Type

Text

Type

Dissertation

Advisor

Bliska, James | Furie, Martha B | Kew, Richard | Thanassi, David G | Monga, Satdarshan.

Date

2013-12-01

Keywords

Cytokine, Francisella tularensis, Hepatocytes | Biology

Department

Department of Genetics.

Language

en_US

Source

This work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.

Identifier

http://hdl.handle.net/11401/77634

Publisher

The Graduate School, Stony Brook University: Stony Brook, NY.

Format

application/pdf

Abstract

ABSTRACT OF THE DISSERTATION Francisella tularensis: Interactions with Hepatocytes and Pathways for the Acquisition of Iron by Cindy A. Thomas-Charles Doctor of Philosophy in Genetics Stony Brook University 2013 Francisella tularensis is a Gram-negative, facultative intracellular bacterium and the causative agent of tularemia. Due to its high virulence, this organism has been classified as a Tier 1 select agent of bioterrorism. Regardless of the route of inoculation, the lungs, spleen, and liver are major targets of infection. Furthermore, this organism replicates to high numbers in hepatocytes, the predominant cells in the liver. Factors that mediate the uptake by and replication of F. tularensis in hepatocytic cell lines or primary mouse hepatocytes were investigated. F. tularensis was observed to be taken up by hepatocytes in a process that required polymerization of the hepatocyte actin cytoskeleton, but not the bacterial type I secretion system or type IV surface pili. Killed bacteria and bacteria rendered incapable of synthesizing protein were still ingested efficiently, suggesting involvement of a pre-formed bacterial surface structure in uptake. F. tularensis transposon mutants were subsequently screened for their ability to be taken up by or replicate in hepatocytes. Two mutants with decreased replicative capacity were identified. Additionally, primary mouse hepatocytes were used to determine the response of these host cells to infection with F. tularensis. Following infection, hepatocytes increased the expression of several genes encoding cytokines involved in inflammation. Furthermore, two potent chemotactic cytokines, CXCL1 and CXCL5, were secreted in increased amounts by infected hepatocytes. The ability to acquire extracellular iron is a key requirement for the replication of F. tularensis in hepatocytes. In some bacterial species, FeoB forms the core of the ferrous iron acquisition system. A mutant strain of F. tularensis lacking FeoB was used to investigate this protein's role in growth and virulence. Loss of FeoB diminished the growth of F. tularensis in medium with restrictive levels of iron and in hepatocytes and epithelial cells. The FeoB-deficient mutant was still capable of causing lethal disease in mice. However, its ability to colonize the liver, spleen, and lungs of mice was markedly impaired. These studies suggest that the interactions between F. tularensis and hepatocytes are important in the pathogenesis of tularemia. | 154 pages

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