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

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 p...

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Autores principales: Lentini, Gaelle, El Hajj, Hiba, Papoin, Julien, Fall, Gamou, Pfaff, Alexander W., Tawil, Nadim, Braun-Breton, Catherine, Lebrun, Maryse
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731766/
https://www.ncbi.nlm.nih.gov/pubmed/29244879
http://dx.doi.org/10.1371/journal.pone.0189556
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author Lentini, Gaelle
El Hajj, Hiba
Papoin, Julien
Fall, Gamou
Pfaff, Alexander W.
Tawil, Nadim
Braun-Breton, Catherine
Lebrun, Maryse
author_facet Lentini, Gaelle
El Hajj, Hiba
Papoin, Julien
Fall, Gamou
Pfaff, Alexander W.
Tawil, Nadim
Braun-Breton, Catherine
Lebrun, Maryse
author_sort Lentini, Gaelle
collection PubMed
description 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 DegP(I) appears dispensable for the establishment of an infection, removal of DegP(II) in a type II strain dramatically impairs the virulence. Finally, we show that KO-DegP(II) 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.
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spelling pubmed-57317662017-12-22 Characterization of Toxoplasma DegP, a rhoptry serine protease crucial for lethal infection in mice Lentini, Gaelle El Hajj, Hiba Papoin, Julien Fall, Gamou Pfaff, Alexander W. Tawil, Nadim Braun-Breton, Catherine Lebrun, Maryse PLoS One Research Article 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 DegP(I) appears dispensable for the establishment of an infection, removal of DegP(II) in a type II strain dramatically impairs the virulence. Finally, we show that KO-DegP(II) 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. Public Library of Science 2017-12-15 /pmc/articles/PMC5731766/ /pubmed/29244879 http://dx.doi.org/10.1371/journal.pone.0189556 Text en © 2017 Lentini et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lentini, Gaelle
El Hajj, Hiba
Papoin, Julien
Fall, Gamou
Pfaff, Alexander W.
Tawil, Nadim
Braun-Breton, Catherine
Lebrun, Maryse
Characterization of Toxoplasma DegP, a rhoptry serine protease crucial for lethal infection in mice
title Characterization of Toxoplasma DegP, a rhoptry serine protease crucial for lethal infection in mice
title_full Characterization of Toxoplasma DegP, a rhoptry serine protease crucial for lethal infection in mice
title_fullStr Characterization of Toxoplasma DegP, a rhoptry serine protease crucial for lethal infection in mice
title_full_unstemmed Characterization of Toxoplasma DegP, a rhoptry serine protease crucial for lethal infection in mice
title_short Characterization of Toxoplasma DegP, a rhoptry serine protease crucial for lethal infection in mice
title_sort characterization of toxoplasma degp, a rhoptry serine protease crucial for lethal infection in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731766/
https://www.ncbi.nlm.nih.gov/pubmed/29244879
http://dx.doi.org/10.1371/journal.pone.0189556
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