Measuring growth, resistance, and recovery after artemisinin treatment of Plasmodium falciparum in a single semi-high-throughput assay

The direct-from-blood 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 potential independent genetic determinants of main effect and overlapping secondary effects. By adapting the method to include DBS, readouts can be easily extended to ex vivo surveillance applications.

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Publication Details

Journal
Malaria Journal
Published
2025-08-14
DOI
https://doi.org/10.1186/s12936-025-05481-9
Citations
2
Primary Topic
Malaria Research and Control
Type
article
Field-Weighted Citation Impact
3.76
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article

Measuring growth, resistance, and recovery after artemisinin treatment of Plasmodium falciparum in a single semi-high-throughput assay

Lisa A. Checkley, Tarrick Qahash, Sudhir Kumar, Zione Cassady et al.
2 citations
Malaria Journal
Malaria Research and Control
3.76
article

Measuring growth, resistance, and recovery after artemisinin treatment of Plasmodium falciparum in a single semi-high-throughput assay

Lisa A. Checkley, Tarrick Qahash, Sudhir Kumar, Zione Cassady, Douglas A. Shoue, Mackenzie A. C. Sievert, Ashley M. Vaughan, Puspendra P. Singh, Michael T. Ferdig, Katelyn M. Vendrely, Jeanne Romero‐Severson, Xue Li, Timothy J. C. Anderson, François Henry Nosten
article en
2 citations

Abstract

The direct-from-blood 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 potential independent genetic determinants of main effect and overlapping secondary effects. By adapting the method to include DBS, readouts can be easily extended to ex vivo surveillance applications.

Malaria JournalVol. 24(1)
University of Notre Dame (US), Texas Biomedical Research Institute (US), Infectious Disease Research Institute (US), Harvard University (US), University of Georgia (US), Iowa State University (US), University of Washington (US), Mahidol University (TH), Indian Council of Medical Research (IN), University of Oxford (GB), Shoklo Malaria Research Unit (TH), Mahidol Oxford Tropical Medicine Research Unit (TH)
Openalex Percentile: Top 7%
Malaria Research and Control
3.76
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