Discovery of D8-03 as an Inhibitor of Intracellular Growth of Francisella tularensis.

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL ACS Infectious Diseases Pub Date : 2024-06-14 DOI:10.1021/acsinfecdis.4c00116
Shannon Whiles, Quanzheng Zhang, Zach Chamberlain, Manish K Singh, Shaun Steele, Linda Zheng, Kristin Rosche, Weigang Huang, Huanyao Gao, Qisheng Zhang, Thomas Kawula
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Abstract

Francisella tularensis is a Gram-negative facultative intracellular bacterial pathogen that is classified by the Centers for Disease Control and Prevention as a Tier 1 Select Agent. F. tularensis infection causes the disease tularemia, also known as rabbit fever. Treatment of tularemia is limited to few effective antibiotics which are associated with high relapse rates, toxicity, and potential emergence of antibiotic-resistant strains. Consequently, new therapeutic options for tularemia are needed. Through screening a focused chemical library and subsequent structure-activity relationship studies, we have discovered a new and potent inhibitor of intracellular growth of Francisella tularensis, D8-03. Importantly, D8-03 effectively reduces bacterial burden in mice infected with F. tularensis. Preliminary mechanistic investigations suggest that D8-03 works through a potentially novel host-dependent mechanism and serves as a promising lead compound for further development.

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发现 D8-03 作为土拉弗氏菌细胞内生长抑制剂。
土拉弗氏菌是一种革兰氏阴性细胞内兼性细菌病原体,被美国疾病控制和预防中心列为一级选择性病原体。土拉菌感染会导致土拉菌病,又称兔热。目前,治疗土拉菌病的有效抗生素不多,而且复发率高、毒性大,还可能出现抗生素耐药菌株。因此,需要针对土拉菌病的新疗法。通过筛选重点化学文库和随后的结构-活性关系研究,我们发现了一种能有效抑制土拉弗氏菌胞内生长的新型抑制剂 D8-03。重要的是,D8-03 能有效减轻土拉弗氏菌感染小鼠的细菌负担。初步的机理研究表明,D8-03 是通过一种潜在的新型宿主依赖机制起作用的,是一种很有希望进一步开发的先导化合物。
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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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