Determinants of GBP recruitment to Toxoplasma gondii vacuoles and the parasitic factors that control it

• Published in: PloS one 2011-09, Vol.6 (9), p.e24434-e24434
• Main Authors: Virreira Winter, Sebastian, Niedelman, Wendy, Jensen, Kirk D, Rosowski, Emily E, Julien, Lindsay, Spooner, Eric, Caradonna, Kacey, Burleigh, Barbara A, Saeij, Jeroen P J, Ploegh, Hidde L, Frickel, Eva-Maria
• Format: Article
• Language: English
• Subjects: Aluminum; Animals; Antigen presentation; Antigens, Protozoan - metabolism; Binding; Binding proteins; Binding sites; Biology; Biomedical research; Borides; Cytokines; Fibroblasts - cytology; Gene Expression Regulation; Genomes; GTP-Binding Proteins - metabolism; GTP-Binding Proteins - physiology; Guanosine Triphosphate - metabolism; Health aspects; Hit & run accidents; Humans; Immune response; Immune system; Immunology; Immunoprecipitation; Infection; Infections; Infectious diseases; Interferon; Interferon-gamma - metabolism; Kinases; Localization; Mediation; Medical research; Medicine; Mice; Mice, Inbred C57BL; Mutagenesis; Mutation; Parasites; Parasitophorous vacuole; Phagosomes; Phagosomes - metabolism; Polymorphism, Genetic; Protein Binding; Protein-Serine-Threonine Kinases - metabolism; Protein-Tyrosine Kinases - metabolism; Proteins; Protozoa; Protozoan Proteins - metabolism; Public health; Recruitment; Rodents; Toxoplasma - metabolism; Toxoplasma gondii; Vacuoles; Vacuoles - metabolism; Vacuoles - parasitology; Virulence; Virulence (Microbiology); Virulence factors; γ-Interferon
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0024434

IFN-γ is a major cytokine that mediates resistance against the intracellular parasite Toxoplasma gondii. The p65 guanylate-binding proteins (GBPs) are strongly induced by IFN-γ. We studied the behavior of murine GBP1 (mGBP1) upon infection with T. gondii in vitro and confirmed that IFN-γ-dependent re-localization of mGBP1 to the parasitophorous vacuole (PV) correlates with the virulence type of the parasite. We identified three parasitic factors, ROP16, ROP18, and GRA15 that determine strain-specific accumulation of mGBP1 on the PV. These highly polymorphic proteins are held responsible for a large part of the strain-specific differences in virulence. Therefore, our data suggest that virulence of T. gondii in animals may rely in part on recognition by GBPs. However, phagosomes or vacuoles containing Trypanosoma cruzi did not recruit mGBP1. Co-immunoprecipitation revealed mGBP2, mGBP4, and mGBP5 as binding partners of mGBP1. Indeed, mGBP2 and mGBP5 co-localize with mGBP1 in T. gondii-infected cells. T. gondii thus elicits a cell-autonomous immune response in mice with GBPs involved. Three parasitic virulence factors and unknown IFN-γ-dependent host factors regulate this complex process. Depending on the virulence of the strains involved, numerous GBPs are brought to the PV as part of a large, multimeric structure to combat T. gondii.