HomeTopics › Microbiome & Gut Health

Microbiome & Gut Health

GMJ News knowledge hub · last reviewed August 2026 · Georgian Medical Journal

SummaryStatisticsGlossaryGMJ newsFAQDocumentsOrganizationsResearch

The human gut microbiome — approximately 100 trillion microorganisms (bacteria, archaea, viruses, fungi) encoding approximately 3 million unique genes vs the ~22,000 of the human genome — communicates bidirectionally with the immune system (70% of immune tissue is gut-associated), the brain (gut-brain axis via vagus nerve, metabolites and immune signalling), and virtually every major organ system, with dysbiosis (disruption of normal microbial ecology) associated — though not always causally proven — with IBD, obesity, type 2 diabetes, depression and colorectal cancer (WHO). The most important clinical advance: faecal microbiota transplantation (FMT) received FDA approval in 2022-2023 (Rebyota — Ferring; Vowst — Seres Therapeutics) specifically for recurrent Clostridioides difficile infection — achieving approximately 90% cure rates vs approximately 30% for repeat antibiotics — while the multi-billion-dollar probiotic supplement market operates largely on marketing rather than clinical evidence for most claimed benefits beyond C. diff and antibiotic-associated diarrhoea.

Key messages

FDA-approved FMT — 90% cure for recurrent C. diff
Faecal microbiota transplantation (FMT) received FDA approval in 2022-2023: Rebyota (Ferring, RBX2660 — enema) November 2022; Vowst (Seres Therapeutics, SER-109 — oral capsules) May 2023 — both for recurrent Clostridioides difficile infection. FMT achieves approximately 90% cure vs approximately 30% for repeated antibiotics. This is the strongest clinical evidence in all of microbiome medicine — and the only FDA-approved microbiome-based therapy.
The gut microbiome — 100 trillion organisms, 3 million genes
The human gut contains approximately 100 trillion microorganisms encoding approximately 3 million unique microbial genes — dwarfing the approximately 22,000 genes in the human genome. These microorganisms co-evolved with humans over millions of years. The dominant phyla: Firmicutes and Bacteroidetes (accounting for approximately 90%); also Actinobacteria, Proteobacteria, Verrucomicrobia.
Gut-brain axis — the second brain
The enteric nervous system (500 million neurons in the gut wall — comparable to the spinal cord) communicates bidirectionally with the brain via the vagus nerve, microbial metabolites (SCFAs, tryptophan metabolites), immune signalling and the HPA stress axis. The microbiome produces approximately 90% of the body's serotonin (in enterochromaffin cells). Germ-free mouse experiments show profound alterations in behaviour, stress response and brain development — establishing a causal microbiome-brain link in animal models.
Probiotics — evidence is condition-specific, not generic
Strong evidence: C. diff prevention during antibiotic therapy (Cochrane 2017: approximately 60% risk reduction; Lactobacillus rhamnosus GG and Saccharomyces boulardii have best evidence); rotavirus and infectious diarrhoea in children; necrotising enterocolitis prevention in premature infants. Modest/inconsistent evidence: IBS (some strains reduce bloating/pain); antibiotic-associated diarrhoea; ulcerative colitis maintenance. Insufficient/no evidence: depression; autism; weight loss; immune function in healthy adults; most other marketed uses. The multi-billion-dollar probiotic market vastly outpaces the evidence.
Fibre — the most evidence-based microbiome intervention
Dietary fibre is metabolised by gut bacteria to produce short-chain fatty acids (SCFAs): butyrate (principal fuel for colonocytes; anti-inflammatory; anti-cancer properties via histone deacetylase inhibition); propionate (liver gluconeogenesis regulation; appetite suppression); acetate (peripheral energy metabolism). Higher fibre intake consistently associated with: lower colorectal cancer risk; lower cardiovascular disease; better insulin sensitivity; greater microbiome diversity. The WHO recommends ≥25g fibre/day for adults; most people in HICs consume approximately 15g.
The hype-evidence gap — microbiome is not a panacea
The microbiome field suffers from a massive hype-evidence gap: preclinical and observational data are exciting; causality from association is frequently over-claimed; "dysbiosis" is loosely defined and varies by condition and study. Interventions with strong evidence: FMT for C. diff; specific probiotic strains for specific conditions. Interventions with insufficient evidence: personalised microbiome testing (direct-to-consumer gut microbiome tests have no validated clinical utility); probiotic supplements for most health claims; prebiotic supplements beyond standard high-fibre diet.

Key statistics

~100T
microorganisms in the human gut — equal to all human cells
Nature 2016
~90%
FMT cure rate for recurrent C. diff (vs ~30% for repeat antibiotics)
FDA/NEJM
FDA 2022-23
Rebyota (RBX2660) and Vowst (SER-109) — first FDA-approved microbiome therapies
FDA
500M neurons
in the enteric nervous system (the "second brain") — communicates with CNS
Neurogastroenterology
~60%
reduction in C. diff with probiotics during antibiotic therapy (Cochrane)
Cochrane 2017
≥25g/day
WHO-recommended dietary fibre for adults — most HICs consume ~15g
WHO

Microbiome intervention evidence — by clinical application (Cochrane/FDA)

Source: Cochrane/FDA. FMT for C. diff is the strongest evidence; most other applications remain investigational.

