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In vitro metabolomic footprint of the Echinococcus multilocularis metacestode
Alveolar echinococcosis (AE) is a zoonotic disease that is deadly if left untreated. AE is caused by the larval metacestode stage of the cestode Echinococcus multilocularis. Better knowledge on the host-parasite interface could yield novel targets for improvement of the treatment against AE. We anal...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6923418/ https://www.ncbi.nlm.nih.gov/pubmed/31857639 http://dx.doi.org/10.1038/s41598-019-56073-y |
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author | Ritler, Dominic Rufener, Reto Li, Jia V. Kämpfer, Urs Müller, Joachim Bühr, Claudia Schürch, Stefan Lundström-Stadelmann, Britta |
author_facet | Ritler, Dominic Rufener, Reto Li, Jia V. Kämpfer, Urs Müller, Joachim Bühr, Claudia Schürch, Stefan Lundström-Stadelmann, Britta |
author_sort | Ritler, Dominic |
collection | PubMed |
description | Alveolar echinococcosis (AE) is a zoonotic disease that is deadly if left untreated. AE is caused by the larval metacestode stage of the cestode Echinococcus multilocularis. Better knowledge on the host-parasite interface could yield novel targets for improvement of the treatment against AE. We analyzed culture media incubated with in vitro grown E. multilocularis metacestodes by (1)H nuclear magnetic resonance spectroscopy to identify the unknown metabolic footprint of the parasite. Moreover, we quantitatively analyzed all amino acids, acetate, glucose, lactate, and succinate in time-course experiments using liquid chromatography and enzymatic assays. The E. multilocularis metacestodes consumed glucose and, surprisingly, threonine and produced succinate, acetate, and alanine as major fermentation products. The metabolic composition of vesicle fluid (VF) from in vitro grown E. multilocularis metacestodes was different from parasite-incubated culture medium with respect to the abundance, but not the spectrum, of metabolites, and some metabolites, in particular amino acids, accumulated in the VF. Overall, this study presents the first characterization of the in vitro metabolic footprint of E. multilocularis metacestodes and VF composition, and it provides the basis for analyses of potentially targetable pathways for future drug development. |
format | Online Article Text |
id | pubmed-6923418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69234182019-12-20 In vitro metabolomic footprint of the Echinococcus multilocularis metacestode Ritler, Dominic Rufener, Reto Li, Jia V. Kämpfer, Urs Müller, Joachim Bühr, Claudia Schürch, Stefan Lundström-Stadelmann, Britta Sci Rep Article Alveolar echinococcosis (AE) is a zoonotic disease that is deadly if left untreated. AE is caused by the larval metacestode stage of the cestode Echinococcus multilocularis. Better knowledge on the host-parasite interface could yield novel targets for improvement of the treatment against AE. We analyzed culture media incubated with in vitro grown E. multilocularis metacestodes by (1)H nuclear magnetic resonance spectroscopy to identify the unknown metabolic footprint of the parasite. Moreover, we quantitatively analyzed all amino acids, acetate, glucose, lactate, and succinate in time-course experiments using liquid chromatography and enzymatic assays. The E. multilocularis metacestodes consumed glucose and, surprisingly, threonine and produced succinate, acetate, and alanine as major fermentation products. The metabolic composition of vesicle fluid (VF) from in vitro grown E. multilocularis metacestodes was different from parasite-incubated culture medium with respect to the abundance, but not the spectrum, of metabolites, and some metabolites, in particular amino acids, accumulated in the VF. Overall, this study presents the first characterization of the in vitro metabolic footprint of E. multilocularis metacestodes and VF composition, and it provides the basis for analyses of potentially targetable pathways for future drug development. Nature Publishing Group UK 2019-12-19 /pmc/articles/PMC6923418/ /pubmed/31857639 http://dx.doi.org/10.1038/s41598-019-56073-y Text en © The Author(s) 2019 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/. |
spellingShingle | Article Ritler, Dominic Rufener, Reto Li, Jia V. Kämpfer, Urs Müller, Joachim Bühr, Claudia Schürch, Stefan Lundström-Stadelmann, Britta In vitro metabolomic footprint of the Echinococcus multilocularis metacestode |
title | In vitro metabolomic footprint of the Echinococcus multilocularis metacestode |
title_full | In vitro metabolomic footprint of the Echinococcus multilocularis metacestode |
title_fullStr | In vitro metabolomic footprint of the Echinococcus multilocularis metacestode |
title_full_unstemmed | In vitro metabolomic footprint of the Echinococcus multilocularis metacestode |
title_short | In vitro metabolomic footprint of the Echinococcus multilocularis metacestode |
title_sort | in vitro metabolomic footprint of the echinococcus multilocularis metacestode |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6923418/ https://www.ncbi.nlm.nih.gov/pubmed/31857639 http://dx.doi.org/10.1038/s41598-019-56073-y |
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