Department of Defense Biotechnology High Performance Computing Software Applications Institute, Telemedicine and Advanced Technology Research Center, U.S. Army Medical Research and Development Command, Fort Detrick, MD, USA.
The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc., Bethesda, MD, USA.
Sci Rep. 2022 Jan 21;12(1):1167. doi: 10.1038/s41598-022-04985-7.
Due to the recurring loss of antimalarial drugs to resistance, there is a need for novel targets, drugs, and combination therapies to ensure the availability of current and future countermeasures. Pyrazoleamides belong to a novel class of antimalarial drugs that disrupt sodium ion homeostasis, although the exact consequences of this disruption in Plasmodium falciparum remain under investigation. In vitro experiments demonstrated that parasites carrying mutations in the metabolic enzyme PfATP4 develop resistance to pyrazoleamide compounds. However, the underlying mechanisms that allow mutant parasites to evade pyrazoleamide treatment are unclear. Here, we first performed experiments to identify the sublethal dose of a pyrazoleamide compound (PA21A092) that caused a significant reduction in growth over one intraerythrocytic developmental cycle (IDC). At this drug concentration, we collected transcriptomic and metabolomic data at multiple time points during the IDC to quantify gene- and metabolite-level alterations in the treated parasites. To probe the effects of pyrazoleamide treatment on parasite metabolism, we coupled the time-resolved omics data with a metabolic network model of P. falciparum. We found that the drug-treated parasites adjusted carbohydrate metabolism to enhance synthesis of myoinositol-a precursor for phosphatidylinositol biosynthesis. This metabolic adaptation caused a decrease in metabolite flux through the pentose phosphate pathway, causing a decreased rate of RNA synthesis and an increase in oxidative stress. Our model analyses suggest that downstream consequences of enhanced myoinositol synthesis may underlie adjustments that could lead to resistance emergence in P. falciparum exposed to a sublethal dose of a pyrazoleamide drug.
由于抗疟药物不断因耐药性而失效,因此需要新的靶标、药物和联合疗法,以确保现有和未来的对策的有效性。吡唑酰胺类药物属于一类新型抗疟药物,可破坏钠离子的动态平衡,尽管这种破坏对恶性疟原虫的具体后果仍在研究中。体外实验表明,携带代谢酶 PfATP4 突变的寄生虫对吡唑酰胺化合物产生耐药性。然而,允许突变寄生虫逃避吡唑酰胺治疗的潜在机制尚不清楚。在这里,我们首先进行了实验,以确定导致一个红细胞内发育周期(IDC)内生长显著减少的吡唑酰胺化合物(PA21A092)的亚致死剂量。在该药物浓度下,我们在 IDC 期间的多个时间点收集转录组和代谢组数据,以量化处理寄生虫中的基因和代谢物水平的变化。为了探究吡唑酰胺处理对寄生虫代谢的影响,我们将时间分辨的组学数据与恶性疟原虫的代谢网络模型相结合。我们发现,药物处理的寄生虫调整了碳水化合物代谢,以增强肌醇的合成-磷脂酰肌醇生物合成的前体。这种代谢适应导致戊糖磷酸途径中的代谢物通量减少,导致 RNA 合成率降低和氧化应激增加。我们的模型分析表明,增强肌醇合成的下游后果可能是导致恶性疟原虫在暴露于吡唑酰胺类药物亚致死剂量时出现耐药性的调整的基础。