Herpesvirus entry mediator is a serotype specific determinant of pathogenesis in ocular herpes

Proc Natl Acad Sci U S A. 2012 Dec 11;109(50):20649-54. doi: 10.1073/pnas.1216967109. Epub 2012 Nov 26.

Abstract

Infection with herpes simplex virus type 1 (HSV-1) and HSV-2 is initiated by viral glycoprotein D (gD) binding to a receptor on the host cell. Two receptors, herpesvirus entry mediator (HVEM) and nectin-1, mediate entry in murine models of HSV-1 and HSV-2. HVEM is dispensable for HSV-2 infection of the vagina and brain, but is required for WT pathogenesis of HSV-1 infection of the cornea. By challenging WT and HVEM KO mice with multiple strains of HSV-1 and HSV-2, we demonstrate that without HVEM, all HSV-1 strains tested do not replicate well in the cornea and infection does not result in severe symptoms, as observed in WT mice. In contrast, all HSV-2 strains tested had no requirement for HVEM to replicate to WT levels in the cornea and still cause severe disease. These findings imply that HSV-2 does not require HVEM to cause disease regardless of route of entry, but HVEM must be present for HSV-1 to cause full pathogenesis in the eye. These findings uncover a unique role for HVEM in mediating HSV-1 infection in an area innervated by the trigeminal ganglion and may explain why the presence of HVEM can lead to severe inflammation in the cornea. Thus, the dependence on HVEM is a dividing point between HSV-1 and HSV-2 that evolved to infect areas innervated by different sensory ganglia.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Disease Models, Animal
  • Female
  • Herpes Genitalis / virology
  • Herpesvirus 1, Human / classification
  • Herpesvirus 1, Human / pathogenicity*
  • Herpesvirus 2, Human / classification
  • Herpesvirus 2, Human / pathogenicity*
  • Herpesvirus 2, Human / physiology
  • Host-Pathogen Interactions
  • Keratitis, Herpetic / etiology*
  • Keratitis, Herpetic / virology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, Tumor Necrosis Factor, Member 14 / deficiency
  • Receptors, Tumor Necrosis Factor, Member 14 / genetics
  • Receptors, Tumor Necrosis Factor, Member 14 / physiology*
  • Serotyping
  • Species Specificity
  • Virulence / physiology
  • Virus Replication

Substances

  • Receptors, Tumor Necrosis Factor, Member 14