Francisella tularensis can cause serious illness and death in humans. F. tularensis is considered to be one of the most likely bioweapons due to ease of dissemination through aerosolization, and the high morbidity and mortality associated with inhalation tularemia. There is currently no tularemia vaccine licensed for general use, and thus human populations are at significant risk from the illicit use of F. tularensis. Very little is known about F. tularensis pathogenesis and host response, and thus fundamental research into F. tularensis biology is critical for the future development of therapeutics and vaccines against tularemia. We have assembled a group of integrated research projects focused on Francisella pathogenesis and immunity from researchers at the University of Texas San Antonio and the University of Texas Health Science Center in San Antonio. The individual projects are designed to be highly integrated with the other projects, and ultimately lead to a synergy that will propel our knowledge of this potential bioweapon such that new antimicrobial strategies can be developed. Virtually nothing is known about aerosol infections of F. tularensis subsp. tularensis (Type A), the most likely bioweapon form of tularemia, and thus this program project focuses almost exclusively on this form of tularemia. Our integrated bacteriological and immunological research approach involves four research projects and three support cores. These projects are designed to 1. identify essential and virulence factors of F. tularensis, 2. detail the immunology of inhalation tularemia in situ, 3. characterize the role of Toll-like receptors in host response, and 4. identify T cell epitopes and characterize T cell mediated responses to F. tularensis. These projects will be supported by an administrative core, a genomics core, and an immunomicroscopy core. The collaborative interactions of the investigators will ultimately lead to a dramatic increase in our understanding of pathogen-host interactions during F. tularensis subsp. tularensis aerosol infections, and facilitate the development of novel therapeutics and vaccines to combat weaponized tularemia.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI057986-04
Application #
7458689
Study Section
Special Emphasis Panel (ZAI1-EC-M (J1))
Program Officer
Mukhopadhyay, Suman
Project Start
2005-07-08
Project End
2010-06-30
Budget Start
2008-07-01
Budget End
2009-06-30
Support Year
4
Fiscal Year
2008
Total Cost
$1,165,484
Indirect Cost
Name
University of Texas Health Science Center San Antonio
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
800189185
City
San Antonio
State
TX
Country
United States
Zip Code
78249
Nguyen, Jesse Q; Gilley, Ryan P; Zogaj, Xhavit et al. (2014) Lipidation of the FPI protein IglE contributes to Francisella tularensis ssp. novicida intramacrophage replication and virulence. Pathog Dis 72:10-8
Chu, Ping; Cunningham, Aimee L; Yu, Jieh-Juen et al. (2014) Live attenuated Francisella novicida vaccine protects against Francisella tularensis pulmonary challenge in rats and non-human primates. PLoS Pathog 10:e1004439
Tsai, Su-Yu; Segovia, Jesus A; Chang, Te-Hung et al. (2014) DAMP molecule S100A9 acts as a molecular pattern to enhance inflammation during influenza A virus infection: role of DDX21-TRIF-TLR4-MyD88 pathway. PLoS Pathog 10:e1003848
Signarovitz, Aimee L; Ray, Heather J; Yu, Jieh-Juen et al. (2012) Mucosal immunization with live attenuated Francisella novicida U112ýýiglB protects against pulmonary F. tularensis SCHU S4 in the Fischer 344 rat model. PLoS One 7:e47639
Arulanandam, Bernard P; Chetty, Senthilnath Lakshmana; Yu, Jieh-Juen et al. (2012) Francisella DnaK inhibits tissue-nonspecific alkaline phosphatase. J Biol Chem 287:37185-94
Hunter, Colleen; Rodriguez, Annette; Yu, Jieh-Juen et al. (2012) Comparison of bone marrow-derived and mucosal mast cells in controlling intramacrophage Francisella tularensis replication. Exp Biol Med (Maywood) 237:617-21
Segovia, Jesus; Sabbah, Ahmed; Mgbemena, Victoria et al. (2012) TLR2/MyD88/NF-?B pathway, reactive oxygen species, potassium efflux activates NLRP3/ASC inflammasome during respiratory syncytial virus infection. PLoS One 7:e29695
Zogaj, Xhavit; Wyatt, Geoff C; Klose, Karl E (2012) Cyclic di-GMP stimulates biofilm formation and inhibits virulence of Francisella novicida. Infect Immun 80:4239-47
Rodriguez, Annette R; Yu, Jieh-Juen; Guentzel, M Neal et al. (2012) Mast cell TLR2 signaling is crucial for effective killing of Francisella tularensis. J Immunol 188:5604-11
Sanapala, Shilpa; Yu, Jieh-Juen; Murthy, Ashlesh K et al. (2012) Perforin- and granzyme-mediated cytotoxic effector functions are essential for protection against Francisella tularensis following vaccination by the defined F. tularensis subsp. novicida ýýfopC vaccine strain. Infect Immun 80:2177-85

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