Foundry120 atlas

Fungal microbiota dysbiosis in IBD PMID: 26843508 RUN2

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Dataset overview

Participants 273
Samples 273
Reuse readiness 4.3/10 evidence-backed score

Fungal microbiota dysbiosis in IBD.

Abstract

<h4>Objective</h4>The bacterial intestinal microbiota plays major roles in human physiology and IBDs. Although some data suggest a role of the fungal microbiota in IBD pathogenesis, the available data are scarce. The aim of our study was to characterise the faecal fungal microbiota in patients with IBD.<h4>Design</h4>Bacterial and fungal composition of the faecal microbiota of 235 patients with IBD and 38 healthy subjects (HS) was determined using 16S and ITS2 sequencing, respectively. The obtained sequences were analysed using the Qiime pipeline to assess composition and diversity. Bacterial and fungal taxa associated with clinical parameters were identified using multivariate association with linear models. Correlation between bacterial and fungal microbiota was investigated using Spearman's test and distance correlation.<h4>Results</h4>We observed that fungal microbiota is skewed in IBD, with an increased Basidiomycota/Ascomycota ratio, a decreased proportion of <i>Saccharomyces cerevisiae</i> and an increased proportion of <i>Candida albicans</i> compared with HS. We also identified disease-specific alterations in diversity, indicating that a Crohn's disease-specific gut environment may favour fungi at the expense of bacteria. The concomitant analysis of bacterial and fungal microbiota showed a dense and homogenous correlation network in HS but a dramatically unbalanced network in IBD, suggesting the existence of disease-specific inter-kingdom alterations.<h4>Conclusions</h4>Besides bacterial dysbiosis, our study identifies a distinct fungal microbiota dysbiosis in IBD characterised by alterations in biodiversity and composition. Moreover, we unravel here disease-specific inter-kingdom network alterations in IBD, suggesting that, beyond bacteria, fungi might also play a role in IBD pathogenesis.

Study facts

Organism
Platform
Age group
Disease groups
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

  • 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

FieldValueEvidence
assay.sequencing_type amplicon_its inferred
Using ITS2 sequencing, we then assessed the composition of the fungal microbiota

Section Results; Altered fungal microbiota diversity in IBD, offset 3900

assay.target_region ITS2
Using ITS2 sequencing, we then assessed the composition of the fungal microbiota

Section Results; Altered fungal microbiota diversity in IBD, offset 3900

Cohort

FieldValueEvidence
cohort.disease_activity_metadata_available True
in flare compared with remission

Section Results; Bacterial dysbiosis in IBD, offset 2850

cohort.non_ibd_controls 38
235 patients with IBD and 38 healthy subjects (HS)

Section study.description, offset —

cohort.total_participants 273 computed
235 patients with IBD and 38 healthy subjects (HS)

Section study.description, offset —

cohort.treatment_exposure_documented True
adjusted all analyses for age, gender, smoking and treatment

Section Materials and methods; Statistical analysis, offset 17800

Specimens

FieldValueEvidence
specimens.body_site faecal
Faecal samples were collected from 235 patients with IBD and 38 HS.

Section Materials and methods; Patients and samples collection, offset 14600

specimens.number_of_samples 273 computed
Faecal samples were collected from 235 patients with IBD and 38 HS.

Section Materials and methods; Patients and samples collection, offset 14600

specimens.sample_type stool
Faecal samples were collected from 235 patients with IBD and 38 HS.

Section Materials and methods; Patients and samples collection, offset 14600