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(1)H-NMR metabolite profiles of different strains of Plasmodium falciparum
Although efforts to understand the basis for inter-strain phenotypic variation in the most virulent malaria species, Plasmodium falciparum, have benefited from advances in genomic technologies, there have to date been few metabolomic studies of this parasite. Using (1)H-NMR spectroscopy, we have com...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240024/ https://www.ncbi.nlm.nih.gov/pubmed/25405893 http://dx.doi.org/10.1042/BSR20140134 |
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author | Teng, Rongwei Lehane, Adele M. Winterberg, Markus Shafik, Sarah H. Summers, Robert L. Martin, Rowena E. van Schalkwyk, Donelly A. Junankar, Pauline R. Kirk, Kiaran |
author_facet | Teng, Rongwei Lehane, Adele M. Winterberg, Markus Shafik, Sarah H. Summers, Robert L. Martin, Rowena E. van Schalkwyk, Donelly A. Junankar, Pauline R. Kirk, Kiaran |
author_sort | Teng, Rongwei |
collection | PubMed |
description | Although efforts to understand the basis for inter-strain phenotypic variation in the most virulent malaria species, Plasmodium falciparum, have benefited from advances in genomic technologies, there have to date been few metabolomic studies of this parasite. Using (1)H-NMR spectroscopy, we have compared the metabolite profiles of red blood cells infected with different P. falciparum strains. These included both chloroquine-sensitive and chloroquine-resistant strains, as well as transfectant lines engineered to express different isoforms of the chloroquine-resistance-conferring pfcrt (P. falciparum chloroquine resistance transporter). Our analyses revealed strain-specific differences in a range of metabolites. There was marked variation in the levels of the membrane precursors choline and phosphocholine, with some strains having >30-fold higher choline levels and >5-fold higher phosphocholine levels than others. Chloroquine-resistant strains showed elevated levels of a number of amino acids relative to chloroquine-sensitive strains, including an approximately 2-fold increase in aspartate levels. The elevation in amino acid levels was attributable to mutations in pfcrt. Pfcrt-linked differences in amino acid abundance were confirmed using alternate extraction and detection (HPLC) methods. Mutations acquired to withstand chloroquine exposure therefore give rise to significant biochemical alterations in the parasite. |
format | Online Article Text |
id | pubmed-4240024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-42400242014-12-01 (1)H-NMR metabolite profiles of different strains of Plasmodium falciparum Teng, Rongwei Lehane, Adele M. Winterberg, Markus Shafik, Sarah H. Summers, Robert L. Martin, Rowena E. van Schalkwyk, Donelly A. Junankar, Pauline R. Kirk, Kiaran Biosci Rep Original Paper Although efforts to understand the basis for inter-strain phenotypic variation in the most virulent malaria species, Plasmodium falciparum, have benefited from advances in genomic technologies, there have to date been few metabolomic studies of this parasite. Using (1)H-NMR spectroscopy, we have compared the metabolite profiles of red blood cells infected with different P. falciparum strains. These included both chloroquine-sensitive and chloroquine-resistant strains, as well as transfectant lines engineered to express different isoforms of the chloroquine-resistance-conferring pfcrt (P. falciparum chloroquine resistance transporter). Our analyses revealed strain-specific differences in a range of metabolites. There was marked variation in the levels of the membrane precursors choline and phosphocholine, with some strains having >30-fold higher choline levels and >5-fold higher phosphocholine levels than others. Chloroquine-resistant strains showed elevated levels of a number of amino acids relative to chloroquine-sensitive strains, including an approximately 2-fold increase in aspartate levels. The elevation in amino acid levels was attributable to mutations in pfcrt. Pfcrt-linked differences in amino acid abundance were confirmed using alternate extraction and detection (HPLC) methods. Mutations acquired to withstand chloroquine exposure therefore give rise to significant biochemical alterations in the parasite. Portland Press Ltd. 2014-11-21 /pmc/articles/PMC4240024/ /pubmed/25405893 http://dx.doi.org/10.1042/BSR20140134 Text en © 2014 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Teng, Rongwei Lehane, Adele M. Winterberg, Markus Shafik, Sarah H. Summers, Robert L. Martin, Rowena E. van Schalkwyk, Donelly A. Junankar, Pauline R. Kirk, Kiaran (1)H-NMR metabolite profiles of different strains of Plasmodium falciparum |
title | (1)H-NMR metabolite profiles of different strains of Plasmodium falciparum |
title_full | (1)H-NMR metabolite profiles of different strains of Plasmodium falciparum |
title_fullStr | (1)H-NMR metabolite profiles of different strains of Plasmodium falciparum |
title_full_unstemmed | (1)H-NMR metabolite profiles of different strains of Plasmodium falciparum |
title_short | (1)H-NMR metabolite profiles of different strains of Plasmodium falciparum |
title_sort | (1)h-nmr metabolite profiles of different strains of plasmodium falciparum |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240024/ https://www.ncbi.nlm.nih.gov/pubmed/25405893 http://dx.doi.org/10.1042/BSR20140134 |
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