Epigenomic alterations are associated with mucosal microbiota and inflammation in inflammatory bowel disease
Download from source ↗Dataset overview
Colonic microbiota is associated with inflammation and host epigenomic alterations in inflammatory bowel disease.
Abstract
Studies of inflammatory bowel disease (IBD) have been inconclusive in relating microbiota with distribution of inflammation. We report microbiota, host transcriptomics, epigenomics and genetics from matched inflamed and non-inflamed colonic mucosa [50 Crohn's disease (CD); 80 ulcerative colitis (UC); 31 controls]. Changes in community-wide and within-patient microbiota are linked with inflammation, but we find no evidence for a distinct microbial diagnostic signature, probably due to heterogeneous host-microbe interactions, and show only marginal microbiota associations with habitual diet. Epithelial DNA methylation improves disease classification and is associated with both inflammation and microbiota composition. Microbiota sub-groups are driven by dominant Enterbacteriaceae and Bacteroides species, representative strains of which are pro-inflammatory in vitro, are also associated with immune-related epigenetic markers. In conclusion, inflamed and non-inflamed colonic segments in both CD and UC differ in microbiota composition and epigenetic profiles.
doi:10.1038/s41467-020-15342-5 ↗ PMID 32251296 ↗ PMC7089947 ↗
Study facts
- Organism
- Homo sapiens
- Platform
- Illumina MiSeq
- Age group
- adult
- Disease groups
- Crohn's disease, Non-IBD controls, Ulcerative colitis
- Anatomical sites
- —
Data availability
Specific data assets have not been resolved from the source yet — see the source repository below for the full file listing.
Strengths & limitations for reuse
Strengths
- Participant-to-sample mapping is available
- Participant counts are documented
- Sample counts are documented
Limitations
- Not documented: raw reads are advertised
- 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.paired_end |
True |
on an Illumina MiSeq for 2 × 300 bp reads Section |
assay.platform |
Illumina MiSeq |
sent for sequencing at Eurofins Genomics on an Illumina MiSeq Section |
assay.primers_reported |
True |
The primers (forward TCGTCGGCAGCGTCAGATGTGTATAAGAGACAGCCTACGGGNGGCWGCAG; reverse GTCTCGTGGGCTCGGAGATGTGTATAAGAGACAGGACTACHVGGGTATCTAATCC) Section |
assay.read_length |
300 |
on an Illumina MiSeq for 2 × 300 bp reads Section |
assay.sequencing_type |
amplicon_16s |
reads of the amplified 16S rRNA V3-V4 gene region Section |
assay.target_region |
16S rRNA V3-V4 |
the amplified 16S rRNA V3-V4 gene region Section |
Cohort
| Field | Value | Evidence |
|---|---|---|
cohort.age_group |
adult |
We studied paired biopsies from inflamed and non-inflamed mucosa of 80 adult patients Section |
cohort.crohns_disease_participants |
50 |
80 adult patients with ulcerative colitis and 50 with Crohn’s disease Section |
cohort.disease_activity_metadata_available |
True |
samples from areas of active (lesions) inflammation and from normal-appearing areas Section |
cohort.non_ibd_controls |
31 |
along with paired biopsies of 31 non-IBD (here: healthy) controls Section |
cohort.study_design |
cross_sectional |
While our study is based on a single time-point Section |
cohort.total_participants |
161 |
Fig. 1 Overall microbiota composition ... from 161 subjects Section |
cohort.treatment_exposure_documented |
True |
Of the 15 patients on biologics (anti-TNFs: Adalimumab and Infliximab) Section |
cohort.ulcerative_colitis_participants |
80 |
80 adult patients with ulcerative colitis and 50 with Crohn’s disease Section |
Data_Assets
| Field | Value | Evidence |
|---|---|---|
data_assets.open_access |
True |
"isOpenAccess": "Y" Section |
data_assets.pipeline_or_tool_versions |
True |
FastQC v0.11.3 ... Trimmomatic v0.33 ... R v3.3.0 ... DADA2 package (v1.03) Section |
data_assets.qc_or_negative_controls_reported |
True |
the quality of the raw reads was visualized with FastQC v0.11.3 followed by read trimming and filtering with Trimmomatic v0.33 Section |
Specimens
| Field | Value | Evidence |
|---|---|---|
specimens.body_site |
colon |
endoscopically-targeted biopsies from paired inflamed and non-inflamed segments of the colon Section |
specimens.inflamed_status_available |
True |
samples from areas of active (lesions) inflammation and from normal-appearing areas Section |
specimens.longitudinal_sampling |
False |
While our study is based on a single time-point Section |
specimens.number_of_samples |
48 |
Bisulphite converted DNA from the 48 samples were hybridised to the Illumina Infinium 450k Human Methylation Beadchip Section |
specimens.participant_to_sample_mapping_available |
True |
For those with CD, colonic biopsies were taken ... (n = 50 biopsy pairs) Section |
specimens.sample_type |
mucosal_biopsy |
Microbiota composition of 346 colonic biopsies were analyzed Section |