Helicobacter pylori has been widely recognized as an important human pathog
en responsible for chronic gastritis, peptic ulcers, gastric cancer, and mu
cose-associated lymphoid tissue (MALT) lymphoma. Little is known about the
natural history of this infection since patients are usually recognized as
having the infection only after years or decades of chronic disease. Severa
l animal models of H. pylori infection, including those with different spec
ies of rodents, nonhuman primates, and germ-free animals, have been develop
ed. Here we describe a new animal model in,which the clinical, pathological
, microbiological, and immunological aspects of human acute and chronic inf
ection are mimicked and which allows us to monitor these aspects of infecti
on within the same individuals. Conventional Beagle dogs were infected oral
ly with a mouse-adapted strain of H. pylori and monitored for up to 24 week
s. Acute infection caused vomiting and diarrhea. The acute phase was follow
ed by polymorphonuclear cell infiltration, interleukin 8 induction, mononuc
lear cell recruitment, and the appearance of a specific antibody response a
gainst H. pylori. The chronic phase was characterized by gastritis, epithel
ial. alterations, superficial erosions, and the appearance of the typical m
acroscopic follicles that in humans are considered possible precursors of M
ALT lymphoma. In conclusion, infection in this model mimics closely human i
nfection and allows us to study those phases that cannot be studied in huma
ns. This new model can be a unique tool for learning more about the disease
and for developing strategies for treatment and prevention.