Vacuolar pathogens present interesting challenges to the host immune system. By residing in specialized organelles, they can evade canonical pathways used for innate immune detection and presentation of microbial antigens. To understand immunity to vacuolar pathogens that reside in unique vacuoles, we are using the respiratory pathogen Legionella pneumophila as a model organism to dissect early events that are important for immune detection. Legionella have an interesting intracellular lifestyle. They reside in a vacuole that initially avoids fusion with lysosomes, and then establish a vacuole derived from the host endoplasmic reticulum that supports bacterial replication. To further understand how mammalian hosts respond to vacuolar pathogens, we are using both Legionella mutants that have specific defects in host trafficking, and mutant mice that lack receptors that play a role in immunity to infection. The overall goal is to determine the function of pattern recognition receptors in the detection and clearance of Legionella pneumophila. Tlr signaling in response to Legionella will be investigated using in vivo and ex vivo assays. The role Nod protein family members play in Legionella detection will also be addressed. Emphasis will be placed on how Bircle-mediated responses restrict Legionella growth.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI048770-08
Application #
7344763
Study Section
Special Emphasis Panel (ZRG1-IDM-J (03))
Program Officer
Sawyer, Richard T
Project Start
2001-01-01
Project End
2011-01-31
Budget Start
2008-02-01
Budget End
2009-01-31
Support Year
8
Fiscal Year
2008
Total Cost
$389,356
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
Shames, Stephanie R; Liu, Luying; Havey, James C et al. (2017) Multiple Legionella pneumophila effector virulence phenotypes revealed through high-throughput analysis of targeted mutant libraries. Proc Natl Acad Sci U S A 114:E10446-E10454
Tørring, Thomas; Shames, Stephanie R; Cho, Wooyoung et al. (2017) Acyl Histidines: New N-Acyl Amides from Legionella pneumophila. Chembiochem 18:638-646
Abshire, Camille F; Dragoi, Ana-Maria; Roy, Craig R et al. (2016) MTOR-Driven Metabolic Reprogramming Regulates Legionella pneumophila Intracellular Niche Homeostasis. PLoS Pathog 12:e1006088
Marion, Chad R; Wang, Jianmiao; Sharma, Lokesh et al. (2016) Chitinase 3-Like 1 (Chil1) Regulates Survival and Macrophage-Mediated Interleukin-1? and Tumor Necrosis Factor Alpha during Pseudomonas aeruginosa Pneumonia. Infect Immun 84:2094-2104
Bradley, William P; Boyer, Mark A; Nguyen, Hieu T et al. (2016) Primary Role for Toll-Like Receptor-Driven Tumor Necrosis Factor Rather than Cytosolic Immune Detection in Restricting Coxiella burnetii Phase II Replication within Mouse Macrophages. Infect Immun 84:998-1015
Kohler, Lara J; Roy, Craig R (2015) Biogenesis of the lysosome-derived vacuole containing Coxiella burnetii. Microbes Infect 17:766-71
Copenhaver, Alan M; Casson, Cierra N; Nguyen, Hieu T et al. (2014) Alveolar macrophages and neutrophils are the primary reservoirs for Legionella pneumophila and mediate cytosolic surveillance of type IV secretion. Infect Immun 82:4325-36
Ivanov, Stanimir S; Roy, Craig R (2013) Pathogen signatures activate a ubiquitination pathway that modulates the function of the metabolic checkpoint kinase mTOR. Nat Immunol 14:1219-28
Sherwood, Racquel Kim; Roy, Craig R (2013) A Rab-centric perspective of bacterial pathogen-occupied vacuoles. Cell Host Microbe 14:256-68
Choy, Augustine; Roy, Craig R (2013) Autophagy and bacterial infection: an evolving arms race. Trends Microbiol 21:451-6

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