Colloids and Surfaces B BiointerfacesMicrobiologyPeer-reviewed journal article
Biophysical properties and phenotypes of cell clusters detached from Staphylococcus epidermidis biofilms after matrix-targeted disruption
Sydney Rachel Packard, Gabriel John Bulacan, Thelge Buddika PeirisiD, Randy Clinton PaffenrothiD, E. Kate StewartiD
Abstract
Bacterial cells detached from Staphylococcus epidermidis biofilms are found to release predominantly as small oblate clusters ([~]1.9 {micro}m) in both untreated biofilms and biofilms treated with matrix-targeted disruptors. Quantitative image analysis common to colloidal science was applied to quantitatively evaluate the physical properties of 9,147 bacterial clusters detached from S. epidermidis biofilms with and without targeted disruption of individual matrix components (polysaccharides, proteins, extracellular DNA) or solubilization of the extracellular polymeric substances (EPS). Concentrations of S. epidermidis biofilm-detached cells are highest after matrix-targeted disruption of polysaccharides. K-means clustering, an unsupervised machine learning technique, was used to reveal that S. epidermidis biofilm-detached cells are released in five distinct phenotypes: small oblate, mid-sized oblate, large oblate, small spherical, and mid-sized prolate clusters. S. epidermidis biofilm detached cell clusters are predominantly oblate across three size groups (79.5%), with the small oblate phenotype representing 60.1% of cell clusters that have 3.1 {+/-} 1.2 cells per cluster, Euclidean diameters of 1.9 {+/-} 0.4 {micro}m, anisotropy indices of 0.98 {+/-} 0.05, and asphericities of -1.75 {+/-} 0.31 on average. The proportion of S. epidermidis cell clusters within each biofilm-detached cell phenotype differs between matrix-targeted disruptors. There are also variations in the abundance of S. epidermidis biofilm detached cells after matrix-targeted disruption between growth conditions and strains. Evaluating the physical properties of biofilm-detached cells after matrix-targeted disruption is critical to understanding their translocation in fluid flow and susceptibility to the host immune response as well as in evaluating matrix-targeted disruption for biofilm control.
- organism: bacteria (other)
- assay: imaging
- research focus: cell type annotation
- approach: statistical model
- Citations
- 1
- FWCI
- 2.05
- Field percentile
- top 17%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- The secreted staphylococcal biofilm protein Sbp forms biomolecular condensates in the presence of DNA
P. Ethan Adkins, Alexander E. Yarawsky, Andrew B. Herr·Protein SciencePeer-reviewed·Jan 23, 2026
- Privatization of biofilm matrix in structurally heterogeneous biofilms
S. B. Otto, M. Martin, … A. T. Kovacs·bioRxiv·Jul 7, 2020
- A branching cell-fate decision in biofilm dispersal enables long-term surface persistence
Sandhya Kasivisweswaran, Jojo A. Prentice, Andrew A. Bridges·bioRxiv·Apr 30, 2026
- Extracellular membrane vesicles - previously unrecognized components of Staphylococcus aureus biofilms
Jinger Lei, Misaki Foster, … Xiaogang Wang·Journal of BacteriologyPeer-reviewed·Aug 7, 2026
- Swarming bacteria undergo localized dynamic phase transition to form stress-induced biofilms
- Mechanical comparison of Escherichia coli biofilms with altered matrix composition: a study combining shear-rheology and microindentation
Macarena Siri, Adrien Sarlet, … Cécile M. Bidan·ACS Biomaterials Science & EngineeringPeer-reviewed·Jun 12, 2025