Persistent colonization of the human stomach with the Gram-negative bacterium Helicobacter pylori is associated with an increased risk for development of gastric adenocarcinoma and peptic ulcer disease. The long-term objective of this project is to understand the molecular mechanisms by which H. pylori contributes to these diseases, and to develop effective means for the prevention and treatment of these diseases. An important virulence factor produced by H. pylori is a secreted toxin known as VacA. Studies in a mouse model indicate that VacA enhances the capacity of H. pylonto colonize the stomach and that it can cause gastric epithelial damage. Analyses of vacA allelic variation in H. pylori isolates from humans suggest that VacA plays a role in the pathogenesis of gastric cancer and peptic ulcer disease. In vitro studies indicate that VacA is a multifunctional toxin. VacA causes multiple alterations in human gastric epithelial cells, including swelling of endosomal compartments (cell vacuolation) and changes in mitochondria! function. In addition to its effects on epithelial cells, VacA inhibits activation and proliferation of T lymphocytes. A current model proposes that VacA intoxicates gastric epithelial cells through a multi- step process, which includes binding of the toxin to the plasma membrane, oligomerization, membrane insertion, membrane channel formation, internalization, intracellular trafficking, and localization in specific intracellular sites. The central hypotheses of the current proposal are that VacA has unique structural features, and that actions required for individual steps in the intoxication process can be mapped to different regions of the VacA protein.
In Aim #1 of this proposal, we will analyze the crystal structure of VacA.
In Aim #2 we will map regions of VacA that have specific functional activities.
In Aim #3, we will analyze the role of VacA in H. pylori colonization of the stomach. These studies should lead to important advances in our understanding of the biology of H. pylori- host interactions, and should ultimately lead to advances in the treatment and prevention of H. py/or/-associated human diseases. Relevance to public health: The presence of a bacterium known as Helicobacter pylori in the human stomach contributes to the development of cancer of the stomach and peptic ulcer disease. This research seeks to understand how a bacterial infection can lead to these diseases, and seeks to develop new approaches for the prevention and therapy of stomach cancer and peptic ulcer disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI039657-15
Application #
7989988
Study Section
Bacterial Pathogenesis Study Section (BACP)
Program Officer
Mills, Melody
Project Start
1996-05-01
Project End
2012-04-30
Budget Start
2010-12-01
Budget End
2012-04-30
Support Year
15
Fiscal Year
2011
Total Cost
$339,268
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Snider, Christina A; Voss, Bradley J; McDonald, W Hayes et al. (2016) Growth phase-dependent composition of the Helicobacter pylori exoproteome. J Proteomics 130:94-107
Cover, Timothy L (2016) Helicobacter pylori Diversity and Gastric Cancer Risk. MBio 7:e01869-15
Pyburn, Tasia M; Foegeding, Nora J; González-Rivera, Christian et al. (2016) Structural organization of membrane-inserted hexamers formed by Helicobacter pylori VacA toxin. Mol Microbiol 102:22-36
Shaffer, Carrie L; Good, James A D; Kumar, Santosh et al. (2016) Peptidomimetic Small Molecules Disrupt Type IV Secretion System Activity in Diverse Bacterial Pathogens. MBio 7:e00221-16
Frick-Cheng, Arwen E; Pyburn, Tasia M; Voss, Bradley J et al. (2016) Molecular and Structural Analysis of the Helicobacter pylori cag Type IV Secretion System Core Complex. MBio 7:e02001-15
Foegeding, Nora J; Caston, Rhonda R; McClain, Mark S et al. (2016) An Overview of Helicobacter pylori VacA Toxin Biology. Toxins (Basel) 8:
Beckett, Amber C; Piazuelo, M Blanca; Noto, Jennifer M et al. (2016) Dietary Composition Influences Incidence of Helicobacter pylori-Induced Iron Deficiency Anemia and Gastric Ulceration. Infect Immun 84:3338-3349
González-Rivera, Christian; Campbell, Anne M; Rutherford, Stacey A et al. (2016) A Nonoligomerizing Mutant Form of Helicobacter pylori VacA Allows Structural Analysis of the p33 Domain. Infect Immun 84:2662-70
Snider, Christina A; Voss, Bradley J; McDonald, W Hayes et al. (2015) Supporting data for analysis of the Helicobacter pylori exoproteome. Data Brief 5:560-3
Voss, Bradley J; Loh, John T; Hill, Salisha et al. (2015) Alteration of the Helicobacter pylori membrane proteome in response to changes in environmental salt concentration. Proteomics Clin Appl 9:1021-34

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