Skip to main content
Log in

BHV-1: New Molecular Approaches to Control a Common and Widespread Infection

  • Review Article
  • Published:
Molecular Medicine Aims and scope Submit manuscript

Abstract

Background

Herpesviruses are widespread viruses, causing severe infections in both humans and animals. Eradication of herpesviruses is extremely difficult because of their ability to establish latent and life-long infections. However, latency is only one tool that has evolved in herpesviruses to successfully infect their hosts; such viruses display a wide (and still incompletely known) panoply of genes and proteins that are able to counteract immune responses of their hosts. Envelope glycoproteins and cytokine inhibitors are two examples of such weapons. All of these factors make it difficult to develop diagnostics and vaccines, unless they are based on molecular techniques.

Materials and Methods

Animal herpesviruses, because of their striking similarity to human ones, are suitable models to study the molecular biology of herpesviruses and develop strategies aimed at designing neurotropic live vectors for gene therapy as well as engineered attenuated vaccines.

Results

BHV-1 is a neurotropic herpesvirus causing infectious rhinotracheitis (IBR) in cattle. It is a major plague in zootechnics and commercial trade, because of its ability to spread through asymptomatic carrier animals, frozen semen, and embryos. Such portals of infections are also important for human herpesviruses, which mainly cause systemic, eye, and genital tract infections, leading even to the development of cancer.

Conclusions

This review covers both the genetics and molecular biology of BHV-1 and its related herpesviruses. Epidemiology and diagnostic approaches to herpesvirus infections are presented. The role of herpesviruses in gene therapy and a broad introduction to classic and engineered vaccines against herpesviruses are also provided.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  1. Metzler AE, Matile H, Gassmann U, Engels M, Wyler E. (1985) European isolates of bovine herpesvirus 1: a comparison of restriction endonuclease sites, polypeptides and reactivity with monoclonal antibodies. Arch. Virol. 85: 57–69.

    Article  PubMed  CAS  Google Scholar 

  2. Misra V, Babiuk LA, Darcel CQ. (1983) Analysis of bovine herpesvirus type 1 isolates by restriction endonuclease fingerprinting. Arch. Virol. 76: 341–354.

    Article  PubMed  CAS  Google Scholar 

  3. Engels M, Steck F, Wyler R. (1981) Comparison of the genomes of infectious bovine rhinotracheitis and infectious pustolar vulvovaginitis virus strains by restriction endonuclease analysis. Arch. Virol. 67: 169–174.

    Article  PubMed  CAS  Google Scholar 

  4. Whetstone CA, Seal BS, Miller JM. (1993) Variability occurs in the inverted repeat region of genomic DNA from bovine herpesvirus 1 respiratory, genital and bovine herpesvirus 5 encephalitic isolates. Vet. Microbiol. 38: 181–189.

    Article  PubMed  CAS  Google Scholar 

  5. Seal BS, Whetstone CA. (1994) Immediate-early gene expression and gene mapping comparisons among isolates of bovine herpesvirus 1 and 5. Vet. Microbiol. 38: 369–384.

    Article  PubMed  CAS  Google Scholar 

  6. Bratanich AC, Sardi SI, Smitsaart EN, Schudel AA. (1991) Comparative studies of BHV-1 variants by in vivo-in vitro tests. J. Vet. Med. B 38: 41–48.

    Article  CAS  Google Scholar 

  7. Mayfield JE, Good PJ, van Oort HJ, Campbell AR, Reed DE. (1983) Cloning and cleavage site mapping of DNA from bovine herpesvirus 1 (cooper strain). J. Virol. 47: 259–264.

    PubMed  PubMed Central  CAS  Google Scholar 

  8. Castrucci G, Frigeri F, Ranucci S, et al. (1984) Comparative studies of strains of infectious bovine rhinotracheitis virus isolated from latently infected calves. Comp. Immunol. Microbiol. Infect. Dis. 7: 1–10.

    Article  PubMed  CAS  Google Scholar 

  9. Engels M, Ackermann M. (1996) Pathogenesis of ruminant herpesvirus infections. Vet. Microbiol. 53: 3–15.

    Article  PubMed  CAS  Google Scholar 

  10. Yates DWG. (1982) A review of infectious bovine rhinotracheitis, shipping fever pneumonia and viral-bacterial synergism in respiratory disease of cattle. Can. J. Comp. Med. 46: 225–263.

    PubMed  PubMed Central  CAS  Google Scholar 

  11. van Oirschot JT. (1995) Bovine herpesvirus 1 in semen of bulls and the risk of transmission: a brief review. Vet. Q. 17: 29–33.

    Article  PubMed  Google Scholar 

  12. Misra PK, Mishra A. (1987) Infectious bovine rhinotracheitis infection and infertility in cows, heifers and bulls. Indian J. Anim. Sci. 57: 267–271.

    Google Scholar 

  13. Parsonson IM, Snowdon WA. (1975) The effect of natural and artificial breeding using bulls infected with, or semen contaminated with, infectious bovine rhinotracheitis virus. Aust. Vet. J. 51: 365–369.

    Article  PubMed  CAS  Google Scholar 

  14. Bielanski A, Loewen KG, Hare WCD. (1988) Inactivation of bovine herpesvirus-1 (BHV-1) from in vitro infected bovine semen. Theriogenology 30: 649–657.

    Article  PubMed  CAS  Google Scholar 

  15. Wyler R, Engels M, Schwyzer M. (1989) Infectious bovine rhinotracheitis/vulvovaginitis (BHV-1). In: Wittman G (ed). Herpesvirus Diseases of Cattle, Horses and Pigs. Kluwer Academic Publishers, Boston, pp.1–72.

    Google Scholar 

  16. Thiry E, Saliki J, Pastoret P-P, Lambert A-F, Ligot J. (1984) Failure to demonstrate infectious bovine rhinotracheitis virus reactivation in parturient cows. Vet. Rec. 8: 248–249.

    Article  Google Scholar 

  17. Van Wuijckhuise L, Bosch J, Franken P, Frankena K, Elbers ARW. (1998) Epidemiological characteristics of bovine herpesvirus 1 infections determined by bulk milk testing of all Dutch dairy herds. Vet. Rec. 142: 181–184.

    Article  PubMed  Google Scholar 

  18. Pastoret P-P, Thiry E. (1985) Diagnosis and prophylaxis of infectious bovine rhinotracheitis: the role of virus latency. Comp. Immun. Microbiol. Infect. Dis. 8: 35–42.

    Article  CAS  Google Scholar 

  19. Thiry E, Saliki J, Bublot M, Pastoret P-P. (1987) Reactivation of infectious bovine rhinotracheitis virus by transport. Comp. Immun. Microbiol. Infect. Dis. 10: 59–63.

    Article  CAS  Google Scholar 

  20. Geng Y, Kashanchi F, Wood C. (1992) Activation of bovine immunodeficiency-like virus expression by bovine herpesvirus type 1. Virology 187: 832–836.

