AMycobacterium tuberculosisMutant Lacking thegroELHomologuecpn60.1Is Viable but Fails To Induce an Inflammatory Response in Animal Models of Infection
- 1 April 2008
- journal article
- Published by American Society for Microbiology in Infection and Immunity
- Vol. 76 (4), 1535-1546
- https://doi.org/10.1128/iai.01078-07
Abstract
The causative agent of tuberculosis, Mycobacterium tuberculosis, has two chaperonin (Cpn60) proteins and one cochaperonin (Cpn10) protein. We show here that cpn60.2 and cpn10, but not cpn60.1, are essential for cell survival. A mutant lacking Cpn60.1 was indistinguishable from the wild-type organism in plate and broth culture and within murine macrophages, although it showed increased sensitivity to high temperature (55 degrees C). However, infection of mice with the Deltacpn60.1 mutant revealed a major difference from the wild-type organism. In spite of having equal numbers of bacteria in infected sites, the Deltacpn60.1 mutant failed to produce granulomatous inflammation in either mice or guinea pigs. This was associated with reduced cytokine expression in infected animals and macrophages. Cell wall lipid acid composition was not altered in the mutant strain. Thus, it appears that Cpn60.1 is an important agent in the regulation of the cytokine-dependent granulomatous response in M. tuberculosis infection.Keywords
This publication has 52 references indexed in Scilit:
- Stress Wars: the Direct Role of Host and Bacterial Molecular Chaperones in Bacterial InfectionInfection and Immunity, 2006
- Proteome-wide Analysis of Chaperonin-Dependent Protein Folding in Escherichia coliCell, 2005
- The Intercellular Signaling Activity of the Mycobacterium tuberculosis Chaperonin 60.1 Protein Resides in the Equatorial DomainJournal of Biological Chemistry, 2005
- Crystal Structure of the 65-Kilodalton Heat Shock Protein, Chaperonin 60.2, ofMycobacterium tuberculosisJournal of Bacteriology, 2004
- Mycobacterium tuberculosis GroEL Homologues Unusually Exist as Lower Oligomers and Retain the Ability to Suppress Aggregation of Substrate ProteinsJournal of Molecular Biology, 2004
- Effect of Mycobacterium tuberculosis chaperonins on bronchial eosinophilia and hyper‐responsiveness in a murine model of allergic inflammationClinical and Experimental Allergy, 2004
- Mycobacterium tuberculosisChaperonin 60.1 Is a More Potent Cytokine Stimulator than Chaperonin 60.2 (Hsp 65) and Contains a CD14-Binding DomainInfection and Immunity, 2001
- Increased levels ofsigJmRNA in late stationary phase cultures ofMycobacterium tuberculosisdetected by DNA array hybridisationFEMS Microbiology Letters, 2001
- Mycobacterial 65-kD heat shock protein induces release of proinflammatory cytokines from human monocytic cellsClinical and Experimental Immunology, 1993
- The 65kDa antigen of mycobacteria—a common bacterial protein?Immunology Today, 1987