大规模并行组合屏幕揭示了抗生素耐药的小分子敏感性 格拉姆阴性ESKAPE病原体
Megan W Tse1,2,3, Meilin Zhu1,2,3, Benjamin Peters2,3
1Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.
bioRxiv : the preprint server for biology
|April 8, 2024
概括
研究人员选了超过3万种化合物,以对抗多抗药性ESKAPE病原体. 他们发现了一种化合物,通过破坏细菌外膜来增强抗生素的有效性,从而提供了对抗性感染的新策略.
科学领域:
- 微生物学与传染病的研究
- 药理学和药物发现
- 遗传学和基因组学 遗传学和基因组学
背景情况:
- 多抗药性ESKAPE病原体的抗生素耐药性是一个关键的全球卫生挑战.
- 组合抗微生物疗法看起来很有前途,但对于大型化学空间,需要有效的选方法.
- 高通量查对于识别抗药性细菌的协同作用药物组合至关重要.
结论:
- 通过DropArray平台,可以对抗生素组合进行大规模的表型查.
- 发现了一种新型的小分子P2-56-3,通过向细菌外膜完整性,与里法协同作用.
- 这些发现突出了高通量查的潜力,以发现针对多药耐药ESKAPE菌株的新抗菌协同作用.
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