Why the study?
Does infection with encephalomyocarditis virus induce a diabetes-like syndrome in DBA/2N male mice?
Does infection with encephalomyocarditis virus induce a diabetes-like syndrome in DBA/2N male mice?
Encephalomyocarditis virus infection in DBA/2N male mice induces a diabetes-like syndrome characterized by hyperglycemia and hypoinsulinemia.
Supports EMCV-induced hyperglycemia model in DBA/2N mice; leaves open relevance to human diabetes pathogenesis.
Infection of DBA/2N male mice with encephalomyocarditis virus resulted in a diabeteslike syndrome characterized by hyperglycemia, glycosuria, hypoinsulinemia, polydipsia, and polyphagia. Blood glucose levels were elevated within 4 days after infection and reached a maximum mean level of 320 mg/100 ml within 12 days. Approximately 60-80% of the animals developed a transient hyperglycemia while 10-15% of the animals remained hyperglycemic for well over 6 mo. The remaining animals failed to become hyperglycemic but many had abnormal glucose tolerance curves. Hyperglycemia was most pronounced when animals were allowed free access to food, and the incidence of byperglycemia was related both to the strain and sex of the animals, with few females developing hyperglycemia. The amount of immunoreactive insulin in the plasma of infected hyperglycemic mice was significantly lower than in appropriate controls, and injection of exogenous insulin resulted in a rapid drop in the blood glucose levels. Despite the fact that certain animals were hyperglycemic for many months, virus could not be recovered from the pancreas after the first 10 days of the infection.
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Boucher et al. (1973) studied this question.
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