Affiliation:
1. Morehouse School of Medicine, Department of Microbiology, Biochemistry & Immunology, Atlanta, Georgia
Abstract
ABSTRACT
Vibrio cholerae
secretes a Zn-dependent metalloprotease, hemagglutinin/protease (HA/protease), which is encoded by
hapA
and displays a broad range of potentially pathogenic activities. Production of HA/protease requires transcriptional activation by the quorum-sensing regulator HapR. In this study we demonstrate that transcription of
hapA
is growth phase dependent and specifically activated in the deceleration and stationary growth phases. Addition of glucose in these phases repressed
hapA
transcription by inducing
V. cholerae
to resume exponential growth, which in turn diminished the expression of a
rpoS-lacZ
transcriptional fusion. Contrary to a previous observation, we demonstrate that transcription of
hapA
requires the
rpoS
-encoded σ
s
factor. The cyclic AMP (cAMP) receptor protein (CRP) strongly enhanced
hapA
transcription in the deceleration phase. Analysis of
rpoS
and
hapR
mRNA in isogenic CRP
+
and CRP
−
strains suggested that CRP enhances the transcription of
rpoS
and
hapR
. Analysis of strains containing
hapR-lacZ
and
hapA-lacZ
fusions confirmed that
hapA
is transcribed in response to concurrent quorum-sensing and nutrient limitation stimuli. Mutations inactivating the stringent response regulator RelA and the HapR-controlled AphA regulator did not affect HA/protease expression. Electrophoretic mobility shift experiments showed that pure cAMP-CRP and HapR alone do not bind the
hapA
promoter. This result suggests that HapR activation of
hapA
differs from its interaction with the
aphA
promoter and could involve additional factors.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
78 articles.
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