# Global metabolic interaction network of the human gut microbiota for   context-specific community-scale analysis

**Authors:** Jaeyun Sung, Seunghyeon Kim, Josephine Jill T. Cabatbat, Sungho Jang,, Yong-Su Jin, Gyoo Yeol Jung, Nicholas Chia, Pan-Jun Kim

arXiv: 1706.01787 · 2017-06-07

## TL;DR

This paper introduces NJS16, a comprehensive interspecies metabolic network of the human gut microbiota, enabling context-specific analysis of microbial communities and their metabolic functions in health and disease.

## Contribution

It provides a curated, large-scale metabolic interaction network and a mathematical framework for analyzing gut microbiota in different health contexts, such as diabetes.

## Key findings

- Identified core microbial entities with significant metabolic influence
- Revealed disease-specific microbial and metabolic features in type 2 diabetes
- Mapped community-wide metabolic interactions in the human gut

## Abstract

A system-level framework of complex microbe-microbe and host-microbe chemical cross-talk would help elucidate the role of our gut microbiota in health and disease. Here we report a literature-curated interspecies network of the human gut microbiota, called NJS16. This is an extensive data resource composed of ~570 microbial species and 3 human cell types metabolically interacting through >4,400 small-molecule transport and macromolecule degradation events. Based on the contents of our network, we develop a mathematical approach to elucidate representative microbial and metabolic features of the gut microbial community in a given population, such as a disease cohort. Applying this strategy to microbiome data from type 2 diabetes patients reveals a context-specific infrastructure of the gut microbial ecosystem, core microbial entities with large metabolic influence, and frequently-produced metabolic compounds that might indicate relevant community metabolic processes. Our network presents a foundation towards integrative investigations of community-scale microbial activities within the human gut.

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Source: https://tomesphere.com/paper/1706.01787