Superinfection Prevents Recombination of the Alphaherpesvirus Bovine Herpesvirus 1

Journal of Virology

Volumn 78, Issue 8, 2004, Pages 3872-3879

  Meurens, François ^a   Schynts, Frédéric ^b   Keil, Günther M ^c   Muylkens, Benoît ^a   Vanderplasschen, Alain ^a   Gallego, Pierre ^a   Thiry, Etienne ^a  

^a UNIVERSITY OF LIÈGE   (Belgium)

^b CER   (Belgium)

^c FEDERAL RESEARCH INSTITUTE FOR ANIMAL HEALTH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BETA GALACTOSIDASE; CELL MARKER; GLYCOPROTEIN E; VACCINE; VIRUS DNA;

ARTICLE; BINDING SITE; ERADICATION THERAPY; FELINE HERPESVIRUS 1; GENE EXPRESSION REGULATION; GENE MUTATION; GENETIC RECOMBINATION; HERPES SIMPLEX VIRUS 1; HERPES SIMPLEX VIRUS 2; HERPES VIRUS; IN VITRO STUDY; IN VIVO STUDY; INOCULATION; NONHUMAN; PRIORITY JOURNAL; PSEUDORABIES HERPETOVIRUS; RISK ASSESSMENT; SPECIES IDENTIFICATION; STRAIN IDENTIFICATION; SUPERINFECTION; TIME; VARICELLA ZOSTER VIRUS; VIRUS INFECTION; VIRUS MUTATION; VIRUS RECOMBINANT; VIRUS RECOMBINATION;

ANIMALS; BETA-GALACTOSIDASE; CATTLE; CELL LINE; DNA, VIRAL; GENE EXPRESSION; HERPESVIRIDAE INFECTIONS; HERPESVIRUS 1, BOVINE; MUTATION; RECOMBINATION, GENETIC; SUPERINFECTION; TIME FACTORS;

EID: 1842536909     PISSN: 0022538X     EISSN: None     Source Type: Journal    
DOI: 10.1128/JVI.78.8.3872-3879.2004     Document Type: Article

References (65)

