Skip to main content
Log in

Chicken strain G-B 1 exhibits a relative resistance to avian osteopetrosis

  • Original Papers
  • Published:
Archives of Virology Aims and scope Submit manuscript

Summary

The disease induced by the avian myeloblastosis associated virus MAV-2-O in the susceptible chicken strains Brown Leghorn (BLH) and Prague CB (CB) was compared with that induced in the resistant G-B 1 strain. Osteopetrosis, stunting and lymphoid organ atrophy were more severe in BLH than in CB chickens. G-B 1 animals remained superficially normal until the end of the experiment. In contrast to the other two strains, the histopathological changes were very mild and there was no sign of immunosuppression. After 4 months, however, nephroblastomas could be detected in more than 50 per cent of the infected G-B 1 chickens. Similar tumors were also found in CB birds kept for up to 5 months. Antibodies against MAV-2-O specific viral proteins were detected in plasma from infected G-B 1 chickens but the titers were less than in plasma of convalescent birds. Virus could be demonstrated in peripheral blood until the end of the experiment (at 8 weeks). Therefore the resistance of the G-B 1 strain is due neither to a restriction at the receptor level nor the result of a humoral immune reaction, but represents a new type of relative resistance at the cellular level. From (CC × G-B 1)F1 and (CC × G-B 1)F2 crosses the resistant phenotype is determined by a single genetic factor. This gene is not linked to the major histocompatibility complex. There is also a sex-dependent factor, possibly hormonal, involved in the resistant phenotype.

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.

Similar content being viewed by others

References

  1. Baba TW, Humphries EH (1984 a) Avian leukosis virus infection: Analysis of viremia and DNA integration in susceptible and resistant chicken lines. J Virol 51: 123–130

    Google Scholar 

  2. Baba TW, Humphries EH (1984 b) Differential response to avian leukosis virus infection exhibited by two chicken lines. Virology 135: 181–188

    Google Scholar 

  3. Banes AJ, Smith RE (1977) Biological characterization of avian osteopetrosis. Infect Immun 16: 876–884

    Google Scholar 

  4. Boyde A, Banes AJ, Dillaman RM, Mechanic GL (1978) A morphological study of avian bone disorder caused by myeloblastosis-associated virus. Metab Bone Dis Rel Res 1: 235–242

    Google Scholar 

  5. Briles WE, Bumstead N, Ewert DL, Gilmour DG, Gogusev J, Hala K, Koch C, Longenecker BM, Nordskog AW, Pink JRL, Schierman LW, Simonsen M, Toivanen A, Toivanen O, Vainio O, Wick G (1982) Nomenclature for chicken major histocompatibility (B) complex. Immunogenetics 15: 441–447

    Google Scholar 

  6. Briles WE, Briles RW, Taffs RE, Stone HA (1983) Resistance to a malignant lymphoma in chickens is mapped to subregion of major histocompatibility (B) complex. Science 219: 977–979

    Google Scholar 

  7. Crittenden LB (1975) Two levels of genetic resistance to lymphoid leukosis. Avian Dis 19: 281–292

    Google Scholar 

  8. Frank RM, Franklin RM (1982) Electron microscopy of avian osteopetrosis induced by retrovirus MAV-2-O. Calcif Tissue Int 34: 382–390

    Google Scholar 

  9. Franklin RM, Martin M-T (1980 a)In ovo tumorigenesis induced by avian osteopetrosis virus. Virology 105: 245–249

    Google Scholar 

  10. Franklin RM, Martin M-T (1980 b) Staining and histochemistry of undecalcified bone embedded in a water-miscible plastic. Stain Technol 55: 313–321

    Google Scholar 

  11. Franklin RM, Martin M-T (1983) An improved formulation of Nocht's azure-eosin stain for plastic embedded material. Stain Technol 58: 353–356

    Google Scholar 

  12. Fung Y-KT, Fadly AM, Crittenden LB, Kung H-J (1981) On the mechanism of retrovirus-induced avian lymphoid leukosis: Deletion and integration of the proviruses. Proc Natl Acad Sci U.S.A. 78: 3418–3422

    Google Scholar 

  13. Fung Y-KT, Fadly AM, Crittenden LB, Kung H-J (1982) Avian lymphoid leukosis virus infection and DNA integration in the preleukotic bursal tissues: a comparative study of susceptible and resistant lines. Virology 119: 411–421

    Google Scholar 

  14. Hirota, Y, Martin M-T, Viljanen M, Toivanen P, Franklin RM (1980) Immunopathology of chickens infectedin ovo and at hatching with the avian osteopetrosis virus MAV-2-O. Eur J Immunol 10: 929–936

