流出
表型
抗菌剂
表达式(计算机科学)
抗菌肽
抗生素耐药性
生物
微生物学
遗传学
抗生素
计算机科学
基因
程序设计语言
作者
Ka Kiu Lee,Urszula Łapińska,Giulia Tolle,Wanida Phetsang,Anthony D. Verderosa,Brandon M. Invergo,Joseph Westley,Attila Bebes,Raif Yuecel,Paul O’Neill,Audrey Farbos,Aaron R. Jeffries,Stineke van Houte,Pierluigi Caboni,Mark A. T. Blaskovich,Benjamin E. Housden,Krasimira Tsaneva‐Atanasova,Stefano Pagliara
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2024-04-22
被引量:2
标识
DOI:10.1101/2024.04.22.590445
摘要
Antimicrobial resistance threatens the viability of modern medical interventions. There is a dire need of developing novel approaches to counter resistance mechanisms employed by starved or slow-growing pathogens that are refractory to conventional antimicrobial therapies. Antimicrobial peptides have been advocated as potential therapeutic solutions due to low levels of genetic resistance observed in bacteria against these compounds. However, here we show that subpopulations of stationary phase Escherichia coli and Pseudomonas aeruginosa survive tachyplesin treatment without genetic mutations. These phenotypic variants induce efflux, outer membrane vesicles secretion and membrane modifications in response to tachyplesin exposure, sequestering the peptide in their membranes where it cannot exert its antimicrobial activity. We discovered that formation of these phenotypic variants could be prevented by administering tachyplesin in combination with sertraline, a clinically used antidepressant, suggesting a novel approach for combatting antimicrobial-refractory stationary phase bacteria.
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