Skip to main content

Pathway of viral spread in herpes zoster: detection of the protein encoded by open reading frame 63 of varicella-zoster virus in biopsy specimens

  • Conference paper
Immunity to and Prevention of Herpes Zoster

Summary

Reactivation of varicella-zoster virus (VZV) in the dorsal root or trigeminal ganglia causes herpes zoster. The pathway of viral spread from the ganglia to the skin and also within the skin is not yet completely understood. Histological studies have revealed that each skin lesion in herpes zoster progresses sequentially through the stages of erythema, vesicles, pustules and finally ulceration. An immunohistochemical study of the early skin lesions of herpes zoster demonstrated a high incidence of hair follicle involvement and the main localization of the virus at the isthmus. This evidence suggests that VZV initially spreads from the ganglia through myelinated nerves, which predominantly end around the isthmus of hair follicles. To further investigate the viral spread within the skin, we analyzed the sequential appearance of the immediate early proteins encoded by ORF 63 of VZV (1E63), using an anti-1E63 antibody raised by immunization of rabbits with a recombinant protein. This antibody could detect 1E63 in a western blot analysis of infected cells and also in immunohistochemical analysis of the skin lesions of herpes zoster. 1E63 initially appeared in the nuclei of the follicular epithelial cells and basal or parabasal epidermal cells. Later, the nuclei and cytoplasm of cells in the epidermis and hair follicles became positive. 1E63 remained in the virus-infected cells even during their degeneration. When we examined the hair follicles in the early erythematous lesions, cells positive for 1E63 were predominantly distributed around the isthmus. In addition, some lymphocytes around the blood vessels were also positive for 1E63, but these cells were seldom positive for the structural antigen. Thus, these observations suggest that VZV arriving through myelinated nerves infects not only permissive cells, but also non-permissive cells in the involved skin of herpes zoster.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 39.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 54.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Hyman RW, Ecker JR, Tenser RB (1983) Varicella-zoster virus RNA in human trigeminal ganglia. Lancet II: 814–816

    Article  Google Scholar 

  2. Gilden DH, Vafai A, Shatram Y, Becker Y, Devlin M, Wellish M (1983) Varicella-zoster virus DNA in human sensory ganglia. Nature 306: 478–480

    Article  PubMed  CAS  Google Scholar 

  3. Cheatham WJ (1953) The relation of heretofore unreported lesions to pathogenesis of herpes zoster. Am J Pathol 29: 401–411

    PubMed  CAS  Google Scholar 

  4. Ghatak NR, Zimmermann HM (1973) Spinal ganglion in herpes zoster: a light and electron microscopic study. Arch Pathol 95: 411–415

    PubMed  CAS  Google Scholar 

  5. Head H, Champbell AW (1900) The pathology of herpes zoster and its bearing on sensory localization. Brain 23: 353–523

    Article  Google Scholar 

  6. Esiri MM, Tomlinson AH (1972) Herpes zoster: demonstration of virus in trigeminal nerve and ganglion by immunofluorescence and electron microscopy. J Neurol Sci 15: 35–48

    Article  PubMed  CAS  Google Scholar 

  7. Shibuta H, Ishikawa T, Aoyama Y, Kurata K, Matsumoto M (1974) Varicella virus isolation from spinal ganglion. Arch Ges Virusforsch 45: 382–385

    Article  PubMed  CAS  Google Scholar 

  8. Nagashima K, Nakazawa M, Endo H, Kurata T, Aoyama Y (1975) Pathology of the human spinal ganglia in varicella-zoster virus infection. Acta Neuropathol 33: 105–117

    Article  PubMed  CAS  Google Scholar 

  9. Bastian FO, Rabson AS, Yee CL, Tralka TS (1974) Herpesvirus varicellae: Isolated from human dorsal root ganglia. Arch Pathol 97: 331–333

    PubMed  CAS  Google Scholar 

  10. Muraki R, Baba T, Iwasaki T, Sata T, Kurata T (1992) Immunohistochemical study of skin lesions in herpes zoster. Virchows Arch (A) 420: 71–76

    Article  CAS  Google Scholar 

  11. Okuno T, Yamanishi K, Shiraki K, Takahashi M (1983) Synthesis and processing of glycoproteins of varicella-zoster virus (VZV) as studied with monoclonal antibodies to VZV antigens. Virology 129: 357–368

    Article  PubMed  CAS  Google Scholar 

  12. Muraki R, Iwasaki T, Sata T, Sato Y, Kurata T (1996) Hair follicle involvement in herpes zoster: pathway of viral spread from ganglia to skin. Virchows Arch 428: 275–280

    Article  PubMed  CAS  Google Scholar 

  13. Cohen JI, Straus SE (1996) Varicella-zoster virus and its replication. In: Fields BN, Knipe DM, Howley PM, Chanock RM, Melnick JL, Monath TP, Roizman B, Straus SE (eds) Fields Virology. Lippincott-Raven, Philadelphia, pp 2525–2545

    Google Scholar 

  14. Debrus S, Sadzot-Delvaux C, Nikkels AF, Piette J, Rentier B (1995) Varicella-zoster virus gene 63 encodes an immediate-early protein that is abundantly expressed during latency. J Virol 69: 3240–3245

    PubMed  CAS  Google Scholar 

  15. Kinchington PR, Bookey D, Turse SE (1995) The transcriptional regulatory proteins encoded by varicella-zoster virus open reading frames (ORFs) 4 and 63, but not ORF61, are associated with purified virus particles. J Virol 69: 4274–4282

    PubMed  CAS  Google Scholar 

  16. Stevenson D, Xue M, Hay J, Ruyechan WT (1996) Phosphorylation and nuclear localization of the varicella-zoster virus gene 63 protein. J Virol 70: 658–662

    PubMed  CAS  Google Scholar 

  17. Vonsover A, Leventon-Kriss S, Langer A, Smetana Z, Zaizov R, Potaznick D, Cohen IJ, Gotlieb-Stematsky T (1987) Detection of varicella-zoster virus in lymphocytes by DNA hybridization. J Med Virol 21: 57–66

    Article  PubMed  CAS  Google Scholar 

  18. Mainka C, Fuß B, Geiger H, Hofelmayr, Wolff MH (1998) Characterization of viremia at different stages of varicella-zoster virus infection. J Med Virol 56: 91–98

    Article  PubMed  CAS  Google Scholar 

  19. Sadzot-Delvaux C, Kinchington PR, Debrus S, Rentier B, Arvin AM (1997) Recognition of the latency-associated immediate early protein IE63 of varicella-zoster virus by human memory T lymphocytes. J Immunol 159: 2802–2806

    PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2001 Springer-Verlag Wien

About this paper

Cite this paper

Iwasaki, T., Muraki, R., Kasahara, T., Sato, Y., Sata, T., Kurata, T. (2001). Pathway of viral spread in herpes zoster: detection of the protein encoded by open reading frame 63 of varicella-zoster virus in biopsy specimens. In: Gershon, A.A., Arvin, A.M., Calisher, C.H. (eds) Immunity to and Prevention of Herpes Zoster. Springer, Vienna. https://doi.org/10.1007/978-3-7091-6259-0_12

Download citation

  • DOI: https://doi.org/10.1007/978-3-7091-6259-0_12

  • Publisher Name: Springer, Vienna

  • Print ISBN: 978-3-211-83555-5

  • Online ISBN: 978-3-7091-6259-0

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics