• Medientyp: E-Artikel
  • Titel: In vitro metabolomic footprint of the Echinococcus multilocularis metacestode
  • Beteiligte: Ritler, Dominic; Rufener, Reto; Li, Jia V.; Kämpfer, Urs; Müller, Joachim; Bühr, Claudia; Schürch, Stefan; Lundström-Stadelmann, Britta
  • Erschienen: Springer Science and Business Media LLC, 2019
  • Erschienen in: Scientific Reports
  • Sprache: Englisch
  • DOI: 10.1038/s41598-019-56073-y
  • ISSN: 2045-2322
  • Schlagwörter: Multidisciplinary
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: <jats:title>Abstract</jats:title><jats:p>Alveolar echinococcosis (AE) is a zoonotic disease that is deadly if left untreated. AE is caused by the larval metacestode stage of the cestode <jats:italic>Echinococcus multilocularis</jats:italic>. Better knowledge on the host-parasite interface could yield novel targets for improvement of the treatment against AE. We analyzed culture media incubated with <jats:italic>in vitro</jats:italic> grown <jats:italic>E. multilocularis</jats:italic> metacestodes by <jats:sup>1</jats:sup>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 <jats:italic>E. multilocularis</jats:italic> metacestodes consumed glucose and, surprisingly, threonine and produced succinate, acetate, and alanine as major fermentation products. The metabolic composition of vesicle fluid (VF) from <jats:italic>in vitro</jats:italic> grown <jats:italic>E. multilocularis</jats:italic> 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 <jats:italic>in vitro</jats:italic> metabolic footprint of <jats:italic>E. multilocularis</jats:italic> metacestodes and VF composition, and it provides the basis for analyses of potentially targetable pathways for future drug development.</jats:p>
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