Foundry120 atlas

Identification of gut microbiome and transcriptome changes in ulcerative colitis and pouchitis

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Dataset overview

Participants 85
Samples None
Reuse readiness 4.4/10 evidence-backed score

Identification of gut microbiome and transcriptome changes in ulcerative colitis and pouchitis.

Abstract

<h4>Background</h4>Pouchitis is the common postoperative complication of ulcerative colitis (UC) and is also considered as inflammatory bowel disease. The aim was to investigate the microbiological and transcriptional differences between the two illnesses.<h4>Methods</h4>Eighty-five participants were enrolled (37 UC, 15 healthy UC pouches, 15 pouchitis and 18 healthy volunteers) and stool samples were collected. Microbial populations were analyzed by pyrosequencing of 16S ribosomal DNA. Furthermore, transcriptome data of 119 UC and 28 pouch patients were obtained from two data sets for bioinformatics analysis.<h4>Results</h4>The results of gut microbiota community analysis showed that with aggravation of UC, intestinal microorganisms were characterized by a gradual decreased in diversity and numbers of butyrate-producing bacteria and <i>Bacteroides</i>. Besides, in addition to the decrease of probiotics, the proliferation of <i>Escherichia-Shigella</i> and <i>Ruminococcus gnavus</i> was observed in pouchitis which is related to multiple infection pathways. The function enrichment of differential expression genes and hub genes, as well as the immunological condition was shown to be distinct using transcriptome bioinformatics analysis between UC and pouchitis. A stronger immune response occurs in UC and may be associated with high expression of tumor necrosis factor and interleukin, while multiple hub genes such as <i>CDK1</i> in pouchitis are associated with cell cycle regulation.<h4>Conclusions</h4>The characteristics of gut microbiota disturbance and transcriptome alteration in UC and pouchitis are different. Our findings suggested that pouchitis may have a unique pathogenesis which was separated from UC.

Study facts

Organism
—
Platform
pyrosequencing
Age group
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Disease groups
Non-IBD controls, Ulcerative colitis
Anatomical sites
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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 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

FieldValueEvidence
assay.platform pyrosequencing
Microbial populations were analyzed by pyrosequencing of 16S ribosomal DNA.

Section descriptions[0].description, offset —

assay.sequencing_type amplicon_16s inferred
Microbial populations were analyzed by pyrosequencing of 16S ribosomal DNA.

Section descriptions[0].description, offset —

Cohort

FieldValueEvidence
cohort.non_ibd_controls 18
Eighty-five participants were enrolled (37 UC, 15 healthy UC pouches, 15 pouchitis and 18 healthy volunteers)

Section descriptions[0].description, offset —

cohort.total_participants 85
Eighty-five participants were enrolled (37 UC, 15 healthy UC pouches, 15 pouchitis and 18 healthy volunteers)

Section descriptions[0].description, offset —

cohort.ulcerative_colitis_participants 37
Eighty-five participants were enrolled (37 UC, 15 healthy UC pouches, 15 pouchitis and 18 healthy volunteers)

Section descriptions[0].description, offset —

Specimens

FieldValueEvidence
specimens.sample_type stool
stool samples were collected

Section descriptions[0].description, offset —