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The bm12 Inducible Model of Systemic Lupus Erythematosus (SLE) in C57BL/6 Mice
Published on: November 1, 2015
[A pathohistological study on experimental brucellosis in inbred mice]
1Laboratory of Pathology, Professional Medical Research Institute of Coal Ministry, Beijing.
Summary
Brucella infection causes chronic lesions, particularly in the reticuloendothelial system. B. abortus infection induced the most significant pathological changes in both BALB/C and C57/BL mice.
Area of Science:
- Pathology
- Infectious Diseases
- Immunology
Background:
- Brucellosis is a significant zoonotic disease caused by Brucella species.
- Understanding the pathological progression and host response is crucial for disease management.
- Inbred mouse models are vital for studying infectious diseases.
Purpose of the Study:
- To investigate the pathohistological changes induced by different Brucella species in BALB/C and C57/BL mice.
- To compare the severity of lesions caused by B. melitensis, B. abortus, and B. suis.
- To identify key organs affected during chronic brucellosis.
Main Methods:
- BALB/C and C57/BL inbred mice were infected with B. melitensis, B. abortus, and B. suis.
- Pathohistological examination of various organs was performed at different stages of infection.
- Comparative analysis of pathological changes between mouse strains and Brucella species.
Main Results:
- Chronic pathological lesions developed in multiple organs due to repeated infectious processes.
- Significant changes were observed in the reticuloendothelial system (lymphocytes, spleen, liver).
- B. abortus infection caused the most significant pathological changes in both mouse models, with BALB/C mice showing more remarkable lesions overall.
Conclusions:
- Brucella infection leads to chronic, progressive pathological changes, primarily affecting the reticuloendothelial system.
- B. abortus is identified as inducing the most severe pathology among the tested species.
- Host genetic background (BALB/C vs. C57/BL) influences the severity of Brucella-induced lesions.

