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Author Correction: Aryl amino acetamides prevent Plasmodium falciparum ring development via targeting the lipid-transfer protein PfSTART1 - Nature Communications
Correction to: Nature Communications https://doi.org/10.1038/s41467-024-49491-8, published online 18 June 2024 The original version of the Supplementary Information associated with this Article contained an error in Supplementary Fig. 7c and d, in which the concentrations of W-991 were provided on the x-axes in the wrong order. The HTML has been updated to include a corrected version of the Supplementary Information.
Aryl amino acetamides prevent Plasmodium falciparum ring development via targeting the lipid-transfer protein PfSTART1 - Nature Communications
Abstract With resistance to most antimalarials increasing, it is imperative that new drugs are developed. We previously identified an aryl acetamide compound, MMV006833 (M-833), that inhibited the ring-stage development of newly invaded merozoites. Here, we select parasites resistant to M-833 and identify mutations in the START lipid transfer protein (PF3D7_0104200, PfSTART1). Introducing PfSTART1 mutations into wildtype parasites reproduces resistance to M-833 as well as to more potent analogues.
Malaria outbreak in Laos caused by formerly rare artemisinin resistant strains of Plasmodium falciparum
These results strongly suggest that the outbreak was driven by a selective sweep, possibly associated with multidrug-resistant phenotypes of the outbreak strains. Established resistant populations can circulate at low frequencies for years before suddenly overwhelming dominant strains when the conditions for selection become favourable—eg, when front-line therapies change.
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