Nagasawa Ryo, Sato Tsutomu, Senpuku Hidenobu
Graduate School of Science and Engineering, Hosei University, Koganei-shi, Tokyo, Japan.
Department of Bacteriology I, National Institute of Infectious Diseases, Tokyo, Japan.
Appl Environ Microbiol. 2017 Jul 17;83(15). doi: 10.1128/AEM.00869-17. Print 2017 Aug 1.
is the primary etiological agent of dental caries and causes tooth decay by forming a firmly attached biofilm on tooth surfaces. Biofilm formation is induced by the presence of sucrose, which is a substrate for the synthesis of extracellular polysaccharides but not in the presence of oligosaccharides. Nonetheless, in this study, we found that raffinose, which is an oligosaccharide with an intestinal regulatory function and antiallergic effect, induced biofilm formation by in a mixed culture with sucrose, which was at concentrations less than those required to induce biofilm formation directly. We analyzed the possible mechanism behind the small requirement for sucrose for biofilm formation in the presence of raffinose. Our results suggested that sucrose contributed to an increase in bacterial cell surface hydrophobicity and biofilm formation. Next, we examined how the effects of raffinose interacted with the effects of sucrose for biofilm formation. We showed that the presence of raffinose induced fructan synthesis by fructosyltransferase and aggregated extracellular DNA (eDNA, which is probably genomic DNA released from dead cells) into the biofilm. eDNA seemed to be important for biofilm formation, because the degradation of DNA by DNase I resulted in a significant reduction in biofilm formation. When assessing the role of fructan in biofilm formation, we found that fructan enhanced eDNA-dependent cell aggregation. Therefore, our results show that raffinose and sucrose have cooperative effects and that this induction of biofilm formation depends on supportive elements that mainly consist of eDNA and fructan. The sucrose-dependent mechanism of biofilm formation in has been studied extensively. Nonetheless, the effects of carbohydrates other than sucrose are inadequately understood. Our findings concerning raffinose advance the understanding of the mechanism underlying the joint effects of sucrose and other carbohydrates on biofilm formation. Since raffinose has been reported to have positive effects on enterobacterial flora, research on the effects of raffinose on the oral flora are required prior to its use as a beneficial sugar for human health. Here, we showed that raffinose induced biofilm formation by in low concentrations of sucrose. The induction of biofilm formation generally generates negative effects on the oral flora. Therefore, we believe that this finding will aid in the development of more effective oral care techniques to maintain oral flora health.
是龋齿的主要病原体,通过在牙齿表面形成牢固附着的生物膜导致蛀牙。生物膜的形成由蔗糖诱导,蔗糖是细胞外多糖合成的底物,但在低聚糖存在时不会诱导生物膜形成。尽管如此,在本研究中,我们发现棉子糖(一种具有肠道调节功能和抗过敏作用的低聚糖)在与蔗糖的混合培养中,以低于直接诱导生物膜形成所需的浓度诱导生物膜形成。我们分析了在棉子糖存在下生物膜形成对蔗糖需求较小的可能机制。我们的结果表明,蔗糖有助于增加细菌细胞表面疏水性和生物膜形成。接下来,我们研究了棉子糖的作用如何与蔗糖对生物膜形成的作用相互作用。我们发现棉子糖的存在通过果糖基转移酶诱导果聚糖合成,并将细胞外DNA(eDNA,可能是从死细胞释放的基因组DNA)聚集到生物膜中。eDNA似乎对生物膜形成很重要,因为DNA酶I对DNA的降解导致生物膜形成显著减少。在评估果聚糖在生物膜形成中的作用时,我们发现果聚糖增强了eDNA依赖性细胞聚集。因此,我们的结果表明棉子糖和蔗糖具有协同作用,并且这种生物膜形成的诱导取决于主要由eDNA和果聚糖组成的支持性成分。在[具体细菌名称未给出]中,蔗糖依赖性生物膜形成机制已得到广泛研究。尽管如此,除蔗糖外的其他碳水化合物的作用仍未得到充分理解。我们关于棉子糖的发现推进了对蔗糖和其他碳水化合物对生物膜形成联合作用机制的理解。由于棉子糖已被报道对肠道细菌菌群有积极影响,在将其用作对人类健康有益的糖之前,需要研究棉子糖对口腔菌群的影响。在这里,我们表明棉子糖在低浓度蔗糖中诱导[具体细菌名称未给出]生物膜形成。生物膜形成的诱导通常对口腔菌群产生负面影响。因此,我们相信这一发现将有助于开发更有效的口腔护理技术以维持口腔菌群健康。