BacArena

BacArena simulates metabolic and spatial dynamics of microbial communities by integrating flux balance analysis (FBA) with individual-based modeling to investigate microbial interactions and community-level metabolic exchanges.


Key Features:

  • Hybrid Modeling Approach: Combines flux balance analysis (FBA) constraint-based modeling with individual-based models to represent metabolism and interactions at single-cell and community scales.
  • Spatial and Temporal Dynamics: Simulates movement, diffusion, chemotaxis, and kinetics to capture spatial and temporal changes in community structure and metabolite gradients.
  • Genome-scale Metabolic Models: Uses genome-scale metabolic models for each organism to represent metabolic capabilities and enable prediction of compound uptake and release.
  • Data Analysis Techniques: Includes analysis routines to interpret simulation outputs and examine metabolic interactions and community dynamics.

Scientific Applications:

  • Pseudomonas aeruginosa Biofilm Formation: Modeled cross-feeding of fermentation products that leads to spatial differentiation of metabolic phenotypes within biofilms.
  • Human Gut Microbiome Modeling: Simulated a seven-species human gut community to examine how mucus glycans generate spatial gradients that influence niche formation and community structure.

Methodology:

Implements genome-scale metabolic models per organism, applies flux balance analysis (FBA) to determine uptake and release of compounds, and simulates individual-based interactions including movement, diffusion, chemotaxis, and kinetics to model spatial-temporal community dynamics.

Topics

Details

Tool Type:
library
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
6/30/2018
Last Updated:
11/25/2024

Operations

Publications

Bauer E, Zimmermann J, Baldini F, Thiele I, Kaleta C. BacArena: Individual-based metabolic modeling of heterogeneous microbes in complex communities. PLOS Computational Biology. 2017;13(5):e1005544. doi:10.1371/journal.pcbi.1005544. PMID:28531184. PMCID:PMC5460873.

PMID: 28531184
PMCID: PMC5460873
Funding: - Deutsche Forschungsgemeinschaft: EXC306 - Fonds National de la Recherche Luxembourg: FNR/6783162, FNR/A12/01

Documentation