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09:49
Experimental Model to Evaluate Resolution of Pneumonia
Published on: February 17, 2023
Sendai viral pneumonia in aged BALB/c mice
R O Jacoby1, P N Bhatt, S W Barthold
1Section of Comparative Medicine, Yale University School of Medicine, New Haven, Connecticut 06510.
Experimental Gerontology
|January 1, 1994
Summary
Sendai virus (SV) infection reveals that aging mice are more susceptible to viral pneumonia. This study highlights aging
Area of Science:
- Immunology
- Virology
- Gerontology
Background:
- Aging is associated with increased susceptibility to infectious diseases.
- Viral pneumonia poses a significant health risk, particularly in older populations.
- Sendai virus (SV) is a common respiratory pathogen that can cause pneumonia.
Purpose of the Study:
- To evaluate aged BALB/c mice as a natural model for age-associated susceptibility to viral pneumonia.
- To investigate the impact of aging on the course and resolution of Sendai virus infection.
- To determine the gradual increase in susceptibility to viral pneumonia during the aging process.
Main Methods:
- Intranasal inoculation of young and aged BALB/c mice with Sendai virus (SV).
- Assessment of viral load through virus titration at multiple time points.
- Histopathological and immunohistochemical analysis of lung tissue.
- Evaluation of immune response via serological antibody titers.
Main Results:
- Aged mice exhibited significantly higher lung virus titers and prolonged infection compared to young mice.
- Development and resolution of pneumonia were delayed in aged mice.
- Aged mice showed significantly lower serum antibody titers, indicating a weaker immune response.
- Intermediate-aged mice displayed a mixed response, with characteristics of both young and aged groups.
Conclusions:
- Sendai virus infection in aged mice serves as a relevant model for studying age-associated susceptibility to viral pneumonia.
- Susceptibility to viral pneumonia in mice increases progressively with age.
- The findings underscore the importance of considering age-related immune decline in managing respiratory viral infections.
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