellular insertions. Virology. 1992;189:285–292. doi: 10.1016/0042-6822(92)90704-s. [DOI] [PubMed] [Google Scholar]
  91. Qvist P., Houe H., Aasted B., Meyling A. Comparison of flow cytometry and virus isolation in cell culture for identification of cattle persistently infected with bovine viral diarrhea virus. Journal of Clinical Microbiology. 1991;29:660–661. doi: 10.1128/jcm.29.3.660-661.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  92. Renard A., Guiot C., Schmetz D. Molecular cloning bovine viral diarrhea viral sequences. DNA. 1985;4:429–438. doi: 10.1089/dna.1985.4.429. [DOI] [PubMed] [Google Scholar]
  93. Ridpath J.F., Bolin S.R. Hybridization analysis of genomic variability among isolates of bovine viral diarrhoea virus using cDNA probes. Molecular and Cellular Probes. 1991;5:291–298. doi: 10.1016/0890-8508(91)90052-l. [DOI] [PubMed] [Google Scholar]
  94. Ridpath J.F., Bolin S.R., Katz J. Comparison Of nucleic acid hybridization and nucleic acid amplification using conserved sequences from the 5′ noncoding region for detection ofbovine viral diarrhea virus. Journal of Clinical Microbiology. 1993;31:986–989. doi: 10.1128/jcm.31.4.986-989.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  95. Roberts D.H., Lucas M.H., Swallow C. Comparison of the agar gel immunodiffusion test and ELISA in the detection of bovine leukosis virus antibody in cattle persistently infected withbovine virus diarrhoea virus. Veterinary Immunology and Immunopathology. 1989;22:275–281. doi: 10.1016/0165-2427(89)90014-7. [DOI] [PubMed] [Google Scholar]
  96. Roeder P.L., Jeffrey M., Drew T. Variable nature of border disease on a single farm: the infection status of affected sheep. Research in Veterinary Science. 1987;43:28–33. [PubMed] [Google Scholar]
  97. Roehe P.M., Woodward M.J., Edwards S. Characterisation of p20 gene sequences from a border disease-like pestivirus isolated from pigs. Veterinary Microbiology. 1992;33:231–238. doi: 10.1016/0378-1135(92)90051-t. [DOI] [PubMed] [Google Scholar]
  98. Rweyemamu M.M., Sylla D., Palya V., Prandota J., Wojciechowski C. Rinderpest vaccine quality control by the Pan African Veterinary Vaccine Centre (PANVAC) Panvac Vaccine Bulletin. 1991;2:21–34. [Google Scholar]
  99. Shannon A.D., Richards S.G., Kirkland P.D., Moyle A. An antigen-capture ELISA detects pestivirus antigens in blood and tissues of immunotolerant carrier cattle. Journal of Virological Methods. 1991;34:1–12. doi: 10.1016/0166-0934(91)90116-h. [DOI] [PubMed] [Google Scholar]
  100. Shannon A.D., Mackintosh S.G., Kirkland P.D. Identification of pestivirus carrier calves by an antigen-capture ELISA. Australian Veterinary Journal. 1992;70:74–76. doi: 10.1111/j.1751-0813.1993.tb15151.x. [DOI] [PubMed] [Google Scholar]
  101. Sopp P., Hooper L.F., Clarke M.C., Howard C.J., Brownlie J. Detection of bovine viral diarrhoea virus p80 protein in subpopulations of bovine leukocytes. Journal of General Virology. 1994;75:1189–1194. doi: 10.1099/0022-1317-75-5-1189. [DOI] [PubMed] [Google Scholar]
  102. Spais A.G., Papadopoulos O., Vantsis J.T. Proceedings of 20th World Veterinary Congress. 1975. An extensive outbreak of border disease in Greece (a preliminary report) pp. 622–623. [Google Scholar]
  103. Steck F., Lazary S., Fey H. Immune responsiveness in cattle fatally affected by bovine virus diarrhea-mucosal disease. Zentralbl fur Veterinaermed. 1980;B27:429–445. doi: 10.1111/j.1439-0450.1980.tb01790.x. [DOI] [PubMed] [Google Scholar]
  104. Straver P.J., Journee D.L.H., Binkhorst G.J. Neurological disorders, virus persistence and hypomyelination in calves clue to intrauterine infections with bovine virus diarrhoea virus. II. Virology and epizootiology. Veterinary Quarterly. 1983;5:156–164. doi: 10.1080/01652176.1983.9693890. [DOI] [PubMed] [Google Scholar]
  105. Tarry D.W., Bernal L., Edwards S. Transmission of bovine virus diarrhoea virus by blood feeding flies. Veterianary Record. 1991;128:82–84. doi: 10.1136/vr.128.4.82. [DOI] [PubMed] [Google Scholar]
  106. Terpstra C. Border disease: a congenital infection of small ruminants. Progress in Veterinary Microbiology and Immunology. 1985;1:175–198. [PubMed] [Google Scholar]
  107. Terpstra C. Hog cholera: an update of present knowledge. British Veterinary Journal. 1991;147:397–406. doi: 10.1016/0007-1935(91)90081-W. [DOI] [PubMed] [Google Scholar]
