{"title":"The influence of cell morphology on the dynamics and stability of model bacterial communities.","authors":"Ing Xhu Lim, Faisal Halabeya, Joshua N Milstein","doi":"10.1371/journal.pcbi.1014874","DOIUrl":null,"url":null,"abstract":"<p><p>Understanding how structures arise in microbial communities remains an outstanding challenge in bacterial ecology. When replicating within dense and confined environments, bacterial populations may collectively self-organize as a result of mechanical interactions. We previously observed that model dual-populations of bacteria, colonizing open-ended microchannels, either quickly fixate to a single population or segregate into long-lived, coexisting populations. This latter quasi-stability results from the alignment of bacteria into lanes, forcing cells to grow toward the open ends of the channel, with inter-lane invasion events driving the boundary dynamics between populations. Here we apply agent-based (AB) simulations to explore the boundary dynamics between dual-bacterial populations of varying morphology and division rate. We find that the simulated boundary dynamics are well-described by a simple drift-diffusion model, which enables us to estimate the mean time to fixation within competitive scenarios where the fixation time is difficult to access by AB simulations. Coccus-like cells display a competitive advantage over bacillus cells as they can more effectively invade and ultimately fixate, while coexisting populations of bacillus cells are \"effectively\" stable. And while faster-dividing cells should have a selective advantage, their morphology determines if this advantage drives fixation or acts as a defensive strategy to maintain their population. These findings highlight the critical role that cell morphology and mechanics play in shaping bacterial communities.</p>","PeriodicalId":20241,"journal":{"name":"PLoS Computational Biology","volume":"22 10","pages":"e1014874"},"PeriodicalIF":3.6000,"publicationDate":"2026-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13674858/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"PLoS Computational Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1371/journal.pcbi.1014874","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/10/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
Understanding how structures arise in microbial communities remains an outstanding challenge in bacterial ecology. When replicating within dense and confined environments, bacterial populations may collectively self-organize as a result of mechanical interactions. We previously observed that model dual-populations of bacteria, colonizing open-ended microchannels, either quickly fixate to a single population or segregate into long-lived, coexisting populations. This latter quasi-stability results from the alignment of bacteria into lanes, forcing cells to grow toward the open ends of the channel, with inter-lane invasion events driving the boundary dynamics between populations. Here we apply agent-based (AB) simulations to explore the boundary dynamics between dual-bacterial populations of varying morphology and division rate. We find that the simulated boundary dynamics are well-described by a simple drift-diffusion model, which enables us to estimate the mean time to fixation within competitive scenarios where the fixation time is difficult to access by AB simulations. Coccus-like cells display a competitive advantage over bacillus cells as they can more effectively invade and ultimately fixate, while coexisting populations of bacillus cells are "effectively" stable. And while faster-dividing cells should have a selective advantage, their morphology determines if this advantage drives fixation or acts as a defensive strategy to maintain their population. These findings highlight the critical role that cell morphology and mechanics play in shaping bacterial communities.
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