Inhibition of Listeria monocytogenes infection by neurological drugs

被引:18
|
作者
Lieberman, Linda A. [1 ]
Higgins, Darren E. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Microbiol & Mol Genet, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
Listeria monocytogenes; Small molecule screen; Intracellular infection; Bepridil; Neurological compounds; Thioridazine; CLINICAL CONCENTRATIONS; BLOCKERS; ENTRY;
D O I
10.1016/j.ijantimicag.2009.10.011
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
To gain insights into the cellular processes required for intracellular bacterial pathogenesis, we previously developed a generalisable screening approach to identify small molecule compounds that alter Listeria monocytogenes infection. In this report, a small molecule library enriched for compounds affecting neurological functions was screened and 68 compounds that disrupted L. monocytogenes infection of macrophages were identified. Many of these compounds were known antimicrobial agents, however 26 compounds were novel inhibitors of intracellular infection. Two of the compounds chosen for further study, the antipsychotic drug thioridazine and the calcium channel blocker bepridil, exhibited dose-dependent inhibition of vacuolar escape and intracellular replication of L. monocytogenes during infection of murine macrophages. These results suggest that clinically approved neurological drugs may provide a novel source of anti-infective agents that are suitable for development as therapeutics against intracellular bacterial infections. (C) 2009 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:292 / 296
页数:5
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