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Infection and Immunity, August 2000, p. 4598-4603, Vol. 68, No. 8
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.
Helicobacter pylori, the
causative agent of gastritis and ulcer disease in humans, relies on its
high motility in viscous environments to colonize and persist in the
human stomach (14, 18). H. pylori carries a
unipolar bundle of sheathed flagella (19). Relatively little
is known about the regulation of flagellar biosynthesis in H. pylori (32, 33). The whole genome sequence of H. pylori strain 26695 (determined by The Institute for Genomic Research [TIGR]) has revealed a conspicuous lack of regulatory elements that are present in other eubacterial species (36). H. pylori does not possess a homolog of the flhCD
master operon which is at the top of the regulatory hierarchy coupling
cell division and motility functions in Salmonella enterica
serovar Typhimurium, Bacillus subtilis, and other
eubacteria (23). H. pylori also appears to lack a
homolog of the flgM gene that in other eubacteria codes for
an antagonist of the flagellar sigma factor, The complete genome sequences of H. pylori strains 26695 and
J99 contain close to 30 genes with simple sequence repeats
(dinucleotide repeats or homopolymeric tracts), either within the
upstream regulatory regions or within the coding sequences (2,
36). Because of the abundance of such sequence repeats,
slipped-strand mispairing has been suggested to be involved in the
control of gene expression in H. pylori (31).
Simple nucleotide repeats are mutational hot spots because they reduce
the fidelity of both DNA replication and transcription. Changes of
repeat length due to slipped-strand mispairing (insertion or deletion
of repeat units) and consequent disruption of open reading frames by
premature stop codons occur at a much higher rate than mutations in
other areas of the chromosome. Slipped-strand mispairing plays a
regulatory role, on both transcriptional and translational levels, in
several other bacteria, mainly for the variation of surface-associated
proteins and related structures such as fimbriae, capsules, or
lipopolysaccharides (13, 25, 39; for a review, see
reference 38). Recently, slipped-strand mispairing
within fucosyltransferase genes of H. pylori has been demonstrated to play a role in the variation of lipopolysaccharide O-specific side chains (4, 40). Among the potentially
phase-variable genes of H. pylori, there is also one
motility-associated gene, fliP, the product of which is
involved in the flagellar export apparatus of eubacteria (27,
31).
In H. pylori strain 26695, whose genome has been sequenced
completely, fliP contains a repeat of nine cytidines
(C9) within its coding region (36). This repeat
causes a frameshift and splits the gene in two parts (HP0684 and
HP0685). In the second complete genome sequence of an H. pylori strain (J99), fliP is a contiguous open reading
frame with a C8 repeat (2).
We therefore wanted to know if the C9 repeat in
fliP might in fact be involved in motility regulation in
H. pylori and if the motility phenotype of the organism is
dependent on expression of a full-length FliP protein. We have studied
the fliP locus in different motile and nonmotile variants of
strain 26695 and in different clinical isolates of H. pylori. In addition, we constructed and characterized isogenic
fliP mutants of different H. pylori strains. The
results make a convincing case for slipped-strand mispairing within the
fliP locus as a novel regulatory feature of H. pylori motility.
Bacterial strains, plasmids, and growth conditions.
H.
pylori strains N6 (11) and 88-3887, a motile
pig-passaged variant of H. pylori 26695 (36), and
the mouse colonizing strain SS1 (21) were used for the
construction of fliP mutants. fliP sequences were
determined for various motile and nonmotile variants of 26695, for N6,
SS1, the nonmotile strain Tx30a (22), and for 20 clinical
isolates from Germany, South Africa, and Singapore (1, 35).
Culture conditions for H. pylori strains were as described
elsewhere (34).
DNA manipulation, PCR, and nucleotide sequencing.
