Evidence map›Paper›PMID 25405893›Full record

ArticleBioscience reports2014

1H-NMR metabolite profiles of different strains of Plasmodium falciparum.

Rongwei Teng, Adele M Lehane, Markus Winterberg, Sarah H Shafik, Robert L Summers, Rowena E Martin, Donelly A van Schalkwyk, Pauline R Junankar, Kiaran Kirk

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.9field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  9. Whole Blood Metabolomics byAnalytical chemistry · 2017
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Rongwei Teng*Research School of Biology, The Australian National University, Canberra, ACT 2601, Australia.
Adele M Lehane*Research School of Biology, The Australian National University, Canberra, ACT 2601, Australia.
Markus Winterberg*Research School of Biology, The Australian National University, Canberra, ACT 2601, Australia.
Sarah H Shafik*Research School of Biology, The Australian National University, Canberra, ACT 2601, Australia.
Robert L Summers*Research School of Biology, The Australian National University, Canberra, ACT 2601, Australia.
Rowena E Martin*Research School of Biology, The Australian National University, Canberra, ACT 2601, Australia.
Donelly A van Schalkwyk*Research School of Biology, The Australian National University, Canberra, ACT 2601, Australia.
Pauline R Junankar*Research School of Biology, The Australian National University, Canberra, ACT 2601, Australia.
Kiaran Kirk*Research School of Biology, The Australian National University, Canberra, ACT 2601, Australia.
Australian National University · AU

Funding

Medical Research Council
6 · The paper itself

Abstract

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 1H-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.

Indexed as

MetabolomeAnimalsAntimalarialsChloroquineChromatography, High Pressure LiquidDrug ResistanceErythrocytesFemaleHost-Parasite InteractionsHumansMembrane Transport ProteinsMetabolomicsMutationOocytesPlasmodium falciparumProton Magnetic Resonance SpectroscopyAntimalarialsChloroquineMembrane Transport ProteinsPfCRT protein, Plasmodium falciparumProtozoan Proteins

Identifiers

PMID25405893
PMCPMC4240024
OpenAlexW2096023665

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.