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Infection and Immunity, April 2000, p. 2016-2023, Vol. 68, No. 4
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Helicobacter pylori Possesses Two CheY
Response Regulators and a Histidine Kinase Sensor, CheA, Which Are
Essential for Chemotaxis and Colonization of the Gastric
Mucosa
Susan
Foynes,1,
Nick
Dorrell,1
Stephen J.
Ward,1,
Richard A.
Stabler,1
Andy A.
McColm,2
Andrew N.
Rycroft,3 and
Brendan
W.
Wren1,*
Pathogen Molecular Biology and Biochemistry
Unit, Department of Infectious and Tropical Diseases, London School of
Hygiene & Tropical Medicine, London,1
Systems Biology Unit, Glaxo Wellcome Research and Development,
Stevenage,2 and Veterinary Bacteriology
Group, Royal Veterinary College, North Mymms,3
United Kingdom
Received 30 August 1999/Returned for modification 21 December
1999/Accepted 20 January 2000
Infection of the mucous layer of the human stomach by
Helicobacter pylori requires the bacterium to be motile and
presumably chemotactic. Previous studies have shown that fully
functional flagella are essential for motility and colonization, but
the role of chemotaxis remains unclear. The two-component regulatory system CheA/CheY has been shown to play a major role in chemotaxis in
other enteric bacteria. Scrutiny of the 26695 genome sequence suggests
that H. pylori has two CheY response regulators: one a
separate protein (CheY1) and the other (CheY2) fused to the histidine
kinase sensor CheA. Defined deletion mutations were introduced into
cheY1, cheY2, and cheA in H. pylori strains N6 and SS1. Video tracking revealed that the
wild-type H. pylori strain moves in short runs with
frequent direction changes, in contrast to movement of
cheY2, cheAY2, and cheAY2 cheY1
mutants, whose motion was more linear. The cheY1 mutant
demonstrated a different motility phenotype of rapid tumbling. All
mutants had impaired swarming and greatly reduced chemotactic responses
to hog gastric mucin. Neither cheY1 nor cheAY2
mutants were able to colonize mice, but they generated a significant
antibody response, suggesting that despite impaired chemotaxis, these
mutants were able to survive in the stomach long enough to induce an
immune response before being removed by gastric flow. Additionally, we demonstrated that cheY1 failed to colonize gnotobiotic
piglets. This study demonstrates the importance of the roles of
cheY1, cheY2, and cheA in motility
and virulence of H. pylori.
*
Corresponding author. Mailing address: Pathogen
Molecular Biology and Biochemistry Unit, Department of Infectious and
Tropical Diseases, London School of Hygiene & Tropical Medicine, Keppel Street, London WC1E 7HT, United Kingdom. Phone: 44 (0)171 927 2288. Fax: 44 (0)171 636 8739. E-mail:
brendan.wren{at}lshtm.ac.uk.

Present address: Department of Biochemistry, Imperial College of
Science, Technology and Medicine, London SW7 2AZ, United
Kingdom.

Present address: Medeva Development, Vaccine Research Unit,
Department of Biochemistry, Imperial College of Science, Technology
and
Medicine, London SW7 2AZ, United
Kingdom.
Infection and Immunity, April 2000, p. 2016-2023, Vol. 68, No. 4
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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