Atovaquone and ELQ-300 Combination Therapy as a Novel Dual-Site Cytochrome bc 1 Inhibition Strategy for Malaria
Abstract
Antimalarial combination therapies play a crucial role in preventing the emergence of drug-resistant Plasmodium parasites. Although artemisinin-based combination therapies (ACTs) comprise the majority of these formulations, inhibitors of the mitochondrial cytochrome bc 1 complex (cyt bc 1 ) are among the few compounds that are effective for both acute antimalarial treatment and prophylaxis. There are two known sites for inhibition within cyt bc 1 : atovaquone (ATV) blocks the quinol oxidase (Q o ) site of cyt bc 1 , while some members of the endochin-like quinolone (ELQ) family, including preclinical candidate ELQ-300, inhibit the quinone reductase (Q i ) site and retain full potency against ATV-resistant Plasmodium falciparum strains with Q o site mutations. Here, we provide the first in vivo comparison of ATV, ELQ-300, and combination therapy consisting of ATV plus ELQ-300 (ATV:ELQ-300), using P. yoelii murine models of malaria. In our monotherapy assessments, we found that ATV functioned as a single-dose curative compound in suppressive tests whereas ELQ-300 demonstrated a unique cumulative dosing effect that successfully blocked recrudescence even in a high-parasitemia acute infection model. ATV:ELQ-300 therapy was highly synergistic, and the combination was curative with a single combined dose of 1 mg/kg of body weight. Compared to the ATV:proguanil (Malarone) formulation, ATV:ELQ-300 was more efficacious in multiday, acute infection models and was equally effective at blocking the emergence of ATV-resistant parasites. Ultimately, our data suggest that dual-site inhibition of cyt bc 1 is a valuable strategy for antimalarial combination therapy and that Q i site inhibitors such as ELQ-300 represent valuable partner drugs for the clinically successful Q o site inhibitor ATV.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Aug 01, 2016
- Source ID
- 10.1128/aac.00791-16
Entities
People
- Aaron Nilsen
- Akhil B. Vaidya
- Allison M Stickles
- Isaac P. Forquer
- Jane X Kelly
- Joanne M. Morrisey
- Martin J. Smilkstein
- Michael K. Riscoe
- Rolf W. Winter
- Sovitj Pou
- Yuexin Li
Organizations
- Drexel University
- National Institutes of Health
- United States Department of Defense
- United States Department of Veterans Affairs
- Veterans Affairs Medical Center (Oregon)