    Article  PubMed  CAS  Google Scholar 

  21. Arthington JD, Corah LR, Blecha F. (1996) The effect of molybdenum-induced copper deficiency on acute-phase protein concentrations, superoxide dismutase activity leukocyte numbers, and lymphocyte proliferation in beef heifers inoculated with bovine herpesvirus-1. J. Anim. Sci. 74: 211–217.

    Article  PubMed  CAS  Google Scholar 

  22. Hage JJ, Schukken YH, Barkema HW, Benedictus G, Rijsewjk FAM, Wentink GH. (1996) Population dynamics of bovine herpesvirus 1 infection in a dairy herd. Vet. Microbiol. 53: 169–180.

    Article  PubMed  CAS  Google Scholar 

  23. Tanyi J, Varga J. (1992) Guidelines for the eradication of bovine rhinotracheitis in Hungary. Acta Vet. Hung. 40: 165–169.

    PubMed  CAS  Google Scholar 

  24. Homan EJ, Easterday BC. (1980) Isolation of bovine herpesvirus-1 from trigeminal ganglia of clinically normal cattle. Am. J. Vet. Res. 41: 1212–1213.

    PubMed  CAS  Google Scholar 

  25. Ackerman M, Peterhans E, Wyler R. (1982) DNA of bovine herpes virus type 1 in the trigeminal ganglia of latently infected calves. Am. J. Vet. Res. 43: 36–40.

    Google Scholar 

  26. Drew TW, Hewitt-Taylor C, Watson L, Edwards S. (1987) Effect of storage conditions and culture technique on the isolation of infectious bovine rhinotracheitis virus from bovine semen. Vet. Rec. 121: 547–548.

    PubMed  CAS  Google Scholar 

  27. Loewen KG, Darcel C. (1985) A comparison of two methods for the isolation of bovine herpesvirus 1 (BHV-1) from extended bovine semen. Theriogenology 23: 935–943.

    Article  Google Scholar 

  28. Brunner D, Engels M, Schwyzer M, Wyler R. (1988) A comparison of three techniques for detecting bovine herpesvirus type 1 (BHV-1) in naturally and experimentally contaminated semen. Zuchthung 23: 1–9.

    Article  CAS  Google Scholar 

  29. Wentink GH, Rutten VPMG, van Exel ACA, De Jong WAC, Vleugel H, Hensen EJ. (1990) Failure of an in vitro lymphoproliferative assay specific for bovine herpesvirus type 1 to detect immunized or latently infected animals. Vet. Q. 12: 175–182.

    Article  PubMed  CAS  Google Scholar 

  30. Florent G, De Marneffe C. (1986) Enzyme linked immunosorbent assay used to monitor serum antibodies to bovine respiratory disease viruses. Vet. Microbiol. 11: 307–317.

    Article  Google Scholar 

  31. Edwards S, Woods SB, Westcott DG, Emmerson M, Jones PC, Phillips AJ. (1986) An evaluation of five serological tests for the detection of antibody to bovine herpesvirus 1 in vaccinated and experimentally infected cattle. Res. Vet. Sci. 41: 378–382.

    Article  PubMed  CAS  Google Scholar 

  32. Kramps JA, Quak S, Weer Dmeester K, van Oirschot JT. (1993) Comparative study on sixteen enzyme-linked immunosorbent assays for the detection of antibodies to bovine herpesvirus 1 in cattle. Vet. Microbiol. 35: 11–21.

    Article  PubMed  CAS  Google Scholar 

  33. Derget D, Cho HJ, Kozub GC. (1993) A comparative evaluation of two sensitive serum neutralizing tests for bovine herpes-1 antibodies. Can. J. Vet. Res. 57: 56–59.

    Google Scholar 

  34. Abdelmagid OY, Mansour MM, Minocha HC, van Drunen Littel-van den Hurk S. (1998) Evaluation of baculovirus-expressed bovine herpesvirus-1 (BHV-1) glycoproteins for detection and analysis of BHV-1-specific antibody responses. Vet. Microbiol. 61: 249–259.

    Article  PubMed  CAS  Google Scholar 

  35. Kramps JA, Perrin B, Edwards S, van Oirschot JT. (1996) A European inter-laboratory trial to evaluate the reliability of serological diagnosis of bovine herpesvirus 1 infections. Vet. Microbiol. 53: 153–161.

    Article  PubMed  CAS  Google Scholar 

  36. van Donkersgoed J, Babiuk L. (1991) Diagnosing and managing the respiratory form of infectious bovine rhinotracheitis. Vet. Med. 1: 86–94.

    Google Scholar 

  37. Andino RH, Torres HN, Polacino PS, Schudel A, Palma EL. (1987) Detection of bovine herpesvirus-1 nucleic acid sequences, using a dot-blot hybridization procedure. Am. J. Vet. Res. 48: 984–987.

    PubMed  CAS  Google Scholar 

  38. Vilcek S, Deliova I, Forgac O, et al. (1993) Detection of bovine herpesvirus 1 with various types of DNA probes. Acta Vet. Hung. 41: 179–190.

    PubMed  CAS  Google Scholar 

  39. van Engelenburg FAC, van Schie FW, Rijsewijk FAM, van Oirschot JT. (1995) Excretion of bovine herpesvirus 1 in semen is detected much longer by PCR than by virus isolation. J. Clin. Microbiol. 33: 308–312.

    PubMed  PubMed Central  Google Scholar 

  40. Kibenge FSB, Harris LM, McKenna PK, Wadowska D, Yason CV. (1994) Amplification of strains of bovine herpesvirus 1 by use of polymerase chain reaction with primers in the thymidine kinase region. Am. J. Vet. Res. 55: 1206–1212.

    PubMed  CAS  Google Scholar 

  41. Yason CV, Harris LM, McKenna PK, Wadowska D, Kibenge FSB. (1995) Establishment of conditions for the detection of bovine herpesvirus-1 by polymerase chain reaction using primers in the thymidine kinase region. Can. J. Vet. Res. 59: 94–101.

    PubMed  PubMed Central  CAS  Google Scholar 

  42. Vilcek S, Nettleton PF, Herring JA, Herring AJ. (1994) Rapid detection of bovine herpesvirus 1 (BHV 1) using the polymerase chain reaction. Vet. Microbiol. 42: 53–64.

    Article  PubMed  CAS  Google Scholar 

  43. van Engelenburg FAC, Maes RK, van Oirschot JT, Rijsewijk FAM. (1993) Development of a rapid and sensitive polymerase chain reaction assay for detection of bovine herpesvirus type 1 in bovine semen. J. Clin. Microbiol. 31: 3129–3135.

    PubMed  PubMed Central  Google Scholar 

  44. Wiedmann M, Brandon R, Wagner P, Dubovi EJ, Batt CA. (1993) Detection of bovine herpesvirus-1 in bovine semen by a nested PCR assay. J. Virol. Methods 44: 129–140.

    Article  PubMed  CAS  Google Scholar 

  45. Masri SA, Olson W, Nguyen PT, Prins S, Deregt D. (1996) Rapid detection of bovine herpesvirus 1 in the semen of infected bulls by a nested polymerase chain reaction assay. Can. J. Vet. Res. 60: 100–107.

