Meridianin D Analogues Display Antibiofilm Activity against MRSA and Increase Colistin Efficacy in Gram-Negative Bacteria

被引:48
作者
Huggins, William M. [1 ]
Barker, William T. [1 ]
Baker, James T. [1 ]
Hahn, Nicholas A. [1 ]
Melander, Roberta J. [1 ]
Melander, Christian [1 ]
机构
[1] North Carolina State Univ, Dept Chem, 2620 Yarbrough Dr, Raleigh, NC 27695 USA
来源
ACS MEDICINAL CHEMISTRY LETTERS | 2018年 / 9卷 / 07期
基金
美国国家卫生研究院;
关键词
Antibiotic resistance; antibiotics; biofilms; antibiotic repotentiation; antibiotic adjuvants; INDOLE ALKALOIDS; RESISTANCE; APLIDIUM; INDOLYLPYRIMIDINES; ANTIMALARIAL; INHIBITORS; SUPPRESS; BIOFILMS;
D O I
10.1021/acsmedchemlett.8b00161
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In the last 30 years, development of new classes of antibiotics has slowed, increasing the necessity for new options to treat multidrug resistant bacterial infections. Development of antibiotic adjuvants that increase the effectiveness of currently available antibiotics is a promising alternative approach to classical antibiotic development. Reports of the ability of the natural product meridianin D to modulate bacterial behavior have been rare. Herein, we describe the ability of meridianin D to inhibit biofilm formation of methicillin-resistant Staphylococcus aureus (MRSA) and to increase the potency of colistin against colistin-resistant and sensitive Gram-negative bacteria. Analogues were identified that are capable of inhibiting and dispersing MRSA biofilms and lowering the colistin MIC to below the CLSI breakpoint against Acinetobacter baumannii, Klebsiella pneumoniae, and Escherichia coli.
引用
收藏
页码:702 / 707
页数:11
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