Francisella tularensis is an extremely virulent Gram negative bacterial pathogen capable of causing rapidly progressing lethal infections in literally hundreds of diverse animal species, including humans. Transmission from infected animals to humans occurs via multiple routes including direct contact, arthropod vectors, ingestion and inhalation. The lowest infective dose, fastest disease progression, and highest mortality rates are associated with inhalation acquired infections. F. tularensis invades (or enters) and replicates within many different host cell types, including macrophages, dendritic cells, neutrophils and at least some epithelial cell types. Following entry the bacteria escape the phagosome and replicate within the cytoplasm of the host cell. We have identified a cytoplasmic membrane protein, RipA, that is conserved among pathogenic Francisella species. Mutants lacking RipA escape the phagosome, but fail to replicate once in the cytoplasm. Gene expression patterns in DripA mutants differ from wild type organisms. Herein we present data demonstrating that the RipA protein associates with a transcriptional regulator, IclR, and IclR regulates a restricted number of genes, most notably an operon containing a response regulator, pmrA, that is required for F. tularensis intracellular growth and pathogenesis.
Three aims are proposed to characterize RipA and discern its function in host cell adaptation, to determine the role of IclR in modulating the expression of virulence associated genes, and to examine the contribution of three RipA - associated genes to F. tularensis virulence and pathogenesis.

Public Health Relevance

We are focused on understanding the bacterial properties of Francisella tularensis that make this organism such a highly virulent pathogen for humans, particularly with respect to pulmonary disease. In this proposal we will study the biological properties of a limited number of cellular components that are unique to Francisella and determine their contribution to Francisella virulence and pathogenesis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56AI082870-01
Application #
7822429
Study Section
Special Emphasis Panel (ZRG1-IDM-Q (03))
Program Officer
Mukhopadhyay, Suman
Project Start
2009-05-22
Project End
2011-04-30
Budget Start
2009-05-22
Budget End
2011-04-30
Support Year
1
Fiscal Year
2009
Total Cost
$363,985
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Steele, Shaun; Radlinski, Lauren; Taft-Benz, Sharon et al. (2016) Trogocytosis-associated cell to cell spread of intracellular bacterial pathogens. Elife 5:
Brunton, J; Steele, S; Miller, C et al. (2015) Identifying Francisella tularensis genes required for growth in host cells. Infect Immun 83:3015-25
LoVullo, Eric D; Miller, Cheryl N; Pavelka Jr, Martin S et al. (2012) TetR-based gene regulation systems for Francisella tularensis. Appl Environ Microbiol 78:6883-9