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© Pierre Gounon
Entrée de Listeria dans une cellule épithéliale (Grossissement X 10000). Image colorisée.
Publication : Tubercle and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease

Protective role of the Mycobacterium smegmatis IdeR against reactive oxygen species and isoniazid toxicity.

Scientific Fields
Diseases
Organisms
Applications
Technique

Published in Tubercle and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease - 01 Jan 1998

Dussurget O, Rodriguez M, Smith I,

Link to Pubmed [PMID] – 10645447

Tuber Lung Dis 1998 ; 79(2): 99-106

To understand the mechanism by which IdeR is necessary for maintaining wild type levels of KatG and SodA enzyme activity and normal isoniazid (INH) resistance.To identify the step(s) of SodA and KatG function that were affected by the ideR mutation, quantitative western immunoassays and ribonucleic acid (RNA) hybridizations were performed. To see if the increased INH sensitivity of the ideR mutant was caused by lower SodA activity, the Mycobacterium smegmatis sod gene was inactivated.The levels of KatG and SodA mRNA and protein in the M. smegmatis IdeR mutant are decreased to approximately 20-40% of those observed in the wild type parent strain. This is quantitatively similar to the decrease in KatG and SodA enzyme activities originally observed in the ideR strain. The M. smegmatis sodA mutant was slightly more sensitive to INH, compared to the wild type strain and was more resistant than the ideR mutant.IdeR is necessary for full expression of the M. smegmatis katG and sodA genes. It is not yet known whether this protein acts directly at the gene level. The lower levels of SodA contribute slightly to the increased susceptibility to INH of the ideR mutant, but cannot explain the magnitude of the INH sensitivity observed when IdeR is not present. These data suggest that IdeR is a regulator of the cellular stress response, as it has a protective role in cells facing environmental stresses, such as increased levels of reactive oxygen species and INH toxic intermediates. These conclusions do not necessarily apply to IdeR’s role in M. tuberculosis physiology, since we have not inactivated its gene in this pathogen.