Lachnospiraceae
Bacteria › Bacillota › Clostridia › Eubacteriales › Lachnospiraceae
MCA-BAC-000004
TaxID: 186803
| Rank: family
Biology & Ecology
Biology
Gram Statusgram-positive
Oxygen Toleranceobligate anaerobe
Ecology
Primary Nichesgut
Reservoirhuman
Clinical Profile
Pathobiont
yes
no
context dependent
unknown
Clinical Rolesprotective commensal
Typical Specimenstool
Clinical Associations:
E2
E3 — Strong human clinical evidence
E2 — Moderate human evidence
E1 — Limited / preliminary
Lachnospiraceae relative abundance was significantly depleted in critically ill ICU patients compared to healthy controls (ANCOM-II p-adj<0.1), contributing to the loss of colonization resistance and gut dysbiosis during critical illness in a prospective cohort of 51 patients.
PMID:
36894652
E2
E3 — Strong human clinical evidence
E2 — Moderate human evidence
E1 — Limited / preliminary
Penalized ridge regression identified Lachnospiraceae as one of the most important families negatively associated with progressive Enterobacteriaceae enrichment between ICU days 1 and 3, consistent with a colonization resistance role against pathobiont expansion during critical illness.
PMID:
36894652
E1
E3 — Strong human clinical evidence
E2 — Moderate human evidence
E1 — Limited / preliminary
In a phase 1 FMT trial (n=10 anti-PD-1-refractory metastatic melanoma patients), both FMT donors who had achieved complete response to anti-PD-1 therapy were characterized by high Lachnospiraceae relative abundance in their stool microbiota; the paper explicitly characterizes this as a previously reported 'immunotherapy-favorable feature' of the gut microbiome associated with response to anti-PD-1 therapy.
PMID:
33303685
D000069467
Fecal Microbiota Transplantation
D000069196
Gastrointestinal Microbiome
D000082082
Immune Checkpoint Inhibitors
D008545
Melanoma
H00038
Melanoma
E1
E3 — Strong human clinical evidence
E2 — Moderate human evidence
E1 — Limited / preliminary
In a murine CDI model, susceptibility to C. difficile colonization following antibiotic treatment was associated with loss of the normal cecal microbial community (mainly Lachnospiraceae) and a relative increase in Enterobacteriaceae; disease severity was related to the recovery dynamics of these families, with more severe outcomes in mice where Lachnospiraceae failed to return post-antibiotic and Enterobacteriaceae continued to dominate.
PMID:
24503131
E1
E3 — Strong human clinical evidence
E2 — Moderate human evidence
E1 — Limited / preliminary
Monocolonization of germ-free mice with a murine Lachnospiraceae isolate significantly reduced levels of C. difficile colonization and severity of colitis compared to mice monocolonized with a murine E. coli isolate, which had no protective effect, formally demonstrating a colonization resistance function for Lachnospiraceae family members against C. difficile intestinal invasion.
PMID:
24503131
Last reviewed: 2026-04-03
Evidence Timeline
Related Taxa
Shared Niche = same body site
Shared Risk = same vulnerable population
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