Mechanisms of PfDNMT2 inhibition and PfATP6-mediated resistance to the antimalarial candidate SC83288 in Plasmodium falciparum
Cecilia P. Sanchez, Maëlle Duffey, Romina V. Celada, Michal Kucharski, Marie Hoarau, Thanaya Saeyang, Sumalee Kamchonwongpaisan, Farzin Sohraby, Svenja de Buhr, Ariane Nunes Alves, Amuza Byaruhanga Lucky, Jun Miao, Clement Regnault, Jerzy M. Dziekan, Zbynek Bozdech
TL;DR
SC83288 is a promising antimalarial drug that kills malaria parasites by blocking DNA replication, and resistance to it is limited due to a costly mechanism involving PfATP6.
Contribution
The study identifies PfDNMT2 as the molecular target of SC83288 and reveals a resistance mechanism involving PfATP6 with a high fitness cost.
Findings
SC83288 disrupts blood-stage development by blocking DNA replication and arresting karyokinesis.
PfDNMT2 is identified as the primary molecular target of SC83288.
Resistance to SC83288 arises through PfATP6 mutations, which sequester the drug into the endoplasmic reticulum.
Abstract
The emergence of multi-drug resistant Plasmodium falciparum underscores the urgent need for new antimalarial therapies. SC83288, a chemically distinct antimalarial compound, is highly effective against P. falciparum both in vivo and in vitro, including strains resistant to artemisinin and partner drugs. Here, we show that SC83288 disrupts blood-stage development by blocking DNA replication and arresting karyokinesis. We identify the parasite’s DNA and tRNAAsp methyltransferase PfDNMT2 as a primary molecular target, linking drug action to impaired epigenetic regulation, altered S-adenosylmethionine fluxes, and compensatory transcriptional responses. Resistance to SC83288 arises through mutations in the parasite’s SERCA-type Ca²⁺ ATPase PfATP6, which enable transport of the compound into the endoplasmic reticulum, away from its nuclear targets. This resistance mechanism carries a…
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Taxonomy
TopicsMalaria Research and Control · Ubiquitin and proteasome pathways · Tuberculosis Research and Epidemiology