DNA
manipulations were done according to standard protocols
(30). H. pylori genomic DNA for sequence
determination was prepared with a QiaAmp tissue kit (Qiagen Inc.,
Hilden, Germany). Plasmid DNA was purified with the Qiagen Midi column
plasmid purification kit. DNA restriction fragments or PCR products
were purified from agarose gels with a QiaQuick DNA purification kit
(Qiagen). Nucleotide sequences were determined by direct sequencing of
PCR products generated using the primers OLHPFliP1
(CCTCATTTGCCCTTTAATATGC) and OLHPFliP2
(GGCAGAGAAATCATTACAGG). PCR consisted of 35 cycles as
follows: denaturation, 94°C for 1 min; annealing, 50°C for 1 min;
and extension, 72°C for 1 min; 75-ng aliquots of PCR products purified using the QiaQuick PCR purification kit (Qiagen) were used in
cycle sequencing reactions from both strands with an ABI Prism dye
terminator cycle sequencing kit (Applied Biosystems), using the same
primers and independent PCR products for each strand. Sequences were
aligned using Seqlab and Pileup from the Wisconsin Package, version 9.1 (Genetics Computer Group, Madison, Wis.). All sequences were reduced to
a common length of 480 nucleotides.
Construction of isogenic fliP mutants of H. pylori.
The complete fliP gene from the motile 26695 variant 88-3887 (fliPC8) including additional
upstream and downstream sequences (1,622 bp) was amplified by PCR with
the primers OLHPFliP3s (TATGGATCCCATAACCTTTAGGGTCAGC) and OLHPFliP4s (TTAGGATCCGACTTTTGGTATTAGCAGC),
which both contained BamHI sites, and cloned into
vectors pILL570 (20) and pUC18 cut with BamHI to
give plasmids pCJ53 and pCJ51, respectively. Subsequently, the cloned
fliP gene was disrupted by insertion of a cassette that
contains a kanamycin resistance gene (aphA-3 [37]). The cassette was inserted in two different
positions. In plasmid pCJ55, a direct derivative of pCJ53, the cassette
was introduced into a natural EcoRI restriction site at
nucleotide position 360 of the fliP locus in H. pylori KE26695, which is 151 nucleotides downstream of the
C8 repeat and 96 nucleotides downstream of the stop codon.
To construct a plasmid where the insertion was located exactly at the
same position of the premature stop codon in C9 strains,
the following strategy was used. Inverse PCR with primers OLHPFliP5s
(TTAAGATCTCTATGATACAGGGATTAAGC) and OLHPFliP6s
(ATTAGATCTCGAGACTAAAATTTGAGTGG) and plasmid pCJ51
(fliP insert in pUC18) as the template was used to generate
a 50-bp deletion in fliP and to introduce a BglII
restriction site at this deletion site just 18 nucleotides downstream
of the C8 repeat. The deletion (nucleotides 229 to 279 of
fliP) includes the stop codon generated by the
fliPC9 locus in 26695 (the TIGR strain). The
aphA-3 cassette (cut from pILL600 with BamHI) was
ligated into this construct, yielding plasmid pCJ57. Since
fliP is not part of an operon and the two genes downstream
of fliP are transcribed in the opposite direction of
fliP, polar effects of these disruptions were extremely
unlikely. Nevertheless, in both plasmids pCJ55 and pCJ57, the
aphA-3 cassette, which has a strong promoter and no
transcription terminator, was inserted in the same transcriptional orientation with respect to fliP, further reducing the
possibility of polar effects. Plasmids pCJ55 and pCJ57 were used to
generate allelic replacement mutants of H. pylori strains
SS1 and N6 and the motile 26695 variant 88-3887 by natural
transformation. Natural transformation of H. pylori was
performed as described elsewhere (6). After natural
transformation, the bacteria were grown on nonselective plates for a
period of 24 h and then transferred to plates containing kanamycin
(20 mg/liter). Recombinant colonies were selected after 3 to 5 days of
growth. The correct genotype of the kanamycin-resistant mutants was
verified by PCRs with primers binding to the target gene and primers
binding to the aphA-3 cassette as previously described
(34) (data not shown).
SDS-PAGE and Western blotting.
Whole-cell lysates of
Helicobacter cells were obtained by sonication, while
flagellar filament proteins were partially purified by mechanical
shearing and ultracentrifugation as described elsewhere (12). Sodium dodecyl sulfate-polyacrylamide gel
electrophoresis and Western blotting were performed as described
elsewhere (32). The blots were incubated with a mixture of
antisera raised against purified recombinant FlaA and FlaB flagellins
of H. pylori, each diluted 1:1,500. Bound antibodies were
visualized with a peroxidase-coupled goat anti-rabbit antibody (diluted
1:3,000; Jackson Biologicals Laboratory, West Grove, Pa.).