1. Babluk, L. A., H. B. Ohmann, G. Gifford, C. W. Czarniecki, V. T. Scialli, and E. B. Hamilton. 1985. Effect of bovine alpha 1 interferon on bovine herpesvirus type 1-induced respiratory disease. J. Gen. Virol. 66:2383-2394.
2. Banfield, B. W., J. D. Kaufman, J. A. Randall, and G. E. Pickard. 2003. Development of pseudorabies virus strains expressing red fluorescent proteins: new tools for multisynaptic labeling applications. J. Virol. 77:10106-10112.
3. Baranowski, E., J. Dubuisson, P.-P. Pastoret, and E. Thiry. 1993. Identification of 108K, 93K, and 42K glycoproteins of bovine herpesvirus-1 by monoclonal antibodies. Arch. Virol. 133:97-111.
4. Campadelli-Fiume, G., F. Cocchi, L. Menotti, and M. Lopez. 2000. The novel receptors that mediate the entry of herpes simplex viruses and animal alphaherpesviruses into cells. Rev. Med. Virol. 10:305-319.
5. Chase, C. C., K. Carter-Allen, C. Lohff, and G. J. Letchworth. 1990. Bovine cells expressing bovine herpesvirus 1 (BHV-1) glycoprotein IV resist infection by BHV-1, herpes simplex virus, and pseudorabies virus. J. Virol. 64:4866-4872.
6. Chase, C. C., C. Lohff, and G. J. Letchworth. 1993. Resistance and susceptibility of bovine cells expressing herpesviral glycoprotein D homologs to herpesviral infections. Virology 194:365-369.
7. Chase, C. C., and G. J. Letchworth. 1994. Bovine herpesvirus 1 gIV-expressing cells resist virus penetration. J. Gen. Virol. 75:177-181.
8. Chowdhury, S. I., C. S. D. Ross, B. J. Lee, V. Hall, H. J. Chu. 1999. Construction and characterization of a glycoprotein E gene-deleted bovine herpesvirus type 1 recombinant. Am. J. Vet. Res. 60:227-232.
9. Czarniecki, C. W., E. B. Hamilton, C. W. Fennie, and R. L. Wolf. 1986. In vitro biological activities of Escherichia coli-derived bovine interferon-alpha, -beta, and -gamma. J. Interferon Res. 6:29-37.
10. Dasika, G. K., and G. J. Letchworth. 1999. Cellular expression of bovine herpesvirus 1 gD inhibits cell-to-cell spread of two closely related viruses without blocking their primary infection. Virology 254:24-36.
11. Dasika, G. K., and G. J. Letchworth. 2000. Homologous and heterologous interference requires bovine herpesvirus-1 glycoprotein D at the cell surface during virus entry. J. Gen. Virol. 81:1041-1049.
12. De Wit, W. J., J. J. Hage, J. Brinkhof, and F. Westenbrink. 1998. A comparative study of serological tests for use in the bovine herpesvirus 1 eradication program in The Netherlands. Vet. Microbiol. 61:153-163.
13. Dispas, M., F. Schynts, M. Lemaire, C. Letellier, E. Vanopdenbosch, E. Thiry, and P. Kerkhofs. 2003. Isolation of a glycoprotein E deleted bovine herpesvirus-1 strain in the field. Vet. Rec. 153:209-212.
14. Dohner, D. E., S. G. Adams, and L. D. Gelb. 1988. Recombination in tissue culture between varicella-zoster virus strains. J. Med. Virol. 24:329-341.
15. Dutta, S. K., A. C. Myrup, and S. R. Thaker. 1986. In vitro interference between equine herpesvirus types 1 and 2. Am. J. Vet. Res. 47:747-750.
16. Fujita, K., K. Maeda, N. Yokoyama, T. Miyazawa, C. Kai, and T. Mikami. 1998. In vitro recombination of feline herpesvirus type 1. Arch. Virol. 143:25-34.
17. Garber, D. A., S. M. Beverley, and D. M. Coen. 1993. Demonstration of circularization of herpes simplex virus DNA following infection using pulsed field gel electrophoresis. Virology 197:459-462.
18. Geraghty, R. J., C. R. Jogger, and P. G. Spear. 2000. Cellular expression of alphaherpesvirus gD interferes with entry of homologous and heterologous alphaherpesviruses by blocking access to a shared gD receptor. Virology 268:147-158.
19. Glazenburg, K. L., R. J. M. Moorman, T. G. Kimman, A. L. J. Gielkens, and B. P. H. Peeters. 1994. In vivo recombination of pseudorabies virus strains in mice. Virus Res. 34:115-126.
20. Henderson, L. M., J. B. Katz, G. A. Erickson, and J. E. Mayfield. 1990. In vivo and in vitro genetic recombination between conventional and gene-deleted vaccine strains of pseudorabies virus. Am. J. Vet. Res. 51:1656-1662.
21. Javier, R. T., F. Sedarati, and J. G. Stevens. 1986. Two avirulent herpes simplex viruses generate lethal recombinants in vivo. Science 234:746-748.
22. Johnson, R. M., and P. G. Spear. 1989. Herpes simplex virus glycoprotein D mediates interference with herpes simplex virus infection. J. Virol. 63:819-827.
