TY - JOUR
T1 - A microfluidics and agent-based modeling framework for investigating spatial organization in bacterial colonies
T2 - The case of Pseudomonas aeruginosa and H1-Type VI secretion interactions
AU - Wilmoth, Jared L.
AU - Doak, Peter W.
AU - Timm, Andrea
AU - Halsted, Michelle
AU - Anderson, John D.
AU - Ginovart, Marta
AU - Prats, Clara
AU - Portell, Xavier
AU - Retterer, Scott T.
AU - Fuentes-Cabrera, Miguel
N1 - Publisher Copyright:
© 2018 Wilmoth, Doak, Timm, Halsted, Anderson, Ginovart, Prats, Portell, Retterer and Fuentes-Cabrera.
PY - 2018/2/6
Y1 - 2018/2/6
N2 - The factors leading to changes in the organization of microbial assemblages at fine spatial scales are not well characterized or understood. However, they are expected to guide the succession of community development and function toward specific outcomes that could impact human health and the environment. In this study, we put forward a combined experimental and agent-based modeling framework and use it to interpret unique spatial organization patterns of H1-Type VI secretion system (T6SS) mutants of P. aeruginosa under spatial confinement. We find that key parameters, such as T6SS-mediated cell contact and lysis, spatial localization, relative species abundance, cell density and local concentrations of growth substrates and metabolites are influenced by spatial confinement. The model, written in the accessible programming language NetLogo, can be adapted to a variety of biological systems of interest and used to simulate experiments across a broad parameter space. It was implemented and run in a high-throughput mode by deploying it across multiple CPUs, with each simulation representing an individual well within a high-throughput microwell array experimental platform. The microfluidics and agent-based modeling framework we present in this paper provides an effective means by which to connect experimental studies in microbiology to model development. The work demonstrates progress in coupling experimental results to simulation while also highlighting potential sources of discrepancies between real-world experiments and idealized models.
AB - The factors leading to changes in the organization of microbial assemblages at fine spatial scales are not well characterized or understood. However, they are expected to guide the succession of community development and function toward specific outcomes that could impact human health and the environment. In this study, we put forward a combined experimental and agent-based modeling framework and use it to interpret unique spatial organization patterns of H1-Type VI secretion system (T6SS) mutants of P. aeruginosa under spatial confinement. We find that key parameters, such as T6SS-mediated cell contact and lysis, spatial localization, relative species abundance, cell density and local concentrations of growth substrates and metabolites are influenced by spatial confinement. The model, written in the accessible programming language NetLogo, can be adapted to a variety of biological systems of interest and used to simulate experiments across a broad parameter space. It was implemented and run in a high-throughput mode by deploying it across multiple CPUs, with each simulation representing an individual well within a high-throughput microwell array experimental platform. The microfluidics and agent-based modeling framework we present in this paper provides an effective means by which to connect experimental studies in microbiology to model development. The work demonstrates progress in coupling experimental results to simulation while also highlighting potential sources of discrepancies between real-world experiments and idealized models.
KW - Agent-based modeling
KW - Microbial organization
KW - Microbial succession
KW - Pseudomonas aeruginosa
KW - Silicon microwell arrays
KW - Spatial confinement
KW - Type VI secretion
UR - http://www.scopus.com/inward/record.url?scp=85041839772&partnerID=8YFLogxK
U2 - 10.3389/fmicb.2018.00033
DO - 10.3389/fmicb.2018.00033
M3 - Article
AN - SCOPUS:85041839772
SN - 1664-302X
VL - 9
JO - Frontiers in Microbiology
JF - Frontiers in Microbiology
IS - FEB
M1 - 33
ER -