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Structural organization and dynamics of exopolysaccharide matrix and microcolonies formation by Streptococcus mutans in biofilms

机译:变形链球菌在生物膜中胞外多糖基质的结构组织和动力学以及微菌落的形成

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Aims:To investigate the structural organization and dynamics of exopolysaccharides (EPS) matrix and microcolonies formation by Streptococcus mutans during the biofilm development process.Methods and Results:Biofilms of Strep. mutans were formed on saliva-coated hydroxyapatite (sHA) discs in the presence of glucose or sucrose (alone or mixed with starch). At specific time points, biofilms were subjected to confocal fluorescence imaging and computational analysis. EPS matrix was steadily formed on sHA surface in the presence of sucrose during the first 8 h followed by a threefold biomass increase between 8 and 30 h of biofilm development. The initial formation and further development of three-dimensional microcolony structure occurred concomitantly with EPS matrix synthesis. Tridimensional renderings showed EPS closely associated with microcolonies throughout the biofilm development process forming four distinct domains (i) between sHA surface and microcolonies, (ii) within, (iii) covering and (iv) filling the spaces between microcolonies. The combination of starch and sucrose resulted in rapid formation of elevated amounts of EPS matrix and faster assembly of microcolonies by Strep. mutans, which altered their structural organization and susceptibility of the biofilm to acid killing (vs sucrose-grown biofilms; P < 0 center dot 05).Conclusions:Our data indicate that EPS modulate the development, sequence of assembly and spatial distribution of microcolonies by Strep. mutans.Significance and Impact of the Study:Simultaneous visualization and analysis of EPS matrix and microcolonies provide a more precise examination of the structural organization of biofilms than labelling bacteria alone, which could be a useful approach to elucidate the exact mechanisms by which Strep. mutans influences oral biofilm formation and possibly identify novel targets for effective antibiofilm therapies.
机译:目的:研究变形链球菌在生物膜形成过程中胞外多糖(EPS)基质的结构组织,动力学以及微菌落的形成。方法与结果:链球菌生物膜。在葡萄糖或蔗糖(单独或与淀粉混合)存在下,在唾液包被的羟基磷灰石(sHA)圆盘上形成变形菌。在特定时间点,对生物膜进行共聚焦荧光成像和计算分析。在最初的8小时内,在蔗糖存在下sHA表面上稳定形成EPS基质,然后在8至30小时的生物膜形成过程中生物量增加了三倍。三维微菌落结构的最初形成和进一步发展与EPS基质合成同时发生。三维渲染图显示EPS在整个生物膜发育过程中与微菌落紧密相关,形成了四个不同的域(i)在sHA表面和微菌落之间,(ii)在内部,(iii)覆盖和(iv)填充微菌落之间的空间。淀粉和蔗糖的结合可快速形成高含量的EPS基质,并通过Strep更快地组装微菌落。变形菌,改变了生物膜的结构组织和对酸杀死的敏感性(相对于蔗糖生长的生物膜; P <0中心点05)。结论:我们的数据表明,EPS可以通过以下方式调节微菌落的发育,组装顺序和空间分布链球菌。这项研究的意义和影响:与单独标记细菌相比,同时对EPS基质和微菌落进行可视化和分析可以更精确地检查生物膜的结构,这可能是阐明链球菌确切机制的有用方法。变形菌会影响口腔生物膜的形成,并可能确定有效抗生物膜疗法的新靶标。

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