Type

Text

Type

Dissertation

Advisor

Bliska, James B | van der Velden, Adrianus WM, Furie, Martha B | Thanassi, David G | Mantis, Nicholas J.

Date

2012-12-01

Keywords

Microbiology | L-asparaginase II, Salmonella, T cell inhibition

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/11401/71532

Publisher

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

Format

application/pdf

Abstract

Bacterial pathogens must avoid clearance by the immune system to establish infection, yet many processes of bacterial immune subversion remain undefined. T cells are a key component of the mammalian immune system and are required for protective immunity against many bacterial pathogens. Salmonella enterica serovar Typhimurium avoid clearance by the host immune system by suppressing T cell responses, yet the mechanisms mediating this immunosuppression are still unknown. We show that S. Typhimurium inhibit T cell responses by producing L-asparaginase II, which catalyzes the hydrolysis of L-asparagine to aspartic acid and ammonia. L-asparaginase II is necessary and sufficient to suppress T cell blastogenesis, cytokine production and proliferation, and to down-modulate expression of the T cell receptor (TCR). Purified L-asparaginase II alters TCR levels and cytokine profiles of T cells in vitro. Furthermore, S. Typhimurium-induced inhibition of T cells in vitro is prevented upon addition of L-asparagine. S. Typhimurium lacking the L-asparaginase II gene (STM3106) are unable to inhibit T cell responses and exhibit attenuated virulence in vivo. L-asparaginases are used to treat acute lymphoblastic leukemia through mechanisms that likely involve amino acid starvation of leukemic cells and these findings indicate that pathogens similarly use L-asparagine depravation to limit T cell responses. | 160 pages

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