Electron microscopy and motility testing.
Transmission
electron microscopy of negatively stained bacteria was performed as
described elsewhere (17). Motility testing of H. pylori strains was performed either in wet mounts or in 0.3%
motility agar plates as described elsewhere (7, 17). Motility plates were incubated for 5 days.
Preparation of RNA from H. pylori.
RNA from H. pylori was prepared by the RNEasy Midi-Prep procedure (Qiagen) or
using a CsCl centrifugation method described by Spohn and Scarlato
(33). RNA was prepared from bacteria grown on two blood agar
plates for 24 h or from 25 ml of liquid culture grown to an
optical density at 600 nm of about 1.0 (mid-log phase, approximately
1010 bacteria). RNA slot blotting was done with a Bio-Dot
slot blotting apparatus (Bio-Rad). The amount of specific mRNA was
detected by hybridization with digoxigenin (DIG)-labeled DNA probes
(flaA, flaB, flgE, and
fliP; PCR-generated fragments; probes were generated with a
DIG-labeling kit from Boehringer/Roche); 2-µg aliquots of RNA were
analyzed on the blots. In all strains, the hybridization signal with a
fliP probe was too weak to be evaluated, even when 5 µg of
RNA was used. Control hybridizations using the four different probes on
an Escherichia coli DH5 Nucleotide sequence accession number.
The nucleotide
sequences described in this paper have been submitted to the GenBank
database (accession no. AJ404379 to AJ404400).
H. pylori 26695C9 (the TIGR strain) is
nonmotile and lacks flagella.
Because the genome sequence of
H. pylori 26695C9 does not contain a full-length
fliP gene, we analyzed whether this strain carried flagella
and was motile. H. pylori 26695C9 was studied by
electron microscopy, and no flagella were detected (data not shown).
Bacteria were completely nonspreading in motility agar, and no motility
was visible by direct microscopy of wet mounts (Fig.
1).
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
ABSTRACT
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
INTRODUCTION
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
28
(15). Except for the gene coding for the major H. pylori flagellin, flaA, most flagellar genes of
H. pylori are governed by 54- or
70-dependent promoters (28, 33, 34). Taken
together, the available data suggest that the regulation of flagellar
biogenesis and motility differs considerably between H. pylori and other bacteria.
MATERIALS AND METHODS
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
RNA gave no detectable background signal. The sequences of the primers used to generate the probes by PCR
are available upon request.
RESULTS
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
View larger version (79K):
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FIG. 1.
Motility tests of H. pylori
26695C9 and the pig-passaged variant, 88-3887. The
nonmotile 26695C9 strain shows only pinpoint colonies
without spreading, while the majority of 88-3887 colonies have a
spreading phenotype. The inset in the upper left corner shows a
magnification of the area of the plate marked by the square.
Different fliP genotypes in motile and nonmotile variants of strain 26695. Previous studies have shown that motility is essential for the ability of H. pylori and other Helicobacter spp. to colonize the gastric mucosa (3, 9, 16). It was therefore surprising that a virulent isolate of H. pylori was nonmotile. H. pylori 26695 was received by one of us in 1986. It was noted that colonies of highly motile and nonmotile bacteria could be identified in soft agar, and both variants were isolated and frozen (8).
To clarify whether the motility of different 26695 variants depended on the length of the fliP repeat sequence, a 642-bp fragment of fliP that contained the homopolymeric repeat was amplified by PCR and sequenced directly from both strands for 26695C9 as well as several motile and nonmotile variant strains (Table 1). 26695C9 contained a C9 repeat and a premature stop codon in fliP 53 nucleotides downstream of the repeat, as reported by Tomb et al. (36) (Fig. 2). An original motile variant (26C) that had been selected because it formed large spreading colonies in motility agar had eight cytidine residues and a continuous fliP gene, while a nonmotile variant (26B) had nine cytidines (Table 1; Fig. 2). We also analyzed six strains each that had been obtained from initial motile or nonmotile variant strains by repeatedly passaging them in vitro without selection for or against motility (up to 10 passages). No changes in the repeat length were detectable in those passaged strains. Three strains (for example, strain 88-3887) that had been reisolated from piglets that had been experimentally infected with the original (mixed) H. pylori 26695 were fully motile and possessed the fliPC8 genotype.
