# A Review of Gut Microbiota Dynamics: From Healthy Gestation to Gestational Diabetes in Human and Mouse Models

**Authors:** Dat Da Ly, Bryony A. McNeill, Kathryn Aston-Mourney, Leni R. Rivera

PMC · DOI: 10.3390/biomedicines14030707 · Biomedicines · 2026-03-18

## TL;DR

This review explores how gut microbiota changes during pregnancy and how these changes may contribute to gestational diabetes, highlighting differences from type 2 diabetes and the need for further research.

## Contribution

The paper provides a comprehensive synthesis of gut microbiota dynamics during healthy and diabetic pregnancies, identifying pregnancy-specific microbial signatures.

## Key findings

- Late pregnancy is marked by increased lactic acid-producing bacteria and reduced Firmicutes-to-Bacteroidetes ratios.
- Gestational diabetes shows dysbiosis with elevated F/B ratios and reduced Bifidobacterium.
- GDM butyrate-producer patterns differ from type 2 diabetes, indicating unique pregnancy-specific mechanisms.

## Abstract

Over the past decades, gut microbiota has emerged as a critical modulator of human health and disease. Pregnancy involves substantial microbiota remodelling that influences offspring development, yet mechanisms linking maternal microbiota changes to gestational diabetes mellitus (GDM) remain unclear. The current literature lacks a comprehensive synthesis of pregnancy microbiota dynamics across healthy gestation to GDM, comparative human–murine analysis, and pregnancy-specific mechanistic frameworks distinct from type 2 diabetes models. This narrative review comprehensively synthesised evidence on gut microbiota composition in healthy pregnancy and GDM (2005–2025, NCBI PubMed) to identify convergent signatures and articulate pregnancy-specific mechanisms. Early pregnancy microbiota resembles non-pregnant individuals, whereas late pregnancy exhibits increased lactic acid-producing bacteria and reduced Firmicutes-to-Bacteroidetes (F/B) ratios. GDM exhibits pathological dysbiosis with elevated F/B ratios and reduced Bifidobacterium. Critically, GDM butyrate-producer patterns diverge from type 2 diabetes, suggesting pregnancy-specific mechanisms beyond glucose homeostasis. Despite these insights, methodological heterogeneity and cross-sectional designs constrain definitive conclusions. Longitudinal studies with standardised sequencing are essential to confirm consistent signatures and enable rational design of microbiota-modulating interventions (prebiotics, probiotics, synbiotics, postbiotics, diet) to optimise maternal health, prevent GDM, and support offspring development.

## Linked entities

- **Diseases:** gestational diabetes mellitus (MONDO:0005406), gestational diabetes (MONDO:0005406), type 2 diabetes (MONDO:0005148)
- **Species:** Homo sapiens (taxon 9606), Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** GDM (MESH:D016640), dysbiosis (MESH:D064806), Diabetes (MESH:D003920), type 2 diabetes (MESH:D003924)
- **Chemicals:** butyrate (MESH:D002087), glucose (MESH:D005947), prebiotics (MESH:D056692), postbiotics (-), lactic acid (MESH:D019344)
- **Species:** Bifidobacterium (genus) [taxon 1678], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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## References

188 references — full list in the complete paper: https://tomesphere.com/paper/PMC13023822/full.md

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Source: https://tomesphere.com/paper/PMC13023822