The taxonomic composition of the donor intestinal microbiota is a major factor influencing the efficacy of faecal microbiota transplantation in therapy refractory ulcerative colitis.
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The taxonomic composition of the donor intestinal microbiota is a major factor influencing the efficacy of faecal microbiota transplantation in therapy refractory ulcerative colitis.
Abstract
<h4>Background</h4>Faecal microbiota transplantation is an experimental approach for the treatment of patients with ulcerative colitis. Although there is growing evidence that faecal microbiota transplantation is effective in this disease, factors affecting its response are unknown.<h4>Aims</h4>To establish a faecal microbiota transplantation treatment protocol in ulcerative colitis patients, and to investigate which patient or donor factors are responsible for the treatment success.<h4>Methods</h4>This is an open controlled trial of repeated faecal microbiota transplantation after antibiotic pre-treatment (FMT-group, n = 17) vs antibiotic pre-treatment only (AB-group, n = 10) in 27 therapy refractory ulcerative colitis patients over 90 days. Faecal samples of donors and patients were analysed by 16SrRNA gene-based microbiota analysis.<h4>Results</h4>In the FMT-group, 10/17 (59%) of patients showed a response and 4/17 (24%) a remission to faecal microbiota transplantation. Response to faecal microbiota transplantation was mainly influenced by the taxonomic composition of the donor's microbiota. Stool of donors with a high bacterial richness (observed species remission 946 ± 93 vs no response 797 ± 181 at 15367 rps) and a high relative abundance of Akkermansia muciniphila (3.3 ± 3.1% vs 0.1 ± 0.2%), unclassified Ruminococcaceae (13.8 ± 5.0% vs 7.5 ± 3.7%), and Ruminococcus spp. (4.9 ± 3.5% vs 1.0 ± 0.7%) were more likely to induce remission. In contrast antibiotic treatment alone (AB-group) was poorly tolerated, probably because of a sustained decrease of intestinal microbial richness.<h4>Conclusions</h4>The taxonomic composition of the donor's intestinal microbiota is a major factor influencing the efficacy of faecal microbiota transplantation in ulcerative colitis patients. The design of specific microbial preparation might lead to new treatments for ulcerative colitis.
Study facts
- Organism
- —
- Platform
- Illumina MiSeq
- Age group
- mixed
- Disease groups
- Ulcerative colitis
- Anatomical sites
- —
Data availability
- Analysis code
Strengths & limitations for reuse
Strengths
- Raw reads are advertised
- Analysis code is available
- Participant counts are documented
- Sample counts are documented
Limitations
- Not documented: feature/otu tables are advertised
- Not documented: taxonomic tables are advertised
Extraction evidence & provenance
Each extracted field is shown with the source excerpt and location used to resolve it.
Assay
| Field | Value | Evidence |
|---|---|---|
assay.platform |
Illumina MiSeq from source |
ENA instrument_model=Illumina MiSeq Section |
assay.read_depth_reported |
15376 |
samples were rarefied to at least 15376 sequences/sample Section |
assay.sequencing_type |
amplicon_16s |
For amplification of bacterial 16S rRNA gene Section |
assay.target_region |
V4 |
targeting the hypervariable region V4 of the 16S rRNA gene Section |
Cohort
| Field | Value | Evidence |
|---|---|---|
cohort.age_group |
mixed inferred |
Eligible patients with chronic active ulcerative colitis were aged between 16 and 80 years. Section |
cohort.disease_activity_metadata_available |
True |
Active ulcerative colitis was defined as a total Mayo score ≥4 and an endoscopic subscore ≥1. Section |
cohort.study_design |
longitudinal |
This is an open prospective trial of repeated faecal microbiota transplantation ... End of follow-up was after 90 days. Section |
cohort.total_participants |
27 |
From June 2012 to July 2014, twenty-seven patients were recruited. Section |
cohort.treatment_exposure_documented |
True |
repeated faecal microbiota transplantation after antibiotic pre-treatment (FMT-group) with a nonrandomised control group with antibiotic pre-treatment only (AB-group) Section |
cohort.treatment_response_metadata_available |
True |
Primary end point was the reduction of the total Mayo score on day 90. Section |
cohort.ulcerative_colitis_participants |
27 |
27 therapy refractory UC patients over 90 days. Section |
Data_Assets
| Field | Value | Evidence |
|---|---|---|
data_assets.analysis_code |
True |
More information on statistics and bioinformatic tools applied to the dataset and metadata information can one found at: https://github.com/LGPW/FMT_in_TRUC_APT2017 Section |
data_assets.open_access |
True from source |
isOpenAccess: "Y" Section |
data_assets.qc_or_negative_controls_reported |
True |
Sequencing errors were reduced ... Chimeras were removed with UCHIME Section |
data_assets.raw_reads |
True |
The datasets generated and analysed during the current study are available in the European nucleotide archive (ENA) repository under the Primary accession number PRJEB11841 Section |
data_assets.sample_metadata |
True |
metadata information can one found at: https://github.com/LGPW/FMT_in_TRUC_APT2017 Section |
Specimens
| Field | Value | Evidence |
|---|---|---|
specimens.body_site |
gastrointestinal tract inferred |
the faecal suspension was applied into the terminal ileum and the right colon Section |
specimens.inflamed_status_available |
True |
Active ulcerative colitis was defined as a total Mayo score ≥4 and an endoscopic subscore ≥1. Section |
specimens.longitudinal_sampling |
True |
Faecal samples for microbiota analyses were collected at each study visit Section |
specimens.number_of_samples |
172 from source |
ENA sample_count=172 Section |
specimens.sample_type |
stool |
Faecal samples for microbiota analyses were collected at each study visit Section |