Shortly after invading host cells, Salmonella resides in vacuoles that fuse with lysosomes. This process is subsequently inhibited, allowing for bacterial survival and replication. Earlier work from the Andrews laboratory showed that permeabilization of the phagosome by the SPI1 type three secretion systems (TTSS) triggers fusion of lysosomes with Salmonella-containing vacuoles shortly after bacterial entry. This process is inhibited in synaptotagmin Vll-deficient macrophages, leading to more vigorous bacterial growth. Synaptotagmin VII, a calcium sensor molecule present on the membrane of lysosomes, interacts with the lysosomal SNARE molecule VAMP7 and facilitates lysosomal fusion. In this project we will test the hypothesis that Salmonella inhibits phagolysosomal fusion by translocating into the host cytosol effector molecules that inhibit the activity of Syt VII, VAMP7 and/or other host cell proteins that regulate phagosome-lysosome fusion.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32AI069785-03
Application #
7561625
Study Section
Special Emphasis Panel (ZRG1-F13-P (20))
Program Officer
Alexander, William A
Project Start
2007-03-01
Project End
2009-08-31
Budget Start
2009-03-01
Budget End
2009-08-31
Support Year
3
Fiscal Year
2009
Total Cost
$24,984
Indirect Cost
Name
Yale University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Idone, Vincent; Tam, Christina; Andrews, Norma W (2008) Two-way traffic on the road to plasma membrane repair. Trends Cell Biol 18:552-9