    Google Scholar 

  15. Holmes JR (1961) Postmortem findings in avian osteopetrosis. J Comp Path 71: 20–27

    Google Scholar 

  16. Koch C, Skjødt K, Toivanen A, Toivanen P (1983) New recombinants within the MHC (B-complex) of the chicken. Tissue Antigens 21: 129–137

    Google Scholar 

  17. Moscovici C, Chi D, Gazzolo L, Moscovici MG (1976) A study of plaque formation with avian RNA tumor viruses. Virology 73: 181–189

    Google Scholar 

  18. Neel BG, Hayward WS, Robinson HL, Fang J, Astrin SM (1981) Avian leukosis virus-induced tumors have common proviral integration sites and synthesize discrete new RNAs: oncogenesis by promotor insertion. Cell 23: 323–334

    Google Scholar 

  19. Paterson RW, Smith RE (1978) Characterization of anemia induced by avian osteopetrosis virus. Infect Immun 22: 891–900

    Google Scholar 

  20. Payne GS, Courtneidge SA, Crittenden LB, Fadly AM, Bishop JM, Varmus HE (1981) Analysis of avian leukosis virus DNA and RNA in bursal tumors: viral gene expression is not required for maintenance of the tumor state. Cell 23: 311–322

    Google Scholar 

  21. Plachý J, Benda V (1981) Location of the gene responsible for Rous sarcoma regression in the B-F region of the B-complex (MHC) of the chicken. Fol Biol (Praha) 27: 363–368

    Google Scholar 

  22. Price JA, Smith RE (1982) Inhibition of concanavalin A response during osteopetrosis virus infection. Cancer Res 42: 3617–3624

    Google Scholar 

  23. Purchase HG, Gilmour DG, Romero CH, Okazaki W (1977) Postinfection genetic resistance to avian lymphoid leukosis resides in B-target cell. Nature 270: 61–62

    Google Scholar 

  24. Robinson HL, Miles BD (1985) Avian leukosis virus-induced osteopetrosis is associated with the persistent synthesis of viral DNA. Virology 141: 130–143

    Google Scholar 

  25. Schiermann LW, Watanabe DH, McBride RA (1977) Genetic control of Rous sarcoma regression in chickens: Linkage with the major histocompatibility complex. Immunogenetics 5: 325–332

    Google Scholar 

  26. Simonsen M (1975) Allo-aggression in chickens. Acta Path Microbiol Scand Sect C 83: 1–14

    Google Scholar 

  27. Simpson CF, Sanger VL (1966) Electron microscopy of the periosteum in experimental avian osteopetrosis. Cancer Res 26: 590–595

    Google Scholar 

  28. Smith RE, Moscovici C (1969) The oncogenic effects of nontransforming viruses from avian myeloblastosis virus. Cancer Res 29: 1356–1366

    Google Scholar 

  29. Smith RE, Davids LJ, Neiman PE (1976) Comparison of an avian osteopetrosis virus with an avian lymphomatosis virus by RNA-DNA hybridization. J Virol 17: 160–167

    Google Scholar 

  30. Smith RE, van Eldik LJ (1978) Characterization of the immunosuppression accompanying virus-induced avian osteopetrosis. Infect Immun 22: 452–461

    Google Scholar 

  31. Smith RE, Schmidt EV (1982) Induction of anemia by avian leukosis viruses of five subgroups. Virology 117: 516–518

    Google Scholar 

  32. Towbin H, Staehelin T, Gordon J (1979) Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci U.S.A. 76: 4350–4354

    Google Scholar 

  33. Vogt PK, Ishizaki R (1965) Reciprocal patterns of genetic resistance to avian tumor viruses in two lines of chickens. Virology 26: 664–672

    Google Scholar 

  34. Voller A, Bidwell PE, Bartlett A (1979) The enzyme linked immunosorbent assay (ELISA). Guernsey: Dynatech Europe

    Google Scholar 

  35. Weiss R (1982) Experimental biology and assay of retroviruses. In:Weiss R, Teich N, Varmus H, Coffin J (eds), Molecular biology of tumor viruses, RNA tumor viruses. Cold Spring Harbor Laboratory, New York, pp 209–260

    Google Scholar 

  36. Zeller R, Nyffeneger T, de Robertis EM (1983) Nucleocytoplasmic distribution of snRNPs and stockpiled snRNA-binding proteins during oogenesis and early development in Xenopus laevis. Cell 32: 425–434

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

With 6 Figures

Rights and permissions

Reprints and permissions

About this article

Cite this article

Böni, J., Böni-Schnetzler, M., Vainio, O. et al. Chicken strain G-B 1 exhibits a relative resistance to avian osteopetrosis. Archives of Virology 91, 21–36 (1986). https://doi.org/10.1007/BF01316725

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01316725

Keywords

Navigation