Foundry120 atlas

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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Dataset overview

Participants 27
Samples 172
Reuse readiness 7.7/10 evidence-backed score

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

FieldValueEvidence
assay.platform Illumina MiSeq from source
ENA instrument_model=Illumina MiSeq

Section ENA study report, offset —

assay.read_depth_reported 15376
samples were rarefied to at least 15376 sequences/sample

Section Microbiota analysis, offset 15380

assay.sequencing_type amplicon_16s
For amplification of bacterial 16S rRNA gene

Section DNA extraction, 16S rRNA gene amplification and sequencing, offset 13800

assay.target_region V4
targeting the hypervariable region V4 of the 16S rRNA gene

Section DNA extraction, 16S rRNA gene amplification and sequencing, offset 13920

Cohort

FieldValueEvidence
cohort.age_group mixed inferred
Eligible patients with chronic active ulcerative colitis were aged between 16 and 80 years.

Section Study population-patients, offset 7240

cohort.disease_activity_metadata_available True
Active ulcerative colitis was defined as a total Mayo score ≥4 and an endoscopic subscore ≥1.

Section Study population-patients, offset 7470

cohort.study_design longitudinal
This is an open prospective trial of repeated faecal microbiota transplantation ... End of follow-up was after 90 days.

Section Study design, offset 3690

cohort.total_participants 27
From June 2012 to July 2014, twenty-seven patients were recruited.

Section Study design, offset 5070

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 Study design, offset 3690

cohort.treatment_response_metadata_available True
Primary end point was the reduction of the total Mayo score on day 90.

Section Study design, offset 4610

cohort.ulcerative_colitis_participants 27
27 therapy refractory UC patients over 90 days.

Section study description, offset —

Data_Assets

FieldValueEvidence
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 study description, offset 1450

data_assets.open_access True from source
isOpenAccess: "Y"

Section publication metadata, offset 1800

data_assets.qc_or_negative_controls_reported True
Sequencing errors were reduced ... Chimeras were removed with UCHIME

Section Microbiota analysis, offset 14700

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 AVAILABILITY OF DATA AND MATERIAL, offset 36000

data_assets.sample_metadata True
metadata information can one found at: https://github.com/LGPW/FMT_in_TRUC_APT2017

Section study.description, offset 900

Specimens

FieldValueEvidence
specimens.body_site gastrointestinal tract inferred
the faecal suspension was applied into the terminal ileum and the right colon

Section Donor stool preparation and protocol for faecal microbiota transplantation, offset 10120

specimens.inflamed_status_available True
Active ulcerative colitis was defined as a total Mayo score ≥4 and an endoscopic subscore ≥1.

Section Study population-patients, offset 7470

specimens.longitudinal_sampling True
Faecal samples for microbiota analyses were collected at each study visit

Section Study design, offset 4290

specimens.number_of_samples 172 from source
ENA sample_count=172

Section ENA study report, offset —

specimens.sample_type stool
Faecal samples for microbiota analyses were collected at each study visit

Section Study design, offset 4290