Mycobacterium tuberculosis DosR is required for activity of the PmbtB and PmbtI promoters under hypoxia

Mycobacterium tuberculosis has the ability to survive for extended periods of time under conditions of low oxygen, low pH, low iron and low nutrients. The mycobactins (M. tuberculosis siderophores) play a key role in scavenging iron from the environment and are induced in response to low iron in an...

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Veröffentlicht in:PloS one 2014-09, Vol.9 (9), p.e107283-e107283
Hauptverfasser: Schreuder, Lise J, Parish, Tanya
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description Mycobacterium tuberculosis has the ability to survive for extended periods of time under conditions of low oxygen, low pH, low iron and low nutrients. The mycobactins (M. tuberculosis siderophores) play a key role in scavenging iron from the environment and are induced in response to low iron in an IdeR-regulated manner. We demonstrate that the promoters of two mycobactin gene (mbt) operons are also expressed during adaptation to low oxygen, and that this expression is dependent on the DosR regulator. Up-regulation of mbt operons induced by low iron was not DosR-dependent. DosR is a member of a two component regulatory system which responds to oxygen availability. Deletion of the DosR regulator led to increased expression of bacterioferritin and increased capacity to grow under iron depletion. These data provide a link between the mycobacterial response to two conditions likely to be encountered in vivo, low iron and low oxygen.
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subjects Adaptation
Adaptation, Physiological
Bacterial Proteins - physiology
Bacterioferritin
Biology and Life Sciences
Dentistry
DNA-Binding Proteins
Gene Expression
Gene Expression Regulation, Bacterial
Genes, Bacterial
Hypoxia
Infections
Iron
Iron - metabolism
Mycobacterium tuberculosis
Mycobacterium tuberculosis - genetics
Mycobacterium tuberculosis - metabolism
Nutrients
Operon
Operons
Oxygen
Oxygen - metabolism
Promoter Regions, Genetic
Promoters
Protein Kinases - physiology
Siderophores
Tuberculosis
title Mycobacterium tuberculosis DosR is required for activity of the PmbtB and PmbtI promoters under hypoxia
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