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Antibacterial Flavonoids from Medicinal Plants Covalently Inactivate Type Ⅲ Protein Secretion Substrates

机译:药用植物中的抗菌类黄酮共价灭活Ⅲ型蛋白分泌基质。

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摘要

Traditional Chinese Medicines (TCMs) have been historically used to treat bacterial infections. However, the molecules responsible for these anti-infective properties and their potential mechanisms of action have remained elusive. Using a high-throughput assay for type Ⅲ protein secretion in Salmonella enterica serovar Typhimurium, we discovered that several TCMs can attenuate this key virulence pathway without affecting bacterial growth. Among the active TCMs, we discovered that baicalein, a specific flavonoid from Scutellaria baicalensis, targets S. Typhimurium pathogenicity island-1 (SPI-1) type Ⅲ secretion system (T3SS) effectors and translocases to inhibit bacterial invasion of epithelial cells. Structurally related flavonoids present in other TCMs, such as quercetin, also inactivated the SPI-l T3SS and attenuated S. Typhimurium invasion. Our results demonstrate that specific plant metabolites from TCMs can directly interfere with key bacterial virulence pathways and reveal a previously unappreciated mechanism of action for anti-infective medicinal plants.
机译:传统中药(TCM)在历史上一直用于治疗细菌感染。但是,负责这些抗感染特性的分子及其潜在的作用机理仍然难以捉摸。通过高通量分析沙门氏菌鼠伤寒沙门氏菌Ⅲ型蛋白的分泌,我们发现几种中药可以减弱这种关键的毒力途径而不会影响细菌的生长。在活跃的中药中,我们发现黄ical素(一种来自黄cut的特定类黄酮)靶向鼠伤寒沙门氏菌致病岛-1(SPI-1)Ⅲ型分泌系统(T3SS)效应子和转座酶,以抑制细菌入侵上皮细胞。存在于其他TCM中的结构相关的类黄酮(例如槲皮素)也使SPI-1 T3SS失活,并减轻了鼠伤寒沙门氏菌的入侵。我们的结果表明,来自中药的特定植物代谢产物可直接干扰关键细菌的毒力途径,并揭示出抗感染药用植物先前未曾了解的作用机理。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2016年第7期|2209-2218|共10页
  • 作者单位

    Laboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University, New York, New York 10065, United States,Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan Town, Miaoli County 35053,Taiwan, R.O.C.;

    Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, Connecticut 06536, United States;

    Laboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University, New York, New York 10065, United States;

    Laboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University, New York, New York 10065, United States;

    Laboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University, New York, New York 10065, United States;

    Laboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University, New York, New York 10065, United States;

    Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, Connecticut 06536, United States;

    Laboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University, New York, New York 10065, United States;

    Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, Connecticut 06536, United States;

    Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06520, United States;

    Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06520, United States;

    Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06520, United States;

    Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, Connecticut 06536, United States;

    Laboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University, New York, New York 10065, 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);
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