Rapid High‐Throughput Discovery of Molecules With Antimicrobial Activity From Natural Products Enabled by a Nanoliter Matrix SlipChip

抗菌剂 抗生素 抗生素耐药性 高通量筛选 药物发现 天然产物 细菌 金黄色葡萄球菌 微生物学 生物 生物化学 遗传学
作者
Qi Wang,Meng‐Ru Wang,Weiyuan Lyu,Xiang Li,Lei Xu,Yuyao Qin,Yongzhi Ren,Zixin Deng,Meifeng Tao,Wei‐Lie Xiao,Feng Shen
出处
期刊:Small methods [Wiley]
卷期号:9 (4): e2402045-e2402045 被引量:4
标识
DOI:10.1002/smtd.202402045
摘要

Improper use of antibiotics has led to the development of antimicrobial resistance, or "superbugs," outpacing the discovery of new antibiotics. The lack of rapid, high-throughput screening methods is a major bottleneck in discovery novel antibiotics. Traditional methods consume significant amounts of samples, making it challenging to discover new antibiotics from limited natural product extracts. Here, a rapid, high-throughput screening method is reported for natural products with antimicrobial activity enabled by a nanoliter matrix SlipChip (nm-SlipChip). This nm-SlipChip creates a screening matrix with nanoliter droplets for 100 drug candidate-bacterium combinations. The effectiveness of candidate antibiotics is assessed by analyzing microbial phenotypic changes. This nm-SlipChip reduces sample consumption by over 5000-fold and shortens the detection time to three hours. Twenty compounds isolated from Callicarpa integerrima were tested against 10 pathogenic bacteria and identified two previously unreported clerodane diterpenes with activity against methicillin-resistant Staphylococcus aureus (MRSA). Molecular docking and fluorescence probe experiments reveals that their antimicrobial effect results from disruption of bacterial cell membranes and biofilms. The nm-SlipChip provides an effective method for discovering new antimicrobial drugs from natural sources, vital in combating antibiotic resistance.
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