Kinetics of IFN-Gamma and TNF-Alpha Gene Expression and Their Relationship with Disease Progression after Infection with Mycobacterium Tuberculosis in Guinea Pigs.
10.3349/ymj.2013.54.3.707
- Author:
In Soon ROH
1
;
Sungae CHO
;
Seok Yong EUM
;
Sang Nae CHO
Author Information
1. Department of Microbiology, Yonsei University College of Medicine, Seoul, Korea. raycho@yuhs.ac
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Mycobacterium tuberculosis;
pathogenesis;
guinea pigs;
IFN-gamma and TNF-alpha
- MeSH:
Animals;
Body Weight;
*Disease Progression;
Female;
Gene Expression;
Gene Expression Regulation;
Guinea Pigs;
Interferon-gamma/genetics/*metabolism;
Kinetics;
Liver/metabolism/pathology;
Lung/metabolism/pathology;
Lymph Nodes/metabolism/pathology;
Mycobacterium tuberculosis;
Spleen/metabolism/pathology;
Tuberculosis/*genetics/pathology;
Tumor Necrosis Factor-alpha/genetics/*metabolism
- From:Yonsei Medical Journal
2013;54(3):707-714
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Guinea pig is one of the most suitable animal models for Mycobacterium tuberculosis (M. tb) infection since it shows similarities to pulmonary infection in humans. Although guinea pig shows hematogenous spread of M. tb infection into the whole body, immunological studies have mainly focused on granulomatous tissues in lungs and spleens. In order to investigate the time-course of disease pathogenesis and immunological profiles in each infected organ, we performed the following approaches with guinea pigs experimentally infected with M. tb over a 22-week post-infection period. MATERIALS AND METHODS: We examined body weight changes, M. tb growth curve, cytokine gene expression (IFN-gamma and TNF-alpha), and histopathology in liver, spleen, lungs and lymph nodes of infected guinea pigs. RESULTS: The body weights of infected guinea pigs did not increase as much as uninfected ones and the number of M. tb bacilli in their organs increased except bronchotracheal lymph node during the experimental period. The gene expression of IFN-gamma and TNF-alpha was induced between 3 and 6 weeks of infection; however, kinetic profiles of cytokine gene expression showed heterogeneity among organs over the study period. Histophathologically granulomatous lesions were developed in all four organs of infected guinea pigs. CONCLUSION: Although IFN-gamma and TNF-alpha gene expression profiles showed heterogeneity, the granuloma formation was clearly observed in every organ regardless of whether the number of bacilli increased or decreased. However, this protective immunity was accompanied with severe tissue damage in all four organs, which may lead to the death of guinea pigs.
