Karaca Basar, Haliscelik Ozan, Gursoy Mervi, Kiran Fadime, Loimaranta Vuokko, Söderling Eva, Gursoy Ulvi Kahraman
Department of Periodontology, Institute of Dentistry, University of Turku, 20520 Turku, Finland.
Department of Biology, Faculty of Science, Ankara University, 06100 Ankara, Turkey.
Microorganisms. 2022 Nov 7;10(11):2200. doi: 10.3390/microorganisms10112200.
Previous studies have indicated that the exopolysaccharides of lactic acid bacteria exhibit antibiofilm activity against non-oral bacteria by preventing their initial adhesion to surfaces and by downregulating the expression of genes responsible for their biofilm formation. The aims of this study were to (1) characterize the exopolysaccharides (EPSs) of EIR/IF-1 postbiotics, (2) test their antibiofilm effect on dual biofilms, and (3) evaluate their bacterial auto-aggregation, co-aggregation, and hydrocarbon-binding inhibitory activity. The EPSs were characterized by FTIR, HPLC, and thermogravimetric analysis. Bacterial auto- and co-aggregation were tested by Kolenbrander's method and hydrocarbon binding was tested by Rosenberg's method. Dual biofilms were formed by culturing ATCC 25586 with one of the following bacteria: ATCC 33185, AHN 33266, ATCC 33277, AHN 24155, and ATCC 35896. The EPSs contained fractions with different molecular weights (51 and 841 kDa) and monosaccharides of glucose, galactose, and fructose. The EPSs showed antibiofilm activity in all the biofilm models tested. The EPSs may have inhibited bacterial aggregation and binding to hydrocarbons by reducing bacterial hydrophobicity. In conclusion, the EPSs of EIR/IF-1, which consists of two major fractions, exhibited antibiofilm activity against oral bacteria, which can be explained by the inhibitory effect of EPSs on the auto-aggregation and co-aggregation of bacteria and their binding to hydrocarbons.
先前的研究表明,乳酸菌的胞外多糖通过阻止非口腔细菌最初黏附于表面以及下调负责其生物膜形成的基因表达,从而展现出针对非口腔细菌的抗生物膜活性。本研究的目的是:(1)表征EIR/IF-1后生元的胞外多糖(EPS);(2)测试它们对双重生物膜的抗生物膜作用;(3)评估它们的细菌自聚集、共聚集以及烃结合抑制活性。通过傅里叶变换红外光谱(FTIR)、高效液相色谱(HPLC)和热重分析对EPS进行表征。采用科伦布兰德方法测试细菌自聚集和共聚集,采用罗森伯格方法测试烃结合。通过将ATCC 25586与以下细菌之一共同培养形成双重生物膜:ATCC 33185、AHN 33266、ATCC 33277、AHN 24155和ATCC 35896。EPS包含不同分子量(51和841 kDa)的组分以及葡萄糖、半乳糖和果糖单糖。EPS在所有测试的生物膜模型中均表现出抗生物膜活性。EPS可能通过降低细菌疏水性抑制细菌聚集和与烃的结合。总之,由两个主要组分组成的EIR/IF-1的EPS对口腔细菌表现出抗生物膜活性,这可以通过EPS对细菌自聚集、共聚集及其与烃结合的抑制作用来解释。