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PMID: 15207493 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Gene expression profile of Mycobacterium tuberculosis in a non-replicating state.

Tuberculosis (Edinburgh, Scotland) ·Vol. 84 ·No. 3-4 ·2004-00-00 ·Pages 239-46

Muttucumaru DG, Roberts G, Hinds J, Stabler RA, Parish T

Abstract

Mycobacterium tuberculosis is able to persist in the human host for decades in an apparently dormant state where it is presumed to reside in an hypoxic environment. This can be mimicked by the Wayne culture model in which progressive oxygen depletion causes the bacteria to shift into a non-replicating state. We investigated global gene expression in aerobic (roller), microaerophilic (NRP1) and anaerobic (NRP2) cultures. A number of genes were significantly up-regulated as compared to aerobic culture; 178 in NRP1, 210 in NRP2, 88 in both. The two states showed distinct gene expression profiles, although a number of membrane and transmembrane proteins were induced in both conditions. A number of regulatory proteins were up-regulated in NRP2. Glycine dehydrogenase, nitrate reductase and alpha-crystallin were induced in both stages, as were fatty acid metabolism genes including fadD26 and mas and genes of the DosR regulon. In a comparison with other stress conditions, there were more similarities between anaerobic conditions and carbon starvation or heat shock than between microaerophilic conditions and carbon starvation or heat shock, but as expected microaerophilic and anaerobic conditions showed the most similar profile. Our results indicate that a large number of genes are up-regulated during the shift into the persistent state.

MeSH Terms
Aerobiosis/physiology Anaerobiosis/physiology Biological Transport/genetics Carbon/metabolism DNA Replication DNA, Bacterial/genetics Fatty Acids/metabolism Gene Expression Profiling/methods Gene Expression Regulation, Bacterial Heat-Shock Response/physiology In Vitro Techniques Isocitrate Lyase/metabolism Mycobacterium tuberculosis/genetics,growth & development,metabolism Oligonucleotide Array Sequence Analysis/methods Up-Regulation
Chemicals
DNA, Bacterial Fatty Acids Carbon Isocitrate Lyase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Muttucumaru D G Niranjala
Centre for Infectious Disease, Institute for Cell and Molecular Science, Barts and the London, Queen Mary's School of Medicine and Dentistry, Turner Street, London E1 2AD, UK.
Roberts Gretta
Hinds Jason
Stabler Richard A
Parish Tanya
Article Info
Journal
Tuberculosis (Edinburgh, Scotland)
Abbr.
Tuberculosis (Edinb)
ISSN
1472-9792
Published
2004-00-00
Pages
239-46
Language
English
Region
Scotland
NLM ID
100971555
Subset
IM
Grants
Wellcome Trust · 062511 · United Kingdom
NIAID NIH HHS · N01 AI-75320 · United States
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