University of Groningen and University Medical Center Groningen, W. J. Kolff Institute, Department of Orthodontics, Groningen, The Netherlands.
University of Groningen and University Medical Center Groningen, W. J. Kolff Institute, Department of Biomedical Engineering, Groningen, The Netherlands.
mBio. 2019 Sep 10;10(5):e01908-19. doi: 10.1128/mBio.01908-19.
Bacterial adhesion is accompanied by altered gene expression, leading to "emergent" properties of biofilm bacteria that are alien to planktonic ones. With the aim of revealing the role of environmental adhesion forces in emergent biofilm properties, genes in UA159 and a quorum-sensing-deficient mutant were identified that become expressed after adhesion to substratum surfaces. Using atomic force microscopy, adhesion forces of initial colonizers on four different substrata were determined and related to gene expression. Adhesion forces upon initial contact were similarly low across different substrata, ranging between 0.2 and 1.2 nN regardless of the strain considered. Bond maturation required up to 21 s, depending on the strain and substratum surface involved, but stationary adhesion forces also were similar in the parent and in the mutant strain. However, stationary adhesion forces were largest on hydrophobic silicone rubber (19 to 20 nN), while being smallest on hydrophilic glass (3 to 4 nN). gene expression in thin (34 to 48 μm) 5-h UA159 biofilms was most sensitive to adhesion forces, while expression of and expressions was weakly sensitive. , , , and expression was insensitive to adhesion forces. In thicker (98 to 151 μm) 24-h biofilms, adhesion-force-induced gene expression and emergent extracellular polymeric substance (EPS) production were limited to the first 20 to 30 μm above a substratum surface. In the quorum-sensing-deficient , adhesion-force-controlled gene expression was absent in both 5- and 24-h biofilms. Thus, initial colonizers of substratum surfaces sense adhesion forces that externally trigger emergent biofilm properties over a limited distance above a substratum surface through quorum sensing. A new concept in biofilm science is introduced: "adhesion force sensitivity of genes," defining the degree up to which expression of different genes in adhering bacteria is controlled by the environmental adhesion forces they experience. Analysis of gene expression as a function of height in a biofilm showed that the information about the substratum surface to which initially adhering bacteria adhere is passed up to a biofilm height of 20 to 30 μm above a substratum surface, highlighting the importance and limitations of cell-to-cell communication in a biofilm. Bacteria in a biofilm mode of growth, as opposed to planktonic growth, are responsible for the great majority of human infections, predicted to become the number one cause of death in 2050. The concept of adhesion force sensitivity of genes provides better understanding of bacterial adaptation in biofilms, direly needed for the design of improved therapeutic measures that evade the recalcitrance of biofilm bacteria to antimicrobials.
细菌黏附伴随着基因表达的改变,导致生物膜细菌出现浮游细菌所没有的“新兴”特性。为了揭示环境黏附力在新兴生物膜特性中的作用,我们鉴定了 UA159 和群体感应缺陷突变体中在黏附到基质表面后表达的基因。使用原子力显微镜,确定了初始定植菌在四种不同基质上的黏附力,并将其与基因表达相关联。无论考虑的是哪种菌株,初始接触时的黏附力在不同基质上都相似较低,范围在 0.2 到 1.2 nN 之间。键的成熟需要长达 21 秒,具体取决于菌株和基质表面,但亲本菌株和突变菌株的固定黏附力也相似。然而,固定黏附力在疏水性硅橡胶上最大(19 到 20 nN),而在亲水性玻璃上最小(3 到 4 nN)。在较薄的(34 到 48 μm)5 小时 UA159 生物膜中,基因表达对黏附力最敏感,而 和 表达的敏感性较弱。 、 、 和 表达对黏附力不敏感。在较厚的(98 到 151 μm)24 小时生物膜中,黏附力诱导的基因表达和新兴胞外聚合物(EPS)的产生仅限于基质表面上方 20 到 30 μm 的范围内。在群体感应缺陷的 中,5 小时和 24 小时生物膜中均不存在黏附力控制的基因表达。因此,基质表面的初始定植菌感知黏附力,这些力通过群体感应在基质表面上方有限的距离之外触发新兴生物膜特性。本文提出了生物膜科学中的一个新概念:“基因对黏附力的敏感性”,定义了不同基因在黏附细菌中的表达受其经历的环境黏附力控制的程度。对生物膜中基因表达与高度的关系进行分析表明,最初黏附的细菌所黏附的基质表面的信息传递到基质表面上方 20 到 30 μm 的生物膜高度,突出了细胞间通讯在生物膜中的重要性和局限性。与浮游生长相比,处于生物膜生长模式的细菌是导致人类绝大多数感染的原因,预计到 2050 年将成为头号死亡原因。基因对黏附力敏感性的概念为更好地理解生物膜中细菌的适应性提供了帮助,这对于设计逃避生物膜细菌对抗微生物药物的顽固性的改进治疗措施是非常必要的。