Lethal encephalitis in myeloid differentiation factor 88-deficient mice infected with herpes simplex virus 1

Am J Pathol. 2005 May;166(5):1419-26. doi: 10.1016/S0002-9440(10)62359-0.

Abstract

Herpes simplex virus 1 (HSV-1), a large DNA virus from the Herpesviridae family, is the major cause of sporadic lethal encephalitis and blindness in humans. Recent studies have shown the importance of Toll-like receptors (TLRs) in the immune response to HSV-1 infection. Myeloid differentiation factor 88 (MyD88) is a critical adaptor protein that is downstream to mediated TLR activation and is essential for the production of inflammatory cytokines. Here, we studied the relationship between MyD88 and HSV-1 using a purified HSV-1 isolated from a natural oral recurrent human infection. We observed the activation of TLR-2 by HSV-1 in vitro using Chinese hamster ovary cells stably transfected with a reporter gene. Interestingly, we found that only peritoneal macrophages from MyD88-/- mice, but not macrophages from TRL2-/- or from wild-type mice, were unable to produce tumor necrosis factor-alpha in response to HSV-1 exposure. Additionally, although TLR2-/- mice showed no enhanced susceptibility to intranasal infection with HSV-1, MyD88-/- mice were highly susceptible to infection and displayed viral migration to the brain, severe neuropathological signs of encephalitis, and 100% mortality by day 10 after infection. Together, our results suggest that innate resistance to HSV-1 is mediated by MyD88 and may rely on activation of multiple TLRs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Animals
  • Antigens, Differentiation
  • CHO Cells
  • Chlorocebus aethiops
  • Cricetinae
  • Cricetulus
  • Disease Susceptibility
  • Encephalitis / metabolism*
  • Encephalitis / mortality
  • Encephalitis / virology*
  • Herpes Simplex* / etiology
  • Herpesvirus 1, Human*
  • Interferon-gamma / deficiency
  • Mice
  • Mice, Knockout
  • Myeloid Differentiation Factor 88
  • Receptors, Immunologic / deficiency*
  • Receptors, Immunologic / metabolism
  • Toll-Like Receptor 2
  • Vero Cells

Substances

  • Adaptor Proteins, Signal Transducing
  • Antigens, Differentiation
  • MYD88 protein, human
  • Myd88 protein, mouse
  • Myeloid Differentiation Factor 88
  • Receptors, Immunologic
  • Tlr2 protein, mouse
  • Toll-Like Receptor 2
  • Interferon-gamma