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Updated: Jul 23, 2026

A Murine Model of Dengue Virus-induced Acute Viral Encephalitis-like Disease
Published on: April 28, 2019
An apparently new lethal virus disease of infant mice
Abstract:
A hitherto unreported disease of infant mice is described. The agent reproduces upon passage, is filterable, is confined mainly to the gastrointestinal tract in infant and adult mice, causes death in infants and inapparent infection in adults, and is sensitive to mild heat, ether, and sodium deoxycholate. Unique and characteristic morphologic changes occur in the epithelial cells of the intestine in infected infant mice. These consist in the development of multinucleated giant cells designated "balloon cells.".
Insights
A novel gastrointestinal disease affects infant mice, causing characteristic "balloon cell" changes in the intestine and leading to death. Adult mice show inapparent infections, and the causative agent is sensitive to heat and ether.
Area of Science:
- Virology
- Pathology
- Animal Models
Background:
- A novel disease affecting infant mice has been identified.
- The disease primarily impacts the gastrointestinal tract.
Purpose of the Study:
- To describe a hitherto unreported disease in infant mice.
- To characterize the agent responsible for the disease and its effects.
Main Methods:
- Passage of the agent in mice.
- Filtration studies to determine agent size.
- Sensitivity testing (heat, ether, sodium deoxycholate).
- Morphological examination of intestinal tissues.
Main Results:
- The agent reproduces upon passage and is filterable.
- Infection is lethal in infant mice but inapparent in adults.
- Characteristic multinucleated giant cells ("balloon cells") develop in the intestinal epithelium of infected infants.
- The agent is sensitive to mild heat, ether, and sodium deoxycholate.
Conclusions:
- A new infectious disease agent affecting the murine gastrointestinal tract has been identified.
- The agent exhibits unique cytopathic effects, forming "balloon cells" in infant mice.
- Differential susceptibility between infant and adult mice suggests age-dependent disease mechanisms.
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