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细胞外DNA和脂磷壁酸与变形链球菌生物膜细胞外基质中的胞外多糖相互作用。

Extracellular DNA and lipoteichoic acids interact with exopolysaccharides in the extracellular matrix of Streptococcus mutans biofilms.

作者信息

Castillo Pedraza Midian C, Novais Tatiana F, Faustoferri Roberta C, Quivey Robert G, Terekhov Anton, Hamaker Bruce R, Klein Marlise I

机构信息

a Department of Dental Materials and Prosthodontics, School of Dentistry , São Paulo State University (Unesp) , Araraquara , Brazil.

b Center for Oral Biology , University of Rochester , Rochester , NY , USA.

出版信息

Biofouling. 2017 Oct;33(9):722-740. doi: 10.1080/08927014.2017.1361412. Epub 2017 Sep 25.

Abstract

Streptococcus mutans-derived exopolysaccharides are virulence determinants in the matrix of biofilms that cause caries. Extracellular DNA (eDNA) and lipoteichoic acid (LTA) are found in cariogenic biofilms, but their functions are unclear. Therefore, strains of S. mutans carrying single deletions that would modulate matrix components were used: eDNA - ∆lytS and ∆lytT; LTA - ∆dltA and ∆dltD; and insoluble exopolysaccharide - ΔgtfB. Single-species (parental strain S. mutans UA159 or individual mutant strains) and mixed-species (UA159 or mutant strain, Actinomyces naeslundii and Streptococcus gordonii) biofilms were evaluated. Distinct amounts of matrix components were detected, depending on the inactivated gene. eDNA was found to be cooperative with exopolysaccharide in early phases, while LTA played a larger role in the later phases of biofilm development. The architecture of mutant strains biofilms was distinct (vs UA159), demonstrating that eDNA and LTA influence exopolysaccharide distribution and microcolony organization. Thus, eDNA and LTA may shape exopolysaccharide structure, affecting strategies for controlling pathogenic biofilms.

摘要

变形链球菌衍生的胞外多糖是导致龋齿的生物膜基质中的毒力决定因素。在致龋生物膜中发现了细胞外DNA(eDNA)和脂磷壁酸(LTA),但其功能尚不清楚。因此,使用了携带可调节基质成分的单基因缺失的变形链球菌菌株:eDNA相关的——ΔlytS和ΔlytT;LTA相关的——ΔdltA和ΔdltD;以及不溶性胞外多糖相关的——ΔgtfB。对单菌种(亲本菌株变形链球菌UA159或单个突变菌株)和混合菌种(UA159或突变菌株、内氏放线菌和戈登链球菌)生物膜进行了评估。根据失活基因的不同,检测到了不同量的基质成分。发现eDNA在早期阶段与胞外多糖协同作用,而LTA在生物膜发育的后期阶段发挥更大作用。突变菌株生物膜的结构与UA159不同,表明eDNA和LTA影响胞外多糖的分布和微菌落组织。因此,eDNA和LTA可能塑造胞外多糖结构,影响控制致病性生物膜的策略。

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