Faecalibacterium

cellular organisms|Bacteria|Bacillati|Bacillota|Clostridia|Eubacteriales|Oscillospiraceae
MCA-BAC-000028
TaxID: 216851 | Rank: genus
Biology & Ecology
Biology
Gram Statusunknown
Oxygen Toleranceobligate anaerobe
Key Traits
  • butyrate-producing
Ecology
Primary Nichesgut
Reservoirhuman
Metabolites

No metabolite relationships documented for this taxon.

Clinical Profile
Pathobiont
yes no context dependent unknown
Clinical Rolesprotective commensal
Typical Specimenstool
Risk Contextsmelanoma patients receiving immune checkpoint inhibitor therapy (ICB)
Clinical Associations:
E2
E3 — Strong human clinical evidence E2 — Moderate human evidence E1 — Limited / preliminary
Faecalibacterium genus relative abundance was significantly higher in anti-PD-1 responders versus non-responders in a newly recruited independent cohort of 132 metastatic melanoma patients (n=87 responders, n=45 non-responders; p=0.018 by Wilcoxon rank sum test), supporting its role as a gut microbiota marker of immunotherapy response.
PMID: 34941392
D000082082 Immune Checkpoint Inhibitors D008545 Melanoma H00038 Melanoma
E2
E3 — Strong human clinical evidence E2 — Moderate human evidence E1 — Limited / preliminary
In melanoma patients treated with ICB (n=123), Faecalibacterium genus abundance was numerically higher in patients reporting sufficient dietary fiber intake (≥20 g/day) and no probiotic use — the subgroup with significantly longer progression-free survival (median PFS not reached versus 13 months, P=0.015 vs. all other groups) — though the Faecalibacterium difference per se did not reach statistical significance due to small group size (n=22 in optimal group).
PMID: 34941392
D004043 Dietary Fiber D000082082 Immune Checkpoint Inhibitors D008545 Melanoma H00038 Melanoma
E2
E3 — Strong human clinical evidence E2 — Moderate human evidence E1 — Limited / preliminary
Faecalibacterium genus was significantly enriched in anti-PD-1 responders versus non-responders in the gut microbiome of 43 metastatic melanoma patients (30R, 13NR; FDR-adjusted pairwise comparisons and LEfSe; p<0.01), establishing the original human evidence for genus-level enrichment as a marker of immunotherapy response.
PMID: 29097493
D000082082 Immune Checkpoint Inhibitors D008545 Melanoma H00038 Melanoma
E2
E3 — Strong human clinical evidence E2 — Moderate human evidence E1 — Limited / preliminary
High Faecalibacterium abundance (above median) was associated with significantly prolonged progression-free survival compared to low abundance in 39 anti-PD-1-treated metastatic melanoma patients (p=0.03; multivariate Cox HR=2.95, 95% CI 1.31–7.29), identifying it as an independent gut microbiome predictor of immunotherapy outcome.
PMID: 29097493
D000082082 Immune Checkpoint Inhibitors D008545 Melanoma D000077982 Progression-Free Survival H00038 Melanoma
E2
E3 — Strong human clinical evidence E2 — Moderate human evidence E1 — Limited / preliminary
Faecalibacterium genus abundance was significantly positively correlated with CD8+ T cell density in pre-treatment tumors of melanoma patients on anti-PD-1 therapy (r²=0.42, p<0.01; n=15 matched tumor-microbiome samples), linking gut microbiome composition to intratumoral anti-tumor immunity.
PMID: 29097493
D000069196 Gastrointestinal Microbiome D000082082 Immune Checkpoint Inhibitors D008545 Melanoma H00038 Melanoma
Last reviewed: 2026-04-03
Evidence Timeline
Related Taxa Shared Niche = same body site   Shared Risk = same vulnerable population