Affiliation:
1. Department of Microbiology and Immunology, Wake Forest University School of Medicine, Winston-Salem, North Carolina
Abstract
ABSTRACT
The response regulator AlgR is required for
Pseudomonas aeruginosa
type IV pilus-dependent twitching motility, a flagellum-independent mode of solid surface translocation. Prior work showed that AlgR is phosphorylated at aspartate 54, and cells expressing an AlgR variant that cannot undergo phosphorylation (AlgRD54N) lack twitching motility. However, the mechanism by which AlgR controls twitching motility is not completely understood. We hypothesized that AlgR functioned by activating genes within the prepilin
fimU-pilVWXY1Y2E
cluster that are necessary for type IV pilin biogenesis. Reverse transcriptase PCR analysis showed that the
fimU-pilVWXY1Y2E
genes are cotranscribed in an operon, which is under the control of AlgR. This supports prior transcriptional profiling studies of wild-type strains and
algR
mutants. Moreover, expression of the
fimU-pilVWXY1Y2
E operon was reduced in strains expressing AlgRD54N. DNase footprinting and electrophoretic mobility shift assays demonstrate that AlgR but not AlgRD54N bound with high affinity to two sites upstream of the
fimU-pilVWXY1Y2E
operon. Altogether, our findings indicate that AlgR is essential for proper pilin localization and that phosphorylation of AlgR results in direct activation of the
fimU-pilVWXY1Y2E
operon, which is required for the assembly and export of a functional type IV pilus.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
63 articles.
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