Cargando…

Metabolomic Profiling of Wildtype and Transgenic Giardia lamblia Strains by (1)H HR-MAS NMR Spectroscopy

Giardia lamblia, a causative agent of persistent diarrhea in humans, domestic animals, and cattle, is usually treated with nitro compounds. Consequently, enzymes involved in anaerobic nitro reduction have been investigated in detail as potential targets. Their role within the normal metabolic contex...

Descripción completa

Detalles Bibliográficos
Autores principales: Müller, Joachim, Vermathen, Martina, Leitsch, David, Vermathen, Peter, Müller, Norbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073884/
https://www.ncbi.nlm.nih.gov/pubmed/32019059
http://dx.doi.org/10.3390/metabo10020053
_version_ 1783506716233564160
author Müller, Joachim
Vermathen, Martina
Leitsch, David
Vermathen, Peter
Müller, Norbert
author_facet Müller, Joachim
Vermathen, Martina
Leitsch, David
Vermathen, Peter
Müller, Norbert
author_sort Müller, Joachim
collection PubMed
description Giardia lamblia, a causative agent of persistent diarrhea in humans, domestic animals, and cattle, is usually treated with nitro compounds. Consequently, enzymes involved in anaerobic nitro reduction have been investigated in detail as potential targets. Their role within the normal metabolic context is, however, not understood. Using (1)H high-resolution magic angle spinning (HR-MAS) NMR spectroscopy, we analyzed the metabolomes of G. lamblia trophozoites overexpressing three nitroreductases (NR1–NR3) and thioredoxin reductase (TrxR), most likely a scavenger of reactive oxygen species, as suggested by the results published in this study. We compared the patterns to convenient controls and to the situation in the nitro drug resistant strain C4 where NR1 is downregulated. We identified 27 metabolites in G. lamblia trophozoites. Excluding metabolites of high variability among different wildtype populations, only trophozoites overexpressing NR1 presented a distinct pattern of nine metabolites, in particular arginine catabolites, differing from the respective controls. This pattern matched a differential pattern between wildtype and strain C4. This suggests that NR1 interferes with arginine and thus energy metabolism. The exact metabolic function of NR1 (and the other nitroreductases) remains to be elucidated.
format Online
Article
Text
id pubmed-7073884
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-70738842020-03-19 Metabolomic Profiling of Wildtype and Transgenic Giardia lamblia Strains by (1)H HR-MAS NMR Spectroscopy Müller, Joachim Vermathen, Martina Leitsch, David Vermathen, Peter Müller, Norbert Metabolites Article Giardia lamblia, a causative agent of persistent diarrhea in humans, domestic animals, and cattle, is usually treated with nitro compounds. Consequently, enzymes involved in anaerobic nitro reduction have been investigated in detail as potential targets. Their role within the normal metabolic context is, however, not understood. Using (1)H high-resolution magic angle spinning (HR-MAS) NMR spectroscopy, we analyzed the metabolomes of G. lamblia trophozoites overexpressing three nitroreductases (NR1–NR3) and thioredoxin reductase (TrxR), most likely a scavenger of reactive oxygen species, as suggested by the results published in this study. We compared the patterns to convenient controls and to the situation in the nitro drug resistant strain C4 where NR1 is downregulated. We identified 27 metabolites in G. lamblia trophozoites. Excluding metabolites of high variability among different wildtype populations, only trophozoites overexpressing NR1 presented a distinct pattern of nine metabolites, in particular arginine catabolites, differing from the respective controls. This pattern matched a differential pattern between wildtype and strain C4. This suggests that NR1 interferes with arginine and thus energy metabolism. The exact metabolic function of NR1 (and the other nitroreductases) remains to be elucidated. MDPI 2020-01-30 /pmc/articles/PMC7073884/ /pubmed/32019059 http://dx.doi.org/10.3390/metabo10020053 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Müller, Joachim
Vermathen, Martina
Leitsch, David
Vermathen, Peter
Müller, Norbert
Metabolomic Profiling of Wildtype and Transgenic Giardia lamblia Strains by (1)H HR-MAS NMR Spectroscopy
title Metabolomic Profiling of Wildtype and Transgenic Giardia lamblia Strains by (1)H HR-MAS NMR Spectroscopy
title_full Metabolomic Profiling of Wildtype and Transgenic Giardia lamblia Strains by (1)H HR-MAS NMR Spectroscopy
title_fullStr Metabolomic Profiling of Wildtype and Transgenic Giardia lamblia Strains by (1)H HR-MAS NMR Spectroscopy
title_full_unstemmed Metabolomic Profiling of Wildtype and Transgenic Giardia lamblia Strains by (1)H HR-MAS NMR Spectroscopy
title_short Metabolomic Profiling of Wildtype and Transgenic Giardia lamblia Strains by (1)H HR-MAS NMR Spectroscopy
title_sort metabolomic profiling of wildtype and transgenic giardia lamblia strains by (1)h hr-mas nmr spectroscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073884/
https://www.ncbi.nlm.nih.gov/pubmed/32019059
http://dx.doi.org/10.3390/metabo10020053
work_keys_str_mv AT mullerjoachim metabolomicprofilingofwildtypeandtransgenicgiardialambliastrainsby1hhrmasnmrspectroscopy
AT vermathenmartina metabolomicprofilingofwildtypeandtransgenicgiardialambliastrainsby1hhrmasnmrspectroscopy
AT leitschdavid metabolomicprofilingofwildtypeandtransgenicgiardialambliastrainsby1hhrmasnmrspectroscopy
AT vermathenpeter metabolomicprofilingofwildtypeandtransgenicgiardialambliastrainsby1hhrmasnmrspectroscopy
AT mullernorbert metabolomicprofilingofwildtypeandtransgenicgiardialambliastrainsby1hhrmasnmrspectroscopy