FliA-Dependent Surface Macromolecules Promote Initial Biofilm Development of Escherichia coli by Influencing the Bacterial Surface Properties

Fatma Pınar GÖRDESLİ DUATEPE
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Abstract

FliA is an important regulatory component for the synthesis of surface macromolecules which are involved in motility and biofilm development of Escherichia coli. In this study, the roles of FliA-dependent surface macromolecules in E. coli surface tension, surface heterogeneity and surface roughness, and initial biofilm development consisting of reversible and irreversible adhesion were investigated using E. coli MG1655 wild-type strain and fliA gene deleted mutant strain. Negative Gibbs free energy change values calculated using bacterial surface tensions obtained by a spectrophotometric method showed that both wild-type and mutant cells in water can reversibly adhere to the surface of the model solid, silicon nitride (Si3N4). The calculations further showed that bacterial reversible auto-adhesion and co-adhesion were also thermodynamically favorable. In comparison, the reversible adhesion and auto-adhesion capacities of wild-type cells were higher than the mutant cells. Direct measurements by atomic force microscopy (AFM) and thorough analysis of the recorded adhesion data showed that the irreversible adhesion strength of wild-type cells to Si3N4 in water was at least 2.0-fold greater than that of the mutants due to significantly higher surface heterogeneity resulting in higher surface roughness for the wild-type cells compared to those obtained for the mutants. These results suggest that strategies aimed at preventing E. coli biofilm development should also consider a combined method, such as modifying the surface of interest with a bacterial repellent layer and targeting the FliA and FliA-dependent surface macromolecules to reduce both reversible and irreversible bacterial adhesion and hence the initial biofilm development of E. coli.
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依赖于flia的表面大分子通过影响细菌表面特性促进大肠杆菌的初始生物膜发育
FliA是大肠杆菌表面大分子合成的重要调控成分,参与大肠杆菌的运动和生物膜发育。本研究以大肠杆菌MG1655野生型菌株和fliA基因缺失突变菌株为研究对象,研究了依赖fliA的表面大分子在大肠杆菌表面张力、表面异质性和表面粗糙度以及由可逆和不可逆粘附组成的初始生物膜发育中的作用。利用分光光度法得到的细菌表面张力计算的负吉布斯自由能变化值表明,野生型和突变型细胞在水中都可以可逆地粘附在模型固体氮化硅(Si3N4)的表面。计算进一步表明,细菌可逆的自粘附和共粘附在热力学上也是有利的。相比之下,野生型细胞的可逆粘附能力和自粘附能力均高于突变型细胞。原子力显微镜(AFM)的直接测量和对记录的粘附数据的深入分析表明,野生型细胞对水中氮化硅的不可逆粘附强度至少是突变体的2.0倍,这是由于与突变体相比,野生型细胞的表面异质性明显更高,导致表面粗糙度更高。这些结果表明,旨在阻止大肠杆菌生物膜发育的策略还应考虑综合方法,例如用细菌排斥层修饰感兴趣的表面,并靶向FliA和依赖FliA的表面大分子,以减少可逆和不可逆的细菌粘附,从而减少大肠杆菌的初始生物膜发育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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