Selection of Plasmodium falciparum cytochrome B mutants by putative PfNDH2 inhibitors

• Published in: Proceedings of the National Academy of Sciences - PNAS 2018-06, Vol.115 (24), p.6285-6290
• Main Authors: Lane, Kristin D., Mu, Jianbing, Lu, Jinghua, Windle, Sean T., Liu, Anna, Sun, Peter D., Wellems, Thomas E.
• Format: Article
• Language: English
• Subjects: Antimalarials - pharmacology; Atovaquone; Biological Sciences; Cytochrome; Cytochrome b; Cytochromes; Cytochromes b - genetics; Drug development; Drug resistance; Drug Resistance - drug effects; Electron transfer; Electron transport; Electron transport chain; Electron Transport Chain Complex Proteins - genetics; Hydroquinone; Inhibitors; Malaria; Malaria, Falciparum - drug therapy; Malaria, Falciparum - genetics; Malaria, Falciparum - parasitology; Mitochondria; Molecular docking; Molecular Docking Simulation - methods; Mutants; Mutation; Mutation - genetics; NADH; NADH dehydrogenase; NADH Dehydrogenase - antagonists & inhibitors; Nicotinamide adenine dinucleotide; Nucleic acids; Oxidation; Parasite resistance; Parasites; Parasitic protozoa; Plasmodium falciparum; Plasmodium falciparum - drug effects; Plasmodium falciparum - genetics; Proguanil; Quinolones; Quinolones - pharmacology; Quinone oxidoreductase; Vector-borne diseases
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1804492115

Malaria control is threatened by a limited pipeline of effective pharmaceuticals against drug-resistant strains of Plasmodium falciparum. Components of the mitochondrial electron transport chain (ETC) are attractive targets for drug development, owing to exploitable differences between the parasite and human ETC. Disruption of ETC function interferes with metabolic processes including de novo pyrimidine synthesis, essential for nucleic acid replication. We investigated the effects of ETC inhibitor selection on two distinct P. falciparum clones, Dd2 and 106/1. Compounds CK-2-68 and RYL-552, substituted quinolones reported to block P. falciparum NADH dehydrogenase 2 (PfNDH2; a type II NADH:quinone oxidoreductase), unexpectedly selected mutations at the quinol oxidation (Qₒ) pocket of P. falciparum cytochrome B (PfCytB). Selection experiments with atovaquone (ATQ) on 106/1 parasites yielded highly resistant PfCytB Y268S mutants seen in clinical infections that fail ATQ-proguanil treatment. In contrast, ATQ pressure on Dd2 yielded moderately resistant parasites carrying a PfCytB M133I or K272R mutation. Strikingly, all ATQ-selected mutants demonstrated little change or slight increase of sensitivity to CK-2-68 or RYL-552. Molecular docking studies demonstrated binding of all three ETC inhibitors to the Qₒ pocket of PfCytB, where Y268 forms strong van der Waals interactions with the hydroxynaphthoquinone ring of ATQ but not the quinolone ring of CK-2-68 or RYL-552. Our results suggest that combinations of suitable ETC inhibitors may be able to subvert or delay the development of P. falciparum drug resistance.