The essential genome of <i>Plasmodium knowlesi</i> reveals determinants of antimalarial susceptibility

Measures to combat the parasites that cause malaria have become compromised because of reliance on a small arsenal of drugs and emerging drug resistance. We conducted a transposon mutagenesis screen in the primate malaria parasite <i>Plasmodium knowlesi</i>, producing the most complete classification of gene essentiality in any <i>Plasmodium</i> spp. to date, with the resolution to define truncatable genes. We found conservation in the druggable genome between <i>Plasmodium</i> spp. and divergences in mitochondrial metabolism. Perturbation analyses with the frontline antimalarial artemisinin revealed modulators that both increase and decrease drug susceptibility. Our findings aid prioritization of drug and vaccine targets for the <i>Plasmodium vivax</i> clade and reveal mechanisms of resistance that can inform therapeutic development.

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Publication Details

Journal
Science
Published
2025-02-06
DOI
https://doi.org/10.1126/science.adq6241
Citations
19
Primary Topic
Malaria Research and Control
Type
article
Field-Weighted Citation Impact
35.69
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article

The essential genome of Plasmodium knowlesi reveals determinants of antimalarial susceptibility

Sheena Dass, Aditya S. Paul, Jacob A. Tennessen, Christof Grüring et al.
19 citations
Science
Malaria Research and Control
35.69
article

The essential genome of Plasmodium knowlesi reveals determinants of antimalarial susceptibility

Sheena Dass, Aditya S. Paul, Jacob A. Tennessen, Christof Grüring, Usheer Kanjee, Marcelo U. Ferreira, Kourosh Zarringhalam, Marc‐Jan Gubbels, Qursheed Sultana, Basil T. Thommen, Sida Ye, Manoj T. Duraisingh, Brendan Elsworth
article en
19 citations

Abstract

Measures to combat the parasites that cause malaria have become compromised because of reliance on a small arsenal of drugs and emerging drug resistance. We conducted a transposon mutagenesis screen in the primate malaria parasite <i>Plasmodium knowlesi</i>, producing the most complete classification of gene essentiality in any <i>Plasmodium</i> spp. to date, with the resolution to define truncatable genes. We found conservation in the druggable genome between <i>Plasmodium</i> spp. and divergences in mitochondrial metabolism. Perturbation analyses with the frontline antimalarial artemisinin revealed modulators that both increase and decrease drug susceptibility. Our findings aid prioritization of drug and vaccine targets for the <i>Plasmodium vivax</i> clade and reveal mechanisms of resistance that can inform therapeutic development.

ScienceVol. 387(6734)
Boston College (US), Center for Biologics Evaluation and Research (US), Harvard University (US), University of Lisbon (PT), Universidade de São Paulo (BR), University of Massachusetts Boston (US)
Good health and well-being
Openalex Percentile: Top 0%
Malaria Research and Control
35.69
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