APC Microbiome Ireland, University College Cork, Western Road, Cork, Ireland.
Current address: NHMRC CRE in Digestive Health, HMRI, Newcastle, NSW, Australia.
Microbiome. 2023 Aug 2;11(1):168. doi: 10.1186/s40168-023-01595-x.
Typically, animal models studying gastrointestinal microbiotas compromised in early life have employed either germ-free animals or mice treated with a cocktail of antibiotics. Such studies intend to mimic scenarios of infants born by caesarean section and/or subjected to antibiotic treatment. However, the antibiotics used in these studies are rarely prescribed to infants. Therefore, an early life model was developed in which the murine gastrointestinal microbiota was severely disrupted by clindamycin treatment.
In this mouse model, we investigated the extent supplementation with a synbiotic mixture of prebiotics, being scGOS/lcFOS with the human milk oligosaccharide 2'-Fucosyllactose (2'-FL), in combination with or without single strain or mix of "infant type" bifidobacteria, can rescue an antibiotic-compromised microbiota. Shotgun metagenomic sequencing showed that the microbiota was severely disrupted by the clindamycin challenge. No recovery was observed 3 weeks post-challenge in the scGOS/lcFOS/2'FL group, while the group that received the synbiotic treatment of scGOS/lcFOS/2'-FL with Bifidobacterium breve NRBB01 showed partial recovery. Strikingly in the scGOS/lcFOS/2'-FL group receiving the mixture of bifidobacteria resulted in a recovery of the microbiota disruption. Histological analyses showed that the clindamycin-treated animals at the end of the experiment still suffered from mild oedema and villi/colonic crypt irregularities which was ameliorated by the synbiotic intervention.
Our study demonstrates that supplementation of synbiotic mixture of scGOS/lcFOS/2'-FL in combination with a specific mix of infant-type bifidobacterial strains is able to partially revive an antibiotic-perturbed gastrointestinal microbiota. Video Abstract.
通常,研究早期生活中胃肠道微生物组受损的动物模型采用无菌动物或用抗生素混合物处理的小鼠。这些研究旨在模拟经剖宫产出生和/或接受抗生素治疗的婴儿的情况。然而,这些研究中使用的抗生素很少用于婴儿。因此,开发了一种早期生活模型,其中用克林霉素处理严重破坏了小鼠的胃肠道微生物组。
在这种小鼠模型中,我们研究了补充益生元混合物(即 scGOS/lcFOS 与母乳低聚糖 2'-岩藻糖基乳糖(2'-FL))与或不与单一菌株或“婴儿型”双歧杆菌混合物联合补充的程度,是否可以挽救抗生素受损的微生物组。 shotgun 宏基因组测序显示,微生物组受到克林霉素挑战的严重破坏。在 scGOS/lcFOS/2'-FL 组中,在挑战后 3 周未观察到恢复,而接受 scGOS/lcFOS/2'-FL 与短双歧杆菌 NRBB01 的合生元治疗的组显示出部分恢复。引人注目的是,在接受双歧杆菌混合物的 scGOS/lcFOS/2'-FL 组中,微生物组的破坏得到了恢复。组织学分析表明,在实验结束时,接受克林霉素治疗的动物仍患有轻度水肿和绒毛/结肠隐窝不规则,这种情况通过合生元干预得到改善。
我们的研究表明,补充 scGOS/lcFOS/2'-FL 合生元与特定的婴儿双歧杆菌菌株混合物联合使用,能够部分恢复抗生素扰乱的胃肠道微生物组。