Literature DB >> 6854716

Secretion from the rhoptries of Toxoplasma gondii during host-cell invasion.

B A Nichols, M L Chiappino, G R O'Connor.   

Abstract

To determine whether the rhoptries of Toxoplasma gondii play a role in the invasion of host cells by this parasite, we inoculated toxoplasmas into the peritoneal cavities of normal mice and into macrophage cultures, fixed the specimens at various intervals thereafter, and analyzed them by electron microscopy. We found that during host-cell invasion, the rhoptry membrane fused with the anterior limiting membrane of the toxoplasma, producing an opening to the exterior. Since such openings were formed when the host-cell membrane was disrupted, it appears that the rhoptries may secrete a lytic product that facilitates invasion through the host-cell membrane. Such a "penetration-enhancing factor" was previously isolated from lysed toxoplasmas (Lycke and Norrby, 1966). Occasionally, when secretion was incomplete, masses of tubules were found in the rhoptries, sometimes as soon as 15 sec after the toxoplasms had been injected into mice. Similar tubules were found in the parasitophorous vacuole that was formed 10-15 min later, and such tubules are typical of vacuoles containing replicating parasites. Because these tubules are in continuity with the vacuolar membrane, it appears to be a hybrid membrane, composed in part of toxoplasma products. We speculate that the hybrid nature of the vacuolar membrane prevents it from fusing with the lysosomes of phagocytes and thereby contributes to the intracellular survival of the parasites.

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Year:  1983        PMID: 6854716     DOI: 10.1016/s0022-5320(83)90067-9

Source DB:  PubMed          Journal:  J Ultrastruct Res        ISSN: 0022-5320


  45 in total

1.  Toxoplasma gondii infection induces gene expression and secretion of interleukin 1 (IL-1), IL-6, granulocyte-macrophage colony-stimulating factor, and intercellular adhesion molecule 1 by human retinal pigment epithelial cells.

Authors:  C N Nagineni; B Detrick; J J Hooks
Journal:  Infect Immun       Date:  2000-01       Impact factor: 3.441

2.  Transmembrane insertion of the Toxoplasma gondii GRA5 protein occurs after soluble secretion into the host cell.

Authors:  L Lecordier; C Mercier; L D Sibley; M F Cesbron-Delauw
Journal:  Mol Biol Cell       Date:  1999-04       Impact factor: 4.138

3.  Daughter cell assembly in the protozoan parasite Toxoplasma gondii.

Authors:  Ke Hu; Tara Mann; Boris Striepen; Con J M Beckers; David S Roos; John M Murray
Journal:  Mol Biol Cell       Date:  2002-02       Impact factor: 4.138

4.  Toxoplasma evacuoles: a two-step process of secretion and fusion forms the parasitophorous vacuole.

Authors:  S Håkansson; A J Charron; L D Sibley
Journal:  EMBO J       Date:  2001-06-15       Impact factor: 11.598

Review 5.  Lytic cycle of Toxoplasma gondii.

Authors:  M W Black; J C Boothroyd
Journal:  Microbiol Mol Biol Rev       Date:  2000-09       Impact factor: 11.056

6.  Monoclonal antibodies identify micronemes and a new population of cytoplasmic granules cross-reacting with micronemes of cystozoites of Sarcocystis muris.

Authors:  R Entzeroth; A König; J F Dubremetz
Journal:  Parasitol Res       Date:  1991       Impact factor: 2.289

Review 7.  Toxoplasma gondii: 25 years and 25 major advances for the field.

Authors:  John C Boothroyd
Journal:  Int J Parasitol       Date:  2009-07-01       Impact factor: 3.981

8.  The late chlamydial inclusion membrane is not derived from the endocytic pathway and is relatively deficient in host proteins.

Authors:  T Taraska; D M Ward; R S Ajioka; P B Wyrick; S R Davis-Kaplan; C H Davis; J Kaplan
Journal:  Infect Immun       Date:  1996-09       Impact factor: 3.441

9.  Toxoplasma gondii sporozoites form a transient parasitophorous vacuole that is impermeable and contains only a subset of dense-granule proteins.

Authors:  M Tilley; M E Fichera; M E Jerome; D S Roos; M W White
Journal:  Infect Immun       Date:  1997-11       Impact factor: 3.441

10.  Host but not parasite cholesterol controls Toxoplasma cell entry by modulating organelle discharge.

Authors:  Isabelle Coppens; Keith A Joiner
Journal:  Mol Biol Cell       Date:  2003-05-29       Impact factor: 4.138

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