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Infection and Immunity, October 1998, p. 4832-4837, Vol. 66, No. 10
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Urease Plays an Important Role in the Chemotactic
Motility of Helicobacter pylori in a Viscous
Environment
Hiroki
Nakamura,1,2
Hironori
Yoshiyama,1
Hiroaki
Takeuchi,1
Tomoko
Mizote,1,3
Kiwamu
Okita,2 and
Teruko
Nakazawa1,*
Department of
Microbiology1 and
First Department of
Internal Medicine,2 Yamaguchi University School
of Medicine, Ube, Yamaguchi 755-8505, and
Department of
Environmental Science, Yamaguchi Prefectural University, Yamaguchi
753-0011,3 Japan
Received 27 March 1998/Returned for modification 6 May
1998/Accepted 8 July 1998
Helicobacter pylori exhibits chemotactic responses to
urea, flurofamide, acetohydroxamic acid, and sodium bicarbonate. In buffer, the chemotactic activities of a urease-positive strain were
higher than those of the isogenic urease-negative strain. Moreover, the
chemotactic activities of the urease-positive strain were increased in
a viscous solution containing 3% polyvinylpyrrolidone, whereas those
of the urease-negative mutant were not. These results are in accordance
with the fact that the mutant strain did not show swarming in motility
agar regardless of having flagella. Incubation of the wild-type strain
with flurofamide resulted in partial inhibition of the chemotactic
activities in the viscous solution. In addition, incubation with
acetohydroxamic acid, a low-molecular-weight, diffusible urease
inhibitor, resulted in complete loss of chemotactic activity in the
viscous solution. The inhibition of the chemotactic activity by urease
inhibitors paralleled the inhibition of urease. The chemotactic
activity of H. pylori was also inhibited by the proton
carrier carbonyl cyanide m-chlorophenylhydrazone, showing
that H. pylori utilizes proton motive force for motility.
These results indicate that cytoplasmic urease plays an important role
in the chemotactic motility of H. pylori under a condition
that mimics the ecological niche of the bacterium, the gastric mucous
layer.
*
Corresponding author. Mailing address: Department of
Microbiology, Yamaguchi University School of Medicine, Ube, Yamaguchi 755-8505, Japan. Phone: (81)836-22-2226. Fax: (81)836-22-2415. E-mail: nakazawa{at}po.cc.yamaguchi-u.ac.jp.
Infection and Immunity, October 1998, p. 4832-4837, Vol. 66, No. 10
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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