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Enrichment and Proteomic Characterization of the Cyst Wall from In Vitro Toxoplasma gondii Cysts
The tissue cyst of Toxoplasma gondii, found in latent infection, serves a critical role in both transmission and reactivation of this organism. Within infected cells, slowly replicating parasites (bradyzoites) are surrounded by a cyst matrix, cyst wall, and cyst membrane. The cyst wall is clearly de...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6495374/ https://www.ncbi.nlm.nih.gov/pubmed/31040239 http://dx.doi.org/10.1128/mBio.00469-19 |
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author | Tu, Vincent Mayoral, Joshua Sugi, Tatsuki Tomita, Tadakimi Han, Bing Ma, Yan Fen Weiss, Louis M. |
author_facet | Tu, Vincent Mayoral, Joshua Sugi, Tatsuki Tomita, Tadakimi Han, Bing Ma, Yan Fen Weiss, Louis M. |
author_sort | Tu, Vincent |
collection | PubMed |
description | The tissue cyst of Toxoplasma gondii, found in latent infection, serves a critical role in both transmission and reactivation of this organism. Within infected cells, slowly replicating parasites (bradyzoites) are surrounded by a cyst matrix, cyst wall, and cyst membrane. The cyst wall is clearly delineated by ultrastructural analysis; however, the composition and function of this layer in host-parasite interactions are not fully understood. In order to understand the composition of the cyst wall, a proteomic analysis of purified cyst wall fragments, that were enriched with Percoll gradients and subsequently immunoprecipitated with CST1 antibody, was performed. Known cyst wall proteins, such as CST1, BPK1, MCP4, MAG1, GRA2, GRA3, and GRA5, were identified in this preparation by liquid chromatography-tandem mass spectrometry (LC-MS/MS). In addition, dense granule proteins (GRAs) not previously shown to associate with the cyst wall, as well as uncharacterized hypothetical proteins, were identified in this cyst wall preparation. Several of these hypothetical cyst wall (CST) proteins were epitope tagged, and immunofluorescence assays confirmed their localization as novel cyst matrix and cyst wall proteins. Expression of two of these newly identified cyst wall proteins was eliminated by gene knockout (CST2-KO and CST3-KO). CST2-KO parasites were highly attenuated in virulence and did not establish detectable cyst burdens. This targeted proteomic approach allowed the identification of new components of the cyst wall that probably have roles in the parasite/host interface. |
format | Online Article Text |
id | pubmed-6495374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-64953742019-05-03 Enrichment and Proteomic Characterization of the Cyst Wall from In Vitro Toxoplasma gondii Cysts Tu, Vincent Mayoral, Joshua Sugi, Tatsuki Tomita, Tadakimi Han, Bing Ma, Yan Fen Weiss, Louis M. mBio Research Article The tissue cyst of Toxoplasma gondii, found in latent infection, serves a critical role in both transmission and reactivation of this organism. Within infected cells, slowly replicating parasites (bradyzoites) are surrounded by a cyst matrix, cyst wall, and cyst membrane. The cyst wall is clearly delineated by ultrastructural analysis; however, the composition and function of this layer in host-parasite interactions are not fully understood. In order to understand the composition of the cyst wall, a proteomic analysis of purified cyst wall fragments, that were enriched with Percoll gradients and subsequently immunoprecipitated with CST1 antibody, was performed. Known cyst wall proteins, such as CST1, BPK1, MCP4, MAG1, GRA2, GRA3, and GRA5, were identified in this preparation by liquid chromatography-tandem mass spectrometry (LC-MS/MS). In addition, dense granule proteins (GRAs) not previously shown to associate with the cyst wall, as well as uncharacterized hypothetical proteins, were identified in this cyst wall preparation. Several of these hypothetical cyst wall (CST) proteins were epitope tagged, and immunofluorescence assays confirmed their localization as novel cyst matrix and cyst wall proteins. Expression of two of these newly identified cyst wall proteins was eliminated by gene knockout (CST2-KO and CST3-KO). CST2-KO parasites were highly attenuated in virulence and did not establish detectable cyst burdens. This targeted proteomic approach allowed the identification of new components of the cyst wall that probably have roles in the parasite/host interface. American Society for Microbiology 2019-04-30 /pmc/articles/PMC6495374/ /pubmed/31040239 http://dx.doi.org/10.1128/mBio.00469-19 Text en Copyright © 2019 Tu et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Tu, Vincent Mayoral, Joshua Sugi, Tatsuki Tomita, Tadakimi Han, Bing Ma, Yan Fen Weiss, Louis M. Enrichment and Proteomic Characterization of the Cyst Wall from In Vitro Toxoplasma gondii Cysts |
title | Enrichment and Proteomic Characterization of the Cyst Wall from In Vitro
Toxoplasma gondii Cysts |
title_full | Enrichment and Proteomic Characterization of the Cyst Wall from In Vitro
Toxoplasma gondii Cysts |
title_fullStr | Enrichment and Proteomic Characterization of the Cyst Wall from In Vitro
Toxoplasma gondii Cysts |
title_full_unstemmed | Enrichment and Proteomic Characterization of the Cyst Wall from In Vitro
Toxoplasma gondii Cysts |
title_short | Enrichment and Proteomic Characterization of the Cyst Wall from In Vitro
Toxoplasma gondii Cysts |
title_sort | enrichment and proteomic characterization of the cyst wall from in vitro
toxoplasma gondii cysts |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6495374/ https://www.ncbi.nlm.nih.gov/pubmed/31040239 http://dx.doi.org/10.1128/mBio.00469-19 |
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