Toxoplasma MIC2 is a major determinant of invasion and virulence

• Published in: PLoS pathogens 2006-08, Vol.2 (8), p.e84-e84
• Main Authors: Huynh, My-Hang, Carruthers, Vern B
• Format: Article
• Language: English
• Subjects: Animal diseases; Animals; Behavior; Cells, Cultured; Chemical properties; Cloning; Cytokines; Deoxyribonucleic acid; Dihydrofolate reductase; Disease Models, Animal; DNA; Eukaryotes; Experiments; Female; Gene Expression; Genetic aspects; Host-bacteria relationships; Host-Parasite Interactions - physiology; Humans; Infections; Infectious Diseases; Locomotion - physiology; Membrane Proteins - deficiency; Membrane Proteins - genetics; Membrane Proteins - metabolism; Mice; Mice, Inbred BALB C; Mice, Knockout; Microbiology; Molecular Sequence Data; Motility; Parasites; Parasitology; Proteins; Protozoan Proteins - genetics; Protozoan Proteins - metabolism; Protozoan Vaccines - immunology; Toxoplasma; Toxoplasma - parasitology; Toxoplasma - pathogenicity; Toxoplasma - physiology; Toxoplasma gondii; Toxoplasmosis - immunology; Toxoplasmosis - parasitology; Toxoplasmosis - physiopathology; Virulence
• ISSN: 1553-7374; 1553-7366; 1553-7374
• DOI: 10.1371/journal.ppat.0020084

Like its apicomplexan kin, the obligate intracellular protozoan Toxoplasma gondii actively invades mammalian cells and uses a unique form of gliding motility. The recent identification of several transmembrane adhesive complexes, potentially capable of gripping external receptors and the sub-membrane actinomyosin motor, suggests that the parasite has multiple options for host-cell recognition and invasion. To test whether the transmembrane adhesin MIC2, together with its partner protein M2AP, participates in a major invasion pathway, we utilized a conditional expression system to introduce an anhydrotetracycline-responsive mic2 construct, allowing us to then knockout the endogenous mic2 gene. Conditional suppression of MIC2 provided the first opportunity to directly determine the role of this protein in infection. Reduced MIC2 expression resulted in mistrafficking of M2AP, markedly defective host-cell attachment and invasion, the loss of helical gliding motility, and the inability to support lethal infection in a murine model of acute toxoplasmosis. Survival of mice infected with MIC2-deficient parasites correlated with lower parasite burden in infected tissues, an attenuated inflammatory immune response, and induction of long-term protective immunity. Our findings demonstrate that the MIC2 protein complex is a major virulence determinant for Toxoplasma infection and that MIC2-deficient parasites constitute an effective live-attenuated vaccine for experimental toxoplasmosis.