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DOI 10.1128/aac.01727-25

Медицинская библиотека · Antimicrobial agents and chemotherapy · 2026

Selective targeting of Plasmodium falciparum hexose transporter by phytochemical Ginsenoside Rg1 disrupts glucose metabolism and blocks development of parasite.

Shafi Sadat, Maurya Preeti, Bansal Ruby, Sharma Jyoti, Mishra Sai Kumar, Najmi Abul Kalam, Singh Shailja

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Аннотация

The emergence of resistance to first-line antimalarial therapies highlights the critical need for next-generation drugs that target distinct molecular pathways and employ novel mechanisms of action. Notably, the intra-erythrocytic parasite development is highly dependent on a sustained glucose supply as their fundamental energy source. Therefore, exploiting a "selective starvation" strategy by targeting the parasite's reliance on glucose metabolism, particularly through the Plasmodium falciparum hexose transporter (PfHT), which is critical for parasite survival, can serve as a promising therapeutic approach to combat multidrug-resistant Plasmodium parasites. Through molecular docking and a structure-based drug design approach, we identified a natural compound, Ginsenoside Rg1 (G-Rg1) from the Drug Bank database library, as a potential PfHT inhibitor. The PfHT specificity of G-Rg1 was validated using a yeast complementation model. Subsequently, to investigate the role of PfHT in drug-resistant Pf parasites, we investigated the stage-specific expression of PfHT in both artemisinin (ART)-sensitive and resistant Pf parasites and reported its elevated expression in resistant parasites, predicting its role in their survival. Notably, in vitro growth inhibition studies demonstrated that G-Rg1 effectively suppressed the growth of both ART-sensitive and resistant Pf parasites. Additionally, G-Rg1 potentiated the efficacy of dihydroartemisinin in combination and ring survival assays, indicating its potential to circumvent resistance mechanisms. G-Rg1 administration alone and in combination with ART, in Plasmodium berghei ANKA-infected mice, reduced parasite multiplication and increased mean survival time. Our findings support G-Rg1 as a promising candidate for drug development against malaria, highlighting the potential of targeting PfHT to combat drug-resistant malaria.

Для цитирования: Shafi Sadat, Maurya Preeti, Bansal Ruby, Sharma Jyoti, Mishra Sai Kumar, Najmi Abul Kalam, Singh Shailja. Selective targeting of Plasmodium falciparum hexose transporter by phytochemical Ginsenoside Rg1 disrupts glucose metabolism and blocks development of parasite.. Antimicrobial agents and chemotherapy. 2026. DOI: 10.1128/aac.01727-25.

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