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Isolation of motile revertants of 26695C9. To demonstrate that the switch from motile (C8) to nonmotile (C9) was reversible, we isolated a motile revertant of 26695C9. The bacteria were diluted in motility agar and poured into petri dishes. Approximately 50,000 colonies were screened before a spreading colony was detected. The spreading colony was isolated and purified through a second round of motility testing. As expected, the motile revertant (26695-R1) had a C8 repeat. A second revertant (26BH) was isolated from strain 26B (C9) by growing a stab preparation of 26B in motility agar for 4 days, swabbing the edge of the streak, and culturing that in broth. That broth produced 117 motile colonies (of 152 total), one of which was colony purified and became 26BH. Like 26695-R1, 26BH had a C8 repeat.
fliP sequence comparison of different H. pylori strains. To determine if the poly(C) repeat within fliP was conserved between different H. pylori strains, we evaluated fliP sequences (480 nucleotides) from 17 clinical isolates of H. pylori and from four widely used laboratory strains of H. pylori (SS1, NCTC11637, NCTC11639, and Tx30a [Table 1; Fig. 2]). With the exception of strain Tx30a, which, consistent with previous reports (7), was nonmotile and lacked flagella, all strains analyzed were motile and carried flagella. Strain Tx30a possessed a C7 stretch instead of the C8 sequence of the motile wild-type strains. All motile strains had a continuous fliP gene; 13 out of the 22 motile strains had an adenine instead of the fifth cytidine within the repeat (CCCCACCC). All five strains from Asia had the CCCCACCC-type allele, while only one out of six strains from the Cape Coloured population in South Africa had that allele.
Construction and characterization of isogenic fliP mutants. To prove that the premature stop of FliP translation in the strains with a fliPC9 or fliPC7 sequence was sufficient to cause the loss of motility and flagellation observed in 26695C9 and Tx30a, isogenic fliP mutants of three different motile H. pylori strains (the mouse-colonizing strains SS1 and N6 and the piglet-passaged motile variant 88-3887 of strain 26695) were constructed by disruption of fliP with an aphA-3 cassette at two different positions, both close to the position of the premature stop codon in fliPC9 strains (Fig. 2A). For each of the wild-type strains, two different fliP mutants were constructed by natural transformation with pCJ55 or pCJ57. Prior to transformation, the wild-type strains were again checked for motility and the presence of flagella to ensure that motility had not accidentally been lost by repeated in vitro passage.
The fliP region of all mutant strains obtained by allelic exchange mutagenesis was resequenced to exclude that the repeat length had changed during the mutant selection process. All mutants had retained the C8 repeat and had integrated the aphA-3 cassette into their genome at the predetermined sites. In all mutant strains, independent of the parent strain, the sequenced part of fliP was identical to the 26695 fliP sequence, because during the double-crossover event, the wild-type fliP sequences had been replaced by the 26695 sequences flanking the aphA-3 cassette in the suicide plasmids. Both types of mutants in the different H. pylori strains were characterized for motility and the presence of flagella, and flagellin expression was checked by Western blot analysis. The phenotypes of both types of fliP mutants (pCJ55 and pCJ57) were identical in all strains and indistinguishable from the phenotype of 26695C9. All fliP mutants failed to form flagella as determined by transmission electron microscopy and were nonmotile. Whole-cell lysates and sheared flagellar material of selected wild-type strains with different fliP genotypes and isogenic fliP mutant strains were analyzed for the presence of flagellins by Western blotting with antisera raised against H. pylori FlaA and FlaB flagellins (Fig. 3). Flagellin synthesis in 26695C9 was very low compared to motile H. pylori wild-type strains, but FlaA was present in whole-cell lysates and, in much lower amounts, in sheared material. To exclude that free flagellin is released into the medium by the nonmotile strains, supernatants of strains grown in liquid culture were precipitated with trichloroacetic acid and analyzed; they did not contain significant amounts of flagellin (data not shown).