23. Johnson, D. C., R. L. Burke, and T. Gregory. 1990. Soluble forms of herpes simplex virus glycoprotein D bind to a limited number of cell surface receptors and inhibit virus entry into cells. J. Virol. 64:2569-2576.
24. Kaashoek, M. J., F. A. Rijsewijk, R. C. Ruuls, G. M. Keil, E. Thiry, P.-P. Pastoret, and J. T. Van Oirschot. 1998. Virulence, immunogenicity and reactivation of bovine herpesvirus 1 mutants with a deletion in the gC, gG, gI, gE, or in both the gI and gE gene. Vaccine 16:802-809.
25. Katz, J. B., L. M. Henderson, and G. A. Erickson. 1990. Recombination in vivo of pseudorabies vaccine strains to produce new virus strains. Vaccine 8:286-288.
26. Keywan, K., and E. Katz. 1999. Co-infection of acyclovir-resistant and acyclovir-sensitive herpes simplex type 2 virus strains in BS-C-1 cells. Intervirology 42:247-251.
27. Kim, J. S., L. W. Enquist, and J. P. Card. 1999. Circuit-specific coinfection of neurons in the rat central nervous system with two pseudorabies virus recombinants. J. Virol. 73:9521-9531.
28. Leung-Tack, P. 1993. L'herpèsvirus bovin de type 1: caractérisation de la région Us du génome viral (souche ST) et étude de mutants délétés. Ph.D. thesis. University Louis Pasteur, Strasbourg, France.
29. Leung-Tack, P., J. C. Audonnet, and M. Rivière. 1994. The complete DNA sequence and the genetic organization of the short unique region (US) of the bovine herpesvirus type 1 (ST strain). Virology 199:409-421.
30. Liang, X. P., L. A. Babiuk, L. A., S. van Drunen Little-van Den Hurk, D. R. Fitzpatrick, and T. J. Zamb. 1991. Bovine herpesvirus 1 attachment to permissive cells is mediated by its major glycoproteins gI, gIII, and gIV. J. Virol. 65:1124-1132.
31. Liang, X., L. A. Babiuk, and T. J. Zamb. 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.
32. Ludwig, G. V., and G. J. Letchworth III. 1987. Temporal control of bovine herpesvirus 1 glycoprotein synthesis. J. Virol. 61:3292-3294.
33. Marcus, P. I. 1999. Interferons, p. 854-862. In A. Granoff and R. G. Webster (ed.), Encyclopedia of virology. Academic Press, Inc., San Diego, Calif.
34. Matis, J., M. Kudelova, and J. Rajcani. 1999. Interference of the low-pH inactivated herpes simplex virus type 1 (HSV-1) strain HSZP with the early shutoff function of superinfecting HSV-1 strain KOS. Virus Res. 60:81-86.
35. McVoy, M. A., and S. P. Adler. 1994. Human cytomegalovirus DNA replicates after early circularization by concatemer formation, and inversion occurs within the concatemer. J. Virol. 68:1040-1051.
36. Metzler, A. E., H. Matile, U. Gassmann, M. Engels, and R. Wyler. 1985. European isolates of bovine herpesvirus 1: a comparison of restriction endonuclease sites, polypeptides, and reactivity with monoclonal antibodies. Arch. Virol. 85:57-69.
37. Meurens, F., B. Muylkens, F. Schynts, I. Bourgot, A. Billiau, and E. Thiry. 2003. L'interférence virale chez les Alphaherpesvirinae. Virologie 7:319-328.
38. Mossman, K. L. 2002. Activation and inhibition of virus and interferon: the herpesvirus story. Viral Immunol. 15:3-15.
39. Nauwynck, H. J., G. G. Labarque, and M. B. Pensaert. 1999. Efficacy of an intranasal immunization with gEgC and gEgI double-deletion mutants of Aujeszky's disease virus in maternally immune pigs and the effects of a successive intramolecular booster with commercial vaccines. J. Vet. Med. B 46:713-722.
40. Nishiyama, Y., H. Kimura, and T. Daikoku. 1991. Complementary lethal invasion of the central nervous system by nonneuroinvasive herpes simplex virus types 1 and 2. J. Virol. 65:4520-4524.
41. Nolan, G. P., S. Fiering, J. F. Nicolas, and L. A. Herzenberg. 1988. Fluorescence activated cell analysis and sorting of viable mammalian cells based on β-D-galactosidase activity after transduction of Escherichia coli lacZ. Proc. Natl. Acad. Sci. USA 85:2603-2607.
42. Pastoret, P.-P., E. Thiry, B. Brochier, G. Derboven, and H. Vindevogel. 1984. The role of latency in the epizootiology of infectious bovine rhinotracheitis, p. 221-227. In G. Wittmann, R. M. Gaskell, and H. J. Rziha (ed.), Latent herpesvirus infections in veterinary medicine. Kluwer Academic Publishers, Boston, Mass.
43. Purifoy, D. J., and K. L. Powell. 1977. Interference between strains of type 1 and type 2 herpes simplex virus. Virology 77:84-94.
