A predicted S-type pyocin shows a bactericidal activity against clinical Pseudomonas aeruginosa isolates through membrane damage

被引:53
作者
Ling, Hua [1 ]
Saeidi, Nazanin [1 ]
Rasouliha, Bahareh Haji [1 ]
Chang, Matthew Wook [1 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, Singapore 637459, Singapore
来源
FEBS LETTERS | 2010年 / 584卷 / 15期
基金
英国医学研究理事会;
关键词
PA0985; Pyocin S5; Bacteriocin; Bactericidal activity; Membrane damage; Pseudomonas aeruginosa; BACTERIOCINS; PAO1;
D O I
10.1016/j.febslet.2010.06.021
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
The nucleic acid sequence at the positions 1067817-1066321 of Pseudomonas aeruginosa PAO1 genome was predicted to encode a novel S-type pyocin, designated S5, based on the genome sequence. However, its antimicrobial spectrum, activity and mechanism have not been investigated. Herein, we report that pyocin S5 has an antimicrobial activity against seven clinical P. aeruginosa isolates (DWW3, InA, InB, In3, In4, In7, and In8). Among them, DWW3 is most sensitive with a minimum inhibitory concentration of 12.6 mu g/ml and a killing percentage of 95.7 at 225 mu g/ml. Further, we demonstrated that the antimicrobial mechanism of pyocin S5 is membrane damage, evidenced by the leakage of intracellular materials, the increase of membrane permeability, and cell surface disruption. (C) 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3354 / 3358
页数:5
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