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Journal of Bacteriology, September 1998, p. 4856-4864, Vol. 180, No. 18
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Oxidative Stress Response and Characterization of the
oxyR-ahpC and furA-katG Loci in
Mycobacterium marinum
E.
Pagán-Ramos,
J.
Song,
M.
McFalone,
M. H.
Mudd, and
V.
Deretic*
Department of Microbiology and Immunology,
University of Michigan Medical School, Ann Arbor, Michigan
48109-0620
Received 30 January 1998/Accepted 1 July 1998
Oxidative stress response in pathogenic mycobacteria is believed to
be of significance for host-pathogen interactions at various stages of
infection. It also plays a role in determining the intrinsic susceptibility to isoniazid in mycobacterial species. In this work, we
characterized the oxyR-ahpC and furA-katG loci
in the nontuberculous pathogen Mycobacterium marinum. In
contrast to Mycobacterium smegmatis and like
Mycobacterium tuberculosis and Mycobacterium
leprae, M. marinum was shown to possess a closely linked and divergently oriented equivalents of the regulator of peroxide stress response oxyR and its subordinate gene
ahpC, encoding a homolog of alkyl hydroperoxide reductase.
Purified mycobacterial OxyR was found to bind to the
oxyR-ahpC promoter region from M. marinum and
additional mycobacterial species. Mobility shift DNA binding analyses
using OxyR binding sites from several mycobacteria and a panel of in
vitro-generated mutants validated the proposed consensus mycobacterial
recognition sequence. M. marinum AhpC levels detected by
immunoblotting, were increased upon treatment with
H2O2, in keeping with the presence of a
functional OxyR and its binding site within the promoter region of
ahpC. In contrast, OxyR did not bind to the sequences
upstream of the katG structural gene, and katG
expression did not follow the pattern seen with ahpC.
Instead, a new open reading frame encoding a homolog of the ferric
uptake regulator Fur was identified immediately upstream of
katG in M. marinum. The furA-katG
linkage and arrangement are ubiquitous in mycobacteria, suggesting the
presence of additional regulators of oxidative stress response and
potentially explaining the observed differences in ahpC and
katG expression. Collectively, these findings broaden our
understanding of oxidative stress response in mycobacteria. They also
suggest that M. marinum will be useful as a model system
for studying the role of oxidative stress response in mycobacterial
physiology, intracellular survival, and other host-pathogen
interactions associated with mycobacterial diseases.
*
Corresponding author. Mailing address: Department of
Microbiology and Immunology, University of Michigan Medical School,
Medical Sciences Building II, Ann Arbor, MI 48109-0620. Phone: (734)
763-1580. Fax: (734) 647-6243. E-mail: Deretic{at}umich.edu.
Journal of Bacteriology, September 1998, p. 4856-4864, Vol. 180, No. 18
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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