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由乳杆菌和双歧杆菌菌株产生的胞外多糖可在体外消除细菌毒素对真核细胞的细胞毒性作用。

Exopolysaccharides produced by Lactobacillus and Bifidobacterium strains abrogate in vitro the cytotoxic effect of bacterial toxins on eukaryotic cells.

机构信息

Department of Microbiology and Biochemistry of Dairy Products, Instituto de Productos Lácteos de Asturias, Consejo Superior de Investigaciones Científicas (IPLA-CSIC), Villaviciosa, Asturias, Spain.

出版信息

J Appl Microbiol. 2010 Dec;109(6):2079-86. doi: 10.1111/j.1365-2672.2010.04839.x. Epub 2010 Sep 16.

Abstract

AIMS

To evaluate the capability of the exopolysaccharides (EPS) produced by lactobacilli and bifidobacteria from human and dairy origin to antagonize the cytotoxic effect of bacterial toxins.

METHODS AND RESULTS

The cytotoxicity of Bacillus cereus extracellular factors on Caco-2 colonocytes in the presence/absence of the EPS was determined by measuring the integrity of the tissue monolayer and the damage to the cell membrane (extracellular lactate dehydrogenase activity). Additionally, the protective effect of EPS against the haemolytic activity of the streptolysin-O was evaluated on rabbit erythrocytes. The EPS produced by Bifidobacterium animalis ssp. lactis A1 and IPLA-R1, Bifidobacterium longum NB667 and Lactobacillus rhamnosus GG were able to counteract the toxic effect of bacterial toxins on the eukaryotic cells at 1mg ml(-1) EPS concentration. The EPS A1 was the most effective in counteracting the effect of B. cereus toxins on colonocytes, even at lower doses (0·5mg ml(-1) ), whereas EPS NB667 elicited the highest haemolysis reduction on erythrocytes.

CONCLUSIONS

The production of EPS by lactobacilli and bifidobacteria could antagonize the toxicity of bacterial pathogens, this effect being EPS and biological marker dependent.

SIGNIFICANCE AND IMPACT OF THE STUDY

This work allows gaining insight about the mechanisms that probiotics could exert to improve the host health.

摘要

目的

评估来源于人和乳制品的乳杆菌和双歧杆菌的胞外多糖 (EPS) 拮抗细菌毒素细胞毒性的能力。

方法和结果

通过测量组织单层的完整性和细胞膜损伤(细胞外乳酸脱氢酶活性)来确定蜡样芽胞杆菌细胞外因子在存在/不存在 EPS 的情况下对 Caco-2 结肠细胞的细胞毒性。此外,还评估了 EPS 对链球菌溶血素-O 的溶血活性的保护作用在兔红细胞上。Bifidobacterium animalis ssp. lactis A1 和 IPLA-R1、Bifidobacterium longum NB667 和 Lactobacillus rhamnosus GG 产生的 EPS 能够在 1mg/ml(-1) EPS 浓度下拮抗细菌毒素对真核细胞的毒性作用。在较低剂量(0.5mg/ml(-1) )下,EPS A1 对抗 B. cereus 毒素对结肠细胞的作用最为有效,而 EPS NB667 对红细胞的溶血减少作用最高。

结论

乳杆菌和双歧杆菌产生的 EPS 可以拮抗细菌病原体的毒性,这种作用依赖于 EPS 和生物标志物。

研究的意义和影响

这项工作使我们能够深入了解益生菌可能发挥作用以改善宿主健康的机制。

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