Evidence map›Paper›PMID 42390640›Full record

ArticleBulletin of mathematical biology2026

Identifiability, Sensitivity, and Genetic Algorithms in Bacterial Biofilm Selection Models.

Stephen Williams, Daravuth Cheam, Michele K Nishiguchi, Suzanne S Sindi, Shilpa Khatri, Erica M Rutter

Abstract read
In one paragraph

Article in Bulletin of mathematical biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Stephen WilliamsDepartment of Applied Mathematics, University of California, Merced, California, US.ORCID http://orcid.org/0000-0001-8848-6372
Daravuth CheamDepartment of Molecular and Cell Biology, University of California, Merced, California, US.
Michele K NishiguchiDepartment of Molecular and Cell Biology, University of California, Merced, California, US.
Suzanne S SindiDepartment of Applied Mathematics, University of California, Merced, California, US.ORCID http://orcid.org/0000-0003-2742-4332
Shilpa KhatriDepartment of Applied Mathematics, University of California, Merced, California, US.
Erica M RutterDepartment of Applied Mathematics, University of California, Merced, California, US. erutter2@ucmerced.edu.ORCID http://orcid.org/0000-0001-7580-2559

Funding

National Science Foundation DBI 2214038
6 · The paper itself

Abstract

Bacteria often develop distinct phenotypes to adapt to environmental stress. In particular, they can produce biofilms, dense communities of bacteria that live in a complex extracellular matrix. While previous studies have investigated how bacterial biofilms are regulated under laboratory conditions, they have not considered (1) the data requirements necessary to estimate model parameters and (2) how bacteria respond to recurring stressors in their natural habitats. To address (1), we adapted a mechanistic population model to explore the dynamics of biofilm formation in the presence of predator stress, using synthetic data. We used a Maximum Likelihood Estimation framework to measure crucial parameters underpinning the biofilm formation dynamics. We used genetic algorithms to propose an optimal data collection schedule that minimised parameter identifiability confidence interval widths. Our sensitivity analysis revealed that, within the explored regimes, we could simplify the binding dynamics and eliminate biofilm detachment. To address (2), we proposed a structured version of our model to capture the long-term behaviour and evolutionary selection. In our extended model, the subpopulations feature different maximal rates of biofilm formation. We compared the selection under different predator types and amounts and identified key parameters that affected the speed of selection via sensitivity analysis.

Indexed as

Bacterial Physiological PhenomenaBiofilmsModels, BiologicalBiological EvolutionComputer SimulationGenetic AlgorithmsLikelihood FunctionsMathematical ConceptsOptimal experimental designParameter identifiability

Identifiers

PMID42390640
PMCPMC13328132

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.