    PubMed  PubMed Central  CAS  Google Scholar 

  46. Asbaugh SE, Thompson KE, Belknap EB, Schultheiss PC, Chowdhury S, Collins JK. (1997) Specific detection of shedding and latency of bovine herpesvirus 1 and 5 using a nested polymerase chain reaction. J. Vet. Diagn. Invest. 9: 387–394.

    Article  Google Scholar 

  47. Lyaku JRS, Vilcek S, Nettieton PF, Marsden HS. (1996) The distinction of serologically related ruminant alphaherpesviruses by the polymerase chain reaction (PCR) and restriction endonuclease analysis. Vet. Microbiol. 48: 135–142.

    Article  PubMed  CAS  Google Scholar 

  48. Rusvai M, Fodor L. (1998) Occurrence of some viruses and bacteria involved in respiratory diseases of ruminants in Hungary. Acta Vet. Hung. 46: 405–414.

    PubMed  CAS  Google Scholar 

  49. Schwyzer M, Ackermann M. (1996) Molecular virology of ruminant herpesviruses. Vet. Microbiol. 53: 17–29.

    Article  PubMed  CAS  Google Scholar 

  50. Tikoo SK, Fitzpatrick DR, Babiuk LA, Zamb TJ. (1990) Molecular cloning, sequencing, and expression of functional bovine herpesvirus 1 glycoprotein gIV in transfected bovine cells. J. Virol. 64: 5132–5142.

    PubMed  PubMed Central  CAS  Google Scholar 

  51. Tikoo SK, Zamb TJ, Babiuk LA. (1993) Analysis of bovine herpesvirus 1 glycoprotein gIV truncation and deletions expressed by recombinant vaccinia viruses. J. Virol. 67: 2103–2109.

    PubMed  PubMed Central  CAS  Google Scholar 

  52. Chase CCL, Lohff C, Letchworth GJ. (1993) Resistance and susceptibility of bovine cells expressing herpesviral glycoprotein D homologous to herpesviral infections. Virology 194: 365–369.

    Article  PubMed  CAS  Google Scholar 

  53. Baranowski E, Keil G, Lyaku J, et al. (1996) Structural and functional analysis of bovine herpesvirus 1 minor glycoproteins. Vet. Microbiol. 53: 91–101.

    Article  PubMed  CAS  Google Scholar 

  54. Liang X, Babiuk LA, Zamb TJ. (1992) An in vivo study of a glycoprotein gIII-negative bovine herpesvirus 1 (BHV-1) mutant expressing β-galactosidase: evaluation of the role of gIII in virus infectivity and its use as a vector for mucosal immunization. Virology 189: 629–639.

    Article  PubMed  CAS  Google Scholar 

  55. Geraghty RJ, Krummenacher C, Cohen GH, Eisenberg RJ, Spear PG. (1998) Entry of alpha herpesviruses mediated by poliovirus receptor-related protein 1 and poliovirus receptor. Science 280: 1618–1620.

    Article  PubMed  CAS  Google Scholar 

  56. Montgomery RI, Warner MW, Lum BJ, Spear PG. (1996) Herpes simplex virus-1 entry into cells mediated by a novel member of the TNF/NGF receptor family. Cell 87: 427–436.

    Article  PubMed  CAS  Google Scholar 

  57. Li Y, van Drunen Littel-van den Hurk S, Babiuk LA, Liang X. (1995) Characterization of cell-binding properties of bovine herpesvirus 1 glycoproteins B, C and D: identification of a dual cell-binding function of gB. J. Virol. 68: 4758–4768.

    Google Scholar 

  58. Varthakavi V, Minocha HC. (1996) Identification of a 56 kDa putative bovine herpesvirus 1 cellular receptor by anti-idiotype antibodies. J. Gen. Virol. 77: 1875–1882.

    Article  PubMed  CAS  Google Scholar 

  59. Liang X, Pyne C, Li Y, Babiuk LA, Kowalski J. (1995) Delineation of the essential function of bovine herpesvirus 1 gD: an indication for the modulatory role of gD in virus entry. Virology 207: 429–441.

    Article  PubMed  CAS  Google Scholar 

  60. Spear PG. (1993) Entry of alphaherpesviruses into cells. Semin. Virol. 4: 167–180.

    Article  CAS  Google Scholar 

  61. Ludwig GV, Letchworth G. (1987) Temporal control of bovine herpesvirus 1 glycoproteins synthesis. J. Virol. 61: 3292–3294.

    PubMed  PubMed Central  CAS  Google Scholar 

  62. Misra V, Bumenthal RM, Babiuk LA. (1981) Proteins specified by bovine herpesvirus 1 (infectious rhinotracheitis virus). J. Virol. 40: 367–378.

    PubMed  PubMed Central  CAS  Google Scholar 

  63. Fitzpatrick DR, Babiuk LA, Zamb TJ. (1989) Nucleotide sequence of bovine herpesvirus type 1 glycoprotein gIII, a structural model for gIII as a new member of the immunoglobulin superfamily, and implications for the homologous glycoproteins of other herpesviruses. Virology 173: 46–57.

    Article  PubMed  CAS  Google Scholar 

  64. Liang X, Babiuk L, Zamb T. (1991) Pseudorabies virus gIII and bovine herpesvirus I gIII share complementary functions. J. Virol. 65: 5553–5557.

    PubMed  PubMed Central  CAS  Google Scholar 

  65. Liang X, Tang M, Zamb TJ, Babiuk LA, Kowalski J, Tykocinski ML. (1993) Expression of glycoprotein gIII-human decay-accelerating factor chimera on the bovine herpesvirus 1 virion via a glycosyl phosphatidylinositol-based membrane anchor. J. Virol. 67: 4896–4904.

    PubMed  PubMed Central  CAS  Google Scholar 

  66. Liang X, Babiuk LA, Zamb TJ. (1993) Mapping of heparin-binding structures on bovine herpesvirus 1 and Pseudorabies virus gIII glycoproteins. Virology 194: 233–243.

    Article  PubMed  CAS  Google Scholar 

  67. Roizman B, Desroisiers R, Fleckenstein B. (1992) The family Herpesviridae: an update. Arch. Virol. 123: 425–449.

    Article  Google Scholar 

  68. Whitbeck JC, Bello LJ, Lawrence WC. (1988) Comparison of the bovine herpesvirus 1 gI gene and the herpes simplex virus type 1 gB gene. J. Virol. 62: 3319–3327.

    PubMed  PubMed Central  CAS  Google Scholar 

  69. Misra V, Blewett EL. (1991) Construction of herpes symplex viruses that are pseudoploid for the glycoprotein B gene: a strategy for studying the function of an essential herpesvirus gene. J. Gen. Virol. 72: 385–392.

    Article  PubMed  CAS  Google Scholar 

  70. Misra V, Nelson R, Smith M. (1988) Sequence of a bovine herpesvirus type-1 glycoprotein gene that is homologous to the herpes simplex gene for glycoprotein B. Virology 166: 542–549.

    Article  PubMed  CAS  Google Scholar 

  71. Rauh I, Weiland F, Fehler F, Keil G, Mettenletter TC. (1991) Pseudorabies virus mutants lacking the essential glycoprotein gII can be complemented by glycoprotein gI of bovine herpesvirus 1. J. Virol. 65: 621–631.

