Zhang Derek, Verstrepen Lynn, De Medts Jelle, Duysburgh Cindy, Van den Abbeele Pieter, Marzorati Massimo, Khoo Christina
Ocean Spray Cranberries, Inc., Lakeville-Middleboro, MA 02349, USA.
ProDigest BV, 9052 Ghent, Belgium.
Pathogens. 2021 Sep 18;10(9):1217. doi: 10.3390/pathogens10091217.
While many beneficial host-microbiota interactions have been described, imbalanced microbiota in the gut is speculated to contribute to the progression and recurrence of chronic inflammatory diseases such as Crohn's disease (CD). This in vitro study evaluated the impact of a cranberry concentrate Type M (CTM) on adherent-invasive (AIEC) LF82, a pathobiont associated with CD. Different stages of pathogenic infection were investigated: (i) colonization of the mucus layer, and (ii) adhesion to and (iii) invasion of the epithelial cells. Following 48 h of fecal batch incubation, 0.5 and 1 mM of CTM significantly altered AIEC LF82 levels in a simulated mucus layer, resulting in a decrease of 50.5% in the untreated blank, down to 43.0% and 11.4%, respectively. At 1 mM of CTM, the significant decrease in the levels of AIEC LF82 coincided with a stimulation of the metabolic activity of the background microbiota. The increased levels of health-associated acetate (+7.9 mM) and propionate levels (+3.5 mM) suggested selective utilization of CTM by host microorganisms. Furthermore, 1 mM of both fermented and unfermented CTM decreased the adhesion and invasion of human-derived epithelial Caco-2 cells by AIEC LF82. Altogether, this exploratory in vitro study demonstrates the prebiotic potential of CTM and supports its antipathogenic effects through direct and/or indirect modulation of the gut microbiome.
虽然已经描述了许多有益的宿主-微生物群相互作用,但据推测,肠道微生物群失衡会导致克罗恩病(CD)等慢性炎症性疾病的进展和复发。这项体外研究评估了蔓越莓浓缩物M型(CTM)对与CD相关的致病共生菌——黏附侵袭性大肠杆菌(AIEC)LF82的影响。研究了致病感染的不同阶段:(i)黏液层的定殖,以及(ii)对上皮细胞的黏附及(iii)侵袭。经过48小时的粪便批次培养后,0.5 mM和1 mM的CTM显著改变了模拟黏液层中AIEC LF82的水平,未处理的空白组中AIEC LF82水平下降了50.5%,分别降至43.0%和11.4%。在1 mM CTM时,AIEC LF82水平的显著下降与背景微生物群代谢活性的刺激同时发生。与健康相关的乙酸盐水平升高(+7.9 mM)和丙酸盐水平升高(+3.5 mM)表明宿主微生物对CTM有选择性利用。此外,1 mM发酵型和未发酵型CTM均降低了AIEC LF82对人源上皮Caco-2细胞的黏附和侵袭。总之,这项探索性的体外研究证明了CTM的益生元潜力,并支持其通过直接和/或间接调节肠道微生物群产生的抗致病作用。