A Multiscale Agent-Based Model for the Investigation of E-coli K12 Metabolic Response During Biofilm Formation
                Authored by Jr Majid Latif, Elebeoba E May
                
                    Date Published: 2018
                
                
                    DOI: 10.1007/s11538-018-0494-3
                
                
                    Sponsors:
                    
                        United States Department of Energy (DOE)
                        
                        United States National Science Foundation (NSF)
                        
                
                
                    Platforms:
                    
                        No platforms listed
                    
                
                
                    Model Documentation:
                    
                        Other Narrative
                        
                        Flow charts
                        
                        Mathematical description
                        
                
                
                    Model Code URLs:
                    
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                Abstract
                Bacterial biofilm formation is an organized collective response to
biochemical cues that enables bacterial colonies to persist and
withstand environmental insults. We developed a multiscale agent-based
model that characterizes the intracellular, extracellular, and cellular
scale interactions that modulate Escherichia coli MG1655 biofilm
formation. Each bacterium's intracellular response and cellular state
were represented as an outcome of interactions with the environment and
neighboring bacteria. In the intracellular model, environment-driven
gene expression and metabolism were captured using statistical
regression and Michaelis-Menten kinetics, respectively. In the cellular
model, growth, death, and type IV pili- and flagella-dependent movement
were based on the bacteria's intracellular state. We implemented the
extracellular model as a three-dimensional diffusion model used to
describe glucose, oxygen, and autoinducer 2 gradients within the biofilm
and bulk fluid. We validated the model by comparing simulation results
to empirical quantitative biofilm profiles, gene expression, and
metabolic concentrations. Using the model, we characterized and compared
the temporal metabolic and gene expression profiles of sessile versus
planktonic bacterial populations during biofilm formation and
investigated correlations between gene expression and biofilm-associated
metabolites and cellular scale phenotypes. Based on our in silico
studies, planktonic bacteria had higher metabolite concentrations in the
glycolysis and citric acid cycle pathways, with higher gene expression
levels in flagella and lipopolysaccharide-associated genes. Conversely,
sessile bacteria had higher metabolite concentrations in the autoinducer
2 pathway, with type IV pili, autoinducer 2 export, and cellular
respiration genes upregulated in comparison with planktonic bacteria.
Having demonstrated results consistent with in vitro static culture
biofilm systems, our model enables examination of molecular phenomena
within biofilms that are experimentally inaccessible and provides a
framework for future exploration of how hypothesized molecular
mechanisms impact bulk community behavior.
                
Tags
                
                    Agent-based modeling
                
                    systems biology
                
                    Quorum sensing
                
                    Mycobacterium-tuberculosis infection
                
                    Gene-expression
                
                    Bacterial biofilms
                
                    Staphylococcus-aureus
                
                    Pseudomonas-aeruginosa biofilms
                
                    Biofilm
                
                    Flux balance analysis
                
                    Escherichia coli k12
                
                    Constraint-based models
                
                    To-cell communication
                
                    Coli k-12 biofilms
                
                    Polysaccharide
adhesin