Characterization of Toxoplasma DegP, a rhoptry serine protease crucial for lethal infection in mice
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Public Library of Science
Abstract
During the infection process, Apicomplexa discharge their secretory organelles called micronemes, rhoptries and dense granules to sustain host cell invasion, intracellular replication and to modulate host cell pathways and immune responses. Herein, we describe the Toxoplasma gondii Deg-like serine protein (TgDegP), a rhoptry protein homologous to High temperature requirement A (HtrA) or Deg-like family of serine proteases. TgDegP undergoes processing in both types I and II strains as most of the rhoptries proteins. We show that genetic disruption of the degP gene does not impact the parasite lytic cycle in vitro but affects virulence in mice. While in a type I strain DegPI appears dispensable for the establishment of an infection, removal of DegPII in a type II strain dramatically impairs the virulence. Finally, we show that KO-DegPII parasites kill immunodeficient mice as efficiently as the wild-type strain indicating that the protease might be involved in the complex crosstalk that the parasite engaged with the host immune response. Thus, this study unravels a novel rhoptry protein in T. gondii important for the establishment of lethal infection. © 2017 Lentini et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Animals, Mice, inbred balb c, Mice, inbred nod, Mice, scid, Protein processing, post-translational, Proteolysis, Protozoan proteins, Serine proteases, Toxoplasma, Toxoplasmosis, Virulence, Deg like serine protein, Serine proteinase, Unclassified drug, Protozoal protein, Animal experiment, Animal model, Article, Bacterial strain, Bacterial virulence, Cell invasion assay, Cellular immunity, Controlled study, Enzyme analysis, Female, Gene disruption, Human, Human cell, Immune complex disease, In vitro study, Mouse, Nonhuman, Toxoplasma gondii, Wild type, Animal, Bagg albino mouse, Enzymology, Genetics, Nonobese diabetic mouse, Parasitology, Pathogenicity, Physiology, Protein degradation, Protein processing, Scid mouse