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In vitro maturation of Toxoplasma gondii bradyzoites in human myotubes and their metabolomic characterization
The apicomplexan parasite Toxoplasma gondii forms bradyzoite-containing tissue cysts that cause chronic and drug-tolerant infections. However, current in vitro models do not allow long-term culture of these cysts to maturity. Here, we developed a human myotube-based in vitro culture model of functio...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897399/ https://www.ncbi.nlm.nih.gov/pubmed/35246532 http://dx.doi.org/10.1038/s41467-022-28730-w |
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author | Christiansen, Céline Maus, Deborah Hoppenz, Ellen Murillo-León, Mateo Hoffmann, Tobias Scholz, Jana Melerowicz, Florian Steinfeldt, Tobias Seeber, Frank Blume, Martin |
author_facet | Christiansen, Céline Maus, Deborah Hoppenz, Ellen Murillo-León, Mateo Hoffmann, Tobias Scholz, Jana Melerowicz, Florian Steinfeldt, Tobias Seeber, Frank Blume, Martin |
author_sort | Christiansen, Céline |
collection | PubMed |
description | The apicomplexan parasite Toxoplasma gondii forms bradyzoite-containing tissue cysts that cause chronic and drug-tolerant infections. However, current in vitro models do not allow long-term culture of these cysts to maturity. Here, we developed a human myotube-based in vitro culture model of functionally mature tissue cysts that are orally infectious to mice and tolerate exposure to a range of antibiotics and temperature stresses. Metabolomic characterization of purified cysts reveals global changes that comprise increased levels of amino acids and decreased abundance of nucleobase- and tricarboxylic acid cycle-associated metabolites. In contrast to fast replicating tachyzoite forms of T. gondii these tissue cysts tolerate exposure to the aconitase inhibitor sodium fluoroacetate. Direct access to persistent stages of T. gondii under defined cell culture conditions will be essential for the dissection of functionally important host-parasite interactions and drug evasion mechanisms. It will also facilitate the identification of new strategies for therapeutic intervention. |
format | Online Article Text |
id | pubmed-8897399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88973992022-03-17 In vitro maturation of Toxoplasma gondii bradyzoites in human myotubes and their metabolomic characterization Christiansen, Céline Maus, Deborah Hoppenz, Ellen Murillo-León, Mateo Hoffmann, Tobias Scholz, Jana Melerowicz, Florian Steinfeldt, Tobias Seeber, Frank Blume, Martin Nat Commun Article The apicomplexan parasite Toxoplasma gondii forms bradyzoite-containing tissue cysts that cause chronic and drug-tolerant infections. However, current in vitro models do not allow long-term culture of these cysts to maturity. Here, we developed a human myotube-based in vitro culture model of functionally mature tissue cysts that are orally infectious to mice and tolerate exposure to a range of antibiotics and temperature stresses. Metabolomic characterization of purified cysts reveals global changes that comprise increased levels of amino acids and decreased abundance of nucleobase- and tricarboxylic acid cycle-associated metabolites. In contrast to fast replicating tachyzoite forms of T. gondii these tissue cysts tolerate exposure to the aconitase inhibitor sodium fluoroacetate. Direct access to persistent stages of T. gondii under defined cell culture conditions will be essential for the dissection of functionally important host-parasite interactions and drug evasion mechanisms. It will also facilitate the identification of new strategies for therapeutic intervention. Nature Publishing Group UK 2022-03-04 /pmc/articles/PMC8897399/ /pubmed/35246532 http://dx.doi.org/10.1038/s41467-022-28730-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Christiansen, Céline Maus, Deborah Hoppenz, Ellen Murillo-León, Mateo Hoffmann, Tobias Scholz, Jana Melerowicz, Florian Steinfeldt, Tobias Seeber, Frank Blume, Martin In vitro maturation of Toxoplasma gondii bradyzoites in human myotubes and their metabolomic characterization |
title | In vitro maturation of Toxoplasma gondii bradyzoites in human myotubes and their metabolomic characterization |
title_full | In vitro maturation of Toxoplasma gondii bradyzoites in human myotubes and their metabolomic characterization |
title_fullStr | In vitro maturation of Toxoplasma gondii bradyzoites in human myotubes and their metabolomic characterization |
title_full_unstemmed | In vitro maturation of Toxoplasma gondii bradyzoites in human myotubes and their metabolomic characterization |
title_short | In vitro maturation of Toxoplasma gondii bradyzoites in human myotubes and their metabolomic characterization |
title_sort | in vitro maturation of toxoplasma gondii bradyzoites in human myotubes and their metabolomic characterization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897399/ https://www.ncbi.nlm.nih.gov/pubmed/35246532 http://dx.doi.org/10.1038/s41467-022-28730-w |
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