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Transcriptional analyses of flagella-associated genes in nonmotile
H. pylori fliP mutant strains and in motile wild-type
strains.
Transcription of the flaA and flaB
flagellin genes and the hook gene, flgE, was measured by RNA
slot blot hybridization in H. pylori 26695C9,
the motile variant of 26695 (88-3887; fliPC8), an isogenic fliP mutant of 88-3887, and the N6 wild-type
strain. In all strains with an interrupted fliP gene,
flaA-, flaB-, and flgE-specific mRNAs
were present in about the same amounts as in the motile wild-type
strains (Fig. 4). These data ruled out the possibility that the observed profound reduction in flagellin in
these strains was due to a downregulation of flagellin gene transcription.
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DISCUSSION |
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Materials and Methods
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Discussion
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fliP genotypes and motility in H. pylori 26695. The data presented here show that H. pylori can use slipped-strand mispairing-mediated frameshifting in fliP to switch the formation of flagella and hence motility off and on. fliP encodes a component of the flagellar basal body and was not previously known to be involved in flagellar regulation of any bacterial species (24). fliP can be reversibly inactivated by addition or deletion of a single cytidine which results in a frameshift and introduces an early stop codon. The consequence of fliP inactivation is a shutdown of flagellar assembly. The observed reduction in the expression of flagellins was not due to transcriptional regulation, because mRNA for major structural flagellar components was present in unchanged amounts in fliP knockout mutants and repeat length variants.
It has been known for a long time that H. pylori loses its motility after prolonged in vitro passage, but the mechanisms responsible for this loss of motility were not known. The H. pylori genome contains relatively few regulatory genes. A striking example is the absence of master regulatory genes (flhCD and flgM) from the flagellar regulatory cascade that have central roles in other bacterial species. In agreement with this, a lack of feedback mechanisms coupling flagellar assembly to the expression of late flagellar genes has been observed in H. pylori hook (flgE) and flagellin (flaA and flaB) mutants (28, 34). The switching mechanism described here may compensate, at least in part, for the lack of other regulatory elements. The fliP-based switching mechanism appears to be relatively specific to H. pylori. A manual search of all available fliP sequences in GenBank for homopolymeric tracts or dinucleotide repeats was performed. No homopolymeric tract was present in the fliP gene of Campylobacter jejuni, whose flagellar system is otherwise quite similar to that of H. pylori, or the fliP genes of any other bacterium with the notable exception of Borrelia burgdorferi, where the potentially frameshiftable sequence T9AT6 is located only few nucleotides downstream of the start codon of fliP (GenBank accession no. L75945). It is tempting to speculate that B. burgdorferi, which, like H. pylori, has very few regulatory genes (e.g., only two two-component signal transduction systems) may employ a similar strategy to switch off motility. Indeed, frameshifts in a motility-associated gene have only recently been shown for the first time to be involved in switching of flagellar biogenesis. Park et al. (29) showed that a nonmotile variant of Campylobacter coli UA585 had an interrupted flhA gene, which was due to a length change in a short homopolymeric T repeat. Motile revertants had corrected the repeat length and restored an intact flhA gene. No repeat was present in C. jejuni flhA or in H. pylori flhA (formerly flbA) (34).fliP mutants. The hypothesis that the nonmotile phenotypes of H. pylori strains 26695 and Tx30a are caused by the frameshifts in fliP was verified by the construction of isogenic fliP knockout mutants of different motile H. pylori strains. Polar effects of the cassette mutagenesis were extremely unlikely, because fliP in H. pylori (unlike in salmonellae) is not part of an operon. The two genes located downstream of fliP are transcribed in the opposite direction. The phenotype of these mutants was indistinguishable from that of 26695C9.
FliP and flagellar assembly. In salmonellae, FliP is an early flagellar protein on the second hierarchical level of flagellar biogenesis and under the direct control of the flhCD master operon, which is not present in H. pylori (27). FliP, of which in salmonellae there are about five subunits per flagellum, is considered a component of the flagellar type III export system in the flagellar basal body (10). It is highly likely that fliP mutants are no longer able to export flagellar components (27). In the H. pylori nonmotile wild-type strains as well as the isogenic fliP mutants, small amounts of flagellin were detected in the cytoplasmic fraction of the bacteria, showing that translation still takes place. In contrast to what was described for H. pylori flgE mutants (28), there was no accumulation of intracellular flagellin, suggesting that flagellin stability is reduced in fliP mutants.
