1887

Abstract

SUMMARY

The herpes simplex virus type 1 (HSV-1) mutant 1403 contains a 2 kb deletion within the sequences encoding the immediate early polypeptide Vmw110. Previous experiments showed that although 1403 exhibits normal patterns of gene expression following infection at an m.o.i. of 5 p.f.u./cell its growth and plaquing efficiency are impaired in low multiplicity infections, particularly in human foetal lung (HFL) cells. We have now investigated the ability of two other human herpesviruses, varicella-zoster virus (VZV) and human cytomegalovirus (HCMV), to compensate for this defect at low m.o.i. in HFL cells. Co-infection with HCMV resulted in greatly increased plaque numbers and the apparent particle/p.f.u. ratios of 1403 stocks were reduced to values similar to those exhibited by wild-type HSV-1 stocks. Complementation of 1403 in low multiplicity infections by HCMV and VZV was also demonstrated by an increased yield of the mutant virus and an increase in synthesis of 1403 DNA. Ultraviolet irradiation of HCMV abolished its ability to complement 1403 and the presence of adenovirus 5 had no stimulatory effect on 1403 DNA replication. When HFL monolayers were infected with dilutions of 403 stocks such that no plaques were produced, replication of the mutant virus could be induced by superinfection with HCMV 7 days after the initial infection. These results indicate that a non-lytic interaction between 1403 and HFL cells is a more likely consequence of a low multiplicity infection than plaque formation.

Keyword(s): Ad5 , HCMV , HSV-1 , immediate early gene Vmw110 and VZV
Loading

Article metrics loading...

/content/journal/jgv/10.1099/0022-1317-70-3-695
1989-03-01
2024-04-19
Loading full text...

Full text loading...

/deliver/fulltext/jgv/70/3/JV0700030695.html?itemId=/content/journal/jgv/10.1099/0022-1317-70-3-695&mimeType=html&fmt=ahah

