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姜黄素与表没食子儿茶素没食子酸酯(EGCG)联合使用对多重耐药鲍曼不动杆菌的体外活性

In vitro activity of curcumin in combination with epigallocatechin gallate (EGCG) versus multidrug-resistant Acinetobacter baumannii.

作者信息

Betts Jonathan W, Wareham David W

机构信息

Antimicrobial Research Group, Centre for Immunology and Infectious Disease, Blizard Institute, Queen Mary University London, 4, Newark Street, Whitechapel, London E1 2AT, UK.

出版信息

BMC Microbiol. 2014 Jun 27;14:172. doi: 10.1186/1471-2180-14-172.

Abstract

BACKGROUND

Acinetobacter baumannii is an opportunistic human pathogen often associated with life-threatening infections in the immunocompromised and the critically ill. Strains are often multidrug-resistant (MDR) and due to the lack of new synthetic antimicrobials in development for treatment, attention is increasingly focused on natural compounds either as stand-alone or adjunctive agents. Curcumin (CCM) is a natural polyphenol found in turmeric and isolated from the plant, Curcuma longa. Curcumin has been found to possess many biological properties, including antibacterial activity. In this study the antimicrobial activity of CCM and synergistic effects with epigallocatechin gallate (EGCG) against multidrug-resistant strains of A. baumannii were investigated and assessed via checkerboard and time-kill assays.

RESULTS

The MIC of CCM was >256 μg/mL against all strains of A. baumannii whilst those for EGCG ranged from 128-1024 μg/mL. In checkerboard studies synergy was observed against 5/9 isolates, with an additive effect noted in the remaining 4. The addition of EGCG reduced the MIC of CCM by 3- to 7-fold, with the greatest interaction resulting in a CCM MIC of 4 μg/mL. Time-kill curves indicated that a CCM-EGCG (1:8 and 1:4) combination was bactericidal with a 4 to 5-log reduction in viable counts after 24 h compared to the most effective polyphenol alone.

CONCLUSIONS

This study demonstrates that despite little antibacterial activity alone, CCM activity is greatly enhanced in the presence of EGCG resulting in antibacterial activity against MDR A. baumannii. The combination may have a potential use in medicine as a topical agent to prevent or treat A. baumannii infections.

摘要

背景

鲍曼不动杆菌是一种机会性人类病原体,常与免疫功能低下和危重症患者的危及生命的感染相关。该菌株通常具有多重耐药性(MDR),由于目前缺乏正在研发的用于治疗的新型合成抗菌药物,人们越来越关注天然化合物,将其作为单独使用或辅助使用的药物。姜黄素(CCM)是一种存在于姜黄中的天然多酚,从植物姜黄中分离得到。已发现姜黄素具有许多生物学特性,包括抗菌活性。在本研究中,通过棋盘法和时间杀菌试验研究并评估了姜黄素对多重耐药鲍曼不动杆菌菌株的抗菌活性以及与表没食子儿茶素没食子酸酯(EGCG)的协同作用。

结果

姜黄素对所有鲍曼不动杆菌菌株的最低抑菌浓度(MIC)均>256μg/mL,而表没食子儿茶素没食子酸酯的MIC范围为128 - 1024μg/mL。在棋盘法研究中,观察到对5/9株分离菌有协同作用,其余4株有相加作用。添加表没食子儿茶素没食子酸酯使姜黄素的MIC降低了3至7倍,最大相互作用使姜黄素的MIC降至4μg/mL。时间杀菌曲线表明,与单独使用最有效的多酚相比,姜黄素 - 表没食子儿茶素没食子酸酯(1:8和1:4)组合具有杀菌作用,24小时后活菌数减少4至5个对数级。

结论

本研究表明,尽管姜黄素单独抗菌活性较低,但在表没食子儿茶素没食子酸酯存在下其活性大大增强,从而对多重耐药鲍曼不动杆菌具有抗菌活性。该组合可能在医学上作为局部用药预防或治疗鲍曼不动杆菌感染具有潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a6/4083870/819839fe3638/1471-2180-14-172-1.jpg

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