Bacterial taxonomic and functional changes following oral lyophilized donor fecal microbiota transplantation in patients with ulcerative colitis

溃疡性结肠炎 基因组 抵抗性 微生物群 粪便细菌疗法 医学 粪便 移植 人体微生物群 口腔微生物群 拟杆菌科 炎症性肠病 失调 内科学 生物 胃肠病学 微生物学 免疫学 结肠炎 细菌 炎症性肠病 霰弹枪测序
作者
Shreeya S. Raich,Marwan E. Majzoub,Craig Haifer,Sudarshan Paramsothy,M. Shamim,Thomas J. Borody,Rupert W. Leong,Nadeem O. Kaakoush
出处
期刊:MSystems [American Society for Microbiology]
卷期号:10 (10): e0099125-e0099125 被引量:3
标识
DOI:10.1128/msystems.00991-25
摘要

spp., was seen in responders treated by either donor. Several of the above outcomes were found to be consistent when data were analyzed at the level of metagenome-assembled genomes. FMT was also found to deplete the resistome within patients treated with antibiotics to levels lower than the UC baseline. Single donor oral lyophilized FMT substantially modifies taxonomic diversity and composition as well as microbiome function and the resistome in patients with UC, with several features identified as strongly linked to response regardless of the donor used. IMPORTANCE: There is a limited amount of work examining the effects of oral lyophilized fecal microbiota transplantation (FMT) on the microbiome of patients with ulcerative colitis (UC), and less so studies examining species-level dynamics and functional changes using this form of FMT. We performed deep shotgun metagenomic sequencing to provide an in-depth species-genome bin-level analysis of the microbiome of patients with UC receiving oral lyophilized FMT from a single donor. We identified key taxonomic and functional features that transferred into patients and were associated with clinical response. We also determined how FMT impacts the resistome of patients with UC. We believe these findings will be important in ongoing efforts to not only improve the efficacy of FMT in UC but also allow for the transition to defined microbial therapeutics, foregoing the need for FMT donors.
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