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L-asparaginase II produced by Salmonella typhimurium inhibits T cell responses and mediates virulence.


ABSTRACT: Salmonella enterica serovar Typhimurium avoids clearance by the host immune system by suppressing T cell responses; however, the mechanisms that mediate this immunosuppression remain 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 downmodulate expression of the T cell receptor. 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 deprivation to limit T cell responses.

SUBMITTER: Kullas AL 

PROVIDER: S-EPMC4361029 | biostudies-literature | 2012 Dec

REPOSITORIES: biostudies-literature

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L-asparaginase II produced by Salmonella typhimurium inhibits T cell responses and mediates virulence.

Kullas Amy L AL   McClelland Michael M   Yang Hee-Jeong HJ   Tam Jason W JW   Torres AnnMarie A   Porwollik Steffen S   Mena Patricio P   McPhee Joseph B JB   Bogomolnaya Lydia L   Andrews-Polymenis Helene H   van der Velden Adrianus W M AW  

Cell host & microbe 20121201 6


Salmonella enterica serovar Typhimurium avoids clearance by the host immune system by suppressing T cell responses; however, the mechanisms that mediate this immunosuppression remain 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 downmodulate express  ...[more]

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