    PubMed  PubMed Central  CAS  Google Scholar 

  72. Kopp A, Mettenleiter TC. (1992) Stable rescue of a gIycoprotein gII deletion mutant of Pseudorabies virus by gIycoprotein gI of bovine herpesvirus 1. J. Virol 66: 2754–2762.

    PubMed  PubMed Central  CAS  Google Scholar 

  73. Fitzpatrick DR, Redmond MJ, Attah-Poku SK, van Drunen Littel-van den Hurk S, Babiuk LA, Zamb TJ. (1990) Mapping of 10 epitopes on bovine herpesvirus type 1 gIycoproteins gI and g III. Virology 176: 145–157.

    Article  PubMed  CAS  Google Scholar 

  74. Vlcek C, Benes V, Lu Z, et al. (1995) Nucleotide sequence analysis of a 30-kb region of the bovine herpesvirus 1 genome which exhibits a colinear gene arrangement with the UL21 to UL4 genes of herpes simplex virus. Virology 210: 100–108.

    Article  PubMed  CAS  Google Scholar 

  75. Wirth UV, Gunkel K, Engels M, Schwyzer M. (1989) Spatial and temporal distribution of bovine herpesvirus-1 transcripts. J. Virol. 63: 4882–4889.

    PubMed  PubMed Central  CAS  Google Scholar 

  76. Wirth UV, Gunkel K, Engels M, Schwyzer M. (1989) Spatial and temporal distribution of bovine herpesvirus 1 transcripts. J. Virol. 63: 4882–4889.

    PubMed  PubMed Central  CAS  Google Scholar 

  77. Seal BS, Whetstone CA, Zamb TJ, Bello LJ, Lawrence WC. (1992) Relationship of bovine herpesvirus 1 immediate-early, early and late gene expression to host cellular gene transcription. Virology 188: 152–159.

    Article  PubMed  CAS  Google Scholar 

  78. Fraefel C, Zeng J, Choffat Y, Engels M, Schwyzer M, Ackermann M. (1994) Identification and zinc dependence of the bovine herpesvirus 1 transactivator protein BICP0. J. Virol. 68: 3154–3162.

    PubMed  PubMed Central  CAS  Google Scholar 

  79. Singh M, Fraefel C, Bello LJ, Lawrence WC, Schwyzer M. (1996) Identification and characterization of BICP27, an early protein of bovine herpesvirus 1 which may stimulate mRNA 3′ processing. J. Gen. Virol. 77: 615–625.

    Article  PubMed  CAS  Google Scholar 

  80. Schwyzer M, Vlcek C, Menkse O, Fraefel C, Paces V. (1993) Promoter, spliced leader, and coding sequence for BICP4, the largest of the immediate-early proteins of bovine herpesvirus 1. Virology 197: 349–357.

    Article  PubMed  CAS  Google Scholar 

  81. Fraefel C, Ackermann M, Schwyzer M. (1994) Identification of the bovine herpesvirus-1 circ protein: a myristylated and virion-associated polypeptyde which is not essential for virus replication in cell culture. J. Virol. 68: 8082–8088.

    PubMed  PubMed Central  CAS  Google Scholar 

  82. Hammerschmidt W, Ludwig H, Buhk H-J. (1988) Specificity of cleavage in replicative-form DNA of bovine herpesvirus 1. J. Virol. 62: 1355–1363.

    PubMed  PubMed Central  CAS  Google Scholar 

  83. Fraefel C, Wirth UV, Vogt B, Schwyzer M. (1993) Immediate-early transcription over covalently joined genome ends of bovine herpesvirus 1: the circ gene. J. Virol. 67: 1328–1333.

    PubMed  PubMed Central  CAS  Google Scholar 

  84. Misra V, Walker S, Hayes S, O’Hare P. (1995) The bovine herpesvirus a gene trans-inducing factor activates transcription by mechanisms different from those of its herpes simplex virus type 1 counterpart V16. J. Virol. 69: 5209–5216.

    PubMed  PubMed Central  CAS  Google Scholar 

  85. Misra V, Bratanich AC, Carpenter D, O’Hare P. (1994) Protein and DNA elements involved in transactivation of the promoter of the bovine herpesvirus (BHV)1 IE-1 transcription unit by the BHV α gene trans-inducing factor. J. Virol. 68: 4898–4909.

    PubMed  PubMed Central  CAS  Google Scholar 

  86. Huang CC, Herr W. (1996) Differential control of transcription by homologous homeodomain co-regulators. Mol. Cell. Biol. 16: 2967–2976.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  87. Wirth UV, Vogt B, Schwyzer M. (1991) The three major immediate-early transcripts of bovine herpesvirus 1 arise from two divergent and spliced transcription units. J. Virol. 65: 195–205.

    PubMed  PubMed Central  CAS  Google Scholar 

  88. van Drunen Littel-van den Hurk S, Garzon S, van den Hurk JV, Babiuk LA, Tijssen P. (1995) The role of the major tegument protein VP8 of bovine herpesvirus-1 in infection and immunity. Virology 206: 413–425.

    Article  PubMed  Google Scholar 

  89. Wirth UV, Fraefel C, Vogt B, Vlcek C, Paces V, Schwyzer M. (1992) Immediate-early RNA 2.9 and early RNA 2.6 of bovine herpesvirus 1 are 3′ coterminal and encode a putative zinc finger transactivator protein. J. Virol. 66: 2763–2772.

    PubMed  PubMed Central  CAS  Google Scholar 

  90. Huemer HP, Larcher C, van Drunen Littel-van den Hurk S, Babiuk L. (1993) Species selective interaction of Alphaherpesvirinae with the “unspecific” immune system of the host. Arch. Virol. 130: 354–364.

    Article  Google Scholar 

  91. Jacobs L. (1994) Glycoprotein E of Pseudorabies virus and homologous proteins of other alphaherpesvirinae. Arch. Virol. 137: 209–228.

    Article  PubMed  CAS  Google Scholar 

  92. Hariharan MJ, Nataraj C, Srikumaran S. (1993) Down regulation of murine MHC class I expression by bovine herpesvirus 1. Viral Immunol. 6: 273–284.

    Article  PubMed  CAS  Google Scholar 

  93. Kutish G, Mainprize T, Rock D. (1990) Characterization of the latency-related transcriptionally active region of the bovine herpesvirus 1 genome. J. Virol. 64: 5730–5737.

    PubMed  PubMed Central  CAS  Google Scholar 

  94. Schang LM, Hossain A, Jones C. (1996) The latency-related gene of bovine herpesvirus-1 encodes a product which inhibits cell cycle progression. J. Virol. 70: 3807–3814.

    PubMed  PubMed Central  CAS  Google Scholar 

  95. Jiang Y, Hossain A, Winkler MT, Holt T, Doster A, Jones C. (1998) A protein encoded by the latency-related gene of bovine herpesvirus 1 is expressed in trigeminal ganglionic neurons of latently infected cattle and interacts with cyclindependent kinase 2 during productive infection. J. Virol. 72: 8133–8142.