  108. Terpstra C., Wensvoort G. Natural infections of pigs with bovine viral diarrhoea virus associated with signs resembling swine fever. Research in Veterinary Science. 1988;45:137–142. [PubMed] [Google Scholar]
  109. Vannier P., Leforban Y., Carnero R., Cariolet R. Contamination of a live virus vaccine against pseudorabies (Aujesky's disease) by an ovine pestivirus pathogenic for the pig. Annales de Recherches Veterinaires. 1988;19:283–290. [PubMed] [Google Scholar]
  110. Van Oirschot J.T. Congenital infections with nonarbo toga-viruses. Veterinary Microbiology. 1983;8:321–361. doi: 10.1016/0378-1135(83)90048-2. [DOI] [PubMed] [Google Scholar]
  111. Vantsis J.T., Rennie J.C., Gardiner A.C., Wells P.W., Barlow R.M., Martin W.B. Immunisation against border disease. Journal of ComparativePathology. 1980;90:349–354. doi: 10.1016/0021-9975(80)90002-x. [DOI] [PubMed] [Google Scholar]
  112. Vilcek S., Herring A.J., Herring J.A., Nettleton P.F., Lowings J.P., Paton D.J. Pestiviruses isolated from pigs, cattle and sheep can be allocated into at least three genogroups using polymrase chain reaction and restriction endonuclease analysis. Archives of Virology. 1994;136:309–323. doi: 10.1007/BF01321060. [DOI] [PubMed] [Google Scholar]
  113. Wengler G. Flaviviridae. In: Francki R.I.B., Fauqet C.M., Knudson D.L., Brown F., editors. Classification and Nomenclature of Viruses. 1991. pp. 223–233. (Archives of Virology). Fifth report of the International Committee on Taxonomy of viruses. (Suppl. 2) [Google Scholar]
  114. Wensvoort G., Terpstra C. Bovine viral diarrhoea virus infections in piglets born to sows vaccinated against swine fever with contaminated virus. Research in Veterinary Science. 1988;45:143–148. [PubMed] [Google Scholar]
  115. Wensvoort G., Terpstra C., De Kluyver E.P. Characterisation of porcine and some ruminant pestiviruses by cross-neutralisation. Veterinary Micobiology. 1989;20:291–306. doi: 10.1016/0378-1135(89)90054-0. [DOI] [PubMed] [Google Scholar]
  116. Westenbrink F., Straver P., Kimman T.G., de Leeuw P. Development of a neutralising antibody response to an inoculated cytopathic strain of bovine virus diarrhoea virus. Veterinary Record. 1989;125:262–265. doi: 10.1136/vr.125.10.262. [DOI] [PubMed] [Google Scholar]
  117. Westbury H.A., Napthine D.V., Straub E. Border disease: persistent infection with the virus. Veterinary Record. 1979;104:406–409. doi: 10.1136/vr.104.18.406. [DOI] [PubMed] [Google Scholar]
  118. Wirz B., Tratshin J.D., Muller H.K., Mitchell D.B. Detection of hog cholera virus and differentiation from other pestiviruses by polymerase chain reaction. Journal of Clinical MIcrobiology. 1993;31:1148–1154. doi: 10.1128/jcm.31.5.1148-1154.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  119. Wiskerchen M., Collett M.S. Pestivirus gene expression: Protein p80 of bovine viral diarrhea virus is a proteinase involved in polyprotein processing. Virology. 1991;184:341–350. doi: 10.1016/0042-6822(91)90850-b. [DOI] [PubMed] [Google Scholar]
  120. Wiskerchen M., Belzer S.K., Collett M.S. Pestivirus gene expression: the first protein product of the bovine viral diarrhea virus large open reading frame, p20, possesses proteolyticactivity. Journal of Virological Methods. 1991;65:4508–4514. doi: 10.1128/jvi.65.8.4508-4514.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  121. Woldehiwet Z., Sharma R. Alterations in lymphocyte subpopulations in peripheral blood of sheep persistently infected with border disease virus. Veterinary Microbiology. 1990;22:153–160. doi: 10.1016/0378-1135(90)90102-2. [DOI] [PubMed] [Google Scholar]
  122. Xue W., Minocha H.C. Identification of the cell surface receptor for bovine viral diarrhoea virus by using anti-idiotypic antibodies. Journal of General Virology. 1993;74:73–79. doi: 10.1099/0022-1317-74-1-73. [DOI] [PubMed] [Google Scholar]
  123. Xue W., Blecha F., Minocha H.C. Antigenic variations in bovine viral diarrhea viruses detected by monoclonal antibodies. Journal of Clinical Microbiology. 1990;28:1688–1693. doi: 10.1128/jcm.28.8.1688-1693.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  124. Yolken R., Dubovi E., Leister F., Reid R., Almeido-Hill J., Santoshan M. Infantile gastroenteritis associated with excretion of pestivirus antigens. Lancet. 1989;i:517–520. doi: 10.1016/s0140-6736(89)90066-4. [DOI] [PubMed] [Google Scholar]

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