Skip to main content
Log in

Role of glycoprotein gD in the adhesion of pseudorabies virus infected cells and subsequent cell-associated virus spread

  • Brief Report
  • Published:
Archives of Virology Aims and scope Submit manuscript

Summary

Pseudorabies virus (PrV) infected cells in suspension are able to adhere to a monolayer of uninfected cells by means of PrV glycoproteins expressed at the outer cell membrane, with gB and gC playing a major role as ligands and a heparinlike substance as receptor. In order to investigate the role of gD in this process and subsequent transmission of infectivity to contact cells, experiments with a gD deletion mutant, heparin and a monoclonal antibody (Mab) against gD were performed. The first indication that gD is active during cell adhesion was found by the observation that the binding of gD PrV infected cells was five times weaker than that of wild type (WT) PrV infected cells. Further evidence was given by the use of a Mab against gD. Preincubation of WT PrV infected cells with this Mab led to a reduction of the percentage adhering cells from 69% to 49%. The same Mab inhibited the heparin independent and heparin resistant binding of WT PrV infected cells indicating that gD is important during both processes. Furthermore, it was demonstrated in a plaque assay that, after contact with a monolayer, gD PrV infected cells in suspension were able to induce plaques with an efficiency of 1%. In conclusion, we can state that beside the interaction of the ligands gB and gC with a heparinlike receptor also the interaction of gD with a receptor which differs from a heparinlike substance mediates the binding of WT PrV infected cells to uninfected cells and that gD is not essential for the subsequent cell-to-cell spread of the virus.

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.

References

  1. Dean HJ, Cheung AK (1993) A 3′ coterminal gene cluster in pseudorabies virus contains herpes simplex virus UL1, UL2, and UL3 gene homologs and a unique UL3.5 open reading frame. J Virol 67: 5955–61

    PubMed  Google Scholar 

  2. Hanssens FP, Nauwynck HJ, Pensaert MB (1993) Involvement of membrane-bound viral glycoproteins in adhesion of pseudorabies virus infected-cells. J Virol 67: 4492–4496

    PubMed  Google Scholar 

  3. Kaplan AS, Vatter A (1959) A comparison of herpes simplex and pseudorabies virus. Virology 7: 394–407

    PubMed  Google Scholar 

  4. Karger A, Mettenleiter TC (1993) Glycoproteins gIII and gp50 play dominant roles in the biphasic attachment of pseudorabies virus. Virology 194: 654–664

    PubMed  Google Scholar 

  5. Klupp BC, Visser N, Mettenleiter TC (1992) Identification and characterization of pseudorabies virus glycoprotein H. J Virol 66: 3048–3055

    PubMed  Google Scholar 

  6. Klupp BC, Baumeister J, Karger A, Visser N, Mettenleiter TC (1994) Identification and characterization of a noval structural glycoprotein in pseudorabies virus, gL. J Virol 68: 3868–3878

    PubMed  Google Scholar 

  7. Ligas MW, Johnson DC (1988) A herpes simplex virus mutant in which glycoprotein D sequences are replaced by beta-galactosidase sequences binds to but is unable to penetrate cells. J Virol 62: 1486–1494

    PubMed  Google Scholar 

  8. Mettenleiter TC, Lukas N, Rziha H-J (1985) Pseudorabies virus avirulent strains fail to express a major glycoprotein. J Virol 56: 307–311

    PubMed  Google Scholar 

  9. Mettenleiter TC, Lukas N, Thiel H-J, Schreurs C, Rziha H-J (1986) Localization of the structural gene of pseudorabies virus glycoprotein gII complex. Virology 152: 66–75

    PubMed  Google Scholar 

  10. Mettenleiter TC, Zsak L, Zuckermann F, Sugg N, Kern H, Ben-Porat T (1990) Interaction of glycoprotein gIII with a cellular heparinlike substance mediates adsorption of pseudorabies virus. J Virol 64: 278–286

    PubMed  Google Scholar 

  11. Nauwynck H (1993) The cell-associated spread of Aujeszky's disease virus and its possible role in the pathogenesis of abortion in vaccinated sows. PhD thesis, University of Gent

