Skip to main content
Log in

Bilateral electroretinographic changes induced by unilateral intra—visual cortex inoculation of herpes simplex virus type 1 in BALB/c mice

  • Published:
Documenta Ophthalmologica Aims and scope Submit manuscript

Abstract

Intra—visual cortex inoculation of 102 plaque—forming units of herpes simplex virus type 1 (KOS—63) induced physiologic and morphologic retinal changes in 62.3% (33/53) of infected animals; of these, 91% were bilateral. In contrast, inoculation of the same viral titers into the frontal lobe induced retinal alterations in only 13.3% (2/15). Initially, there was a decrease of the b—wave amplitude and retinal sensitivity and necrotic changes of the ganglion cells and nuclei in the inner nuclear layer. Immunoperoxidase staining for virus—specific antigens showed positive staining of the same cell type. Over time, there was a progressive decrease in the electroretinogram until it was extinguished and the retina was replaced by gliotic tissue. Parallel viral recovery studies demonstrated detectable infectious virus in one of eight eyes on day 2 after inoculation and in three of eight eyes on day 4. Thereafter, there was an increase in the percentage of eyes with infectious virus and a concomitant increase in viral titers. Immunoperoxidase staining of brain sections obtained on days 6 through 8 demonstrated virus—specific antigens on cells in the lateral geniculate nuclei and the suprachiasmatic nuclei bilaterally.

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

Abbreviations

HSV:

herpes simplex virus

IVC:

intra—visual cortex

References

  1. Peiffer RL JR, Dekker CD, Siegel FL. Ocular lesions in mice following intracerebral injection of herpes simplex virus type 1. Invest Ophthalmol Vis Sci 1983; 24: 1070–78.

    PubMed  Google Scholar 

  2. Anderson JR, Field HJ. An animal model of ocular herpes keratitis, retinitis and cataract in the mouse. Br J Exp Pathol 1984; 65: 283–97.

    PubMed  Google Scholar 

  3. Anderson JR, Field HJ. The distribution of herpes simplex type 1 antigen in mouse central nervous system after different routes of inoculation. J Neurol Sci 1983; 60: 181–95.

    PubMed  Google Scholar 

  4. Minckler DS, McLean EB, Shaw CM, Hendrickson A.Herpesvirus hominis encephalitis and retinitis. Arch Ophthalmol 1976; 94: 89–95.

    PubMed  Google Scholar 

  5. Johnson BL, Wisotzkey HM. Neuroretinitis associated with herpes simplex encephalitis in an adult. Am J Ophthalmol 1977; 83: 481–9.

    PubMed  Google Scholar 

  6. Lewis ML, Culbertson W, Post JD, Miller M, Kokame GT, Dix RD. Herpes simplex virus type 1: A cause of the acute retinal necrosis syndrome. Ophthalmology 1989; 96: 875–78.

    PubMed  Google Scholar 

  7. Dix RD, McKendell RR, Baringer JR. Comparative neurovirulence of herpes simplex virus type 1 strains after peripheral or intracerebral inoculation of BALB/c mice. Infect Immun 1983; 40: 103–12.

    PubMed  Google Scholar 

  8. Whittum JA, McCulley JP, Niederkorn JY, Streilein JW. Ocular disease induced in mice by anterior chamber inoculation of herpes simplex virus. Invest Ophthalmol Vis Sci 1984; 25: 1065–73.

    PubMed  Google Scholar 

  9. Atherton SS, Streilein JW. Two waves of virus following anterior chamber inoculation of HSV—1. Invest Ophthalmol Vis Sci 1987; 28: 571–79.

    PubMed  Google Scholar 

  10. Hamasaki DI, Dix RD, Atherton SS. Bilateral alterations of the ERG and retinal histology following unilateral HSV—1 inoculation. Invest Ophthalmol Vis Sci 1988; 29: 1242–54.

    PubMed  Google Scholar 

  11. Hamasaki DI, Atherton SS Dix RD. HSV—2 alters retinal physiology and morphology bilaterally in mice. Invest Ophthalmol Vis Sci 1990; 31: 1056–69.

    PubMed  Google Scholar 

  12. Drager UC, Olsen JF. Origins of crossed and uncrossed retinal projections in pigmented and albino mice. J Comp Neurol 1980; 191: 383–412.

    PubMed  Google Scholar 

  13. LaVail JH, Nixon RA, Sidman RL. Genetic control of retinal ganglion cell projections. J Comp Neurol 1978; 182: 399–422.

    PubMed  Google Scholar 

  14. Ekstrom P, Sanyal S. Narfstrom K, Chader GJ, van Veen T. Accumulation of glial fibrillary acidic protein in Muller radial glia during retinal degeneration. Invest Ophthalmol Vis Sci 1988; 29: 1363–71.

    PubMed  Google Scholar 

  15. Dix RD, Hamasaki DI, Hurst L, Culbertson WW, Lewis ML. Bilateral retinal necrosis following unilateral inoculation of mice with an HSV—1 isolated from a patient with acute retinal necrosis. Invest Ophthalmol Vis Sci 1990; 31 (suppl): 314.

    Google Scholar 

  16. Hurst L, Hamasaki DI, Stewart R, Dix RD. Comparative neuroinvasiveness, neurovirulence and retinovirulence of two KOS strains of herpes simplex virus type 1. Invest Ophthalmol Vis Sci 1991; 32 (suppl): 801.

    Google Scholar 

  17. McLean JH, Shipley MT, Bernstein DI. Golgi—like, transneuronal retrograde labeling with CNS injections of herpes simplex virus type 1. Brain Res Bull 1989; 22: 867–81.

    PubMed  Google Scholar 

  18. Kristensson K, Ghetti B, Wisniewski HK. Study of the propogation of herpes simplex virus (type 2) into the brain after intraocular injection. Brain Res 1974; 69: 189–201.

    PubMed  Google Scholar 

  19. Margolis T, Togni B, LaVail JH, Dawson CR. Identifying HSV infected neurons after ocular inoculation. Curr Eye Res 1987; 6: 119–26.

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mizota, A., Dix, R.D. & Hamasaki, D.I. Bilateral electroretinographic changes induced by unilateral intra—visual cortex inoculation of herpes simplex virus type 1 in BALB/c mice. Doc Ophthalmol 84, 213–230 (1993). https://doi.org/10.1007/BF01203654

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01203654

Key words

Navigation