Toxoplasma gondii autophagy-related protein ATG9 is crucial for the survival of parasites in their host

Abstract

Autophagy is a conserved, life-promoting, catabolic process involved in the recycling of nonessential cellular components in response to stress. The parasite Toxoplasma gondii is an early-diverging eukaryote in which part of the autophagy machinery is not exclusively involved in a catabolic process but instead has been repurposed for an original function in organelle inheritance during cell division. This function, depending essentially on protein TgATG8 and its membrane conjugation system, is crucial for parasite survival and prevented an in depth study of autophagy in the mutants generated so far in Toxoplasma. Thus, in order to decipher the primary function of canonical autophagy in the parasites, we generated a cell line deficient for TgATG9, a protein thought to be involved in the early steps of the autophagy process. Although the protein proved to be dispensable for the development of these obligate intracellular parasites in vitro, the absence of TgATG9 led to a reduced ability to sustain prolonged extracellular stress. Importantly, depletion of the protein significantly reduced parasites survival in macrophages and markedly attenuated their virulence in mice. Altogether, this shows TgATG9 is important for the fate of Toxoplasma in immune cells and contributes to the overall virulence of the parasite, possibly through an involvement in a canonical autophagy pathway. © 2016 John Wiley & Sons Ltd

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Atg9, Autophagy, Stress response, Toxoplasma, Virulence, Animals, Autophagy-related proteins, Cell division, Cell line, Female, Gene knockout techniques, Macrophages, Membrane proteins, Mice, Mice, inbred balb c, Protozoan proteins, Autophagy related protein, Autophagy related protein 9, Messenger rna, Unclassified drug, Atg9 protein, toxoplasma gondii, Membrane protein, Protozoal protein, Animal experiment, Animal model, Article, Autophagosome, Cell compartmentalization, Controlled study, Human, Human cell, In vitro study, In vivo study, Mouse, Murine toxoplasmosis, Nonhuman, Parasite load, Parasite survival, Parasite viability, Parasite virulence, Priority journal, Promoter region, Protein degradation, Protein localization, Toxoplasma gondii, Trans golgi network, Animal, Bagg albino mouse, Gene knockout, Genetics, Macrophage, Parasitology, Pathogenicity, Physiology

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