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Prebiotic fibre mixtures counteract the manifestation of gut microbial dysbiosis induced by the chemotherapeutic 5-Fluorouracil (5-FU) in a validated in vitro model of the colon

益生元 抗性淀粉 肠道菌群 双歧杆菌 生物 丁酸盐 失调 阿拉伯木聚糖 菊粉 微生物学 食品科学 乳酸菌 多糖 生物化学 淀粉 发酵
作者
Janine Ziemons,Lars Hillege,Romy Aarnoutse,Judith de Vos‐Geelen,Liselot Valkenburg‐van Iersel,Jasper Mastenbroek,Robin M.J.M. van Geel,David Barnett,Sander S. Rensen,Ardy van Helvoort,Lotte H. J. Dopheide,Guus Roeselers,John Penders,Marjolein L. Smidt,Koen Venema
出处
期刊:BMC Microbiology [BioMed Central]
卷期号:24 (1)
标识
DOI:10.1186/s12866-024-03384-4
摘要

Abstract Background 5-Fluorouracil (5-FU) is used as an antineoplastic agent in distinct cancer types. Increasing evidence suggests that the gut microbiota might modulate 5-FU efficacy and toxicity, potentially affecting the patient’s prognosis. The current experimental study investigated 5-FU-induced microbiota alterations, as well as the potential of prebiotic fibre mixtures (M1-M4) to counteract these shifts. Methods A pooled microbial consortium was derived from ten healthy donors, inoculated in an in vitro model of the colon, and treated with 5-FU, with or without prebiotic fibre mixtures for 72 h. Four different prebiotic fibre mixtures were tested: M1 containing short-chain galacto-oligosaccharides (sc GOS), long-chain fructo-oligosaccharides (lcFOS), and low viscosity pectin (lvPect), M2 consisting of arabinoxylan, beta-glucan, pectin, and resistant starch, M3 which was a mixture of scGOS and lcFOS, and M4 containing arabinoxylan, beta-glucan, pectin, resistant starch, and inulin. Results We identified 5-FU-induced changes in gut microbiota composition, but not in microbial diversity. Administration of prebiotic fibre mixtures during 5-FU influenced gut microbiota composition and taxa abundance. Amongst others, prebiotic fibre mixtures successfully stimulated potentially beneficial bacteria ( Bifidobacterium , Lactobacillus, Anaerostipes, Weissella , Olsenella , Senegalimassilia ) and suppressed the growth of potentially pathogenic bacteria ( Klebsiella , Enterobacter ) in the presence of 5-FU. The short-chain fatty acid (SCFA) acetate increased slightly during 5-FU, but even more during 5-FU with prebiotic fibre mixtures, while propionate was lower due to 5-FU with or without prebiotic fibre mixtures, compared to control. The SCFA butyrate and valerate did not show differences among all conditions. The branched-chain fatty acids (BCFA) iso-butyrate and iso-valerate were higher in 5-FU, but lower in 5-FU + prebiotics, compared to control. Conclusions These data suggest that prebiotic fibre mixtures represent a promising strategy to modulate 5-FU-induced microbial dysbiosis towards a more favourable microbiota, thereby possibly improving 5-FU efficacy and reducing toxicity, which should be evaluated further in clinical studies.

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