A geometry-dependent, force balance-driven model of Staphylococcus epidermidis biofilm cell cluster detachment
Yuehui Xu, Jasmine A.F. Kreig, Zhuoran Wang, Elizabeth J. Stewart, Rayanne A. Luke, Sarah D. Olson

TL;DR
This paper introduces a geometry-dependent, force balance-based model for biofilm detachment that incorporates cluster properties and EPS disruption, providing new insights into detachment dynamics.
Contribution
The model uniquely accounts for cluster geometry, local bacterial and EPS arrangements, and EPS disruption effects, advancing predictive understanding of biofilm detachment.
Findings
Cluster size and shape are influenced by EPS disruption levels.
Model predictions align with experimental biofilm microstructure data.
EPS weakening increases detachment frequency and alters cluster morphology.
Abstract
Biofilms, bacteria cells surrounded by a self-produced polymeric matrix, are common on medical devices and lead to many hospital infections. The biofilm lifecycle includes disassembly and dispersion, where bacteria clusters detach from the biofilm, circulate in the bloodstream, and potentially colonize secondary infection sites. Existing models often simplify detachment to a function of biofilm thickness or extracellular polymeric substance (EPS) density, without tracking properties of detached clusters that impact their biological fate, including cluster size and morphology. Addressing this gap, our detachment model accounts for drag and adhesion in tagged sections of the biofilm determined by the cluster geometry and local arrangement of bacteria and EPS. A stickiness parameter controls local EPS adhesion strength, which is modulated to disrupt (or compromise) EPS biomass. We…
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