| Literature DB >> 23541881 |
Michael J Brumlik1, Srilakshmi Pandeswara, Sara M Ludwig, Duane P Jeansonne, Michelle R Lacey, Kruthi Murthy, Benjamin J Daniel, Rong-Fu Wang, Suzanne R Thibodeaux, Kristina M Church, Vincent Hurez, Mark J Kious, Bin Zhang, Adebusola Alagbala, Xiaojun Xia, Tyler J Curiel.
Abstract
The parasite Toxoplasma gondii controls tissue-specific nitric oxide (NO), thereby augmenting virulence and immunopathology through poorly-understood mechanisms. We now identify TgMAPK1, a Toxoplasma mitogen-activated protein kinase (MAPK), as a virulence factor regulating tissue-specific parasite burden by manipulating host interferon (IFN)-γ-mediated inducible nitric oxide synthase (iNOS). Toxoplasma with reduced TgMAPK1 expression (TgMAPK1(lo)) demonstrated that TgMAPK1 facilitates IFN-γ-driven p38 MAPK activation, reducing IFN-γ-generated NO in an MKK3-dependent manner, blunting IFN-γ-mediated parasite control. TgMAPK1(lo) infection in wild type mice produced ≥ten-fold lower parasite burden versus control parasites with normal TgMAPK1 expression (TgMAPK1(con)). Reduced parasite burdens persisted in IFN-γ KO mice, but equalized in normally iNOS-replete organs from iNOS KO mice. Parasite MAPKs are far less studied than other parasite kinases, but deserve additional attention as targets for immunotherapy and drug discovery.Entities:
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Year: 2013 PMID: 23541881 PMCID: PMC4226171 DOI: 10.1016/j.exppara.2013.03.016
Source DB: PubMed Journal: Exp Parasitol ISSN: 0014-4894 Impact factor: 2.011