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Genetically determined resistance to murine cytomegalovirus and herpes simplex virus in newborn mice
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.
Insights
Newborn mice show genetically determined resistance to herpesviruses, similar to adults but requiring lower viral doses. This innate immunity may protect newborns across species, including humans.
Area of Science:
- Immunology
- Virology
- Genetics
Background:
- Herpesviruses, including murine cytomegalovirus (MCMV) and herpes simplex virus type 1 (HSV-1), pose significant health risks.
- Understanding innate resistance mechanisms in newborns is crucial for preventing severe disease.
Purpose of the Study:
- To investigate genetically determined resistance to MCMV and HSV-1 in newborn mice.
- To determine if postnatal maternal factors influence this resistance.
Main Methods:
- Infection of newborn mice from various strains with MCMV and HSV-1.
- Assessment of lethal disease development, viral titers in organs, and survival rates.
- Comparison of resistance patterns between newborn and adult mice.
Main Results:
- Mouse strain-dependent differences in lethal disease susceptibility were observed for both viruses.
- Genetic resistance patterns in newborns mirrored those in adult mice, though lower viral doses were needed.
- Murine cytomegalovirus resistance involved both H-2-associated and non-H-2 genes; herpes simplex virus type 1 resistance in C57BL/6 mice was linked to non-H-2 genes.
- Resistance correlated with lower viral titers in spleen/liver and improved survival for MCMV-infected mice.
- Postnatal maternal factors did not confer resistance.
Conclusions:
- Newborn mice possess autonomous, virus-specific genetic resistance to herpesviruses.
- This innate resistance acts as a barrier against natural infections in genetically resistant strains.
- Similar genetically regulated mechanisms likely protect human newborns against herpesvirus infections.