Abstract
Coxsackievirus B4 (CB4) replicated to equally high titers in the pancreas and other tissues of the C57BL/Ks (+/+) mouse and its genetic variants that were either heterozygous (db/+) or homozygous (db/db) for the autosomal recessive gene for diabetes, db. In contrast, the insulin-producing beta cells of both diabetic variants, but not the +/+ mice, completely degranulated during acute infection and resulted in hypoglycemia and hyperinsulemia. All db/db mice died within 13 days, with signs of severe endocrine pancreas involvement. Surviving +/+ mice maintained relatively normal glucose homeostasis. Surviving db/+ variants exhibited prolonged periods of diabetes-like disease with hypoinsulemia and abnormal glucose tolerance, even though the db gene is not phenotypically expressed in the heterozygous state.
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Webb, S.R., Loria, R.M., Madge, G.E. et al. Coxsackievirus B infection in the mouse: Effects associated with the diabetes gene, db. Current Microbiology 3, 15–19 (1979). https://doi.org/10.1007/BF02603127
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DOI: https://doi.org/10.1007/BF02603127