Goll Rasmus, Johnsen Peter Holger, Hjerde Erik, Diab Joseph, Valle Per Christian, Hilpusch Frank, Cavanagh Jorunn Pauline
Research Group of Gastroenterology and Nutrition, Department of Clinical Medicine, UiT the Arctic University of Norway , Tromsø, Norway.
Department of Gastroenterology, Division of Internal Medicine, University Hospital of North Norway , Tromsø, Norway.
Gut Microbes. 2020 Nov 9;12(1):1794263. doi: 10.1080/19490976.2020.1794263.
Irritable bowel syndrome (IBS) is a common disorder of the lower gastrointestinal tract. The pathophysiology is far from settled, but a gut microbial dysbiosis is hypothesized to be a contributing factor. We earlier published a randomized double-blind placebo-controlled clinical trial on fecal microbiota transplantation (FMT) for IBS - the REFIT trial. The present data set describes the engraftment and includes participants from the study who received active FMT; 14 participants with effect of FMT () and 8 without (). Samples were collected at baseline, after 6 and 12 months. Samples from the transplants () served as a comparator. In total 66 recipient samples and 17 donor samples were subjected to deep metagenomic sequencing, and taxonomic and functional analyses were performed. Alpha diversity measures showed a significantly increased diversity and evenness in the IBS groups compared to the donors. Taxonomic profiles showed higher relative abundance of phylum Firmicutes, and lower relative abundance of phylum Bacteroidetes, compared to donors at baseline. This profile was shifted toward the donor profile following FMT. Imputed growth rates showed that the resulting growth pattern was a conglomerate of donor and recipient activity. Thirty-four functional subclasses showed distinct differences between baseline samples and donors, most of which were shifted toward a donor-like profile after FMT. All of these changes were less pronounced in the group. We conclude that FMT induces long-term changes in gut microbiota, and these changes mirror the clinical effect of the treatment. The study was registered in ClinicalTrials.gov (NCT02154867).
肠易激综合征(IBS)是下消化道的一种常见疾病。其病理生理学尚未完全明确,但据推测肠道微生物群失调是一个促成因素。我们之前发表了一项关于粪便微生物群移植(FMT)治疗IBS的随机双盲安慰剂对照临床试验——REFIT试验。本数据集描述了植入情况,并纳入了该研究中接受活性FMT的参与者;14名有FMT效果的参与者( )和8名无效果的参与者( )。在基线、6个月和12个月后采集样本。移植样本( )用作对照。总共对66份受体样本和17份供体样本进行了深度宏基因组测序,并进行了分类学和功能分析。α多样性测量结果显示,与供体相比,IBS组的多样性和均匀度显著增加。分类学图谱显示,与基线时的供体相比,厚壁菌门的相对丰度较高,而拟杆菌门的相对丰度较低。FMT后,这种图谱向供体图谱转变。估算的生长速率表明,最终的生长模式是供体和受体活性的混合体。34个功能亚类在基线样本和供体之间表现出明显差异,其中大多数在FMT后向类似供体的图谱转变。在 组中,所有这些变化都不太明显。我们得出结论,FMT可诱导肠道微生物群的长期变化,这些变化反映了治疗的临床效果。该研究已在ClinicalTrials.gov(NCT02154867)注册。