Medrano Micaela, Hamet Maria F, Abraham Analía G, Pérez Pablo F
Centro de Investigación y Desarrollo en Criotecnología de Alimentos, CCT La Plata-CONICET, UNLP. 47 y 116 (s/n), La Plata 1900, Argentina.
Antonie Van Leeuwenhoek. 2009 Nov;96(4):505-13. doi: 10.1007/s10482-009-9366-z. Epub 2009 Jul 25.
The aim of this work was to evaluate the ability of kefiran to antagonize cytopathic effects triggered by Bacillus cereus strain B10502 on cultured human enterocytes (Caco-2 cells). Cell damage was evaluated by F-actin labelling, scanning electron microscopy and determination of ratios of necrotic and detached cells. To assess the interaction between kefiran and bacteria or eukaryotic cells, flow cytometric analysis was conducted with FITC-labelled kefiran. Kefiran significantly protected infected cells from cytopathic effects induced by B. cereus such as cell necrosis, F-actin disorganisation and microvilli effacement, although presence of kefiran did not modify the adhesion of microorganisms to cultured human enterocytes. Results could be ascribed to the ability of kefiran to interact with both bacteria and eukaryotic cells thus antagonizing interactions necessary for maximal biological effects. Our findings encourage further research on the use of bacterial exopolysaccharides to antagonize virulence factors associated to direct bacteria-cell interactions.
这项工作的目的是评估开菲尔多糖拮抗蜡样芽孢杆菌菌株B10502对培养的人肠上皮细胞(Caco-2细胞)引发的细胞病变效应的能力。通过F-肌动蛋白标记、扫描电子显微镜以及坏死和脱落细胞比例的测定来评估细胞损伤。为了评估开菲尔多糖与细菌或真核细胞之间的相互作用,使用异硫氰酸荧光素标记的开菲尔多糖进行流式细胞术分析。开菲尔多糖显著保护受感染细胞免受蜡样芽孢杆菌诱导的细胞病变效应,如细胞坏死、F-肌动蛋白紊乱和微绒毛缺失,尽管开菲尔多糖的存在并未改变微生物对培养的人肠上皮细胞的粘附。结果可归因于开菲尔多糖与细菌和真核细胞相互作用的能力,从而拮抗最大生物学效应所需的相互作用。我们的研究结果鼓励进一步研究使用细菌胞外多糖来拮抗与细菌-细胞直接相互作用相关的毒力因子。