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dc.contributor.authorWilmoth, Jared L.
dc.contributor.authorDoak, Peter W.
dc.contributor.authorTimm, Andrea
dc.contributor.authorHalsted, Michelle
dc.contributor.authorAnderson, John D.
dc.contributor.authorGinovart Gisbert, Marta
dc.contributor.authorPrats Soler, Clara
dc.contributor.authorPortell Canal, Xavier
dc.contributor.authorRetterer, Scott T.
dc.contributor.authorFuentes-Cabrera, Miguel
dc.contributor.otherUniversitat Politècnica de Catalunya. Departament de Matemàtiques
dc.contributor.otherUniversitat Politècnica de Catalunya. Departament de Física
dc.date.accessioned2018-02-06T16:01:05Z
dc.date.available2018-02-06T16:01:05Z
dc.date.issued2018-02-06
dc.identifier.citationWilmoth, J., Doak, P., Timm, A., Halsted, M., Anderson, J., Ginovart, M., Prats, C., Portell, X., Retterer, S., Fuentes-Cabrera, M. A microfluidics and agent-based modeling framework for investigating spatial organization in bacterial colonies: the case of Pseudomonas Aeruginosa and H1-Type VI secretion interactions. "Frontiers in Microbiology", 6 Febrer 2018, vol. 9, núm. 33, p. 1-11.
dc.identifier.issn1664-302X
dc.identifier.urihttp://hdl.handle.net/2117/113818
dc.description.abstractThe factors leading to changes in the organization of microbial assemblages at fine spatial scales are not well characterized or understood. However, they are expected to guide the succession of community development and function toward specific outcomes that could impact human health and the environment. In this study, we put forward a combined experimental and agent-based modeling framework and use it to interpret unique spatial organization patterns of H1-Type VI secretion system (T6SS) mutants of P. aeruginosa under spatial confinement. We find that key parameters, such as T6SS-mediated cell contact and lysis, spatial localization, relative species abundance, cell density and local concentrations of growth substrates and metabolites are influenced by spatial confinement. The model, written in the accessible programming language NetLogo, can be adapted to a variety of biological systems of interest and used to simulate experiments across a broad parameter space. It was implemented and run in a high-throughput mode by deploying it across multiple CPUs, with each simulation representing an individual well within a high-throughput microwell array experimental platform. The microfluidics and agent-based modeling framework we present in this paper provides an effective means by which to connect experimental studies in microbiology to model development. The work demonstrates progress in coupling experimental results to simulation while also highlighting potential sources of discrepancies between real-world experiments and idealized models.
dc.format.extent11 p.
dc.language.isoeng
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Spain
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subjectÀrees temàtiques de la UPC::Matemàtiques i estadística
dc.subject.lcshMathematical modelling--theory and applications
dc.subject.otheragent-based modeling
dc.subject.otherPseudomonas aeruginosa
dc.subject.otherType VI secretion
dc.subject.othersilicon microwell arrays
dc.subject.othermicrobial succession
dc.subject.othermicrobial organization
dc.subject.otherspatial confinement
dc.titleA microfluidics and agent-based modeling framework for investigating spatial organization in bacterial colonies: the case of Pseudomonas Aeruginosa and H1-Type VI secretion interactions
dc.typeArticle
dc.subject.lemacModels matemàtics
dc.contributor.groupUniversitat Politècnica de Catalunya. BIOCOM-SC - Grup de Biologia Computacional i Sistemes Complexos
dc.identifier.doi10.3389/fmicb.2018.00033
dc.relation.publisherversionhttps://www.frontiersin.org/articles/10.3389/fmicb.2018.00033/full
dc.rights.accessOpen Access
local.identifier.drac21891504
dc.description.versionPostprint (published version)
local.citation.authorWilmoth, J.; Doak, P.; Timm, A.; Halsted, M.; Anderson, J.; Ginovart, M.; Prats, C.; Portell, X.; Retterer, S.; Fuentes-Cabrera, M.
local.citation.publicationNameFrontiers in Microbiology
local.citation.volume9
local.citation.number33
local.citation.startingPage1
local.citation.endingPage11
dc.identifier.pmid29467721


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