Major histocompatibility complex haplotype determines hsp70-dependent protection against measles virus neurovirulence

J Virol. 2009 Jun;83(11):5544-55. doi: 10.1128/JVI.02673-08. Epub 2009 Mar 25.

Abstract

In vitro studies show that hsp70 promotes gene expression for multiple viral families, although there are few reports on the in vivo significance of virus-hsp70 interaction. Previously we showed that hsp70-dependent stimulation of Edmonston measles virus (Ed MeV) transcription caused an increased cytopathic effect and mortality in transgenic hsp70-overexpressing C57BL/6 mice (H-2(b)). The response to MeV infection is influenced by the major histocompatibility complex haplotype; H-2(d) mice are resistant to brain infection due to robust antiviral immune responses, whereas H-2(b) mice are susceptible due to deficiencies in this response. We therefore tested the hypothesis that the outcome of MeV-hsp70 interaction may be dependent upon the host H-2 haplotype. The impact of selective neuronal hsp70 overexpression on Ed MeV brain infection was tested with congenic C57BL/10 H-2(d) neonatal mice. In this context, hsp70 overexpression conferred complete protection against virus-induced mortality, compared to >30% mortality in nontransgenic mice. Selective depletion of T-cell populations showed that transgenic mice exhibit a diminished reliance on T cells for protection. Brain transcript analysis indicated enhanced innate immune activation and signaling through Toll-like receptors 2 and 4 at early times postinfection for transgenic infected mice relative to those for nontransgenic infected mice. Collectively, results suggest that hsp70 can enhance innate antiviral immunity through Toll-like receptor signaling, supporting a protective role for physiological responses that enhance tissue levels of hsp70 (e.g., fever), and that the H-2 haplotype determines the effectiveness of this response.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Brain Diseases / genetics
  • Brain Diseases / immunology*
  • Brain Diseases / metabolism
  • Brain Diseases / pathology
  • Cells, Cultured
  • Female
  • Gene Expression Regulation
  • HSP72 Heat-Shock Proteins / genetics
  • HSP72 Heat-Shock Proteins / immunology*
  • HSP72 Heat-Shock Proteins / metabolism*
  • Haplotypes
  • Humans
  • Immunity, Innate / immunology
  • Major Histocompatibility Complex / immunology*
  • Male
  • Measles / genetics
  • Measles / immunology*
  • Measles / metabolism
  • Measles / pathology
  • Measles virus / immunology*
  • Measles virus / pathogenicity*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Survival Rate
  • T-Lymphocyte Subsets / immunology
  • Virulence

Substances

  • HSP72 Heat-Shock Proteins