Literature DB >> 18315533

Apicomplexa in mammalian cells: trafficking to the parasitophorous vacuole.

Marie-France Cesbron-Delauw1, Claire Gendrin, Laetitia Travier, Pauline Ruffiot, Corinne Mercier.   

Abstract

Most Apicomplexa reside and multiply in the cytoplasm of their host cell, within a parasitophorous vacuole (PV) originating from both parasite and host cell components. Trafficking of parasite-encoded proteins destined to membrane compartments beyond the confine of the parasite plasma membrane is a process that offers a rich territory to explore novel mechanisms of protein-membrane interactions. Here, we focus on the PVs formed by the asexual stages of two pathogens of medical importance, Plasmodium and Toxoplasma. We compare the PVs of both parasites, with a particular emphasis on their evolutionary divergent compartmentalization within the host cell. We also discuss the existence of peculiar export mechanisms and/or sorting determinants that are potentially involved in the post-secretory targeting of parasite proteins to the PV subcompartments.

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Year:  2008        PMID: 18315533     DOI: 10.1111/j.1600-0854.2008.00728.x

Source DB:  PubMed          Journal:  Traffic        ISSN: 1398-9219            Impact factor:   6.215


  24 in total

1.  Protein targeting to the parasitophorous vacuole membrane of Plasmodium falciparum.

Authors:  Saliha Eksi; Kim C Williamson
Journal:  Eukaryot Cell       Date:  2011-04-15

2.  The obligate intracellular parasite Toxoplasma gondii secretes a soluble phosphatidylserine decarboxylase.

Authors:  Nishith Gupta; Anne Hartmann; Richard Lucius; Dennis R Voelker
Journal:  J Biol Chem       Date:  2012-05-04       Impact factor: 5.157

3.  Intervacuolar transport and unique topology of GRA14, a novel dense granule protein in Toxoplasma gondii.

Authors:  Michael E Rome; Josh R Beck; Jay M Turetzky; Paul Webster; Peter J Bradley
Journal:  Infect Immun       Date:  2008-09-02       Impact factor: 3.441

4.  Immunodominant, protective response to the parasite Toxoplasma gondii requires antigen processing in the endoplasmic reticulum.

Authors:  Nicolas Blanchard; Federico Gonzalez; Marie Schaeffer; Nathalie T Joncker; Tiffany Cheng; Anjali J Shastri; Ellen A Robey; Nilabh Shastri
Journal:  Nat Immunol       Date:  2008-06-29       Impact factor: 25.606

Review 5.  Toxoplasma Effectors Targeting Host Signaling and Transcription.

Authors:  Mohamed-Ali Hakimi; Philipp Olias; L David Sibley
Journal:  Clin Microbiol Rev       Date:  2017-07       Impact factor: 26.132

6.  Type II Toxoplasma gondii KU80 knockout strains enable functional analysis of genes required for cyst development and latent infection.

Authors:  Barbara A Fox; Alejandra Falla; Leah M Rommereim; Tadakimi Tomita; Jason P Gigley; Corinne Mercier; Marie-France Cesbron-Delauw; Louis M Weiss; David J Bzik
Journal:  Eukaryot Cell       Date:  2011-04-29

7.  Dynamic development of parasitophorous vacuole of Eimeria tenella transfected with the yellow fluorescent protein gene fused to different signal sequences from apicomplexan parasites.

Authors:  Tuanyuan Shi; Wenchao Yan; Huaibin Ren; Xianyong Liu; Xun Suo
Journal:  Parasitol Res       Date:  2008-09-25       Impact factor: 2.289

8.  The arginine-rich N-terminal domain of ROP18 is necessary for vacuole targeting and virulence of Toxoplasma gondii.

Authors:  Sarah J Fentress; Tobias Steinfeldt; Jonathan C Howard; L David Sibley
Journal:  Cell Microbiol       Date:  2012-09-20       Impact factor: 3.715

9.  Further aspects of Toxoplasma gondii elimination in the presence of metals.

Authors:  Laís Pessanha de Carvalho; Edésio José Tenório de Melo
Journal:  Parasitol Res       Date:  2018-02-18       Impact factor: 2.289

Review 10.  Immune response and immunopathology during toxoplasmosis.

Authors:  Christopher D Dupont; David A Christian; Christopher A Hunter
Journal:  Semin Immunopathol       Date:  2012-09-07       Impact factor: 9.623

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