Affiliation:
1. Department of Microbiology and Molecular Genetics
2. Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin 53226
Abstract
ABSTRACT
The genetic mechanisms mediating the adaptation of
Mycobacterium tuberculosis
within the host are poorly understood. The best-characterized regulatory systems in this organism include sigma factors and two-component signal transduction systems.
mprAB
is a two-component system required by
M. tuberculosis
for growth in vivo during the persistent stage of infection. In this report, we demonstrate that MprAB is stress responsive and regulates the expression of numerous stress-responsive genes in
M. tuberculosis
. With DNA microarrays and quantitative real-time reverse transcription-PCR, genes regulated by MprA in
M. tuberculosis
that included two stress-responsive sigma factors were identified. Response regulator MprA bound to conserved motifs in the upstream regions of both
sigB
and
sigE
in vitro and regulated the in vivo expression of
sigB
and
sigE
in
M. tuberculosis
. In addition,
mprA
itself was induced following exposure to stress, establishing a direct role for this regulatory system in stress response pathways of
M. tuberculosis
. Induction of
mprA
and
sigE
by MprA in response to stress was mediated through the cognate sensor kinase MprB and required expression of the extracytoplasmic loop domain. These results provide the first evidence that recognition of and adaptation to specific stress in
M. tuberculosis
are mediated through activation of a two-component signal transduction system that directly regulates the expression of stress-responsive determinants.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
144 articles.
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