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绿原酸通过增强RsmA的表达抑制铜绿假单胞菌生物被膜的形成

  • 唐小丽1 ,
  • 韦俊彬2 ,
  • 封毅3 ,
  • 乐宁3 ,
  • 梁丹娜4 ,
  • 卓少元3 ,
  • 尚立国3
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  • 1. 广西中医药大学护理学院,广西 南宁 530200; 2. 广西中医药大学教学与实验中心,广西 南宁 530200; 3. 广西中医药大学基础医学院,广西 南宁 530200; 4. 广西中医药大学赛恩斯新医药学院,广西 南宁 530222

收稿日期: 2020-08-31

  网络出版日期: 2021-10-25

基金资助

广西自然科学基金青年基金(2019GXNSFBA245078),广西中医药大学2018年引进博士科研启动基金(2018BS008),广西中医药大学校级科研项目(2019QN008)

Chlorogenic acid represses biofilm formation of Pseudomonas aeruginosa via increasing RsmA expression

  • TANG Xiaoli1 ,
  • WEI Junbin2 ,
  • FENG Yi3 ,
  • LE Ning3 ,
  • LIANG Danna4 ,
  • ZHUO Shaoyuan3 ,
  • SHANG Liguo3
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  • 1. Faculty of Nursing, Guangxi University of Chinese Medicine, Nanning 530200, Guangxi, China; 2. Teaching and Experimental Center, Guangxi University of Chinese Medicine, Nanning 530200, Guangxi, China; 3. School of Basic Medical Science, Guangxi University of Chinese Medicine, Nanning 530200, Guangxi, China; 4. Faculty of Chinese Medicine Science, Guangxi University of Chinese Medicine, Nanning 530222, Guangxi, China

Received date: 2020-08-31

  Online published: 2021-10-25

摘要

铜绿假单胞菌是常见的人类条件致病菌,其生物被膜的形成会增强菌体的耐药性。已有文献报道绿原酸可抑制铜绿假单胞菌生物被膜的形成,本研究在此基础上主要探究了其对全局性次级代谢调控系统Gac-Rsm表达的影响。结果显示,绿原酸可抑制铜绿假单胞菌生物被膜形成的能力,降低胞外总多糖合成量,但关键胞外多糖psl的合成酶基因pslA转录未受影响,还可增强Gac-Rsm系统中关键调控因子RsmA的表达水平,降低细胞内关键信使分子环二鸟苷酸(cyclic dimeric guanosine monophosphate,c-di-GMP)水平。结果表明,绿原酸可通过增强RsmA的表达来抑制铜绿假单胞菌生物被膜的形成。

本文引用格式

唐小丽1 , 韦俊彬2 , 封毅3 , 乐宁3 , 梁丹娜4 , 卓少元3 , 尚立国3 . 绿原酸通过增强RsmA的表达抑制铜绿假单胞菌生物被膜的形成[J]. 微生物与感染, 2021 , 16(5) : 322 -330 . DOI: DOI:10.3969/j.issn.1673-6184.2021.05.005

Abstract

Pseudomonas aeruginosa (P. aeruginosa) is a common human opportunistic pathogen, and the biofilm formation could enhance its antibiotic tolerance. Chlorogenic acid (CA) has been reported to repress the biofilm formation of P. aeruginosa, so the present study aims to further explore the regulatory mechanism of CA, especially the effect of CA on the expression of Gac-Rsm (global secondary metabolism regulation system). The results showed that CA could repress the biofilm formation of P. aeruginosa, reduce exopolysaccharide production, although the transcription level of pslA (synthetase gene of key exopolysaccharide psl) was not significantly changed. The expression of RsmA (core regulator in Gac-Rsm system) was enhanced and the level of key signal molecule cyclic dimeric guanosine monophosphate (c-di-GMP) was reduced. It is suggested that CA represses the biofilm formation of P. aeruginosa via increasing the expression of RsmA.
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