Enteropathogenic Escherichia coli (EPEC) strains are a leading cause of severe diarrhea worldwide. These strains use a type III secretion system (T3SS) to inject proteins into host cells, produce the attaching effacing effect, initiate the mitochondrial death pathway, and disrupt intestinal barrier function. Prior work has led to the discovery of the EspADB protein translocation apparatus and the EspF effector protein. With the overall goal of better understanding the mechanisms of EPEC pathogenesis, this proposal has four specific aims. (1) to determine the role of Abcf2 in EspF-induced apoptosis. The host Abcf2 protein is a target of EspF. Experiments will be conducted to test the hypothesis that Abcf2 is an anti-apoptotic protein that is degraded directly or indirectly by EspF. An abcf2 knockout mouse model will be used to study the effects of Abcf2 on apoptosis in tissue culture and in vivo. (2) to determine the role of EspF in alterations in barrier function. The evidence suggests that EspF is a bifunctional protein with separate effects on apoptosis that depend on mitochondrial targeting and on tight junctions that are independent of mitochondrial targeting. The role of Abcf2 in EspF mediated disruption of barrier function will be determined and alternative pathways that lead to this effect will be identified. (3) to define interactions among translocon components EspA, EspD and EspB. The prevailing model of the EPEC translocon proposes that the EspD and EspB proteins form a complex at the tip of the EspA filament that forms a pore in the host membrane through which effector molecules pass. Purified functional proteins will be used to test whether EspB and EspD form a complex and whether this complex is located at the tip of the EspA filament. (4) to determine the roles of EspB and EspD pore formation and in translocation of effector proteins through the pore. The abiity of purified proteins to form pores will be tested. The identification of a recessive espB allele that results in normal hemolytic activity but no effector translocation suggests a role for EspB in translocation that is separate from its role in pore formation. Whether this phenotype is due to a defect in connecting to the EspA filament or to a defect in assisting effector proteins to translocate the host membrane will be determined. The significance of this work is that it will lead to a better understanding of how bacteria inject proteins into host cells and interfere with pathways that protect the cells from death and maintain barrier function. E. coli strains are a leading cause of severe diarrhea worldwide. Some of these strains inject proteins into host cells, resulting in cell death and disrupting intestinal barrier function. By studying the specific proteins involved in these processes the work outlined in this proposal will lead to a better understanding of how bacteria inject proteins into host cells and interfere with pathways that protect the cells from death and maintain barrier function.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI032074-20
Application #
8249091
Study Section
Bacterial Pathogenesis Study Section (BACP)
Program Officer
Baqar, Shahida
Project Start
1992-02-01
Project End
2013-06-28
Budget Start
2012-03-01
Budget End
2013-06-28
Support Year
20
Fiscal Year
2012
Total Cost
$367,538
Indirect Cost
$122,513
Name
University of Maryland Baltimore
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
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