Type

Text

Type

Dissertation

Advisor

Benach, Jorge | Thanassi, David G. | van der Velden, Adrianus | Zong, Wei-Xing | Maurelli, Anthony.

Date

2014-12-01

Keywords

Microbiology | Apoptosis, Cell death, Francisella tularensis, LVS, Schu S4, TolC

Department

Department of Molecular Genetics and Microbiology.

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/11401/76542

Publisher

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

Format

application/pdf

Abstract

Francisella tularensis is a Gram-negative, facultative intracellular pathogen and the causative agent of tularemia. F. tularensis is a Tier 1 agent of bioterrorism that is highly lethal via the pulmonary route of infection. F. tularensis invades host cells, escapes the phagosome, and replicates in the cytosol prior to being released upon host cell death. The molecular mechanisms behind the virulence of F. tularensis are largely unknown. Among the described virulence factors of F. tularensis is a functional type I secretion system (T1SS). The T1SS is important for the secretion of virulence factors from the bacterial cytoplasm to the extracellular environment. The F. tularensis T1SS consists of a periplasm-spanning outer membrane protein, TolC, which interacts with inner membrane adapter and transport proteins to form a contiguous channel. TolC has been shown to be important for the virulence of multiple F. tularensis subspecies. Infection of host cells with a F. tularensis live vaccine strain (LVS) ∆ tolC mutant leads to increased caspase-3 activation and host cell death compared to cells infected with the wildtype LVS. The LVS Δ tolC mutant also elicits increased secretion of proinflammatory cytokines from infected cells when compared to cells infected with the wildtype LVS. The work described here investigates the temporal induction of host cell apoptosis during LVS infection and the role that TolC plays in modulating this process. I show that the LVS delays activation of the intrinsic apoptotic pathway to allow for bacterial replication during infection and that TolC is necessary for this inhibition. Chromosomal deletion of tolC in the highly virulent, human pathogenic Schu S4 strain showed that TolC is necessary for virulence and inhibiting cell death during infection, demonstrating that TolC function is conserved across F. tularensis subspecies. Finally, I investigated the efficacy of the LVS ∆ tolC mutant strain as a live vaccine against tularemia. My results suggest that the ∆ tolC mutant strain may be a safer, more effective tularemia vaccine compared to the parental LVS. Taken together, my work characterizes the role of TolC as a major F. tularensis virulence factor aimed at suppressing innate immune responses during infection. | 139 pages

Share

COinS
 
 

To view the content in your browser, please download Adobe Reader or, alternately,
you may Download the file to your hard drive.

NOTE: The latest versions of Adobe Reader do not support viewing PDF files within Firefox on Mac OS and if you are using a modern (Intel) Mac, there is no official plugin for viewing PDF files within the browser window.