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Infection and Immunity, October 1998, p. 4856-4866, Vol. 66, No. 10
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Experimental Infection of Mongolian Gerbils with
Wild-Type and Mutant Helicobacter pylori Strains
Hans-Peter
Wirth,1,2
Michael H.
Beins,1
Manqiao
Yang,1,2
Kyi T.
Tham,3,4 and
Martin J.
Blaser1,4,*
Division of Infectious Diseases, Department
of Medicine,1 and
Department of
Pathology,3 Vanderbilt University School of
Medicine, and
Department of Veterans Affairs Medical
Center,4 Nashville, Tennessee, and
Division of Gastroenterology, University Hospital, Zurich,
Switzerland2
Received 5 March 1998/Returned for modification 22 June
1998/Accepted 22 July 1998
Experimental Helicobacter pylori infection was studied
in Mongolian gerbils with fresh human isolates that carry or do not carry cagA (cagA-positive or
cagA-negative, respectively), multiply passaged laboratory
strains, wild-type strain G1.1, or isogenic ureA,
cagA, or vacA mutants of G1.1. Animals were
sacrificed 1 to 32 weeks after challenge, the stomach was removed from
each animal for quantitative culture, urease test, and histologic
testing, and blood was collected for antibody determinations. No
colonization occurred after
20 in vitro passages of wild-type strain
G1.1 or with the ureA mutant of G1.1. In contrast,
infection occurred in animals challenged with wild-type G1.1 (99 of 101 animals) or the cagA (25 of 25) or vacA (25 of
29) mutant of G1.1. Infection with G1.1 persisted for at least 8 months. All 15 animals challenged with any of three fresh human
cagA-positive isolates became infected, in contrast to only
6 (23%) of 26 animals challenged with one of four fresh human
cagA-negative isolates (P < 0.001).
Similar to infection in humans, H. pylori colonization of
gerbils induced gastric inflammation and a systemic antibody response
to H. pylori antigens. These data confirm the utility of
gerbils as an animal model of H. pylori infection and
indicate the importance of bacterial strain characteristics for
successful infection.
*
Corresponding author. Mailing address: Vanderbilt
University School of Medicine, A-3310 Medical Center North, Nashville,
TN 37232-2605. Phone: (615) 322-2035. Fax: (615) 343-6160. E-mail: Martin.Blaser{at}mcmail.vanderbilt.edu.
Infection and Immunity, October 1998, p. 4856-4866, Vol. 66, No. 10
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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