海藻酸寡糖对体外肠道菌群的调节作用

Grégoire Bouillon, O. Gåserød, Łukasz Krych, J. Castro-Mejía, W. Kot, M. Saarinen, A. Ouwehand, D. Nielsen, F. Rattray
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引用次数: 1

摘要

褐藻酸盐寡糖(AOS)是来自褐藻的不可消化的碳水化合物。因此,它们是膳食纤维,可能具有益生元的潜力。因此,我们研究了肠道细菌利用AOS的单菌株培养能力和作为一个复杂的细菌群落的能力。青少年双歧杆菌、干酪乳杆菌和副干酪乳杆菌的生长较弱(相对于未添加培养基;p < 0.05),而以海藻酸盐为碳水化合物源时卵形拟杆菌生长旺盛(p < 0.01)。粪肠球菌和扁平肠球菌是首次报道能够在AOS上生长。此外,在体外肠道模型中,AOS作为底物在复杂的细菌群落中进行了结肠发酵研究。体外肠道模型表明,AOS增加了内源性短链脂肪酸(SCFA)水平,但与菊粉的水平不同。以海藻酸盐为底物进行体外肠道模拟后,发现拟杆菌属菌群占主导地位。此外,在三分之二的供体肠道模型中,观察到AOS对拟杆菌的刺激,第三个供体对变化的抵抗力更强。我们的结果允许在常见的肠道物种中确定AOS的利用者。结果还表明,在体外模拟结肠发酵过程中,AOS能够提高SCFA水平,并积极调节肠道微生物群,尽管一些受试者似乎对底物变化的扰动具有弹性。
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Modulating the Gut Microbiota with Alginate Oligosaccharides In Vitro
Alginate oligosaccharides (AOS) are non-digestible carbohydrates from brown kelp. As such, they are dietary fibers and may have prebiotic potential. Therefore, we investigated the capacity of gut bacteria to utilize AOS with single-strain cultures and as a complex bacterial community. Bifidobacterium adolescentis, Lacticaseibacillus casei and Lacticaseibacillus paracasei showed weak growth (relative to unsupplemented medium; p < 0.05) in the presence of AOS and alginate, while strong growth (p < 0.01) was observed for Bacteroides ovatus when grown with alginate as carbohydrate source. Enterococcus faecium and Enterococcus hirae were for the first time reported to be able to grow on AOS. Further, AOS as substrate was investigated in a complex bacterial community with colonic fermentations in an in vitro gut model. The in vitro gut model indicated that AOS increased short-chain fatty acid (SCFA) levels in donors with a low endogenous SCFA production, but not to the same level as inulin. Bacteroides was found to dominate the bacteria community after in vitro gut simulation with alginate as substrate. Further, stimulation of Bacteroides was observed with AOS in the gut model for two out of three donors with the third donor being more resistant to change. Our results allowed the identification of AOS utilizers among common gut species. The results also demonstrated the capacity of AOS to elevate SCFA levels and positively modulate the gut microbiota during in vitro simulated colon fermentations, although some subjects appear to be resilient to perturbation via substrate changes.
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