    PubMed  PubMed Central  CAS  Google Scholar 

  96. Jones C, Delhon G, Bratanich A, Kutish G, Rock D. (1990) Analysis of the transcriptional promoter which regulates the latency-related transcript of bovine herpesvirus 1. J. Virol. 64: 1164–1170.

    PubMed  PubMed Central  CAS  Google Scholar 

  97. Bratanich AC, Jones CJ. (1992) Localization of cis-acting sequences in the latency-related promoter of bovine herpesvirus 1 which are regulated by memorial cell type factors and immediate-early genes. J. Virol. 66: 6099–6106.

    PubMed  PubMed Central  CAS  Google Scholar 

  98. Bratanich AC, Hanson ND, Jones CJ. (1992) The latency-related gene of bovine herpesvirus 1 inhibits the activity of immediate-early transcription unit 1. Virology 191: 988–991.

    Article  PubMed  CAS  Google Scholar 

  99. Devireddy LR, Jones C. (1998) Alternative splicing of the latency-related transcript of bovine herpesvirus 1 yields RNAs containing unique open reading frames. J. Virol 72: 7294–7301.

    PubMed  PubMed Central  CAS  Google Scholar 

  100. Schang LM, Jones C. (1997) Analysis of bovine herpesvirus 1 transcripts during a primary infection of trigeminal ganglia of cattle. J. Virol. 71: 6786–6795.

    PubMed  PubMed Central  CAS  Google Scholar 

  101. Whetstone CA, Miller IM, Seal BS, Bello LJ, Lawrence WC. (1992) Latency and reactivation of a thymidine kinase-negative bovine herpesvirus 1 deletion mutant. Arch. Virol. 122: 207–214.

    Article  PubMed  CAS  Google Scholar 

  102. Rock D, Lokensgard J, Lewis T, Kutish G. (1992) Characterization of dexamethasone-induced reactivation of latent bovine herpesvirus 1. J. Virol. 66: 2484–2490.

    PubMed  PubMed Central  CAS  Google Scholar 

  103. van Engelenburg FAC, Kaashoek MJ, van Oirschot JT, Rijsewijk FAM. (1995) A glycoprotein E deletion mutant of bovine herpesvirus 1 infects the same limited number of tissue in calves as wild-type virus, but for a shorter period. J. Gen. Virol. 76: 2387–2392.

    Article  PubMed  Google Scholar 

  104. Bielefeldt O, Babiuk LA, Harland R. (1991) Cytokine synergy with viral cytopathic effects and bacterial products during the pathogenesis of respiratory tract infection. Clin. Immunol. Immunopathol. 60: 153–170.

    Article  Google Scholar 

  105. Campos M, Bielefeldt Ohmann H, et al. (1989) Role of interferon-γ in inducing cytotoxicity of peripheral blood mononuclear leukocytes to bovine herpesvirus type 1 (BHV-1)-infected cells. Cell. Immunol. 120: 259–269.

    Article  PubMed  CAS  Google Scholar 

  106. Hutchings DL, van Drunen Littel-van den Hurk S, Babiuk LA. (1990) Lymphocyte proliferative responses to separate bovine herpesvirus-1 proteins in immune cattle. J. Virol. 64: 5114–5122.

    PubMed  PubMed Central  CAS  Google Scholar 

  107. Babiuk LA, van Drunen Littel-van den Hurk S, Tikoo SK. (1996) Immunology of bovine herpesvirus 1 infection. Vet. Microbiol. 53: 31–42.

    Article  PubMed  CAS  Google Scholar 

  108. Choi S-H, Splitter GA. (1994) Induction of MHC-unrestricted cytolytic CD4+ T cells against virally infected target cells by cross-linking CD4 molecules. J. Immunol. 153: 3874–3881.

    PubMed  CAS  Google Scholar 

  109. Denis M, Slaoui M, Keil G, et al. (1993) Identification of different target glycoproteins for bovine herpesvirus-1 specific cytotoxic T lymphocytes depending on the method of in vitro stimulation. Immunology 78: 7–13.

    PubMed  PubMed Central  CAS  Google Scholar 

  110. Wang C, Splitter GA. (1998) CD4+ cytotoxic T-lymphocyte activity against macrophages pulsed with bovine herpesvirus 1 polypeptides. J. Virol. 72: 7040–7047.

    PubMed  PubMed Central  CAS  Google Scholar 

  111. Hanon E, Meyer G, Vanderplasschen A, Dessy-Doize C, Thiry E, Pastoret P-P. (1998) Attachment but not penetration of bovine herpesvirus 1 is necessary to induce apoptosis in target cells. J. Virol. 72: 7638–7641.

    PubMed  PubMed Central  CAS  Google Scholar 

  112. Ryan AM, Womack JE. (1997) A molecular genetic approach to improved animal health. Vet. Clin. North Am: Food Anim. Pract. 13: 401–409.

    CAS  Google Scholar 

  113. Yu Z, Manickan E, Rouse BT. (1996) Role of interferon-γ in immunity to herpes simplex virus. J. Leukoc. Biol. 60: 528–532.

    Article  PubMed  CAS  Google Scholar 

  114. Milligan GN, Bernstein DI. (1997) Interferon-γ enhances resolution of herpes simplex virus type 2 infection of the murine genital tract. Virology 229: 259–268.

    Article  PubMed  CAS  Google Scholar 

  115. Otsuka H, Qavi H, Kit S. (1982) Inhibition by interferon of biochemical transformation induced by cloned herpesvirus thymidine kinase genes. Antiviral Res. 2: 301–311.

    Article  PubMed  CAS  Google Scholar 

  116. Hughes HPA, Campos M, Godson DL, van Drunen Littel-van den Hurk S, McDougall L, Rapin N. (1991) Immunopotentiation of bovine herpesvirus subunit vaccination by interleukin-2. Immunology 74: 461–466.

    PubMed  PubMed Central  CAS  Google Scholar 

  117. Reddy PG, Blecha F, Minocha HC, et al. (1989) Bovine recombinant interleukin-2 augment immunity and resistance to bovine herpesvirus infection. Vet. Immunol. Immunopathol. 23: 61–74.

    Article  PubMed  CAS  Google Scholar 

  118. Hughes HPA, Campos M, van Drunen Littel-van den Hurk S, et al. (1992) Multiple administration with interleukin-2 potentiates antigen-specific responses to subunit vaccination with herpesvirus-1 glycoprotein IV. Vaccine 10: 226–230.

    Article  PubMed  CAS  Google Scholar 

  119. Reddy DN, Reddy PG, Minocha HC, et al. (1990) Adjuvancity of recombinant bovine interleukin-1β: influence on immunity, infection, and latency in bovine herpesvirus-1 infection. Lymphokine Res. 9: 295–307.

    PubMed  CAS  Google Scholar 

  120. Reddy DN, Reddy PG, Xue W, Minocha HC, Daley MJ, Becha F. (1993) Immunopotentiation of bovine respiratory disease virus vaccines by interleukin-1β and interleukin-2. Vet. Immunol. Immunopathol. 37: 25–38.

