Infection with Helicobacter pylori causes a histological gastritis that in some individuals is associated with the development of peptic ulcer disease or gastric malignancy. H. pylori infection may be more common than infection with any other bacterial agent. Yet despite what must be repeated exposures, some individuals do not become infected. What accounts for the fact that some individuals become persistently infected while others remain uninfected, and perhaps still others have a transient infection? Presumably, bacterial as well as host variables are important. Because experimental infection of humans with H. pylori is not possible, the investigators propose to use the rhesus monkey as a model of H. pylori infection to address this question. They hypothesize that inoculation of human H. pylori in rhesus monkeys will result in diverse outcomes that will be associated with conditions of bacterial inoculation as well as host variables. A type strain of human H. pylori will be selected by in vitro characterization and in vivo passage through rhesus monkeys. The effects on infection of inoculum size, gastric acid suppression, and bacterial growth phase will be examined. Animals will be orogastrically inoculated with a standard dose of the type strain and acute and chronic infection will be studied. The outcome of infection will be determined by serial endoscopy, urea breath test, and examination of bacterial shedding in saliva and feces by culture and PCR. The host immune response will be assessed by immunophenotyping of gastric lymphocytes and peripheral blood mononuclear cells, immunohistochemistry of gastric mucosal inflammation, T cell proliferative responses from peripheral blood and gastric mucosa, and cytokine secretion by T cells. Gastric physiology will be examined by assay of serum gastrin levels and gastric basal acid output. The results will be compared in juvenile and adult animals. These studies will further understanding of the host-pathogen relationship in acute and chronic H. pylori infection.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI042081-04
Application #
6328757
Study Section
Bacteriology and Mycology Subcommittee 2 (BM)
Program Officer
Hamilton, Frank A
Project Start
1997-12-01
Project End
2002-11-30
Budget Start
2000-12-01
Budget End
2002-11-30
Support Year
4
Fiscal Year
2001
Total Cost
$340,120
Indirect Cost
Name
University of California Davis
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
094878337
City
Davis
State
CA
Country
United States
Zip Code
95618
Martin, Miriam E; Dieter, Jacquelyn A; Luo, Zheng et al. (2012) Predicting the outcome of infectious diseases: variability among inbred mice as a new and powerful tool for biomarker discovery. MBio 3:e00199-12
Ta, Linda H; Hansen, Lori M; Sause, William E et al. (2012) Conserved transcriptional unit organization of the cag pathogenicity island among Helicobacter pylori strains. Front Cell Infect Microbiol 2:46
Perry, Sharon; de Jong, Bouke C; Solnick, Jay V et al. (2010) Infection with Helicobacter pylori is associated with protection against tuberculosis. PLoS One 5:e8804
Styer, Cathy M; Hansen, Lori M; Cooke, Cara L et al. (2010) Expression of the BabA adhesin during experimental infection with Helicobacter pylori. Infect Immun 78:1593-600
Cooke, Cara L; An, Hyun Joo; Kim, Jaehan et al. (2009) Modification of gastric mucin oligosaccharide expression in rhesus macaques after infection with Helicobacter pylori. Gastroenterology 137:1061-71, 1071.e1-8
Axsen, Wendy S; Styer, Cathy M; Solnick, Jay V (2009) Inhibition of heat shock protein expression by Helicobacter pylori. Microb Pathog 47:231-6
Raffatellu, Manuela; George, Michael D; Akiyama, Yuko et al. (2009) Lipocalin-2 resistance confers an advantage to Salmonella enterica serotype Typhimurium for growth and survival in the inflamed intestine. Cell Host Microbe 5:476-86
Amundsen, Susan K; Fero, Jutta; Hansen, Lori M et al. (2008) Helicobacter pylori AddAB helicase-nuclease and RecA promote recombination-related DNA repair and survival during stomach colonization. Mol Microbiol 69:994-1007
Tsolis, Renee M; Young, Glenn M; Solnick, Jay V et al. (2008) From bench to bedside: stealth of enteroinvasive pathogens. Nat Rev Microbiol 6:883-92
Hornsby, Michael J; Huff, Jennifer L; Kays, Robert J et al. (2008) Helicobacter pylori induces an antimicrobial response in rhesus macaques in a cag pathogenicity island-dependent manner. Gastroenterology 134:1049-57

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