Institute of Cell and Molecular Biology, University of Edinburgh, Edinburgh, UK.
J Appl Microbiol. 1998 Dec;85 Suppl 1:13S-18S. doi: 10.1111/j.1365-2672.1998.tb05278.x.
A plasmid encoding the green fluorescent protein (GFP) of Aequorea victoria was transformed into a biofilm-forming strain of Enterobacter agglomerans originally isolated from an industrial environment. The transformed strain, EntGFP, could then be identified in dual species biofilms by direct visualization, plate counts and quantitiative fluorescence measurements. A variety of cell constituents and products may be involved in the adhesion and accumulation process and exopolysaccharides (EPS) represent one of these factors. The involvement of EPS in the initial adhesion events and the role in dual species biofilm development was investigated. Cells of EntGFP and Klebsiella pneumoniae Gl interact forming biofilms more successfully in a mixture than in isolation. The co-resistance results in enhanced biofilm formation and increased resistance to disinfection. Microscopic examination showed that the two species were often closely juxtaposed in microcolonies, suggesting the interactions involve surface-associated macromolecules. Fluorescence was used to measure the adhesion of EntGFP cells to Kleb, pneumoniae Gl (Gl) EPS. The results showed EntGFP adhered better to Gl EPS that Ent EPS. Polysaccharde depolymerases isolated from a bacteriophage for Ent. agglomerans were used to degrade Ent EPS specifically. Following polysaccharase treatment, the adhaesion of EntGFP to Gl cells was reduced. This suggests both types of EPS mediate adhesion. The two types of EPS were dissolved in dimethylsulphoxide and when mixed, their viscosity increased, reaching a maximum after ∼+40 min. This may partially explain the increased protection of dual species biofilms from disinfectants. The depolymerases were used to treat dual species biofilms and this resulted in the effective removal of both species from the surface. This may suggest Ent contributes more EPS to the biofilm matrix. The EPS play an important role in EntGFP and Gl dual species biofilm formation both as adhesins and as the EPS interact, changing their physical properties.
一个编码维多利亚水母绿色荧光蛋白(GFP)的质粒被转化到一种原本从工业环境中分离出来的成团肠杆菌的生物膜形成菌株中。通过直接可视化、平板计数和定量荧光测量,可以在双物种生物膜中识别转化后的菌株 EntGFP。各种细胞成分和产物可能参与到粘附和积累过程中,而胞外多糖(EPS)就是其中之一。我们研究了 EPS 在初始粘附事件中的作用及其在双物种生物膜形成中的作用。EntGFP 细胞和肺炎克雷伯菌 Gl 在混合物中比在分离状态下更成功地相互作用形成生物膜。共同耐药导致生物膜形成增强和对消毒的抵抗力增加。显微镜检查表明,这两个物种经常在微群落中紧密相邻,表明这些相互作用涉及表面相关的大分子。荧光用于测量 EntGFP 细胞对肺炎克雷伯菌 Gl(Gl)EPS 的粘附。结果表明,EntGFP 对 Gl EPS 的粘附性优于 Ent EPS。从噬菌体中分离的多糖解聚酶被用于特异性降解 Ent 团聚杆菌的 Ent EPS。多糖酶处理后,EntGFP 对 Gl 细胞的粘附减少。这表明两种类型的 EPS 都介导了粘附。将两种类型的 EPS 溶解在二甲基亚砜中,当混合时,它们的粘度增加,在大约+40 分钟后达到最大值。这可能部分解释了双物种生物膜对消毒剂的保护增加。使用这些酶处理双物种生物膜,结果导致两种物种都从表面有效去除。这可能表明 Ent 对生物膜基质的贡献更多的是 EPS。EPS 在 EntGFP 和 Gl 双物种生物膜形成中都起着重要作用,既是粘附剂,也是 EPS 相互作用,改变它们的物理性质。