The long-term? objective of these studies are to determine how an enteropathogenic? bacterium is able to enter within host cells and to evaluate the role? of mammalian cell receptors in promoting uptake. As a model system,? Yersinia pseudotuberculosis is being studied in order to gain detailed? information on the function of bacterial- and host-encoded? internalization factors. Specifically, Y. pseudotuberculosis invasin-? integrin interaction will be studied, and host-encoded factors that? modulate receptor-mediated bacterial internalization will be identified.? Uptake promoted by invasin depends upon high affinity binding to its? receptors, regulated by the concentration of receptor available to? participate in uptake. To further investigate the molecular mechanism? of uptake, the following experiments will be performed: 1) A model for? the binding of a single invasin molecule to multiple host receptors will? be tested, by analyzing the subunit structure of invasin and determining? the stoichiometry of invasin-receptor interaction; 2) the region of the? integrin heterodimer involved in invasin binding will be determined by? performing two novel mutant selection for altered receptor interaction;? 3)the role in bacterial uptake of the beta-1 integrin will be? investigated by analyzing the binding of mammalian cell cytoplasmic? components to hybrid protein harboring this domain; 4) functional? studies on the role of mammalian cytoplasmic components will be? performed using a newly-developed perforated cell assay, allowing? evaluation of the biological roles of factors identified in other Aims;? and5) the role of invasin in intestinal infections will be analyzed,? using invasin mutations resulting in partially functional proteins.? Bacterial uptake by host cells is a common step in establishing disease? by a number of bacterial pathogens. Investigation of this process will? result in important information on how enteric diseases are initiated,? and provide a potential source for the development of new chemotherapies? that block this step in the infection process. In addition,? identification of the components that allow a simple organism to enter? an animal cell could result in new techniques to introduce therapeutic? agents that would otherwise not be able to enter the host cell.?

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37AI023538-21
Application #
7234074
Study Section
Special Emphasis Panel (NSS)
Program Officer
Alexander, William A
Project Start
1986-06-01
Project End
2010-05-31
Budget Start
2007-06-01
Budget End
2008-05-31
Support Year
21
Fiscal Year
2007
Total Cost
$348,811
Indirect Cost
Name
Tufts University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
039318308
City
Boston
State
MA
Country
United States
Zip Code
02111
Mohammadi, Sina; Isberg, Ralph R (2013) Cdc42 interacts with the exocyst complex to promote phagocytosis. J Cell Biol 200:81-93
De Jesús, Dennise A; O'Connor, Tamara J; Isberg, Ralph R (2013) Analysis of Legionella infection using RNAi in Drosophila cells. Methods Mol Biol 954:251-64
Crimmins, Gregory T; Isberg, Ralph R (2012) Analyzing microbial disease at high resolution: following the fate of the bacterium during infection. Curr Opin Microbiol 15:23-7
Rajagopal, Soumitra; Ji, Yuxin; Xu, Kun et al. (2010) Scaffold proteins IRSp53 and spinophilin regulate localized Rac activation by T-lymphocyte invasion and metastasis protein 1 (TIAM1). J Biol Chem 285:18060-71
Mohammadi, Sina; Isberg, Ralph R (2009) Yersinia pseudotuberculosis virulence determinants invasin, YopE, and YopT modulate RhoG activity and localization. Infect Immun 77:4771-82
Auerbuch, Victoria; Golenbock, Douglas T; Isberg, Ralph R (2009) Innate immune recognition of Yersinia pseudotuberculosis type III secretion. PLoS Pathog 5:e1000686
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Conover, Gloria M; Martinez-Morales, Fernando; Heidtman, Matthew I et al. (2008) Phosphatidylcholine synthesis is required for optimal function of Legionella pneumophila virulence determinants. Cell Microbiol 10:514-28

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