The candidate is presently a resident in the Pathology Department at the Massachusetts General Hospital and has a strong research and clinical interest in bacterial pathogens. He spent two years at the National Institutes of Health learning bacterial genetics, and in elective time this year, is studying Listeria and Salmonella pathogenesis at the Whitehead Institute. The candidate's career development plan will be under the mentorship of Ralph Isberg, Ph.D., in the Molecular Biology and Microbiology Department at Tufts University School of Medicine. This department has a strong microbial pathogenesis group and has extensive interactions with the Infectious Disease Department at New England Medical Center. The candidate's immediate career goal is to acquire skills necessary for independent study of pathogen host interactions. During his career development plan, he will, therefore, take course work to expand his knowledge of bacterial pathogenesis and related disciplines of cell biology and immunology. In the research project, he will study virulence mechanisms of Leqionella pneumophila, a cause of severe pneumonia and a model for pathogens that survive and replicate inside phagocytic vacuoles. An animal model will be used to identify virulence mutants that fail to survive during the course of infection. Assays of the host immune response and bacterial survival during infection will be used to rapidly categorize virulence mutants and plan further experiments to define virulence gene function. The candidate's long term career goal is to become an independent bacterial pathogenesis researcher associated with an academic pathology department.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Clinical Investigator Award (CIA) (K08)
Project #
7K08AI001402-05
Application #
6127083
Study Section
Microbiology and Infectious Diseases B Subcommittee (MID)
Program Officer
Heyse, Stephen P
Project Start
1996-07-01
Project End
2001-06-30
Budget Start
1999-08-01
Budget End
2000-06-30
Support Year
5
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Beth Israel Deaconess Medical Center
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
02215
Kirby, James E; Nekorchuk, Dawn M (2002) Bartonella-associated endothelial proliferation depends on inhibition of apoptosis. Proc Natl Acad Sci U S A 99:4656-61
Watarai, M; Derre, I; Kirby, J et al. (2001) Legionella pneumophila is internalized by a macropinocytotic uptake pathway controlled by the Dot/Icm system and the mouse Lgn1 locus. J Exp Med 194:1081-96
Kirby, J E; Vogel, J P; Andrews, H L et al. (1998) Evidence for pore-forming ability by Legionella pneumophila. Mol Microbiol 27:323-36
Kirby, J E; Isberg, R R (1998) Legionnaires' disease: the pore macrophage and the legion of terror within. Trends Microbiol 6:256-8