Affiliation:
1. Department of Medicine/Infectious Diseases, University of Florida, Gainesville, Florida 32610
Abstract
ABSTRACT
The single polar flagellum of
Pseudomonas aeruginosa
plays an important role in the pathogenesis of infection by this organism. However, regulation of the assembly of this organelle has not been delineated. In analyzing the sequence available at the
Pseudomonas
genome database, an open reading frame (ORF), flanked by flagellar genes
flhF
and
fliA
, that coded for a protein (280 amino acids) with an ATP-binding motif at its N terminus was found. The ORF was inactivated by inserting a gentamicin cassette in
P. aeruginosa
PAK and PAO1. The resulting mutants were nonmotile on motility agar plates, but under a light microscope they exhibited random movement and tumbling behavior. Electron microscopic studies of the wild-type and mutant strains revealed that the mutants were multiflagellate, with three to six polar flagella per bacterium as rather than one as in the wild type, indicating that this ORF was involved in regulating the number of flagella and chemotactic motility in
P. aeruginosa
. The ORF was named
fleN
. An intact copy of
fleN
on a plasmid complemented the mutant by restoring motility and monoflagellate status. The β-galactosidase activities of eight flagellar operon or gene promoters in the wild-type and
fleN
mutant strains revealed a direct correlation between six promoters that were upregulated in the
fleN
mutant (
fliLMNOPQ
,
flgBCDE
,
fliEFG
,
fliDS orf126
,
fleSR
, and
fliC
) and positive regulation by FleQ, an NtrC-like transcriptional regulator for flagellar genes. Based on these results, we propose a model where FleN influences FleQ activity (directly or indirectly) in regulating flagellar number in
P. aeruginosa
.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
143 articles.
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