Karimianghadim Ramin, Satokari Reetta, Yeo Sam, Arkkila Perttu, Kao Dina, Pakpour Sepideh
School of Engineering, University of British Columbia, Kelowna, BC, Canada.
Human Microbiome Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Front Microbiol. 2025 May 9;16:1589704. doi: 10.3389/fmicb.2025.1589704. eCollection 2025.
Fecal microbiota transplantation (FMT) is highly effective in preventing recurrence by restoring gut microbiota composition and function. However, the impact of recent antibiotic use, a key exclusion criterion for stool donors, on gut microbiota recovery is poorly understood.
We investigated microbial recovery dynamics following antibiotic use in three long-term stool donors from Canada and Finland. Using longitudinal stool sampling, metagenomic sequencing, and qPCR, we assessed changes in bacterial diversity, community composition, microbial functions, the gut phageome, and the risk of transmitting antibiotic-resistant genes (ARGs).
Antibiotics caused lasting disruption to bacterial communities, significantly reducing important taxa like , , , sp. , and , with effects persisting for months. Functional analyses revealed alterations in housekeeping genes critical for energy production and biosynthesis, with no direct links to key health-related pathways. Antibiotics also disrupted viral populations, decreasing diversity and increasing abundance, reflecting disrupted host-bacteriophage dynamics. No significant increase in clinically important ARGs was detected.
These findings highlight the unpredictable and complex recovery of gut microbiota post-antibiotics. Individualized suspension periods in donor programs, guided by metagenomic analyses, are recommended to optimize FMT outcomes in various indications by considering antibiotic spectrum, duration, and host-specific factors.
粪便微生物群移植(FMT)通过恢复肠道微生物群的组成和功能,在预防复发方面非常有效。然而,近期使用抗生素这一粪便供体的关键排除标准对肠道微生物群恢复的影响却知之甚少。
我们调查了来自加拿大和芬兰的三名长期粪便供体在使用抗生素后微生物的恢复动态。通过纵向粪便采样、宏基因组测序和定量聚合酶链反应,我们评估了细菌多样性、群落组成、微生物功能、肠道噬菌体组以及抗生素抗性基因(ARG)传播风险的变化。
抗生素对细菌群落造成了持久的破坏,显著减少了如 、 、 、 菌属和 等重要分类群,其影响持续数月。功能分析揭示了对能量产生和生物合成至关重要的管家基因发生了改变,与关键的健康相关途径没有直接联系。抗生素还扰乱了病毒群体,降低了多样性并增加了 丰度,反映出宿主 - 噬菌体动态受到破坏。未检测到临床上重要的ARG显著增加。
这些发现凸显了抗生素后肠道微生物群恢复的不可预测性和复杂性。建议在供体计划中根据宏基因组分析指导设定个体化的暂停期,通过考虑抗生素谱、持续时间和宿主特异性因素,优化各种适应症的FMT结果。