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A Microfluidics and Agent-Based Modeling Framework for Investigating Spatial Organization in Bacterial Colonies: The Case of Pseudomonas Aeruginosa and H1-Type VI Secretion Interactions

机译:用于研究细菌菌落空间组织的微流控和基于代理的建模框架:铜绿假单胞菌和H1型VI分泌相互作用的案例

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摘要

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.
机译:导致微生物集合体组织在精细空间尺度上变化的因素尚未得到很好的表征或理解。但是,它们有望指导社区发展和功能的继承,以实现可能影响人类健康和环境的特定成果。在这项研究中,我们提出了一个基于实验和基于代理的组合建模框架,并用它来解释在空间限制下铜绿假单胞菌H1型VI分泌系统(T6SS)突变体的独特空间组织模式。我们发现关键参数,如T6SS介导的细胞接触和裂解,空间定位,相对物种丰度,细胞密度以及生长底物和代谢产物的局部浓度受空间限制的影响。用可访问的编程语言NetLogo编写的模型可以适应各种感兴趣的生物系统,并用于在宽泛的参数空间中模拟实验。通过在多个CPU上部署它,可以实现并以高通量模式运行,每个模拟代表高通量微孔阵列实验平台中的单个孔。我们在本文中介绍的基于微流体和基于代理的建模框架提供了一种有效的手段,可以将微生物学的实验研究与模型开发联系起来。这项工作展示了将实验结果与模拟结合起来的进展,同时还强调了实际实验与理想模型之间差异的潜在根源。

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