Francisella tularensis (Ft), a Gram negative intracellular bacterium, the etiologic agent of tularemia, and is classified as a Category A agent because it can contracted with low inocula by the respiratory route and causes rapid morbidity and mortality if untreated. While attenuated for humans, mice infected i.n. or i.p. with Ft Live Vaccine Strain (LVS), a type B strain, contract a tularemia-like disease. In this grant cycle, we reported that Ft LVS induces in mice a potent inflammatory response in vivo and in vitro. Using Ft LVS mutants that fail to escape from the phagosome or fail to replicate intracellularly in murine macrophages, we identified the signaling pathways by the host innate immune system is activated. Ft LVS induces TLR2- mediated signaling;however, once Ft escapes from the phagosome into the cytosol, IFN-J3 is produced and reutilized, and the inflammasome activated. Despite this robust inflammatory response, the host succumbs to infection. Our data indicate that Ft LVS initiates a strong inflammatory response leading to development of "classically activated" macrophages (CA-M0);however, once IL-4 and IL-13 are induced by infected macrophages, they differentiate into "alternatively activated" (AA-M0), thereby facilitating intracellular replication. Ft LVS-infected IL-4Ra~'~ and STAT6"'" macrophages fail to differentiate into AA-M0 and control intracellular replication, while Ft LVS-infected macrophages treated with rIFN-p restrict bacterial growth. Ft LVS lipopolysaccharide (LPS), a poor TLR4 agonist, fails to induce an inflammatory response. However, when mice are vaccinated with Ft LVS LPS 2 days prior to lethal i.p. challenge, a protective anti-LPS antibody response is induced by splenic B-1a cells. We will now seek novel ways to control respiratory infection with Ft LVS and Schu S4, a virulent type A strain, by testing the hypotheses that (1) Schu S4, like Ft LVS, drives AA-M0 to evade host responses;(2) agents that interfere with development ofAA-M0 will increase the anti-microbial response in vivo;and, (3) increasing the immunogenicity of a Ft LVS LPS vaccine will protect mice against respiratory and systemic challenge with Ft LVS and Schu S4. The main objective of this proposal is to develop novel therapies for tularemia based on interfering with development of AA-M0, as well as improve development of a safe vaccine(s) that protects against both type A and B strains.

Public Health Relevance

F. tularensis (Ft) is a bacterial pathogen that replicates intracellularly in macrophages. It is classified as a Category A agent based on its ease of aerosolization, low infectious dose, and rapid onset of debilitating disease. By understanding the interplay between the innate and adaptive immune response to Ft, we may be able to identify mechanisms whereby the host response to this agent can be manipulated, allowing more time for intervention with antibiotics and the host's own adaptive immune response to control the pathogen.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54AI057168-10
Application #
8442359
Study Section
Special Emphasis Panel (ZAI1-DDS-M)
Project Start
Project End
2015-02-28
Budget Start
2013-03-01
Budget End
2015-02-28
Support Year
10
Fiscal Year
2013
Total Cost
$217,586
Indirect Cost
$26,417
Name
University of Maryland Baltimore
Department
Type
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
Freedman, John C; Theoret, James R; Wisniewski, Jessica A et al. (2015) Clostridium perfringens type A-E toxin plasmids. Res Microbiol 166:264-79
Li, Jihong; McClane, Bruce A (2014) Contributions of NanI sialidase to Caco-2 cell adherence by Clostridium perfringens type A and C strains causing human intestinal disease. Infect Immun 82:4620-30
Moy, Ryan H; Gold, Beth; Molleston, Jerome M et al. (2014) Antiviral autophagy restrictsRift Valley fever virus infection and is conserved from flies to mammals. Immunity 40:51-65
Cuevas, Christian D; Ross, Susan R (2014) Toll-like receptor 2-mediated innate immune responses against Junín virus in mice lead to antiviral adaptive immune responses during systemic infection and do not affect viral replication in the brain. J Virol 88:7703-14
Boyd, Mary Adetinuke; Tennant, Sharon M; Saague, Venant A et al. (2014) Serum bactericidal assays to evaluate typhoidal and nontyphoidal Salmonella vaccines. Clin Vaccine Immunol 21:712-21
Su, Yi-Hsuan; Tsegaye, Mikiyas; Varhue, Walter et al. (2014) Quantitative dielectrophoretic tracking for characterization and separation of persistent subpopulations of Cryptosporidium parvum. Analyst 139:66-73
Xu, Jie; Cherry, Sara (2014) Viruses and antiviral immunity in Drosophila. Dev Comp Immunol 42:67-84
Uzal, Francisco A; Freedman, John C; Shrestha, Archana et al. (2014) Towards an understanding of the role of Clostridium perfringens toxins in human and animal disease. Future Microbiol 9:361-77
Weir, Dawn L; Laing, Eric D; Smith, Ina L et al. (2014) Host cell virus entry mediated by Australian bat lyssavirus G envelope glycoprotein occurs through a clathrin-mediated endocytic pathway that requires actin and Rab5. Virol J 11:40
Weir, Dawn L; Annand, Edward J; Reid, Peter A et al. (2014) Recent observations on Australian bat lyssavirus tropism and viral entry. Viruses 6:909-26

Showing the most recent 10 out of 299 publications