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Updated: May 12, 2026

09:02
An Experimental Model to Study Tuberculosis-Malaria Coinfection upon Natural Transmission of Mycobacterium tuberculosis and Plasmodium berghei
Published on: February 17, 2014
Tuberculosis in CBA/J mice.
1Department of Infectious Disease and Global Health, Tufts University, 200 Westboro Rd, Bldg 20, Grafton, MA 01536, USA.
Veterinary Pathology
|March 28, 2013
Summary
Tuberculosis (TB) development is unclear. In Mycobacterium tuberculosis (M.tb)-infected CBA/J mice, weight loss correlated with increased lung inflammation, necrosis, and fibrosis, suggesting neutrophils may drive TB disease progression.
Area of Science:
- Immunology
- Pathology
- Microbiology
Background:
- Tuberculosis (TB) affects 5-10% of Mycobacterium tuberculosis (M.tb) infected individuals, but disease development mechanisms remain poorly understood.
- CBA/J mice exhibit TB-like symptoms including weight loss, M.tb growth, granulomatous infiltrates, neutrophils, necrosis, and fibrosis, potentially modeling human TB.
- Understanding TB pathogenesis is crucial for developing effective treatments and interventions.
Purpose of the Study:
- To investigate the association between clinical status (weight loss) and lung pathology in M.tb-infected CBA/J mice.
- To determine if CBA/J mice can serve as a relevant model for studying TB disease progression.
- To explore the role of neutrophils in the development of TB lesions.
Main Methods:
- Mice infected with M.tb were clinically assessed and categorized based on weight loss (none vs. 10%).
- Lung tissues were examined for the type, distribution, and extent of inflammatory infiltrates, necrosis, and fibrosis.
- Histopathological analysis was performed to compare lesions between clinically distinct groups of mice.
Main Results:
- Lung infiltrates (granulomatous with lymphoid aggregates and neutrophils) were similar in type and distribution between mice with and without weight loss.
- Mice experiencing 10% weight loss showed significantly higher infiltration and neutrophil foci compared to asymptomatic mice.
- Necrosis and fibrosis were exclusively observed in M.tb-infected CBA/J mice that exhibited weight loss.
Conclusions:
- CBA/J mice with M.tb infection develop distinct lung pathologies correlating with clinical signs of disease.
- The presence of weight loss in M.tb-infected CBA/J mice is associated with increased inflammation, necrosis, and fibrosis.
- These findings support the utility of CBA/J mice as a model to investigate the contribution of neutrophils to TB disease progression.

