Shafiei Morvarid, Abdi-Ali Ahya, Shahcheraghi Fereshteh, Vali Hojatollah, Shahbani Zahiri Hossein, Akbari Noghabi Kambiz
Department of Microbiology, Faculty of Biological Sciences, Alzahra University, Tehran, Iran.
Department of Bacteriology, Pasteur Institute of Iran, Tehran, Iran.
Appl Biochem Biotechnol. 2017 Aug;182(4):1444-1457. doi: 10.1007/s12010-017-2409-4. Epub 2017 Jan 30.
Pseudomonas aeruginosa biofilm-related infections are the major cause of premature death in cystic fibrosis patients. Strategies to induce biofilm dispersal are of interest, because of their potential in preventing biofilm-related infections. Our previous work demonstrated that n-butanolic Cyclamen coum extract with ciprofloxacin could eliminate 1- and 3-day-old P. aeruginosa PAO1 biofilms. To gain new insights into the role of C. coum extract and its synergistic effect with ciprofloxacin in eliminating P. aeruginosa PAO1 biofilms, two-dimensional gel electrophoresis (2-DE) in combination with mass spectrometry-based protein identification were used. Changes in the bacterial protein expression were analyzed when 3-day-old biofilm cells were exposed to the C. coum extract alone and in combination with ciprofloxacin. Proteins involved in alginate biosynthesis, quorum sensing, adaptation/protection, carbohydrate and amino acid metabolism showed a weaker expression in the C. coum extract-ciprofloxacin-treated biofilm cells compared to those in the untreated cells. Interestingly, the proteome of C. coum extract-ciprofloxacin-treated biofilm revealed more resemblance to the planktonic phenotype than to the biofilm phenotype. It appears that saponin extract in combination with ciprofloxacin causes biofilm disruption due to several mechanisms such as motility induction, cell envelope integrity perturbation, stress protein expression reduction, and more importantly, signal transduction perturbation. In conclusion, exposure to a combination of biofilm dispersal such as saponin extract and antimicrobial agents may offer a novel strategy to control preestablished, persistent P. aeruginosa biofilms and biofilm-related infections.
铜绿假单胞菌生物膜相关感染是囊性纤维化患者过早死亡的主要原因。诱导生物膜分散的策略备受关注,因为它们在预防生物膜相关感染方面具有潜力。我们之前的研究表明,正丁醇提取的仙客来提取物与环丙沙星联合使用可以消除1天龄和3天龄的铜绿假单胞菌PAO1生物膜。为了深入了解仙客来提取物的作用及其与环丙沙星在消除铜绿假单胞菌PAO1生物膜中的协同效应,采用了二维凝胶电泳(2-DE)结合基于质谱的蛋白质鉴定方法。当3天龄的生物膜细胞单独暴露于仙客来提取物以及与环丙沙星联合暴露时,分析细菌蛋白质表达的变化。与未处理的细胞相比,参与藻酸盐生物合成、群体感应、适应/保护、碳水化合物和氨基酸代谢的蛋白质在仙客来提取物-环丙沙星处理的生物膜细胞中表达较弱。有趣的是,仙客来提取物-环丙沙星处理的生物膜的蛋白质组与浮游表型的相似性高于生物膜表型。似乎皂苷提取物与环丙沙星联合使用通过多种机制导致生物膜破坏,如诱导运动性、扰乱细胞膜完整性、降低应激蛋白表达,更重要的是,扰乱信号转导。总之,暴露于皂苷提取物等生物膜分散剂与抗菌剂的组合可能为控制已形成的、持续性的铜绿假单胞菌生物膜及生物膜相关感染提供一种新策略。