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

被引:0
|
作者
Whiles, Shannon [1 ]
Zhang, Quanzheng [2 ]
Chamberlain, Zach [1 ]
Singh, Manish K. [2 ]
Steele, Shaun [1 ]
Zheng, Linda [2 ]
Rosche, Kristin [3 ]
Huang, Weigang [2 ]
Gao, Huanyao [2 ]
Zhang, Qisheng [2 ,4 ]
Kawula, Thomas [1 ]
机构
[1] Washington State Univ, Paul G Allen Sch Global Hlth, Pullman, WA 99164 USA
[2] Univ N Carolina, Eshelman Sch Pharm, Div Chem Biol & Med Chem, Chapel Hill, NC 27599 USA
[3] Washington State Univ, Dept Vet Microbiol & Pathol, Program Vector Borne Dis, Pullman, WA 99164 USA
[4] Univ N Carolina, Sch Med, Dept Pharmacol, Chapel Hill, NC 27599 USA
来源
ACS INFECTIOUS DISEASES | 2024年 / 10卷 / 08期
基金
美国国家卫生研究院;
关键词
host-directed therapy; intracellular pathogen; tularemia; antibiotic; Francisella tularensis; cyclodextrin; GENTAMICIN; EVOLUTION;
D O I
10.1021/acsinfecdis.4c00116
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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.
引用
收藏
页码:2775 / 2784
页数:10
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