Characterization of Toxoplasma DegP, a rhoptry serine protease crucial for lethal infection in mice

PLoS One. 2017 Dec 15;12(12):e0189556. doi: 10.1371/journal.pone.0189556. eCollection 2017.

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.

MeSH terms

  • Animals
  • Mice, Inbred BALB C
  • Mice, Inbred NOD
  • Mice, SCID
  • Protein Processing, Post-Translational
  • Proteolysis
  • Protozoan Proteins / physiology*
  • Serine Proteases / physiology*
  • Toxoplasma / enzymology*
  • Toxoplasma / genetics
  • Toxoplasma / pathogenicity
  • Toxoplasmosis / parasitology*
  • Virulence

Substances

  • Protozoan Proteins
  • Serine Proteases

Grants and funding

This research was supported by the Laboratoire d’Excellence (LabEx) (ParaFrap ANR-11-LABX-0024), by the Fondation pour la Recherche Médicale (Equipe FRM DEQ20130326508) and The Cèdre France-Lebanon program (Project N2177) to M.L., by the Cèdre France-Lebanon program (Project N21774) and the American University of Beirut Medical Practice Plan and the National Council for Scientific Research (CNRS-L) to H.E.H and M.L. Hiba El Hajj (H.E.H.) is funded by the American University of Beirut Faculty of Medicine Medical Practice Plan and the Centre National de Recherche Scientifique Libanais (CNRS-L) and The Cèdre France-Lebanon program (Project N2177) and The Centre National de Recherche Scientifique Libanais (CNRS-L). Gaelle Lentini received a fellowship through the FRM FDT20140931002. Gamou Fall was supported by a fellowship from the Fonds Inkerman Fondation de France. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.