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DCAP: A Broad-Spectrum Antibiotic That Targets the Cytoplasmic Membrane of Bacteria

机译:DCAP:一种针对细菌细胞质膜的广谱抗生素

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摘要

Persistent infections are frequently caused by dormant and biofilm-associated bacteria, which often display characteristically slow growth. Antibiotics that require rapid cell growth may be ineffective against these organisms and thus fail to prevent reoccurring infections. In contrast to growth-based antimicrobial agents, membrane-targeting drugs effectively kill slow-growing bacteria. Herein we introduce 2-((3-(3,6-dichloro-9H-carbazol-9-yl)-2-hydroxypropyl)amino)-2-(hydroxymethyl)propane-1,3-diol (DCAP), a potent broad-spectrum antibiotic that reduces the transmembrane potential of Gram-positive and Gram-negative bacteria and causes mislocalization of essential membrane-associated proteins, including MinD and FtsA. Importantly, DCAP kills nutrient-deprived microbes and sterilizes bacterial biofilms. DCAP is lethal against bacterial cells, has no effect on red blood cell membranes, and only decreases the viability of mammalian cells after ≥6 h. We conclude that membrane-active compounds are a promising solution for treating persistent infections. DCAP expands the limited number of compounds in this class of therapeutic small molecules and provides new opportunities for the development of potent broad-spectrum antimicrobial agents.
机译:持久性感染通常是由休眠和生物膜相关细菌引起的,这些细菌通常表现出缓慢的生长。需要快速细胞生长的抗生素可能对这些生物无效,因此无法预防再次发生的感染。与基于生长的抗菌剂相反,靶向膜的药物可有效杀死生长缓慢的细菌。在这里,我们介绍一种有效的2-((3-(3,6-二氯-9H-咔唑-9-基)-2-羟丙基)氨基)-2-(羟甲基)丙烷-1,3-二醇(DCAP)广谱抗生素,可降低革兰氏阳性和革兰氏阴性细菌的跨膜潜能,并引起必需的膜相关蛋白(包括MinD和FtsA)的错误定位。重要的是,DCAP可以杀死营养缺乏的微生物,并对细菌生物膜进行灭菌。 DCAP对细菌细胞具有致死性,对红细胞膜无影响,并且仅在≥6h后降低哺乳动物细胞的活力。我们得出结论,膜活性化合物是治疗持续感染的有前途的解决方案。 DCAP在这类治疗性小分子中扩展了有限数量的化合物,并为开发有效的广谱抗菌剂提供了新的机会。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2012年第28期|p.11322-11325|共4页
  • 作者单位

    Department of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States;

    Department of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States;

    Max Planck Institute for Terrestrial Microbiology, Philipps University 35043 Marburg, Germany,LOEWE Center for Synthetic Microbiology, and Philipps University 35043 Marburg, Germany;

    Cellular and Molecular Biology Program, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States;

    National Magnetic Resonance Facility at Madison, and University of Wisconsin-Madison, Madison, Wisconsin 53706, United States;

    Max Planck Institute for Terrestrial Microbiology, Philipps University 35043 Marburg, Germany,LOEWE Center for Synthetic Microbiology, and Philipps University 35043 Marburg, Germany,Faculty of Biology, Philipps University 35043 Marburg, Germany;

    Department of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States,Department of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:13:33

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