Evidence map›Paper›PMID 39605531›Full record

ArticlebioRxiv : the preprint server for biology2024

Measuring Growth, Resistance, and Recovery after Artemisinin Treatment of Plasmodium falciparum in a single semi-high-throughput Assay.

Mackenzie A C Sievert, Puspendra P Singh, Douglas A Shoue, Lisa A Checkley, Katelyn M Brenneman, Tarrick Qahash, Zione Cassady, Sudhir Kumar, Xue Li, François H Nosten and 4 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Mackenzie A C SievertEck Institute for Global Health, Dept. of Biological Sciences, University of Notre Dame, Notre Dame, Indiana, USA.
Puspendra P SinghEck Institute for Global Health, Dept. of Biological Sciences, University of Notre Dame, Notre Dame, Indiana, USA.
Douglas A ShoueEck Institute for Global Health, Dept. of Biological Sciences, University of Notre Dame, Notre Dame, Indiana, USA.
Lisa A CheckleyEck Institute for Global Health, Dept. of Biological Sciences, University of Notre Dame, Notre Dame, Indiana, USA.
Katelyn M BrennemanEck Institute for Global Health, Dept. of Biological Sciences, University of Notre Dame, Notre Dame, Indiana, USA.
Tarrick QahashEck Institute for Global Health, Dept. of Biological Sciences, University of Notre Dame, Notre Dame, Indiana, USA.
Zione CassadyEck Institute for Global Health, Dept. of Biological Sciences, University of Notre Dame, Notre Dame, Indiana, USA.
Sudhir KumarCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, USA.
Xue LiTexas Biomedical Research Institute, San Antonio, Texas, USA.
François H NostenShoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Mae Sot, Thailand.
Timothy J C AndersonTexas Biomedical Research Institute, San Antonio, Texas, USA.ORCID 0000-0002-0191-0204
Ashley M VaughanCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, USA.
Jeanne Romero-SeversonEck Institute for Global Health, Dept. of Biological Sciences, University of Notre Dame, Notre Dame, Indiana, USA.
Michael T FerdigEck Institute for Global Health, Dept. of Biological Sciences, University of Notre Dame, Notre Dame, Indiana, USA.

Funding

Systems genetics of artemisinin resistanceP01AI127338 · NIAID · UNIVERSITY OF NOTRE DAME · PI Michael T Ferdig · 2017 to 2026
$21.3M
Mapping Drug Resistance Genes in Plasmodium falciparumR37AI048071 · NIAID · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI ANDERSON, TIM J · 2012 to 2021
$7.9M
NIAID NIH HHS P01 AI127338NIAID NIH HHS R37 AI048071Wellcome Trust
6 · The paper itself

Abstract

Background: Artemisinin partial resistance (ART-R) has spread throughout Southeast Asia and mutations in Results: The assay determined growth between 6 h and 96 h, resistance at 120 h, and recovery from 120 h and 192 h. Growth can be accurately captured by qPCR and is shown by reproduction of previous growth phenotypes from HB3 × Dd2. Resistance measured at 120 h continually shows the most consistent phenotype for ring stage susceptibility. Recovery identifies an additional response to drug than parasites that are determined sensitive by Fold Change at 120 h. Comparison of progeny phenotypes for Growth vs Resistance showed a minor but significant correlation, whereas Growth vs Recovery and Resistance vs Recovery showed no significant correlation. Additionally, dried blood spot (DBS) samples matched Fold Change measured from liquid samples demonstrating Resistance can be easily quantified using either storage method. Conclusions: The qPCR-based methodology provides the throughput needed to quickly measure large numbers of parasites for multiple relevant phenotypes. Growth can reveal fitness defects and illuminate relationships between proliferation rates and drug response. Recovery serves as a complementary phenotype to resistance that quantifies the ability of sensitive parasites to tolerate drug exposure. All three phenotypes offer a comprehensive assessment of parasite-drug interaction each with independent genetic determinants of main effect and overlapping secondary effects that should be further. By adapting our method to include DBS, readouts can be easily extended to

Indexed as

Artemisinin resistanceGenetic crossKelch13PhenotypesPlasmodium falciparumRing-stage survival assay

Identifiers

PMID39605531
PMCPMC11601240

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.