Herpes simplex virus DNA in normal corneas: persistence without viral shedding from ganglia

H Openshaw1, J I McNeill, X H Lin

  • 1Department of Neurology, City of Hope National Medical Center, Duarte, California 91010, USA.

Insights

Herpes simplex virus type 1 (HSV-1) DNA was found in 10 of 24 donor corneas, primarily in the peripheral cornea. A rabbit model showed transplanted corneas with HSV-1 DNA did not cause viral shedding or seroconversion.

Area of Science:

  • Ophthalmology
  • Virology
  • Molecular Biology

Background:

  • Herpes simplex virus type 1 (HSV-1) DNA can persist in the cornea.
  • Corneal HSV-1 DNA has been observed in patients with and without known eye disease.

Purpose of the Study:

  • To investigate the presence and distribution of HSV-1 DNA in eye bank corneas.
  • To determine the biological role of corneal HSV-1 DNA using a rabbit model.

Main Methods:

  • Polymerase chain reaction (PCR) was used to detect HSV-1 thymidine kinase (TK) and glycoprotein D (gD) gene sequences.
  • Eye bank corneas were trephined to separate central and peripheral sections.
  • A rabbit model involved transplantation of corneas with HSV-1 DNA into naive recipients.

Main Results:

  • HSV-1 DNA was detected in 10 out of 24 (41.7%) eye bank corneas.
  • Viral DNA was found predominantly in the corneal rim (8/10 eyes) versus the central cornea (2/10 eyes).
  • Rabbit recipients showed no HSV-1 shedding or seroconversion, and viral DNA persisted in grafts.

Conclusions:

  • HSV-1 DNA is present in a significant proportion of donor corneas, often in peripheral regions.
  • Corneal HSV-1 DNA in grafts does not appear to lead to viral reactivation or transmission in a short-term rabbit model.
  • The clinical significance of latent HSV-1 DNA in donor corneas requires further investigation.

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