First Author | Degrandi D | Year | 2013 |
Journal | Proc Natl Acad Sci U S A | Volume | 110 |
Issue | 1 | Pages | 294-9 |
PubMed ID | 23248289 | Mgi Jnum | J:192526 |
Mgi Id | MGI:5465342 | Doi | 10.1073/pnas.1205635110 |
Citation | Degrandi D, et al. (2013) Murine guanylate binding protein 2 (mGBP2) controls Toxoplasma gondii replication. Proc Natl Acad Sci U S A 110(1):294-9 |
abstractText | IFN-gamma orchestrates the host response against intracellular pathogens. Members of the guanylate binding proteins (GBP) comprise the most abundant IFN-gamma-induced transcriptional response. mGBPs are GTPases that are specifically up-regulated by IFN-gamma, other proinflammatory cytokines, toll-like receptor agonists, as well as in response to Listeria monocytogenes and Toxoplasma gondii infection. mGBP2 localizes at the parasitophorous vacuole (PV) of T. gondii; however, the molecular function of mGBP2 and its domains in T. gondii infection is not known. Here, we show that mGBP2 is highly expressed in several cell types, including T and B cells after stimulation. We provide evidence that the C-terminal domain is sufficient and essential for recruitment to the T. gondii PV. Functionally, mGBP2 reduces T. gondii proliferation because mGBP2-deficient cells display defects in the replication control of T. gondii. Ultimately, mGBP2-deficient mice reveal a marked immune susceptibility to T. gondii. Taken together, mGBP2 is an essential immune effector molecule mediating antiparasitic resistance. |