Gut multi-omics profiling in Crohn’s disease: A preliminary study
Download from source ↗Dataset overview
In search for interplay between stool microRNAs, microbiota and short chain fatty acids in Crohn's disease - a preliminary study.
Abstract
<h4>Background</h4>Inflammatory bowel diseases are classic polygenic disorders, with genetic loads that reflect immunopathological processes in response to the intestinal microbiota. Herein we performed the multiomics analysis by combining the large scale surveys of gut bacterial community, stool microRNA (miRNA) and short chain fatty acid (SCFA) signatures to correlate their association with the activity of Crohn's disease (CD).<h4>Methods</h4>DNA, miRNA, and metabolites were extracted from stool samples of 15 CD patients, eight with active disease and seven in remission, and nine healthy individuals. Microbial, miRNA and SCFA profiles were assessed using datasets from 16S rRNA sequencing, Nanostring miRNA and GC-MS targeted analysis, respectively.<h4>Results</h4>Pairwise comparisons showed that 9 and 23 taxa differed between controls and CD patients with active and inactive disease, respectively. Six taxa were common to both comparisons, whereas four taxa differed in CD patients. α-Diversity was lower in both CD groups than in controls. The levels of 13 miRNAs differed (p-value < 0.05; FC > 1.5) in CD patients and controls before FDR correction and 4 after. Of six SCFAs, the levels of two differed significantly (p-value < 0.05, FC > 1.5) in CD patients and controls, and the levels of four differed in patients with active and inactive CD. PLS-DA revealed models with smallest error rate for controls in bacterial component and inactive disease in metabolites.<h4>Conclusion</h4>A complex interrelationship may exist between gut dysbiosis, miRNA profiling and SCFA level in response to intestinal inflammation.
doi:10.1186/s12876-020-01444-3 ↗ PMID 32958038 ↗ PMC7507689 ↗
Study facts
- Organism
- Homo sapiens
- Platform
- Ion Torrent Personal Genome Machine (PGM)
- Age group
- adult
- Disease groups
- Crohn's disease, Non-IBD controls
- 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
- Raw reads are advertised
- Feature/OTU tables are advertised
- Taxonomic tables are advertised
- Participant-to-sample mapping is available
- Participant counts are documented
- Sample counts are documented
Extraction evidence & provenance
Each extracted field is shown with the source excerpt and location used to resolve it.
Assay
| Field | Value | Evidence |
|---|---|---|
assay.platform |
Ion Torrent Personal Genome Machine (PGM) |
16S rRNA was sequenced on an Ion Torrent Personal Genome Machine (PGM) platform Section |
assay.read_depth_reported |
92000 |
An average of 92,000 reads were generated Section |
assay.sequencing_type |
amplicon_16s |
16S rRNA was sequenced on an Ion Torrent Personal Genome Machine (PGM) platform Section |
assay.target_region |
V2, V3, V4, V6–7, V8 and V9 |
a consensus view across 6 regions V2, V3, V4, V6–7, V8 and V9 Section |
Cohort
| Field | Value | Evidence |
|---|---|---|
cohort.age_group |
adult inferred |
median age 32 years (range, 20–62 years) ... median age 36 years (range, 26–41 years) Section |
cohort.crohns_disease_participants |
15 |
The study cohort consisted of 15 CD patients Section |
cohort.disease_activity_metadata_available |
True |
seven patients in remission or with mild CD ... eight patients with moderate to severe CD Section |
cohort.non_ibd_controls |
9 |
and nine healthy control individuals Section |
cohort.study_design |
cross_sectional inferred |
A stool sample from a single bowel movement was collected and immediately frozen Section |
cohort.total_participants |
24 computed |
The study cohort consisted of 15 CD patients... and nine healthy control individuals. Section |
cohort.treatment_exposure_documented |
True |
Previous treatment Immunosupressants Glucocorticoids Biological therapy Section |
Data_Assets
| Field | Value | Evidence |
|---|---|---|
data_assets.feature_or_otu_table |
True inferred |
Of the 432 taxa identified in these samples, 81 were present at level higher than 0.1% of reads Section |
data_assets.open_access |
True |
"isOpenAccess": "Y" Section |
data_assets.pipeline_or_tool_versions |
True |
Additional steps of the analysis were performed using Mothur version 1.38 software. Section |
data_assets.qc_or_negative_controls_reported |
True |
only the sequences that were 200–300 bases in length, with an average base quality of 20... were kept Section |
data_assets.raw_reads |
True |
Unmapped BAM files were converted to FASTQ using Picard’s SamToFastq Section |
data_assets.sample_metadata |
True |
The study cohort consisted of 15 CD patients ... and nine healthy control individuals Section |
data_assets.taxonomic_table |
True |
Of the 432 taxa identified in these samples Section |
Specimens
| Field | Value | Evidence |
|---|---|---|
specimens.body_site |
gastrointestinal tract |
Microbial communities of the gastro-intestinal tract Section |
specimens.inflamed_status_available |
True |
Disease activity was determined by measuring the CD activity index (CDAI) Section |
specimens.longitudinal_sampling |
False inferred |
A stool sample from a single bowel movement was collected Section |
specimens.number_of_samples |
24 inferred |
stool samples of 15 CD patients... and nine healthy individuals Section |
specimens.participant_to_sample_mapping_available |
True inferred |
A stool sample from a single bowel movement was collected Section |
specimens.sample_type |
stool |
A stool sample from a single bowel movement was collected Section |