    Article  PubMed  CAS  Google Scholar 

  121. Baca-Estrada ME, Godson DL, Hughes HPA, et al. (1995) Effect of recombinant bovine interleukin-1β on viral/bacterial pneumonia in cattle. J. Interferon Cytokine Res. 15: 431–439.

    Article  PubMed  CAS  Google Scholar 

  122. Leib DA, Olivo PD. (1993) Gene delivery to neurons: is herpes simplex virus the right tool for the job? Bioassays 15: 547–554.

    Article  CAS  Google Scholar 

  123. Glorioso JC, DeLuca NA, Fink DJ. (1995) Development and application of herpes simplex virus vectors for human gene therapy. Annu. Rev. Microbiol. 49: 675–710.

    Article  PubMed  CAS  Google Scholar 

  124. Bello LJ, Whitbeck JC, Lawrence WC. (1992) Bovine herpesvirus 1 as live virus vector for expression of foreign genes. Virology 190: 666–673.

    Article  PubMed  CAS  Google Scholar 

  125. Kit M, Kit S, Little SP, Di Marchi RD, Gale C. (1991) Bovine herpesvirus-1 (infectious bovine rhinotracheitis virus) based viral vector which express foot-and-mouth disease epitopes. Vaccine 9: 564–572.

    Article  PubMed  CAS  Google Scholar 

  126. Kit S, Otsuka H, Kit M. (1992) Expression of porcine Pseudorabies virus genes by a bovine herpesvirus-1 (infectious bovine rhinotracheitis virus) vector. Arch. Virol. 124: 1–20.

    Article  PubMed  CAS  Google Scholar 

  127. Otsuka H, Xuan X. (1996) Construction of bovine herpesvirus-1 (BHV-1) recombinants which express pseudorabies virus (PRV) glycoproteins gB, gC and gE. Arch. Virol. 141: 57–71.

    Article  PubMed  CAS  Google Scholar 

  128. Ackermann M, Belak S, Bitsch V, et al. (1990) Round table on infectious bovine rhinotracheitis/infectious postural vulvovaginitis virus infection diagnosis and control. Vet. Microbiol. 23: 361–363.

    Article  PubMed  CAS  Google Scholar 

  129. Lemaire M, Schynts F, Meyer G, Thiry E. (1999) Antibody response to glycoprotein E after bovine herpesvirus type 1 infection in passively immunised, glycoprotein E-negative calves. Vet Rec 144: 172–176.

    Article  PubMed  CAS  Google Scholar 

  130. Lemairie M, Meyer G, Ernst E, et al. (1995) Latent bovine herpesvirus 1 infection in calves protected by colostral immunity. Vet. Rec. 137: 70–71.

    Article  Google Scholar 

  131. van Oirshot JT, Kaashoek MJ, Rijsewijk FAM. (1996) Advances in the development and evaluation of bovine herpesvirus 1 vaccines. Vet. Microbiol. 53: 43–54.

    Article  Google Scholar 

  132. Madin SH, York CJ, McKercher DG. (1956) Isolation of infectious bovine rhinotracheitis virus. Science 124: 721–722.

    Article  PubMed  CAS  Google Scholar 

  133. Kendrick JW, York CJ, McKercher DG. (1956) A controlled field trial of a vaccine for infectious bovine rhinotracheitis. Proc. U.S. Livestock San. Assoc. 60: 155–158.

    Google Scholar 

  134. Straub OC, Mawhinney IC. (1988) Vaccination to protect calves against infectious bovine rhinotracheitis. Vet. Rec. 122: 407–411.

    Article  PubMed  CAS  Google Scholar 

  135. Zygraich N, Lobmann M, Vascoboinic E, Berge E, Huygelen C. (1974) In vivo and in vitro properties of a temperature sensitive mutant in infectious bovine rhinotracheitis virus. Res. Vet. Sci. 16: 328–335.

    PubMed  CAS  Google Scholar 

  136. Whetstone CA, Wheeler JG, Reed DE. (1986) Investigation of possible vaccine induced epizootics of infectious rhinotracheitis, using restriction endonuclease analysis of viral DNA. Am. J. Vet. Res. 47: 1789–1795.

    PubMed  CAS  Google Scholar 

  137. Whetstone C, Miller J, Bortner D, van Der Maaten MJ. (1989) Changes in the restriction endonuclease patterns of four modified-live infectious bovine rhinotracheitis virus (IBRV) vaccines after one passage in host animal. Vaccine 7: 527–532.

    Article  PubMed  CAS  Google Scholar 

  138. Duque H, Marshall RL, Israel BA, Letchworth GJ. (1989) Effect of formalin inactivation on bovine herpesvirus 1 glycoproteins and antibody response elicited by formalin-inactivated vaccines in rabbits. Vaccine 7: 513–520.

    Article  PubMed  CAS  Google Scholar 

  139. Brun A, Dauvergine M, Languet B, Reynaud G. (1988) Studies of an inactivated vaccine prepared from viral subunits against infectious bovine rhinotracheitis virus. Med. Vet. 5: 583–586.

    Google Scholar 

  140. Frerichs GN, Woods SB, Lucas MH, Sands J-J. (1982) Safety and efficacy of live and inactivated infectious bovine rhinotracheitis vaccines. Vet. Rec. 111: 116–122.

    Article  PubMed  CAS  Google Scholar 

  141. Bryan LA, Fenton RA, Misra V, Haines DM. (1994) Fatal, generalized bovine herpesvirus type 1 infection associated with a modified-live infectious bovine rhinotracheitis parainfluenza-3 vaccine administered to neonatal calves. Can. Vet. J. 35: 223–228.

    PubMed  PubMed Central  CAS  Google Scholar 

  142. Backer JC, Rust RS, Walker RD. (1989) Transmission of a vaccinal strain of infectious bovine rhinotracheitis virus from intranasally vaccinated steers commingled with non vaccinated steers. Am. J. Vet. Res. 50: 814–816.

    Google Scholar 

  143. Pastoret P-P, Babiuk LA, Misra V, Griebel P. (1980) Reactivation of temperature-sensitive and non-temperature sensitive infectious bovine rhinotracheitis vaccine virus with dexamethasone. Infect. Immunol. 29: 483–488.

    CAS  Google Scholar 

  144. George LW, Ardans A, Mihalyi S, Guerra MR. (1988) Enhancement of infectious bovine keratoconjunctivitis by modified-live infectious bovine rhinotracheitis virus vaccine. Am. J. Vet. Res. 49: 1800–1806.

    PubMed  CAS  Google Scholar 

  145. Kelling CL, Schipper IA, Strum GE, Carlson RB, Tilton GE. (1973) Infectious bovine rhinotracheitis (IBR) abortion; observations on incidence in vaccinated and non-vaccinated and exposed cattle. Cornell Vet. 63: 383–389.

    PubMed  CAS  Google Scholar 

  146. van Der Maaten MJ, Miller JM, Whetstone CA. (1985) Ovarian lesions induced in heifers by intravenous inoculation with modified-live infectious bovine rhinotracheitis virus on the day after breeding. Am. J. Vet. Res. 46: 1996–1999.

