Lau Peter C Y, Lindhout Theresa, Beveridge Terry J, Dutcher John R, Lam Joseph S
Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada.
J Bacteriol. 2009 Nov;191(21):6618-31. doi: 10.1128/JB.00698-09. Epub 2009 Aug 28.
Bacterial biofilms are responsible for the majority of all microbial infections and have profound impact on industrial and geochemical processes. While many studies documented phenotypic differentiation and gene regulation of biofilms, the importance of their structural and mechanical properties is poorly understood. Here we investigate how changes in lipopolysaccharide (LPS) core capping in Pseudomonas aeruginosa affect biofilm structure through modification of adhesive, cohesive, and viscoelastic properties at an early stage of biofilm development. Microbead force spectroscopy and atomic force microscopy were used to characterize P. aeruginosa biofilm interactions with either glass substrata or bacterial lawns. Using isogenic migA, wapR, and rmlC mutants with defined LPS characteristics, we observed significant changes in cell mechanical properties among these strains compared to wild-type strain PAO1. Specifically, truncation of core oligosaccharides enhanced both adhesive and cohesive forces by up to 10-fold, whereas changes in instantaneous elasticity were correlated with the presence of O antigen. Using confocal laser scanning microscopy to quantify biofilm structural changes with respect to differences in LPS core capping, we observed that textural parameters varied with adhesion or the inverse of cohesion, while areal and volumetric parameters were linked to adhesion, cohesion, or the balance between them. In conclusion, this report demonstrated for the first time that changes in LPS expression resulted in quantifiable cellular mechanical changes that were correlated with structural changes in bacterial biofilms. Thus, the interplay between architectural and functional properties may be an important contributor to bacterial community survival.
细菌生物膜是大多数微生物感染的罪魁祸首,对工业和地球化学过程有着深远影响。虽然许多研究记录了生物膜的表型分化和基因调控,但对其结构和力学性质的重要性却知之甚少。在此,我们研究了铜绿假单胞菌脂多糖(LPS)核心封端的变化如何通过在生物膜发育早期改变其粘附性、内聚性和粘弹性来影响生物膜结构。微珠力谱法和原子力显微镜被用于表征铜绿假单胞菌生物膜与玻璃基质或细菌菌苔之间的相互作用。使用具有特定LPS特征的同基因migA、wapR和rmlC突变体,我们观察到与野生型菌株PAO1相比,这些菌株的细胞力学性质有显著变化。具体而言,核心寡糖的截短使粘附力和内聚力增强了多达10倍,而瞬时弹性的变化与O抗原的存在相关。使用共聚焦激光扫描显微镜来量化生物膜结构随LPS核心封端差异的变化,我们观察到纹理参数随粘附力或内聚力的倒数而变化,而面积和体积参数与粘附力、内聚力或它们之间的平衡有关。总之,本报告首次证明LPS表达的变化导致了可量化的细胞力学变化,这些变化与细菌生物膜的结构变化相关。因此,结构和功能性质之间的相互作用可能是细菌群落生存的一个重要因素。