44. Rebordosa, X., J. Pinol, J. A. Perez-Pons, J. Lloberas, J. Naval, X. Serra-Hartmann, E. Espuna, and E. Querol. 1996. Glycoprotein E of bovine herpesvirus type 1 is involved in virus transmission by direct cell-to-cell spread. Virus Res. 45:59-68.
45. Roizman, B. 1963. The programming of herpes virus multiplication in doubly-infected and in puromycin-treated cells. Proc. Natl. Acad. Sci. USA 49:165-171.
46. Roizman, B., and D. M. Knipe. 2001. Herpes simplex viruses and their replication, p. 2399-2461. In D. M. Knipe and P. M. Howley (ed.), Fields virology, 4th ed. Lippincott/The Williams & Wilkins Co., Philadelphia, Pa.
47. Savan, M., A. B. Angulo, and J. B. Derbyshire. 1979. Interferon, antibody responses and protection induced by an intranasal infectious bovine rhinotracheitis vaccine. Can. Vet. J. 20:207-210.
48. Schynts, F., E. Baranowski, M. Lemaire, and E. Thiry. 1999. A specific PCR to differentiate between gE negative vaccine and wild-type bovine herpesvirus type 1 strains. Vet. Microbiol. 66:187-195.
49. Schynts, F., A. Vanderplasschen, E. Hanon, F. A. Rijsewijk, J. T. Van Oirschot, and E. Thiry. 2001. Use of PCR and immunofluorescence to detect bovine herpesvirus 1 recombinants. J. Virol. Methods 92:99-104.
50. Schynts, F., M. A. McVoy, F. Meurens, B. Detry, A. L. Epstein, and E. Thiry. 2003. The structures of bovine herpesvirus 1 virion and concatemeric DNA: implications for cleavage and packaging of herpesvirus genomes. Virology 314:326-335.
51. Schynts, F., F. Meurens, B. Detry, A. Vanderplasschen, and E. Thiry. 2003. Rise and survival of bovine herpesvirus 1 recombinants after primary infection and reactivation from latency. J. Virol. 77:12535-12542.
52. Sedarati, F., R. T. Javier, and J. G. Stevens. 1988. Pathogenesis of a lethal mixed infection in mice with two nonneuroinvasive herpes simplex virus strains. J. Virol. 62:3037-3039.
53. Slobedman, B., X. Zhang, and A. Simmons. 1999. Herpes simplex virus genome isomerization: origins of adjacent long segments in concatemeric viral DNA. J. Virol. 73:810-813.
54. Smith, G. A., S. T. Gross, and L. W. Enquist. 2001. Herpesviruses use bidirectionnal fast-axonal transport to spread in sensory neurons. Proc. Natl. Acad. Sci. USA 98:3466-3470.
55. Spear, P. G., R. J. Eisenberg, and G. H. Cohen. 2000. Three classes of cell surface receptors for alphaherpesvirus entry. Virology 275:1-8.
56. Stegeman, A. 1995. Pseudorabies virus eradication by area-wide vaccination is feasible. Ph.D. thesis. University of Utrecht, Utrecht, The Netherlands.
57. Strube, W., S. Auer, W. Block, E. Heinen, D. Kretzdorn, C. Rodenbach, and N. Schmeer. 1996. A gE deleted infectious bovine rhinotracheitis marker vaccine for use in improved bovine herpesvirus 1 control programs. Vet. Microbiol. 53:181-189.
58. Tikoo, S. K., M. Campos, and L. A. Babiuk. 1995. Bovine herpesvirus 1 (BHV-1): biology, pathogenesis, and control. Adv. Virus Res. 45:191-223.
59. Van Engelenburg, E. F., M. J. Kaashoek, F. A. Rijsewijk, D. B. van den Burg, A. Moerman, A. L. Gielkens, and J. T. Van Oirschot. 1994. A glycoprotein E deletion mutant of bovine herpesvirus 1 is avirulent in calves. J. Gen. Virol. 75:2311-2318.
60. Van Oirschot, J. T., M. J. Kaashoek, M. A. Maris-Veldhuis, K. Weerdmeester, and F. A. Rijsewijk. 1997. An enzyme-linked immunosorbent assay to detect antibodies against glycoprotein gE of bovine herpesvirus 1 allows differentiation between infected and vaccinated cattle. J. Virol. Methods 67:23-34.
61. Wyler, R., M. Engels, and M. Schwyzer. 1989. Infectious bovine rhinotracheitis/vulvovaginitis (BHV-1), p. 1-72. In G. Wittmann (ed.), Herpesvirus diseases of cattle, horses and pig. Kluwer Academic Publishers, Boston, Mass.
62. Xiao, C. Z., Z. L. Chen, and B. Z. Wu. 1989. Kinetics of antiviral state in cells activated by interferons in vitro. Arch. Immunol. Ther. Exp. 37:508-513.
63. Youngner, J. S., and P. Whitaker-Dowling. 1999. Interference, p. 850-862. In A. Granoff and R. G. Webster (ed.), Encyclopedia of virology. Academic Press, Inc., San Diego, Calif.
64. Zelena, D., J. Roubal, and V. Vonka. 1976. Inhibitory effect of herpes simplex virus type 1 on type 2 virus replication. J. Gen. Virol. 33:249-257.
65. Zsak, L., F. Zuckermann, N. Sugg, and T. Ben-Porat. 1992. Glycoprotein gI of pseudorabies virus promotes cell fusion and virus spread via direct cell-to-cell transmission. J. Virol. 66:2316-2325.