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使用全动物感染模型进行新型抗菌药物的高通量筛选。

High-throughput screen for novel antimicrobials using a whole animal infection model.

作者信息

Moy Terence I, Conery Annie L, Larkins-Ford Jonah, Wu Gang, Mazitschek Ralph, Casadei Gabriele, Lewis Kim, Carpenter Anne E, Ausubel Frederick M

机构信息

Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.

出版信息

ACS Chem Biol. 2009 Jul 17;4(7):527-33. doi: 10.1021/cb900084v.

Abstract

The nematode Caenorhabditis elegans is a unique whole animal model system for identifying small molecules with in vivo anti-infective properties. C. elegans can be infected with a broad range of human pathogens, including Enterococcus faecalis, an important human nosocomial pathogen. Here, we describe an automated, high-throughput screen of 37,200 compounds and natural product extracts for those that enhance survival of C. elegans infected with E. faecalis. Using a robot to dispense live, infected animals into 384-well plates and automated microscopy and image analysis, we identified 28 compounds and extracts not previously reported to have antimicrobial properties, including six structural classes that cure infected C. elegans animals but do not affect the growth of the pathogen in vitro, thus acting by a mechanism of action distinct from antibiotics currently in clinical use.

摘要

线虫秀丽隐杆线虫是一种独特的全动物模型系统,用于鉴定具有体内抗感染特性的小分子。秀丽隐杆线虫可被多种人类病原体感染,包括粪肠球菌,一种重要的人类医院病原体。在此,我们描述了一项对37200种化合物和天然产物提取物进行的自动化高通量筛选,以寻找那些能提高感染粪肠球菌的秀丽隐杆线虫存活率的物质。利用机器人将感染了病原体的活线虫分注到384孔板中,并通过自动化显微镜和图像分析,我们鉴定出28种以前未报道具有抗菌特性的化合物和提取物,其中包括六个结构类别,它们能治愈受感染的秀丽隐杆线虫,但在体外不影响病原体的生长,因此其作用机制不同于目前临床使用的抗生素。

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