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
Research Project (R01)
Project #
5R01AI023538-13
Application #
2855937
Study Section
Bacteriology and Mycology Subcommittee 2 (BM)
Project Start
1986-06-01
Project End
1999-12-31
Budget Start
1999-01-01
Budget End
1999-12-31
Support Year
13
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Tufts University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02111
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Isberg, R R; Barnes, P (2001) Subversion of integrins by enteropathogenic Yersinia. J Cell Sci 114:21-28
Alrutz, M A; Srivastava, A; Wong, K W et al. (2001) Efficient uptake of Yersinia pseudotuberculosis via integrin receptors involves a Rac1-Arp 2/3 pathway that bypasses N-WASP function. Mol Microbiol 42:689-703
Dersch, P; Isberg, R R (2000) An immunoglobulin superfamily-like domain unique to the Yersinia pseudotuberculosis invasin protein is required for stimulation of bacterial uptake via integrin receptors. Infect Immun 68:2930-8
Isberg, R R; Hamburger, Z; Dersch, P (2000) Signaling and invasin-promoted uptake via integrin receptors. Microbes Infect 2:793-801
Krukonis, E S; Isberg, R R (2000) Integrin beta1-chain residues involved in substrate recognition and specificity of binding to invasin. Cell Microbiol 2:219-30
Dersch, P; Isberg, R R (1999) A region of the Yersinia pseudotuberculosis invasin protein enhances integrin-mediated uptake into mammalian cells and promotes self-association. EMBO J 18:1199-213
Alrutz, M A; Isberg, R R (1998) Involvement of focal adhesion kinase in invasin-mediated uptake. Proc Natl Acad Sci U S A 95:13658-63
Krukonis, E S; Dersch, P; Eble, J A et al. (1998) Differential effects of integrin alpha chain mutations on invasin and natural ligand interaction. J Biol Chem 273:31837-43
Krukonis, E S; Isberg, R R (1998) SWIM analysis allows rapid identification of residues involved in invasin-mediated bacterial uptake. Gene 211:109-16

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