An off-lattice discrete model to characterise filamentous yeast colony morphology

We combine an off-lattice agent-based mathematical model and experimentation to explore filamentous growth of a yeast colony. Under environmental stress, Saccharomyces cerevisiae yeast cells can transition from a bipolar (sated) to unipolar (pseudohyphal) budding mechanism, where cells elongate and bud end-to-end. This budding asymmetry yields spatially non-uniform growth, where filaments extend away from the colony centre, foraging for food. We use approximate Bayesian computation to quantify how individual cell budding mechanisms give rise to spatial patterns observed in experiments. We apply this method of parameter inference to experimental images of colonies of two strains of S. cerevisiae, in low and high nutrient environments. The colony size at the transition from sated to pseudohyphal growth, and a forking mechanism for pseudohyphal cell proliferation are the key features driving colony morphology. Simulations run with the most likely inferred parameters produce colony morphologies that closely resemble experimental results.

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Publication Details

Journal
PLoS Computational Biology
Published
2024-11-21
DOI
https://doi.org/10.1371/journal.pcbi.1012605
Citations
3
Primary Topic
Fungal and yeast genetics research
Type
article
Field-Weighted Citation Impact
0.70

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article

An off-lattice discrete model to characterise filamentous yeast colony morphology

Jennifer M. Gardner, Vladimir Jiranek, J. E. F. Green, Benjamin J. Binder et al.
3 citations
PLoS Computational Biology
Fungal and yeast genetics research
0.70
article

An off-lattice discrete model to characterise filamentous yeast colony morphology

Jennifer M. Gardner, Vladimir Jiranek, J. E. F. Green, Benjamin J. Binder, Andrew J. Black, Kai Li, Hayden Tronnolone, Alexander Tam, Joanna F. Sundstrom
article en
3 citations

Abstract

We combine an off-lattice agent-based mathematical model and experimentation to explore filamentous growth of a yeast colony. Under environmental stress, Saccharomyces cerevisiae yeast cells can transition from a bipolar (sated) to unipolar (pseudohyphal) budding mechanism, where cells elongate and bud end-to-end. This budding asymmetry yields spatially non-uniform growth, where filaments extend away from the colony centre, foraging for food. We use approximate Bayesian computation to quantify how individual cell budding mechanisms give rise to spatial patterns observed in experiments. We apply this method of parameter inference to experimental images of colonies of two strains of S. cerevisiae, in low and high nutrient environments. The colony size at the transition from sated to pseudohyphal growth, and a forking mechanism for pseudohyphal cell proliferation are the key features driving colony morphology. Simulations run with the most likely inferred parameters produce colony morphologies that closely resemble experimental results.

PLoS Computational BiologyVol. 20(11)
Flinders University (AU), University of South Australia (AU), University of Southampton (GB), The University of Adelaide (AU)
Australian Government, Department for Education and Child Development South Australian, Australian Research Council
Life in Land
Openalex Percentile: Top 29%
Fungal and yeast genetics research
0.70
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