1887

Abstract

SUMMARY

The present paper reports on the induction of two cell surface markers on human lymphoid cells following herpes simplex virus (HSV) infection. While both primary and chronic infections of human lymphoid cells led to the induction of receptors for the Fc region of 7S IgG, chronic HSV infection was also characterized by the induction of surface-bound IgM. Surface and intracellular Fc receptors were detected in the human lymphoid cell line, Raji, infected with HSV types 1 and 2. Under optimal conditions with a multiplicity of infection (m.o.i.) of 50 to 100 p.f.u. per cell, this marker was inducible in only about 53% of the infected cells. Kinetic studies revealed the appearance of these receptors at around 5 h following HSV infection and they reached a plateau 16 to 18 h p.i. Interestingly, this Fc receptor expression (i.e. percentage of positive cells) was found to be similar in primary and chronically HSV-infected Raji cells. Both human leukocyte interferon and phosphonoacetic acid (PAA), an inhibitor of herpesvirus DNA polymerase activity, effectively inhibited Fc receptor synthesis during primary HSV-infection and these two agents suppressed its induction in chronically HSV-infected Raji (Raji-HSV) cells. This inhibitory or suppressive effect, particularly of PAA, suggests that this HSV-induced Fc receptor may represent a late virus function in the infected cell. Unlike primary HSV infection, about 80% of the chronically HSV-infected Raji cells were found to express surface-bound IgM. This IgM induction was suppressed by long-term interferon treatment but not with PAA-treatment. Superinfection studies of interferon and PAA-treated Raji-HSV cells indicated that only the former would develop Fc receptors suggesting a protective role of this IgM against superinfection by HSV.

Loading

Article metrics loading...

/content/journal/jgv/10.1099/0022-1317-44-2-361
1979-08-01
2024-04-19
Loading full text...

Full text loading...

/deliver/fulltext/jgv/44/2/JV0440020361.html?itemId=/content/journal/jgv/10.1099/0022-1317-44-2-361&mimeType=html&fmt=ahah

References

  1. Costa J., Yee C., Nakamura Y., Rabson A. 1978; Characteristics of the Fc receptor induced by herpes simplex virus. Intervirology 10:32–39
    [Google Scholar]
  2. Flanagan J. P. 1967; Virus-specific ribonucleic acid synthesis in KB cells infected with herpes simplex virus. Journal of Virology 1:583–590
    [Google Scholar]
  3. Furukawa T., Hornberger E., Sakuma S., Plotkin S. A. 1975; Demonstration of immunoglobulin G receptors induced by human cytomegalovirus. Journal of Clinical Microbiology 3:332–336
    [Google Scholar]
  4. Honess R. W., Watson D. H. 1977; Herpes simplex virus resistance and sensitivity to phosphonoacetic acid. Journal of Virology 21:584–600
    [Google Scholar]
  5. Jondal M., Klein G. 1973; Surface markers on human B and T lymphocytes. II. Presence of Epstein-Barr virus receptors on B lymphocytes. Journal of Experimental Medicine 138:1365–1378
    [Google Scholar]
  6. Keller R., Peitchel R., Goldman J. N., Goldman M. 1976; An IgG-Fc receptor induced in cytomegalovirus-infected human fibroblasts. Journal of Immunology 116:772–777
    [Google Scholar]
  7. Kerbel R. S., Davies A. J. S. 1974; The possible biological significance of Fc receptors on mammalian lymphocytes and tumor cells. cell 3:105–112
    [Google Scholar]
  8. McTaggart S. P., Burns W. H., White D. O., Jackson D. 1978; Fc receptors induced by herpes simplex virus. I. Biologic and biochemical properties. Journal of Immunology 121:726–730
    [Google Scholar]
  9. Mao J. C. H., Ribushaw E. E., Overby L. R. 1975; Inhibition of DNA polymerase from herpes simplex virus-infected Wi-38 cells by phosphonoacetic acid. Journal of Virology 15:1281–1283
    [Google Scholar]
  10. Menezes J., Leibold W., Klein G. 1975; Biological differences between EBV strains with regard to lymphocyte transforming ability, superinfection and antigen induction. Experimental Cell Research 92:478–484
    [Google Scholar]
  11. Menezes J., Jondal M., Leibold W., Dorval G. 1976a; Epstein-Barr virus interactions with human lymphocyte subpopulations: virus adsorption, kinetics of expression of EBV-associated nuclear antigen (EBNA) and lymphocyte transformation. Infection and Immunity 13:303–310
    [Google Scholar]
  12. Menezes J., Patel P., Dussault H., Joncas J. 1976b; The effect of interferon on lymphocyte-transformation and induction of nuclear antigen (EBNA) by Epstein-Barr virus (EBV). Nature, London 260:430–432
    [Google Scholar]
  13. Menezes J., Patel P., Dussault H., Bourkas A. E. 1978; Comparative studies on the induction of virus-associated nuclear antigen and early antigen by lymphocyte transforming (B95-8) and nontransforming (P3HR-1) strains of Epstein-Barr virus. Intervirology 9:86–94
    [Google Scholar]
  14. Pulvertaft R. J. V. 1965; A study of malignant tumors in Nigeria by short term tissue culture. Journal of Clinical Pathology 18:261–273
    [Google Scholar]
  15. Rahman A. A., Teschner M., Sethi K. K., Brandis H. 1976; Appearance of IgG (Fc) receptor(s) on cultured human fibroblasts infected with human cytomegalovirus. Journal of Immunology 117:253–258
    [Google Scholar]
  16. Roizman B., Spear P. G., Kieff E. D. 1973; Herpes simplex viruses I and II: a biochemical definition. Perspectives in Virology 8:129–169
    [Google Scholar]
  17. Seigneurin J. M., Desgranges C., Lavoue M. F., De Thé G. 1976; Herpes simplex-Raji (A44) a new cell line for serologic testing by immunofluorescence. Journal of Immunology 117:950–952
    [Google Scholar]
  18. Simon M. 1977; Exclusion of false positive reactions due to IgG-binding Fc receptor(s) in herpesvirus serology. Acta Microbiologica Academiae Scientiarum Hungariacae 24:307–316
    [Google Scholar]
  19. Watkins J. F. 1964; Adsorption of sensitized sheep erythrocytes to HeLa cells infected with herpes simplex virus. Nature, London 202:1364–1365
    [Google Scholar]
  20. Watkins J. F. 1965; The relationship of the herpes simplex haemadsorption phenomenon to the virus growth cycle. Virology 26:746–753
    [Google Scholar]
  21. Westmoreland D., Watkins J. F. 1974; The IgG receptor induced by herpes simplex virus: studies using radioiodinated IgG. Journal of General Virology 24:167–178
    [Google Scholar]
  22. Westmoreland D., Watkins J. F., Rapp F. 1974; Demonstration of a receptor for IgG in Syrian hamster cells transformed with herpes simplex virus. Journal of General Virology 25:167–170
    [Google Scholar]
  23. Westmoreland D., St Jeor S., Rapp F. 1976; The development of cytomegalovirus-infected cells binding affinity for normal human immunoglobulin. Journal of Immunology 116:1566–1670
    [Google Scholar]
  24. Yasuda J., Milgrom F. 1968; Hemadsorption by herpes simplex-infected cell cultures. International Archives of Allergy and Applied Immunology 33:151–170
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/jgv/10.1099/0022-1317-44-2-361
Loading
/content/journal/jgv/10.1099/0022-1317-44-2-361
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error