http://jcps.bjmu.edu.cn

中国药学(英文版) ›› 2016, Vol. 25 ›› Issue (4): 310-315.DOI: 10.5246/jcps.2016.04.035

• 【研究论文】 • 上一篇    下一篇

KL-0153, 一种新型铜绿假单胞菌MexAB-OprM外排泵抑制剂

刘忆霜1, 王颖1, 郑佳音2, 李兴华1, 关艳1, 黄树超1, 肖春玲1*   

  1. 1. 中国医学科学院 北京协和医学院 医药生物技术研究所 国家新药(微生物)筛选实验室, 北京 100050
    2. 首都医科大学 神经生物学系, 北京 100069
  • 收稿日期:2016-01-05 修回日期:2016-02-24 出版日期:2016-04-21 发布日期:2016-02-29
  • 通讯作者: Tel.: 86-10-63020226, E-mail: xiaocl318@163.com
  • 基金资助:

    National High-tech R&D Program (863 Program, Grant No. 2015AA020911), and National Natural Science Foundation (Grant No. 81102353).

KL-0153, a novel inhibitor of Pseudomonas aeruginosa MexAB-OprM efflux pump

Yishuang Liu1, Ying Wang1, Jiayin Zheng2, Xinghua Li1, Yan Guan1, Shuchao Huang1, Chunling Xiao1*   

  1. 1. National Key Lab for Screening New Microbial Drugs, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China
    2. Department of Neurobiology, Capital Medical University, Beijing 100069, China
  • Received:2016-01-05 Revised:2016-02-24 Online:2016-04-21 Published:2016-02-29
  • Contact: Tel.: 86-10-63020226, E-mail: xiaocl318@163.com
  • Supported by:

    National High-tech R&D Program (863 Program, Grant No. 2015AA020911), and National Natural Science Foundation (Grant No. 81102353).

摘要:

铜绿假单胞菌是一种具有高发病率和死亡率的条件致病菌。以MexAB-OprM外排泵为主的耐药节结化细胞分化家族多药耐药外排系统的存在是铜绿假单胞菌产生多药耐药的主要原因。MexAB-OprM外排泵抑制剂可以显著增强被MexAB-OprM外排的抗生素的活性, 作为抗菌药物增效剂, 具有良好的临床应用前景。在本研究中, 通过小分子库筛选得到了一种新型的MexAB-OprM外排泵抑制剂KL-0153, 通过与抗生素的协同活性研究以及EB积累检测证明了其对于MexAB-OprM的抑制活性。在表达MexAB-OprM的铜绿假单胞菌菌株, 特别是MexAB-OprM高表达株中, KL-0153与被MexAB-OprM外排的抗生素有协同作用, 并且在EB积累检测中, 其活性强于阳性药羰基---氯苯腙。尽管KL-0153也具有明显的肝肾毒性, 但作为先导化合物, 对于KL-0153的进一步研究将有助于新型MexAB-OprM外排泵抑制剂的研发。

关键词: 铜绿假单胞菌, 多药耐药, 外排泵, MexAB-OprM, 抑制剂, 抗菌药物增效剂

Abstract:

Pseudomonas aeruginosa is an opportunistic pathogen that contributes to high morbidity and mortality. MexAB-OprM is the main efflux pump among the Resistance-Nodulation-Division family multi-drug efflux systems, which contribute greatly to the multidrug resistance of P. aeruginosa. Efflux pump inhibitors (EPIs) of MexAB-OprM could enhance the activity of the antibiotics effluxed by MexAB-OprM, and thus they might be useful in the clinic as antibacterial synergistic agents. In this work, a new EPI of MexAB-OprM, KL-0153, was discovered by screening of a small molecular library. Its inhibition of MexAB-OprM was confirmed by assays of synergistic activity and EB accumulation. The activity of KL-0153 was shown to be synergistic with antibiotics effluxed by MexAB-OprM when they were tested against strains expressing MexAB-OprM, especially so for the strains that express MexAB-OprM at high levels. KL-0153 showed more activity than the positive drug carbonyl cyanide m-chlorophenylhydrazone in the EB accumulation assay. It cannot be neglected that KL-0153 has significant liver and kidney toxicity. However, KL-0153 may be a lead compound for the research and development of new types of EPIs.

Key words: Pseudomonas aeruginosa, Multi-drug resistance, Efflux pump, MexAB-OprM, Inhibitor, Antibacterial drug synergistic agent

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