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Infection and Immunity, August 2000, p. 4598-4603, Vol. 68, No. 8
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Switching of Flagellar Motility in Helicobacter pylori
by Reversible Length Variation of a Short Homopolymeric Sequence
Repeat in fliP, a Gene Encoding a Basal Body
Protein
Christine
Josenhans,1,2
Kathryn A.
Eaton,3
Tracy
Thevenot,3 and
Sebastian
Suerbaum1,2,*
Institute of Hygiene and Microbiology, University of
Würzburg, D-97080 Würzburg,1 and
Department of Medical Microbiology, Ruhr-Universität
Bochum, D-44780 Bochum,2 Germany, and
Department of Veterinary Biosciences, Ohio State
University, Columbus, Ohio3
Received 28 January 2000/Returned for modification 24 March
2000/Accepted 15 May 2000
The genome of Helicobacter pylori contains numerous
simple nucleotide repeats that have been proposed to have regulatory
functions and to compensate for the conspicuous dearth of master
regulatory pathways in this highly host-adapted bacterium. H. pylori strain 26695, whose genomic sequence was determined by The
Institute for Genomic Research (TIGR), contains a repeat of nine
cytidines in the fliP flagellar basal body gene that splits
the open reading frame in two parts. In this work, we demonstrate that
the 26695C9 strain with a split fliP gene as
sequenced by TIGR was nonflagellated and nonmotile. In contrast,
earlier isolates of strain 26695 selected by positive motility testing
as well as pig-passaged derivatives of 26695 were all flagellated and
highly motile. All of these motile strains had a C8 repeat
and consequently a contiguous fliP reading frame. By
screening approximately 50,000 colonies of 26695C9 for
motility in soft agar, a motile revertant with a C8 repeat could be isolated, proving that the described switch is reversible. The
fliP genes of 20 motile clinical H. pylori
isolates from different geographic regions possessed intact
fliP genes with repeats of eight cytidines or the sequence
CCCCACCC in its place. Isogenic fliP mutants of
a motile, C8 repeat isolate of strain 26695 were constructed by allelic exchange mutagenesis and found to be defective in flagellum biogenesis. Mutants produced only small amounts of flagellins, while the transcription of flagellin genes appeared unchanged. These results strongly suggest a unique mechanism regulating motility in H. pylori which relies on slipped-strand
mispairing-mediated mutagenesis of fliP.
*
Corresponding author. Mailing address: Institute of
Hygiene and Microbiology, University of Würzburg,
Josef-Schneider-Str. 2, D-97080 Würzburg, Germany. Phone:
49 931 201 3949. Fax: 49 931 201 3445. E-mail:
ssuerbaum{at}hygiene.uni-wuerzburg.de.
Infection and Immunity, August 2000, p. 4598-4603, Vol. 68, No. 8
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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