Frequency of motility switching.
The switching frequencies of
the motility phenotype had previously been determined to be 1.6 × 10
4 for the motile-to-nonmotile switch and less than
107 for the inverse event (8). We could not
measure the rate of the fliP off switch, because when motile
strains of H. pylori are tested in soft agar, many colonies
appear nonmotile (such as the pinpoint colonies in the left panel of
Fig. 1). Most of these either still express flagellins or, if they do
not, still have a C8 genotype (data not shown). Thus,
frameshifting in fliP does not seem to be the only mechanism
responsible for loss of motility in H. pylori. With more
than 50 genes involved in motility and flagellar biosynthesis, there
are many different possible events that could cause a nonmotile
phenotype. We succeeded in detecting the fliP on switch.
Screening of a fliPC9 strain for back-mutation
to C8 yielded two independent revertants with two different
screening approaches. However, this event was so infrequent (1 revertant in 50,000 colonies screened) that it was impossible to
determine an exact switching frequency.
such as when bacteria are grown in vitroleads to a frequent loss of this energy-consuming property. It is not clear which role this
propensity for a relatively frequent switch to a nonmotile phenotype by
mutation in fliP or by other mechanisms might play in vivo.
It is conceivable that there is a niche for a proportion of the
H. pylori bacteria where motility is no longer needed. In
certain parts of the stomach mucosa not directly exposed to the
shedding forces of mucus production or peristalsis, the energy-saving loss of motility might be advantageous for a lifestyle of low nutrient
requirements, continuous slow growth, and tight adherence to cells.
Sequence polymorphisms and recombination in fliP. Thirteen out of 22 motile strains studied had an adenosine residue in the fifth position of the repeat. This mutation would greatly reduce the probability of slipped-strand mispairing mutagenesis. The relevance of this polymorphism in the repeat sequence is not known. Since motility is essential for colonization, it seems unlikely that a hypermutatable nucleotide sequence that renders the motility system more susceptible to functional inactivation would occur so frequently unless this had biological significance. However, the occurrence of the CCCCACCC sequence in more than half of the strains analyzed, including all of the Asian strains, shows that the presence of the C8 repeat is not essential, at least not in all hosts. It is conceivable that there are subgroups of strains or strains in particular hosts where loss of motility is particularly detrimental, and strains with a CCCCACCC sequence therefore have a selective advantage. Given the frequency of recombination in H. pylori (35), this mutation in the repeat sequence would not have to be a dead end for a given strain because the C8 repeat could be reacquired by recombination. Analysis of the fliP sequences with the Homoplasy test (26) shows that fliP has been involved in frequent recombination events (data not shown). Finally, it has recently been shown in Neisseria meningitidis that the frequency of slipped-strand mispairing-mediated phase variation of capsule biosynthesis is strongly dependent on the presence or absence of the mutator gene dam (5). Although nothing is yet known about the occurrence of mutator phenotypes in H. pylori, it is possible that similar differences of mutation frequencies exist in H. pylori, and these might strongly affect the frequency of fliP-mediated motility switching.
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ACKNOWLEDGMENTS |
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We gratefully acknowledge expert technical assistance by Susanne Friedrich, Doris Jaromin, and Barbara Beuerle. We thank M. Heep and N. Lehn for the strains from Singapore and E. Kunstmann and P. van Helden for strains from South Africa. We thank Chi Aizawa for critical reading of the manuscript.
The work in S.S.'s laboratory was supported by grants SU 133/2-3 (Gerhard Hess award) and SU 133/3-1 from the Deutsche Forschungsgemeinschaft. Work in K.A.E.'s laboratory was supported by Public Health Service grants R01 AI43643 and R29 DK-45340 from the NIH.
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FOOTNOTES |
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* 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.
Editor: J. T. Barbieri
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Infection and Immunity, August 2000, p. 4598-4603, Vol. 68, No. 8
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