Murine Irgm Paralogs Regulate Nonredundant Functions To Execute Host Defense to Toxoplasma gondii

• Published in: Infection and immunity Vol. 89; no. 11; p. e0020221
• Main Authors: Dockterman, Jacob, Fee, Brian E, Taylor, Gregory A, Coers, Jörn
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 15.10.2021
• Subjects: Animals; Apoptosis Regulatory Proteins - physiology; Cellular Microbiology: Pathogen-Host Cell Molecular Interactions; GTP Phosphohydrolases - physiology; GTP-Binding Proteins - physiology; Mice; Mice, Inbred C57BL; Microbial Pathogenesis; Microtubule-Associated Proteins - physiology; Toxoplasmosis - immunology; Ubiquitin - physiology; Vacuoles - physiology; Toxoplasma; immunity-related GTPases; intracellular parasites; autophagy; interferons; ubiquitination; guanylate binding proteins; GABARAP; cell-autonomous immunity; GBPs
• ISSN: 0019-9567; 1098-5522; 1098-5522
• DOI: 10.1128/IAI.00202-21

Gamma interferon (IFN-γ)-induced immunity-related GTPases (IRGs) confer cell-autonomous immunity to the intracellular protozoan pathogen Toxoplasma gondii. Effector IRGs are loaded onto the -containing parasitophorous vacuole (PV), where they recruit ubiquitin ligases, ubiquitin-binding proteins, and IFN-γ-inducible guanylate-binding proteins (Gbps), prompting PV lysis and parasite destruction. Host cells lacking the regulatory IRGs Irgm1 and Irgm3 fail to load effector IRGs, ubiquitin, and Gbps onto the PV and are consequently defective for cell-autonomous immunity to . However, the role of the third regulatory IRG, Irgm2, in cell-autonomous immunity to Toxoplasma has remained unexplored. Here, we report that Irgm2 unexpectedly plays a limited role in the targeting of effector IRGs, ubiquitin, and Gbps to the PV. Instead, Irgm2 is instrumental in the decoration of PVs with γ-aminobutyric acid receptor-associated protein-like 2 (GabarapL2). Cells lacking Irgm2 are as defective for cell-autonomous host defense to as pan- cells lacking all three Irgm proteins, and mice succumb to infections as readily as pan- mice. These findings demonstrate that, relative to Irgm1 and Irgm3, Irgm2 plays a distinct but critically important role in host resistance to .