IRSD, INSERM, INRA, INP-ENVT, Toulouse University 3 Paul Sabatier, Toulouse, France.
Farncombe Family Digestive Health Institute, McMaster University Faculty of Health Sciences, Hamilton, Ontario, Canada.
Gut. 2021 Jun;70(6):1088-1097. doi: 10.1136/gutjnl-2020-321173. Epub 2020 Sep 25.
Data from clinical research suggest that certain probiotic bacterial strains have the potential to modulate colonic inflammation. Nonetheless, these data differ between studies due to the probiotic bacterial strains used and the poor knowledge of their mechanisms of action.
By mass-spectrometry, we identified and quantified free long chain fatty acids (LCFAs) in probiotics and assessed the effect of one of them in mouse colitis.
Among all the LCFAs quantified by mass spectrometry in Nissle 1917 (EcN), a probiotic used for the treatment of multiple intestinal disorders, the concentration of 3-hydroxyoctadecaenoic acid (C18-3OH) was increased in EcN compared with other strains tested. Oral administration of C18-3OH decreased colitis induced by dextran sulfate sodium in mice. To determine whether other bacteria composing the microbiota are able to produce C18-3OH, we targeted the gut microbiota of mice with prebiotic fructooligosaccharides (FOS). The anti-inflammatory properties of FOS were associated with an increase in colonic C18-3OH concentration. Microbiota analyses revealed that the concentration of C18-3OH was correlated with an increase in the abundance in , and . In culture, produced high concentration of C18-3OH. Finally, using TR-FRET binding assay and gene expression analysis, we demonstrated that the C18-3OH is an agonist of peroxisome proliferator activated receptor gamma.
The production of C18-3OH by bacteria could be one of the mechanisms implicated in the anti-inflammatory properties of probiotics. The production of LCFA-3OH by bacteria could be implicated in the microbiota/host interactions.
临床研究数据表明,某些益生菌菌株具有调节结肠炎症的潜力。然而,由于使用的益生菌菌株不同以及对其作用机制的了解不足,这些数据在不同的研究中存在差异。
通过质谱法,我们鉴定和定量了益生菌中的游离长链脂肪酸(LCFA),并评估了其中一种在小鼠结肠炎中的作用。
在用于治疗多种肠道疾病的益生菌 Nissle 1917(EcN)中,通过质谱定量的所有 LCFA 中,3-羟基十八碳烯酸(C18-3OH)的浓度高于其他测试菌株。口服 C18-3OH 可降低葡聚糖硫酸钠诱导的小鼠结肠炎。为了确定组成微生物群的其他细菌是否能够产生 C18-3OH,我们用益生元果寡糖(FOS)靶向小鼠的肠道微生物群。FOS 的抗炎特性与结肠 C18-3OH 浓度的增加有关。微生物组分析显示,C18-3OH 的浓度与 、 和 的丰度增加相关。在培养中, 产生了高浓度的 C18-3OH。最后,通过 TR-FRET 结合测定和基因表达分析,我们证明了 C18-3OH 是过氧化物酶体增殖物激活受体 γ 的激动剂。
细菌产生的 C18-3OH 可能是益生菌抗炎特性的机制之一。细菌产生的 LCFA-3OH 可能与微生物群/宿主相互作用有关。