Genetically determined resistance to murine cytomegalovirus and herpes simplex virus in newborn mice

J Virol. 1986 Apr;58(1):152-6. doi: 10.1128/JVI.58.1.152-156.1986.

Abstract

Mice which were infected with the herpesvirus murine cytomegalovirus or herpes simplex virus type 1 on the day of birth exhibited mouse strain-dependent differences in the development of lethal disease. The pattern of resistance among the strains was distinct for each virus and closely resembled that reported in adult mice. However, much lower doses of the viruses were required in newborn mice to reveal these resistance patterns. For murine cytomegalovirus, both H-2-associated and non-H-2 genes conferred resistance, and, as has been shown for adults, there was a 25-fold difference in the dose required to kill 50% of the animals belonging to the most resistant and susceptible strains. The resistance of newborn mice to herpes simplex virus type 1 was conferred by non-H-2 genes in C57BL/6 mice, as has been reported for adults, and newborn C57BL/6 mice were considerably more resistant than mice of susceptible strains. Resistance was also reflected in the titer of these viruses in the spleen or liver early in infection and, with murine cytomegalovirus, in the survival time of infected mice. The resistance of newborn mice to lethal disease was not conferred postnatally by the mother. This appears to be the first report of genetically determined resistance to herpesviruses in newborn mice. Such autonomous virus-specific resistance may provide a significant barrier to naturally acquired infection in genetically resistant strains. Similar genetically regulated mechanisms may protect the newborns of many species, including humans, against infection with herpesviruses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn / genetics
  • Animals, Newborn / immunology*
  • Cytomegalovirus / immunology
  • Cytomegalovirus / pathogenicity
  • Cytomegalovirus Infections / genetics*
  • Cytomegalovirus Infections / immunology
  • Female
  • Herpes Simplex / genetics*
  • Herpes Simplex / immunology
  • Immunity, Innate
  • Maternal-Fetal Exchange
  • Mice
  • Mice, Inbred Strains / genetics
  • Mice, Inbred Strains / immunology*
  • Milk / immunology
  • Pregnancy
  • Simplexvirus / immunology
  • Simplexvirus / pathogenicity