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PRJNA1169537 SRP536866

Multi-omic gut microbiome in Japanese UC and Crohn's disease

Multi-biome analysis of Cron's disease and ulcerative colitis patients

654 fecal samples from a Japanese cohort (4D study), comparing ulcerative colitis and Crohn's disease patients with healthy controls using shotgun metagenomics of bacteria, phages, and fungi; case-control design. machine-written summary

654 samples · 654 runs · Age unknown · 2024 · 1.20 Gbp / sample · cohort Multi-biome analysis identifies distinct gut micro

Sources
✓Sequence archive 654○Abstract / description○Full text–Supplementary tables–External resources–User contribution–Human verified

Checked this project's papers and archive records yourself? Mark it human-verified.

what each source gave
✓ Sequence archive654 sample values (subject id)
○ Abstract / descriptionread; no usable statement
○ Full textread; no usable statement or table · PMC11603027
– Supplementary tablesno supplementary tables available (or none open access)
– External resourcesnot covered by the external resources we ingest
– User contributionnothing uploaded yet · share metadata
– Human verifiednot yet checked by a person · I checked this project — verify it
Samples at a glance
Age
unknown654
Body site
primary654
Sequencing depth per sample · this project all projects
all projects, 0–0.03 Gbp: 25,080 samples (4 %)all projects, 0.03–0.1 Gbp: 17,066 samples (3 %)all projects, 0.1–0.3 Gbp: 29,179 samples (5 %)all projects, 0.3–1 Gbp: 47,044 samples (8 %)this project, 0.3–1 Gbp: 51 samplesall projects, 1–3 Gbp: 124,983 samples (22 %)this project, 1–3 Gbp: 603 samplesall projects, 3–10 Gbp: 253,728 samples (44 %)all projects, 10–30 Gbp: 72,533 samples (13 %)all projects, 30–100 Gbp: 3,024 samples (1 %)all projects, 100–300 Gbp: 106 samples (0 %)all projects, ≥ 300 Gbp: 9 samples (0 %)project median 1.20 Gbp per sample0130Gbp
Community composition
Bifidobacterium 10.0%Blautia_A 7.1%Phocaeicola 6.7%Bacteroides 5.7%Faecalibacterium 5.0%Prevotella 3.9%Collinsella 3.8%Roseburia 3.6%Mediterraneibacter 3.5%Fusicatenibacter 2.9%Streptococcus 2.9%Ruminococcoides 2.6%not assigned to a genus 9.2%other genera 32.9%

Genera, mean relative abundance over 586 profiled gut samples of this project (Sandpiper SingleM profiles, GTDB R232; low-depth and non-metagenome profiles left out).

Field coverage
fieldsamplescoverageR1R2R3R4
age_category0 0%
country0 0%
health_condition0 0%
subject_id654 100%654
Papers (1)
  • Multi-biome analysis identifies distinct gut microbial signatures and their crosstalk in ulcerative colitis and Crohn's disease. 2024 PMID 39604394 PMC11603027 unsure
Details
Archive description

Gut microbial dysbiosis has been implicated in the pathogenesis of Inflammatory bowel disease. However, comprehensive analyses of the interactions between various components of the gut microbiome, including the bacteriome, virome, and mycobiome, in ulcerative colitis (UC) and Crohn's disease (CD) remain fully understood. Here, we performed shotgun metagenomic sequencing of feces from patients with UC and CD, and healthy controls in the Japanese 4D cohort, and profiled bacterial taxa, gene functions, and antibacterial genes, bacteriophages, and fungi. External metagenomic datasets from the US, Spain, the Netherlands, and China were analyzed to validate our multi-biome findings. Our analysis showed that Enterococcus faecium and Bifidobacterium spp. were enriched in both diseases. Enriched Escherichia coli was particularly characteristic of CD and was significantly linked to numerous antibiotic-resistance genes involved in efflux pumps and adherent-invasive Escherichia coli virulence factors. Changes in the virome were correlated with the shifts in the bacteriome, including the increased abundance of phages encoding pathogenic genes. Saccharomyces paradoxus and Saccharomyces cerevisiae were significantly enriched in UC and CD, respectively. Saccharomyces cerevisiae and Escherichia coli had specific negative associations with SCFA-producing bacteria in CD. Multi-biome signatures and their interactions in UC and CD showed high similarities between Japan and other countries. Since several bacteria, phages, and fungi formed a hub of an intra- or trans-kingdom network with SCFA producers as well as pathobionts in UC and CD, an approach targeting the interaction network may hold therapeutic promise.

How this project entered the registry

Classified as human gut / stool shotgun DNA metagenome of age unknown by sonnet_x2 with confidence 0.85. Assay shotgun_dna.

  • host run.host_tax_id · “9606”
  • body site study.description · “shotgun metagenomic sequencing of feces”
Evidence examples (one per field × route)
samplefieldvaluerouteconf.sourcequote
SAMN44682188subject_idJP4D_11R10.85sample.attr.host_subject_idJP4D_11
Sequencing

654 runs over 654 samples · mean 1.23 Gbp per run (median 1.20 Gbp, total 801.20 Gbp; 654 runs with a base count) · layout PAIRED 654 · platform ILLUMINA 654 · models Illumina HiSeq 4000 (654) · 90% of runs with a Sandpiper profile · first public 2024-11-16

Authors (13)

Akiyama S first · Nishijima S · Kojima Y · Kimura M · Ohsugi M · Ueki K · Mizokami M · Hattori M · Tsuchiya K · Uemura N · Kawai T · Bork P · Nagata N last

Help complete this project

3 of the 4 core fields are below 50% coverage: age_category, country, health_condition. Share metadata

Downloads

PRJNA1169537.csv.gz (16.5 KB) · parquet (95.3 KB) — all 654 samples, every field with route and confidence · PRJNA1169537_determinations.csv.gz (7.5 KB) — 654 evidence rows

Samples (654 · every field this project has values for · hover a cell for its source)
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