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Published on: June 20, 2014
Selenium deficiency contributes to the chronic myocarditis in coxsackievirus-infected mice
1Department of Microbiology, University of Ulsan College of Medicine, Seoul, Korea.
Insights
Selenium deficiency worsens coxsackievirus B3 (CVB3) heart disease. Se-deficient mice had higher mortality, increased viral replication, and chronic myocarditis, indicating Se deficiency promotes active CVB3 infection.
Area of Science:
- Cardiology
- Virology
- Nutritional Science
Background:
- Keshan disease is linked to coxsackievirus B3 (CVB3) infection and selenium (Se) deficiency.
- Se deficiency exacerbates CVB3-induced myocarditis in acute and subacute phases.
- The impact of Se deficiency on chronic CVB3 myocarditis remains unexamined.
Purpose of the Study:
- To investigate the effect of Se deficiency on chronic CVB3-induced myocarditis in a mouse model.
- To assess viral replication and cardiac pathology in Se-deficient and Se-replete mice over 90 days post-infection.
Main Methods:
- Mice were fed Se-replete or Se-deficient diets for 28 days before CVB3 intraperitoneal infection.
- Diets were maintained post-infection, and mice were monitored for 90 days.
- Parameters assessed included mortality, serum glutathione peroxidase (GPx) activity, histopathology, and cardiac viral RNA levels.
Main Results:
- Se-deficient mice exhibited significantly higher mortality rates compared to Se-replete mice.
- Lower serum GPx activity was observed in Se-deficient mice, indicating compromised antioxidant status.
- Histopathological examination revealed more severe myocarditis, and higher viral RNA levels were detected in the hearts of Se-deficient mice.
Conclusions:
- Se deficiency promotes chronic myocarditis by fostering active coxsackievirus B3 replication.
- Maintaining adequate selenium levels is crucial for mitigating the severity of CVB3-induced heart disease.
- These findings highlight the critical role of selenium in managing viral myocarditis and preventing chronic cardiac pathology.
Abstract:
Both coxsackievirus B3 (CVB3) infection and selenium (Se) deficiency play a pivotal role in Keshan disease of the heart. The Se deficiency was known to contribute to the CVB3-induced myocarditis in acute and subacute phase of infection. However, its effect on the myocarditis in chronic phase of infection has not been examined yet. To address this question, we kept mice on a Se-replete or Se-deficient diet for 28 days, infected them intraperitoneally with CVB3 and maintaining previous diets, we examined them for next 90 days for several parameters indicative of the infection or disease. We found out that the mice on the Se-deficient diet exhibited a higher mortality, lower serum glutathione peroxidase (GPx) activity, evident histopathological changes indicative of myocarditis, and a higher level of viral RNA in the heart. Summing up, these data suggest that the Se-deficiency creates a chronic myocarditis-prone condition by fostering the active virus replication.
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