Graduate School of Science, Technology and Innovation, Kobe University, 1-1 Rokkodai-cho, Nada-ku, Kobe, Hyogo, 657-8501, Japan.
Division of Gastroenterology, Department of Internal Medicine, Graduate School of Medicine, Kobe University, 7-5-2 Kusunoki-cho, Chuo-ku, Kobe, Hyogo, 650-0017, Japan.
Appl Microbiol Biotechnol. 2020 May;104(9):3859-3867. doi: 10.1007/s00253-020-10506-1. Epub 2020 Mar 7.
The aim of this study was to clarify the effect of the spore-forming and lactic acid-producing probiotic strain, Bacillus coagulans SANK 70258, on human colonic microbiota of healthy subjects and ulcerative colitis patients. A model culture system was employed to construct the in vitro human colonic microbiota, to retain the bacterial species richness and simulate the patient's disordered composition, from the fecal inoculum. Bacterial 16S rRNA gene sequencing confirmed that administration of B. coagulans SANK 70258 (at an initial concentration of 4 × 10-total cells/mL) suppressed bacteria related to the family Enterobacteriaceae in the microbiota models for both healthy subjects (P = 0.016) and ulcerative colitis patients (P = 0.023). In addition, administration of B. coagulans SANK 70258 increased bacteria related to the family Lachnospiraceae (P = 0.031), thereby enhancing butyrate production (P = 0.031) in the microbiota models of healthy subjects. However, these changes were not observed in the microbiota models of ulcerative colitis patients, likely owing to the low abundance of Lachnospiraceae species. This study demonstrates the potential of B. coagulans SANK 70258 to exhibit antimicrobial activity against harmful organisms in patients with ulcerative colitis, while improving the intestinal microenvironment by increasing butyrogenesis in healthy persons. KEY POINTS: • B. coagulans SANK 70258 treatment reduced colonic Enterobacteriaceae species. • B. coagulans SANK 70258 treatment enhanced butyrogenesis in healthy individuals. • B. coagulans SANK 70258 treatment increased Lachnospiraceae in healthy persons. • B. coagulans SANK 70258 improves the colonic microenvironment in ulcerative colitis.
本研究旨在阐明产孢子和产乳酸益生菌菌株凝结芽孢杆菌 SANK 70258 对健康受试者和溃疡性结肠炎患者的人类结肠微生物群的影响。采用模型培养系统从粪便接种物中构建体外人类结肠微生物群,保留细菌物种丰富度并模拟患者紊乱的组成。细菌 16S rRNA 基因测序证实,凝结芽孢杆菌 SANK 70258(初始浓度为 4×10-总细胞/mL)的给药抑制了健康受试者(P=0.016)和溃疡性结肠炎患者(P=0.023)微生物群模型中与肠杆菌科相关的细菌。此外,凝结芽孢杆菌 SANK 70258 的给药增加了与lachnospiraceae 科相关的细菌(P=0.031),从而增强了健康受试者微生物群模型中的丁酸产生(P=0.031)。然而,在溃疡性结肠炎患者的微生物群模型中未观察到这些变化,这可能是由于lachnospiraceae 物种的丰度较低。本研究表明,凝结芽孢杆菌 SANK 70258 具有针对溃疡性结肠炎患者有害生物的抗菌活性的潜力,同时通过增加丁酸生成来改善健康个体的肠道微环境。关键点: • 凝结芽孢杆菌 SANK 70258 治疗减少了结肠肠杆菌科物种。 • 凝结芽孢杆菌 SANK 70258 治疗增强了健康个体的丁酸生成。 • 凝结芽孢杆菌 SANK 70258 治疗增加了健康个体中的lachnospiraceae。 • 凝结芽孢杆菌 SANK 70258 改善溃疡性结肠炎的结肠微环境。