Synergy between the clavanins as a weapon against multidrug-resistant Enterobacter cloacae

被引:0
|
作者
Naing, Marvin D. [1 ]
Juliano, Samuel A. [1 ]
Angeles-Boza, Alfredo M. [1 ,2 ]
机构
[1] Univ Connecticut, Dept Chem, Storrs, CT 06269 USA
[2] Univ Connecticut, Inst Mat Sci, Storrs, CT 06269 USA
来源
RSC MEDICINAL CHEMISTRY | 2024年 / 15卷 / 06期
关键词
ANTIMICROBIAL PEPTIDES; PH;
D O I
10.1039/d4md00070f
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Finding new antibiotics that can act synergistically with each other offers many benefits such as lower dosages used for each drug, improved pathogen clearance, and ability to act against multi-drug resistant strains. In this study, six peptides isolated from the tunicate Styela clava were evaluated for their synergistic interaction using the checkerboard assay and the time kill kinetics assay. Using two different tests, we report synergy between clavanin D and clavaspirin in both tests and synergy between clavanin A and B only in the checkerboard test when used against the multidrug resistant E. cloacae 0136. This work demonstrates the possible cooperativity between homologous AMPs from a single organism and the advantage of using two susceptibility tests instead of one when testing synergistic combinations.
引用
收藏
页码:2160 / 2164
页数:5
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