References

  1. Brown S. M., Harland J. 1987; Three mutants of herpes simplex virus type 2: one lacking the genes US10, US 11 and US 12 and two in which Rs has been extended by 6kb to 0·91 map units with the loss of Us sequences between 0·94 and the US/TRS junction. Journal of General Virology 68:1–18
    [Google Scholar]
  2. Colberg-Poley A. M., Isom H. C., Rapp F. 1981; Involvement of an early cytomegalovirus function in reactivation of quiescent herpes simplex virus type 2. Journal of Virology 37:1051–1059
    [Google Scholar]
  3. Davison A. J., Scott J. E. 1986; The complete DNA sequence of varicella-zoster virus. Journal of General Virology 67:1759–1816
    [Google Scholar]
  4. Dixon R. A. F., Schaffer P. A. 1980; Fine structure mapping and functional analysis of temperature-sensitive mutants in the gene encoding the herpes simplex virus type 1 immediate early protein VP175. Journal of Virology 36:189–203
    [Google Scholar]
  5. Everett R. D. 1984; Transactivation of transcription by herpes virus products; requirements for two HSV-1 immediate early polypeptides for maximum activity. EMBO Journal 3:3135–3141
    [Google Scholar]
  6. Everett R. D. 1986; The products of herpes simplex virus type 1 (HSV-1) immediate early genes 1, 2 and 3 can activate HSV-1 gene expression in trans. Journal of General Virology 67:2507–2513
    [Google Scholar]
  7. Everett R. D. 1987; The regulation of viral and cellular genes by herpesvirus immediate-early gene products. Anticancer Research 7:589–604
    [Google Scholar]
  8. Felser J. M., Straus S. E., Ostrove J. M. 1987; Varicella-zoster virus complements herpes simplex virus type 1 temperature-sensitive mutants. Journal of Virology 61:225–228
    [Google Scholar]
  9. Felser J. M., Kinchington P. R., Inchauspe G., Straus S., Ostrove J. M. 1988; Cell lines containing varicella-zoster virus open reading frame 62 and expressing “IE” 175 protein complement ICP4 mutants of herpes simplex virus type 1. Journal of Virology 62:2076–2082
    [Google Scholar]
  10. Gelman I. H., Silverstein S. 1985; Identification of immediate early genes from herpes simplex virus that transactivate the virus thymidine kinase gene. Proceedings of the National Academy of SciencesU.S.A 825265–5269
    [Google Scholar]
  11. Lafemina R. L., Hayward G. S. 1988; Differences in cell type-specific blocks to immediate early gene expression and DNA replication of human, simian and murine cytomegalovirus. Journal of General Virology 69:355–374
    [Google Scholar]
  12. Longnecker R., Roizman B. 1986; Generation of an inverting herpes simplex virus 1 mutant lacking the L-S junction a sequences, an origin of DNA synthesis, and several genes including those specifying glycoproteins E and the α47 gene. Journal of Virology 58:583–591
    [Google Scholar]
  13. Mcgeoch D. J., Dalrymple M. A., Davison A. J., Dolan A., Frame M. C., Mcnab D., Perry L. J., Scott I. E., Taylor P. 1988; The complete DNA sequence of the long unique region in the genome of herpes simplex virus type 1. Journal of General Virology 69:1531–1574
    [Google Scholar]
  14. Matthews R. E. F. 1982; Classification and nomenclature of viruses. Intervirology 17:1–199
    [Google Scholar]
  15. Notarianni E. L., Preston C. M. 1982; Activation of cellular stress protein genes by herpes simplex virus temperature-sensitive mutants which overproduce immediate early polypeptides. Virology 123:113–122
    [Google Scholar]
  16. O’hare P., Hayward G. S. 1985; Three trans-acting regulatory proteins of herpes simplex virus immediate-early gene expression in a pathway involving positive and negative feedback regulation. Journal of Virology 56:723–733
    [Google Scholar]
  17. Perry L. J., Rixon F. J., Everett R. D., Frame M. C., Mcgeoch D. J. 1986; Characterization of the IE110 gene of herpes simplex virus type 1. Journal of General Virology 67:2365–2380
    [Google Scholar]
  18. Pizzorno M. C., O’hare P., Sha L., Lafemina R. L., Hayward G. S. 1988; Trans-activation and autoregulation of gene expression by the immediate-early region 2 gene products of human cytomegalovirus. Journal of Virology 62:1167–1179
    [Google Scholar]
  19. Preston C. M. 1979; Control of herpes simplex virus type 1 mRNA synthesis in cells infected with wild-type virus or the temperature-sensitive mutant tsK. Journal of Virology 29:275–284
    [Google Scholar]
  20. Quinlan M. P., Knipe D. M. 1985; Stimulation of expression of a herpes simplex virus DNA-binding protein by two viral functions. Molecular and Cellular Biology 5:957–963
    [Google Scholar]
  21. Russell J., Preston C. M. 1986; An in vitro latency system for herpes simplex virus type 2. Journal of General Virology 67:397–403
    [Google Scholar]
  22. Russell J., Stow N. D., Stow E. C., Preston C. M. 1987; Herpes simplex virus genes involved in latency in vitro . Journal of General Virology 68:3009–3018
    [Google Scholar]
  23. Sacks W. R., Schaffer P. A. 1987; Deletion mutants in the gene encoding the herpes simplex virus type 1 immediate-early protein ICP0 exhibit impaired growth in cell culture. Journal of Virology 61:829–839
    [Google Scholar]
  24. Sacks W. R., Greene C. C., Aschman D. P., Schaffer P. A. 1985; Herpes simplex virus type 1 ICP27 is an essential regulatory protein. Journal of Virology 55:796–805
    [Google Scholar]
  25. Sears A. E., Halliburton I. W., Meignier B., Silver S., Roizman B. 1985; Herpes simplex virus 1 mutant deleted in the alpha 22 gene: growth and gene expression in permissive and restrictive cells and establishment of latency in mice. Journal of Virology 55:338–346
    [Google Scholar]
  26. Stow N. D., Davison A. J. 1986; Identification of a varicella-zoster virus origin of DNA replication and its activation by herpes simplex virus type 1 gene products. Journal of General Virology 67:1613–1623
    [Google Scholar]
  27. Stow N. D., Stow E. C. 1986; Isolation and characterization of a herpes simplex virus type 1 mutant containing a deletion within the gene encoding the immediate early polypeptide Vmw110. Journal of General Virology 67:2571–2585
    [Google Scholar]
  28. Stow N. D., Mcmonagle E. C., Davison A. J. 1983; Fragments from both termini of the herpes simplex virus type 1 genome contain signals required for the encapsidation of viral DNA. Nucleic Acids Research 11:8205–8220
    [Google Scholar]
  29. Umene K. 1986; Conversion of a fraction of the unique sequence to part of the inverted repeats in the S component of the herpes simplex virus type 1 genome. Journal of General Virology 67:1035–1048
    [Google Scholar]
  30. Wagner E. K. 1985; Individual HSV Transcripts: Characterisation of Specific Genes. In The Herpesviruses 345–104 Roizman B. New York & London: Plenum Press;
    [Google Scholar]
  31. Watson R. J., Clements J. B. 1980; A herpes simplex virus type 1 function continuously required for early and late virus RNA synthesis. Nature, London 285:329–330
    [Google Scholar]
  32. Wigdahl B. L., Isom H. C., Declerc E., Rapp F. 1982; Activation of herpes simplex virus (HSV) type 1 genome by temperature-sensitive mutants of HSV type 2. Virology 116:468–479
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/jgv/10.1099/0022-1317-70-3-695
Loading
/content/journal/jgv/10.1099/0022-1317-70-3-695
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