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Volume 90, Issue 4, Pages 236-244 (July 2010)


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Individual Mycobacterium tuberculosis universal stress protein homologues are dispensable in vitro

S.M. Hingley-Wilson1, K.E.A. Lougheed1, K. Ferguson, S. Leiva, H.D. WilliamsCorresponding Author Informationemail address

Received 1 December 2009; received in revised form 16 March 2010; accepted 31 March 2010. published online 14 June 2010.

Summary 

Mycobacterium tuberculosis has 10 universal stress proteins, whose function is unknown. However, proteomic and transcriptomic analyses have shown that a number of usp genes are significantly upregulated under hypoxic conditions and in response to nitric oxide and carbon monoxide, as well as during M. tuberculosis infection of macrophage cell lines. Six of these USPs are part of the DosR regulon and this, along with their expression pattern and the phenotypes of usp mutants in other bacterial species, suggests a potential role in the persistence and/or intracellular survival of Mtb. Knock-out mutants of individual usp genes encoding the USPs Rv1996, Rv2005c, Rv2026c and Rv2028c were generated and their growth and survival under hypoxic and other stress conditions examined. Although the majority of usp genes are highly induced in hypoxic conditions, mutation did not affect the long term survival of Mtb under these conditions, or in response to a range of stress conditions chosen to represent the environmental onslaughts experienced by the bacillus during an infection, nor during infection of mouse and human – derived macrophage cell lines. The possibility remains that these USPs are functionally redundant in Mtb.

Department of Life Sciences, Faculty of Natural Sciences, Imperial College London, Sir Alexander Fleming Building, London SW7 2AZ, UK

Corresponding Author InformationCorresponding author. Tel.: +44 (020) 75945383; fax: +44 (020) 75842056.

1 These authors contributed equally to this work.

PII: S1472-9792(10)00044-2

doi:10.1016/j.tube.2010.03.013


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