    PubMed  Google Scholar 

  147. Smith PC, Nusbaum KE, Kwapien RP, Stringfellow DA, Driggers K. (1990) Necrotic oophoritis in heifers vaccinated intravenously with infectious bovine rhinotracheitis virus vaccine during estrus. Am. J. Vet. Res. 51: 969–972.

    PubMed  CAS  Google Scholar 

  148. Harasawa R. (1995) Advention pestivirus RNA in live virus vaccine against bovine and swine diseases. Vaccine 13: 100–103.

    Article  PubMed  CAS  Google Scholar 

  149. Babiuk LA, L’Italien J, van Drunen Littel-van den Hurk S, et al. (1987) Protection of cattle from bovine herpesvirus type-1 (BHV-1) infection by immunization with individual glycoproteins. Virology 159: 57–66.

    Article  PubMed  CAS  Google Scholar 

  150. Van Drunen Littel-van den Hurk S, van Den Hurk JV, Gilchrist JE, Misra V, Babiuk LA. (1984) Interactions of monoclonal antibodies and bovine herpesvirus type 1 (BHV-1) glycoproteins: characterization of their biochemical and immunological properties. Virology 135: 466–479.

    Article  PubMed  Google Scholar 

  151. Collins JK, Butcher AC, Riegel CA. (1985) Immune response to bovine herpesvirus type-1 infections: virus-specific antibodies in sera from infected animals. J. Clin. Microbiol. 21: 546–552.

    PubMed  PubMed Central  CAS  Google Scholar 

  152. Ayers VK, Collins JK, Purdy CW. (1994) Epitope-specific antibody responses in market-stressed calves to bovine herpesvirus type 1. Vaccine 12: 940–946.

    Article  PubMed  CAS  Google Scholar 

  153. Israel BA, Marshall RL, Letchworth GL. (1988) Epitope specificity and protective efficacy of the bovine immune response to bovine herpesvirus-1 gIycoprotein vaccine. Vaccine 6: 349–356.

    Article  PubMed  CAS  Google Scholar 

  154. Kaashoek MJ, Moerman A, Madic J, et al. (1995) An inactivated vaccine based on a glycoprotein gE-negative strain of bovine herpesvirus 1 induces protective immunity and allows serological differentiation. Vaccine 13: 342–346.

    Article  PubMed  CAS  Google Scholar 

  155. Zhu X, Letchworth GJ. (1996) Mucosal and systemic immunity to bovine herpesvirus-1 glycoprotein D confer resistance to viral replication and latency in cattle. Vaccine 14: 61–69.

    Article  PubMed  Google Scholar 

  156. Babiuk LA, van Drunen Littel-van den Hurk S, Tikoo SK, Lewis PJ, Liang X. (1996) Novel viral vaccines for livestock. Vet. Immunol. Immunopathol. 54: 355–363.

    Article  PubMed  CAS  Google Scholar 

  157. Fitzpatrick DR, Zamb T, Parker MD, van Drunen Littel-van den Hurk S, Babiuk LA, Lawman MJP. (1988) Expression of bovine herpesvirus 1 glycoproteins gI and gIII in transfected murine cells. J. Virol. 62: 4239–4248.

    PubMed  PubMed Central  CAS  Google Scholar 

  158. van Drunen Littel-van den Hurk S, Zamb TJ, Babiuk LA. (1989) Synthesis, cellular location and immunogenicity of bovine herpesvirus-1 glycoproteins gI and gIII expressed by recombinant vaccinia virus. J. Virol. 63: 2159–2168.

    PubMed  PubMed Central  Google Scholar 

  159. Leary TP, Gao Y, Splitter GA. (1992) Constitutively expressing cell lines which secrete bovine herpesvirus-1 glycoprotein I stimulate T lymphocyte responsiveness. Immunology 76: 367–372.

    PubMed  PubMed Central  CAS  Google Scholar 

  160. van Drunen Littel-van den Hurk S, Parker MD, Massie B, van den Hurk JV, Harland R, Babiuk LA. (1993) Protection of cattle from BHV-1 infection by immunization with recombinant glycoprotein gIV. Vaccine 11: 25–36.

    Article  PubMed  Google Scholar 

  161. van Drunen Littel-van den Hurk S, Parker MD, Fitzpatrick DR, et al. (1991) Expression of bovine herpesvirus 1 glycoprotein gIV by recombinant baculovirus and analysis of its immunogenic properties. J. Virol. 65: 263–271.

    PubMed  PubMed Central  Google Scholar 

  162. van Drunen Littel-van den Hurk S, van Donkersgoed J, Kowalski J, et al. (1994) A subunit gIV vaccine produced by transfected mammalian cells in culture, induces mucosa immunity against bovine herpesvirus-1 in cattle. Vaccine 12: 1295–1302.

    Article  PubMed  Google Scholar 

  163. Merza M, Tibor S, Kucsera L, Bognar G, Morein B. (1991) ISCOM of BHV-1 envelope glycoproteins protected calves against both disease and infection. J. Vet. Med. 38: 306–314.

    Article  CAS  Google Scholar 

  164. Garcia-Valcarcel M, Fowler WJ, Harper DR, Jeffries DJ, Layton GT. (1997) Cloning, expression and immunogenicity of the assembly protein of varicella-zoster virus and detection of the products of open reading frame 33. J. Med. Virol. 53: 332–339.

    Article  PubMed  CAS  Google Scholar 

  165. Trudel M, Nadon F, Seguin C, Boulay G, Lussier G. (1987) Vaccination of rabbits with a bovine herpesvirus type 1 subunit vaccine: adjuvant effect of ISCOMs. Vaccine 5: 239–243.

    Article  PubMed  CAS  Google Scholar 

  166. Moser CA, Speaker TJ, Offit PA. (1997) Effect of microencapsulation on immunogenicity of a bovine herpes virus glycoprotein and inactivated influenza virus in mice. Vaccine 15: 1767–1772.

    Article  PubMed  CAS  Google Scholar 

  167. Young PL, Smith GA. (1995) Genetically altered herpesviruses as vaccines. Vet. Microbiol. 46: 175–179.

    Article  PubMed  CAS  Google Scholar 

  168. Rijsewijk FAM, Kaashoek MJ, Keil G, et al. (1994) In vitro and in vivo phenotypes and immunogenic properties of bovine herpesvirus 1 mutants with a deletion in the gC, gG, gI or gE gene. In: Proceedings of the 19th Herpesvirus Workshop, Vancouver, July 30-August 5, p. 419.

  169. Kit S, Qavi H, Gaines JD, Billingsley P, McConnell S. (1985) Thymidine kinase-negative bovine herpesvirus type 1 mutant is stable and highly attenuated in calves. Arch. Virol. 86: 63–83.

    Article  PubMed  CAS  Google Scholar 

  170. Smith GA, Young PL, Rodwell BJ, et al. (1994) Development and trial of a bovine herpesvirus-1-thymidine kinase deletion virus as a vaccine. Austr. Vet. J. 71: 65–70.

