Malapaka Venkata R R, Barrese Albert A, Tripp Brian C, Tripp Brian C
Biological Sciences, Western Michigan University, Kalamazoo, MI 49008, USA.
J Biomol Screen. 2007 Sep;12(6):849-54. doi: 10.1177/1087057107304478. Epub 2007 Jul 20.
There is a pressing need to develop new antimicrobial drugs because of the increasing resistance of pathogenic bacteria to existing antibiotics. The preliminary development and validation of a novel methodology for the high-throughput screening of antimicrobial compounds and inhibitors of bacterial motility is described. This method uses a bacterial motility swarming agar assay, combined with the use of offset inoculation of the wells in a standard, clear, 96-well plate, to enable rapid screening of compounds for potential antibiotic and antimotility properties with a standard absorbance microplate reader. Thus, the methodology should be compatible with 96-well laboratory automation technology used in drug discovery and chemical biology studies. To validate the screening method, the Genesis Plus structurally diverse library of 960 biologically active compounds was screened against a motile strain of the gram-negative bacterial pathogen Salmonella typhimurium. The average Z' value for the positive and negative motility controls on all 12 compound plates was 0.67 +/- 0.14, and the signal-to-baseline ratio calculated from the positive and negative controls was 5.9 +/- 1.1. A collection of 70 compounds with well-known antimicrobial properties was successfully identified using this assay.
由于致病细菌对现有抗生素的耐药性不断增加,开发新型抗菌药物的需求迫在眉睫。本文描述了一种用于高通量筛选抗菌化合物和细菌运动抑制剂的新方法的初步开发和验证。该方法采用细菌运动群集琼脂试验,并结合在标准的透明96孔板中对孔进行偏移接种,以便使用标准吸光酶标仪快速筛选具有潜在抗生素和抗运动特性的化合物。因此,该方法应与药物发现和化学生物学研究中使用的96孔实验室自动化技术兼容。为了验证筛选方法,针对革兰氏阴性细菌病原体鼠伤寒沙门氏菌的运动菌株,对包含960种生物活性化合物的Genesis Plus结构多样文库进行了筛选。所有12个化合物板上阳性和阴性运动对照的平均Z'值为0.67±0.14,根据阳性和阴性对照计算的信号与基线比为5.9±1.1。使用该试验成功鉴定了一组70种具有已知抗菌特性的化合物。