Glossary of key terms

Faecal microbiota transplantation (FMT)
FDA/NEJM
Transfer of processed donor faecal material (containing gut microbiota) into a recipient's gastrointestinal tract to restore a healthy microbial community. Methods: colonoscopic infusion (most established); nasal-jejunal tube; enema (Rebyota, RBX2660); oral capsules (Vowst, SER-109 — spore-based, heat-treated). Donor screening (strict): HIV, HBV, HCV, CMV, EBV, parasites, C. diff, multidrug-resistant organisms. FDA-approved only for recurrent C. diff. Under clinical trial for: IBD (ulcerative colitis — promising Phase 2 results); metabolic syndrome; autism (pilot studies); ME/CFS; multiple sclerosis.
Short-chain fatty acids (SCFAs)
Microbiology/Physiology
Microbial metabolites produced by fermentation of dietary fibre (particularly resistant starch and pectin) in the colon. The three main SCFAs: Butyrate (n-butyric acid): the primary fuel for colonocytes; anti-inflammatory (inhibits NF-κB); epigenetic effects (histone deacetylase inhibitor — anti-cancer potential); maintains gut barrier integrity; reduced in IBD and colorectal cancer patients. Propionate: regulates hepatic gluconeogenesis; appetite suppression (stimulates GLP-1 and PYY release from enteroendocrine cells). Acetate: peripheral metabolism; appetite modulation; anti-inflammatory.
Gut-brain axis
Neurogastroenterology
The bidirectional communication network between the gut microbiome and the central nervous system. Pathways: Vagus nerve (primary bidirectional highway — carries signals from enteroendocrine cells and enteric neurons to brainstem); Microbial metabolites (SCFAs, tryptophan/serotonin precursors, GABA precursors cross the gut-brain barrier); Immune system (gut-associated lymphoid tissue — GALT — releases cytokines that cross the blood-brain barrier); HPA axis (stress responses alter gut motility and microbiome composition; microbiome composition affects cortisol). Relevance: germ-free mice show profoundly altered behaviour, anxiety and social interaction; FMT in animals transfers behavioural traits; clinical evidence in humans is growing but largely associational.
Dysbiosis
Microbiology
A disruption of the normal gut microbiome composition — characterised by: reduced microbial diversity (Shannon diversity index); overgrowth of potentially pathogenic bacteria; reduced abundance of health-associated genera (Bacteroides, Faecalibacterium prausnitzii, Akkermansia muciniphila). Associated with (causation uncertain): IBD (Crohn's, UC); obesity; type 2 diabetes; colorectal cancer (Fusobacterium nucleatum as a driver); depression and anxiety; autism spectrum disorder (observational). Important caveat: "dysbiosis" is poorly defined, varies by study and condition, and correlation ≠ causation. Many dysbiosis findings may reflect consequences of disease rather than causes.
Direct-to-consumer microbiome testing
Evidence/Regulatory
Companies offer gut microbiome analysis from stool samples, providing reports on microbial composition with personalised diet and supplement recommendations. Current limitations: no standardised reference range for a "healthy" microbiome; microbiome composition varies enormously between healthy individuals; the same person's microbiome varies by day and season; no clinical validation that modifying composition based on these tests produces health benefits; no regulatory oversight for clinical claims. Clinical utility: essentially none currently established beyond research settings. GMJ position: direct-to-consumer microbiome testing is interesting science but not yet a basis for clinical decisions or personalised nutrition.
Akkermansia muciniphila
Emerging/Research
A mucin-degrading bacterium (Verrucomicrobia phylum) that colonises the mucus layer of the gut. Reduced in: obesity, type 2 diabetes, IBD, metabolic syndrome. Associated with: gut barrier integrity; reduced metabolic endotoxaemia; reduced inflammation. Pasteurised A. muciniphila has been marketed as a probiotic in some markets. Clinical trial evidence: one Phase 1/2 trial (2019, Nature Medicine) — pasteurised A. muciniphila improved insulin sensitivity and metabolic parameters in overweight/obese adults vs placebo. Regulatory status as a probiotic: novel food approval pending in EU. Evidence: promising but early — far from established clinical application.

Latest GMJ coverage

How Gut Dysbiosis Triggers Systemic Inflammation: A Mechanistic Overview
06/08/2026
Resistant Starch and Gut Health: Why Fiber Type Matters More Than You Think
16/07/2026
Sugar-free diets may worsen blood glucose control, new study finds
29/06/2026
The Human Gut Microbiome: Trillions of Microorganisms Shape Health and Disease
26/06/2026
Aging Immune System Fails to Control Gut Microbiome, New Research Shows
23/06/2026
Gut Parasites May Manipulate Human Behavior, New Research Suggests
15/06/2026

Frequently asked questions 12 Q&A — structured for Google featured snippets and AI discovery

Knowledge hub: guidelines, conventions and reports

Organizations working in migration and health

Related health topics

Clostridioides difficile (FMT primary indication)Nutrition and dietIBD (FMT trials)Mental health (gut-brain axis)Antibiotics and microbiomeObesity (microbiome associations)

About this hub. Produced by the GMJ News Editorial Team as a public-good service. Every statistic is linked to its primary source. Documents are preserved in the GMJ Repository with full attribution. Georgian Medical Journal · Contact the editorial team
GMJ BriefsView all →