将 Brusatol 重新定位为疟疾寄生虫的传播阻断剂。

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL ACS Infectious Diseases Pub Date : 2024-10-11 Epub Date: 2024-10-01 DOI:10.1021/acsinfecdis.4c00434
Amelia Cox, Neelima Krishnankutty, Steven Shave, Virginia M Howick, Manfred Auer, James J La Clair, Nisha Philip
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引用次数: 0

摘要

目前,伯氨喹是世卫组织推荐的唯一一种疟疾传播阻断药物。最近的努力凸显了发现能调节疟疾传播的新药的重要性,人们对能以单次小剂量给药的药物尤其感兴趣,这些药物最好具有离散性和疟原虫选择性作用机制。在这里,我们的团队展示了一种通过体外筛选和体内分析相结合来确定疟疾传播阻断剂的方法。我们利用一组天然产品,发现了强效的传播阻断剂,发现 brusatol 有阻断传播的功效就说明了这一点。作为生物活性天然产品大家族中的一员,这一发现为下一步开发快速鉴定具有宝贵药理治疗特性的喹西诺酮类及相关制剂的方法提供了关键的一步。
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Repositioning Brusatol as a Transmission Blocker of Malaria Parasites.

Currently, primaquine is the only malaria transmission-blocking drug recommended by the WHO. Recent efforts have highlighted the importance of discovering new agents that regulate malarial transmission, with particular interest in agents that can be administered in a single low dose, ideally with a discrete and Plasmodium-selective mechanism of action. Here, our team demonstrates an approach to identify malaria transmission-blocking agents through a combination of in vitro screening and in vivo analyses. Using a panel of natural products, our approach identified potent transmission blockers, as illustrated by the discovery of the transmission-blocking efficacy of brusatol. As a member of a large family of biologically active natural products, this discovery provides a critical next step toward developing methods to rapidly identify quassinoids and related agents with valuable pharmacological therapeutic properties.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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