  12. Peeters B, de Wind N, Hooisma M, Wagenaar F, Gielkens A, Moormann R (1992a) Pseudorabies virus envelope glycoproteins gp50 and gII are essential for virus penetration, but only gII is involved in membrane fusion. J Virol 66: 894–905

    PubMed  Google Scholar 

  13. Peeters B, de Wind N, Broer R, Gielkens A, Moormann R (1992b) Glycoprotein H of pseudorabies virus is essential for entry and cell-to-cell spread of the virus. J Virol 66: 3888–3892

    PubMed  Google Scholar 

  14. Petrovskis EA, Timmins JG, Armentrout A, Marchioli CC, Yancey RJ, Post LE (1986a) DNA sequence of the gene for pseudorabies virus gp50, a glycoprotein without N-linked glycosylation. J Virol 59: 216–223

    PubMed  Google Scholar 

  15. Petrovskis EA, Timmins JG, Post LE (1986b) Use of lambda-gt11 to isolate genes for two pseudorabies virus glycoproteins with homology to herpes simplex virus and varicella-zoster virus glycoproteins. J Virol 60: 185–193

    PubMed  Google Scholar 

  16. Petrovskis EA, Duffus PM, Thomsen DR, Meyer AL, Post LE (1988) Sequence of pseudorabies virus and infectious bovine rhinotracheitis virus glycoprotein gH genes, p 217. Abstracts 13th International Herpesvirus Workshop, Irvine California

  17. Rauh I, Weiland F, Fehler F, Keil GM, Mettenleiter 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  Google Scholar 

  18. Rauh I, Mettenleiter TC (1991) Pseudorabies virus gII and gp50 are essential for virus penetration. J Virol 65: 5348–5356

    PubMed  Google Scholar 

  19. Rea TJ, Timmins JG, Long GW, Post LE (1985) Mapping and sequence of the gene for the pseudorabies virus glycoprotein which accumulates in the medium of infected cells. J Virol 54: 21–29

    PubMed  Google Scholar 

  20. Robbins AK, Watson RJ, Whealy ME, Hays WW, Enquist LW (1986) Characterization of pseudorabies virus glycoprotein gene with homology to herpes simplex virus type 1 and type 2 glycoprotein C. J Virol 58: 339–347

    PubMed  Google Scholar 

  21. Robbins AK, Dorney DJ, Wathen MW, Whealy ME, Gold C, Watson RJ, Holland LE, Weed SD, Levine M, Glorioso JC, Enquist LW (1987) The pseudorabies virus gII gene is closely related to the gB glycoprotein gene of herpes simplex virus. J Virol 61: 2691–2701

    PubMed  Google Scholar 

  22. Schreurs C, Mettenleiter TC, Zuckermann F, Sugg N, Ben-Porat T (1988) Glycoprotein gIII of pseudorabies virus is multifunctional. J Virol 62: 2251–2257

    PubMed  Google Scholar 

  23. Vandeputte J, Chappuis G, Fargeaud D, Precausta P, Guillemin F, Brun A, Desmettre P, Stellmann C (1990) Vaccination against pseudorabies with glycoprotein gI+ or glycoprotein gI− vaccine. Am J Vet Res 51: 1100–1106

    PubMed  Google Scholar 

  24. Wathen MW, Wathen LMK (1984) Isolation, characterization, and physical mapping of a pseudorabies virus mutant containing antigenically altered gp50. J Virol 5: 57–62

    Google Scholar 

  25. Zsak L, Zuckermann F, Sugg N, Ben-Porat T (1992) Glycoprotein gI of pseudorabies virus promotes cell fusion and virus spread via direct cell-to-cell transmission. J Virol 66: 2316–2325

    PubMed  Google Scholar 

  26. Zuckermann F, Zsak L, Reilly L, Sugg N, Ben-Porat T (1989) Early interactions of pseudorabies virus with host cells: functions of glycoprotein gIII. J Virol 63: 3323–3329

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hanssens, F.P., Nauwynck, H.J. & Mettenleiter, T.C. Role of glycoprotein gD in the adhesion of pseudorabies virus infected cells and subsequent cell-associated virus spread. Archives of Virology 140, 1855–1862 (1995). https://doi.org/10.1007/BF01384348

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01384348

Keywords

Navigation