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A human gut metagenome-assembled genome catalogue spanning 41 countries supports genome-scale metabolic models.

Nature microbiology2025-12-05PubMed
Total: 83.0Innovation: 8Impact: 8Rigor: 8Citation: 10

Summary

HRGM2 delivers 155,211 near-complete gut genomes from 4,824 species across 41 countries, substantially expanding diversity and quality over prior catalogues. The resource improves species/strain profiling and underpins automated, high-confidence genome-scale metabolic models, facilitating analysis of disease-associated microbial metabolic networks.

Key Findings

  • Compiled 155,211 non-redundant, near-complete genomes (≥90% completeness, ≤5% contamination) from 4,824 species across 41 countries.
  • Expanded genome count by 66% and species diversity by 50% versus UHGG, improving species/strain resolution and resistome surveys.
  • Exclusive use of near-complete genomes enabled high-confidence, automated genome-scale metabolic models and revealed disease-associated microbial metabolic interactions.

Clinical Implications

Enhances translational microbiome research for metabolic syndrome, diabetes, and obesity by enabling reliable prediction of microbial metabolic capacities and interactions that influence host endocrine-metabolic homeostasis.

Why It Matters

Provides a foundational, globally representative genomic resource that enables robust metabolic modeling—critical for mechanistic studies and interventions in metabolic and endocrine-related diseases.

Limitations

  • Potential sampling biases remain despite broad geographic coverage.
  • MAG-based reconstructions, while near-complete, may still miss plasmids or low-abundance genomic regions affecting metabolic inference.

Future Directions

Expand underrepresented populations and longitudinal sampling; link models to host phenotypes and metabolomics; validate predicted microbial metabolic interactions experimentally and clinically.

Study Information

Study Type
Resource/Data paper
Research Domain
Pathophysiology
Evidence Level
III - High-quality genomic resource enabling downstream mechanistic and translational studies
Study Design
OTHER