    Article  CAS  Google Scholar 

  171. Yu-Su K, Liu C, Manning J-RS. (1986) Identification of the thymidine kinase gene of infectious bovine rhinotracheitis virus and its function in Escherichia coli hosts. Gene 44: 279–285.

    Article  Google Scholar 

  172. Bello L, Whitbeck JC, Lawrence WC. (1987) Map location of the thymidine kinase gene of bovine herpesvirus 1. J. Virol. 61: 4023–4025.

    PubMed  PubMed Central  CAS  Google Scholar 

  173. Kaashoek MJ, Moerman A, Madic J, et al. (1994) A conventionally attenuated glycoprotein E-negative strain of bovine herpesvirus type 1 is an efficacious and safe vaccine. Vaccine 12: 439–444.

    Article  PubMed  CAS  Google Scholar 

  174. van Oirschot JT. (1994) Vaccination in food animal population. Vaccine 12: 415–418.

    Article  PubMed  Google Scholar 

  175. Kaashoek MJ, van Engelenburg FAC, Moerman A, Gielkens ALJ, Rijsewijk FAM, van Oirschot JT. (1996) Virulence and immunogenicity in calves of thymidine kinase- and glycoprotein E-negative bovine herpesvirus 1 mutants. Vet. Microbiol. 48: 143–153.

    Article  PubMed  CAS  Google Scholar 

  176. Flores EF, Osorio FA, Zanella EL, Kits S, Kit M. (1993) Efficacy of a deletion mutant bovine herpesvirus-1 (BHV-1) vaccine that allows serologic differentiation of vaccinated from naturally infected animals. J. Vet. Diagn. Invest. 5: 534–540.

    Article  PubMed  CAS  Google Scholar 

  177. Bosch JC, Frankena K, van Oirschot JT. (1996) Effect on milk production of vaccination with a bovine herpesvirus 1 gene-deleted inactivated vaccine. Vet. Rec. 140: 196–199.

    Article  Google Scholar 

  178. Strube W, Auer S, Block W, et al. (1996) A gE deleted infectious bovine rhinotracheitis marker vaccine for use in improved bovine herpesvirus 1 control programs. Vet. Microbiol. 53: 181–189.

    Article  PubMed  CAS  Google Scholar 

  179. Denis M, Hanon E, Rijsewijk FAM, et al. (1996) The role of glycoproteins gC, gE, gI and gG in the induction of cell-mediated immune responses to bovine herpesvirus 1. Vet. Microbiol. 53: 121–132.

    Article  PubMed  CAS  Google Scholar 

  180. Chowdhury SI. (1996) Construction and characterization of an attenuated bovine herpesvirus type 1 (BHV-1) recombinant virus. Vet. Microbiol. 52: 13–23.

    Article  PubMed  CAS  Google Scholar 

  181. Kuhnle G, Collins RA, Scott JE, Keil M. (1996) Bovine interleukins 2 and 4 expressed in recombinant bovine herpesvirus 1 are biologically active secreted glycoproteins. J. Gen. Virol. 77: 2231–2240.

    Article  PubMed  Google Scholar 

  182. Dinarello CA. (1991) Interleukin-1 and interleukin-1 antagonism. Blood 77: 1627–1652.

    PubMed  CAS  Google Scholar 

  183. Raggo C, Fitzpatrick DR, Babiuk LA, Liang X. (1996) Expression of bovine interleukin-1 β in a bovine herpesvirus-1 vector: in vitro analysis. Virology 221: 78–86.

    Article  PubMed  CAS  Google Scholar 

  184. Cox GJM, Zamb TJ, Babiuk LA. (1993) Bovine herpesvirus 1: immune responses in mice and cattle injected with plasmid DNA. J. Virol. 67: 5664–5667.

    PubMed  PubMed Central  CAS  Google Scholar 

  185. Terpstra C, Kroese AH. (1996) Potency control of modified live vaccines for veterinary use. Vaccine 14: 13–18.

    Article  PubMed  CAS  Google Scholar 

  186. Strube W, Abar B, Bergle RD, et al. (1995) Safety aspects in the development of an infectious bovine rhinotracheitis marker vaccine. Dev. Biol. Stand. 84: 75–81.

    PubMed  CAS  Google Scholar 

  187. Mettenleiter TC. (1996) Conclusions from the symposium. Vet. Microbiol. 53: 207–211.

    Article  PubMed  CAS  Google Scholar 

  188. van Drunen Littel-van den Hurk S, Khattar S, Tikoo SK, et al. (1996) Glycoprotein H (gII/gp108) and glycoprotein L form a functional complex which plays a role in penetration, but not in attachment, of bovine herpesvirus 1. J. Gen. Virol. 11: 1515–1520.

    Article  Google Scholar 

  189. Baranowski E, Dubuisson J, van Drunen Littelvan den Hurk S, et al. (1995) Synthesis and processing of bovine herpesvirus-1 glycoprotein H. Virology 206: 651–654.

    Article  PubMed  CAS  Google Scholar 

  190. Chowdhury SI. (1997) Fine mapping of bovine herpesvirus 1 (BHV-1) glycoprotein C neutralizing epitopes by type-specific monoclonal antibodies and synthetic peptides. Vet. Microbiol. 58: 309–314.

    Article  PubMed  CAS  Google Scholar 

  191. Keil GM, Engelhardt T, Karger A, Enz M. (1996) Bovine herpesvirus 1 Us open reading frame 4 encodes a glycoproteoglycan. J. Virol. 70: 3032–3038.

    PubMed  PubMed Central  CAS  Google Scholar 

  192. Kuhnle G, Heinze A, Schmitt J, et al. (1998) The class II membrane glycoprotein G of bovine respiratory syncytial virus, expressed from a synthetic open reading frame, is incorporated into virions of recombinant bovine herpesvirus 1. J. Virol. 72: 3804–3811.

    PubMed  PubMed Central  CAS  Google Scholar 

  193. Khadr A, Tikoo SK, Babiuk LA, van Drunen Littel-van den Hurk S. (1996) Sequence and expression of a bovine herpesvirus-1 gene homologous to the glycoprotein K-encoding gene of herpes simplex virus-1. Gene 168: 189–193.

    Article  PubMed  CAS  Google Scholar 

  194. Wu SX, Zhu XP, Letchworth GJ. (1998) Bovine herpesvirus 1 glycoprotein M forms a disulfidelinked heterodimer with the UL 49.5 protein. J. Virol. 72: 3029–3036.

    PubMed  PubMed Central  CAS  Google Scholar 

  195. Khattar SK, van Drunen Littel-van den Hurk S, Attah-Poku SK, Babiuk LA, Tikoo SK. (1996) Identification and characterization of a bovine herpesvirus-1 (BHV-1) glycoprotein gL which is required for proper antigenicity, processing, and transport of BHV-1 glycoprotein gH. Virology 219: 66–76.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Lauretta Turin.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Turin, L., Russo, S. & Poli, G. BHV-1: New Molecular Approaches to Control a Common and Widespread Infection. Mol Med 5, 261–284 (1999). https://doi.org/10.1007/BF03402063

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF03402063

Keywords

Navigation