Endika Martha F, Barnett David J M, Olmos Emiliana M, Ter Braak Cajo J F, Arts Ilja C W, Penders John, Nauta Arjen, Leemhuis Hans, Venema Koen, Smidt Hauke
Laboratory of Microbiology, Wageningen University & Research, 6708 PE Wageningen, The Netherlands.
Maastricht Centre for Systems Biology (MaCSBio), Maastricht University, 6229 EN Maastricht, The Netherlands.
FEMS Microbiol Ecol. 2025 Mar 18;101(4). doi: 10.1093/femsec/fiaf028.
Environmental factors like diet and antibiotics modulate the gut microbiota in early life. During weaning, gut microbiota progressively diversifies through exposure to non-digestible carbohydrates (NDCs) from diet, while antibiotic perturbations might disrupt this process. Supplementing an infant's diet with prebiotic NDCs may mitigate the adverse effects of antibiotics on gut microbiota development. This study evaluated the influence of supplementation with 2-fucosyllactose (2'-FL), galacto-oligosaccharides (GOS), or isomalto/malto-polysaccharides containing 87% of α(1→6) linkages (IMMP-87), on the recovery of antibiotic-perturbed microbiota. The TIM-2 in vitro colon model inoculated with fecal microbiota of 9-month-old infants was used to simulate the colon of weaning infants exposed to the antibiotics amoxicillin/clavulanate or azithromycin. Both antibiotics induced changes in microbiota composition, with no signs of recovery in azithromycin-treated microbiota within 72 h. Moreover, antibiotic exposure affected microbiota activity, indicated by a low valerate production, and azithromycin treatment was associated with increased succinate production. The IMMP-87 supplementation promoted the compositional recovery of amoxicillin/clavulanate-perturbed microbiota, associated with the recovery of Ruminococcus, Ruminococcus gauvreauii group, and Holdemanella. NDC supplementation did not influence compositional recovery of azithromycin-treated microbiota. Irrespective of antibiotic exposure, supplementation with 2'-FL, GOS, or IMMP-87 enhanced microbiota activity by increasing short-chain fatty acids production (acetate, propionate, and butyrate).
饮食和抗生素等环境因素会在生命早期调节肠道微生物群。在断奶期间,肠道微生物群通过接触饮食中的不可消化碳水化合物(NDCs)而逐渐多样化,而抗生素干扰可能会破坏这一过程。在婴儿饮食中补充益生元NDCs可能会减轻抗生素对肠道微生物群发育的不利影响。本研究评估了补充2-岩藻糖基乳糖(2'-FL)、低聚半乳糖(GOS)或含有87%α(1→6)键的异麦芽/麦芽多糖(IMMP-87)对受抗生素干扰的微生物群恢复的影响。使用接种了9个月大婴儿粪便微生物群的TIM-2体外结肠模型来模拟暴露于阿莫西林/克拉维酸或阿奇霉素的断奶婴儿的结肠。两种抗生素均引起微生物群组成的变化,在72小时内,阿奇霉素治疗的微生物群没有恢复的迹象。此外,抗生素暴露影响微生物群活性,表现为戊酸产量低,阿奇霉素治疗与琥珀酸产量增加有关。补充IMMP-87促进了阿莫西林/克拉维酸干扰的微生物群的组成恢复,这与瘤胃球菌、高夫瘤胃球菌群和霍尔德曼菌的恢复有关。补充NDCs对阿奇霉素治疗的微生物群的组成恢复没有影响。无论是否接触抗生素,补充2'-FL、GOS或IMMP-87都能通过增加短链脂肪酸(乙酸、丙酸和丁酸)的产生来增强微生物群活性。