The spatial ecology of microbes
| dc.contributor.advisor | Keymer, Juan E. | |
| dc.contributor.author | Wetherington, Miles T. | |
| dc.contributor.other | Pontificia Universidad Católica de Chile. Facultad de Ciencias Biológicas | |
| dc.date | 2021-10-02 | |
| dc.date.accessioned | 2021-05-25T13:40:22Z | |
| dc.date.issued | 2021 | |
| dc.date.updated | 2021-05-20T11:49:01Z | |
| dc.description | Tesis (Doctoral of Philosophy degree in Biological Sciences : Ecology)--Pontificia Universidad Católica de Chile, 2021 | |
| dc.description.abstract | Guided by cell biophysics experimentation and equipped with toolsets from theoretical ecology, the aim of my thesis is to explore the ways in which spatial structure influences the dynamics and distributions of microbial cells, populations and communities. In my first project, we highlighted range expansion experiments of a colicin producing-colicin sensitive E.coli community on solid agar; The process of colony formation is driven by colicin production, cell lysis and division all driving the dynamical structure and ecological composition of the colony. Making analogies to percolation theory from statistical physics, we were able to develop a spatial model to quantify regimes of strain coexistence, competitive exclusion and extinction. Next we aimed to understand the spatial conditions under which microbial common goods games could persist. A particular bacterial system motivating this study was Pseudomonas aeruginosa, which excretes a costly ‘iron-scavenging’ compound (siderophore) in order to bind and transport iron across the cell membrane. This compound represents a common-pool resource, susceptible to exploitation by nearby bacteria free from producing this metabolically costly resource. With this system in mind we asked the following question: what spatial conditions permit these common-pool resources to be monopolized by a cooperator strategy in competition with an exploiter strategy? By developing a stochastic spatial model, we quantified the phase transition from monopolized to exploited and predicted which circumstances to expect coexistence between niche constructing and exploiter strategies as a result of differences in niche monopolization and colonization rates, respectively, and when to expect a collapse of the niche and a ‘tragedy of the commons’. Following this work, I began to apply newly acquired expertise in microfluidics, microfabrication techniques, microscopy and experimental cell biophysics in order to observe and study the spatial colonization dynamics of E.coli and P.aeruginosa in structured microfabricated landscapes. We showed how these two bacterial species enact a competition-colonization tradeoff where the faster colonizing E.coli can be overwhelmed locally by the slower but superior competitor, P.aeruginosa. This work constituted the first evidence of an abstract ecological theory in a spatial bacterial community. Furthermore, these results showed the importance of spatial structure in leading to coexistence as E.coli is able to effectively localize P.aeruginosa populations when competing in a patchy landscape via priority-effects. Conversely, in well-mixed ‘mean-field’ conditions the superior competitor always wins. In order to address the priority effects observed by E.coli, we made analogies to the Kronig-Penny model of solid state physics to our patchy landscape. To help understand the role habitat structure plays in the process of ecological colonization via invading wave populations, we represented our patchy landscapes as a periodic potential. An interesting result of such interpretation is the opening for the possibility of Anderson localization phenomena to take place; whereby species modulate each other’s dynamic habitat landscape. In this scenario E. coli cells modulate the potential seen by P.aeruginosa and introduce randomness to ecological corridors. In this way E. coli can induce strong localization in the spatial distribution of the P.aeruginosa metapopulation. This work highlights the importance of invisible corridor interactions and their potential to determine patterns of patch occupancy. Building on these results we next made an explicit connection between the topological properties of spatially structured microbial landscapes and Taylor’s Law, which asserts that the fluctuations within a metapopulation is a power law function of the mean. This statistical phenomena of populations, while well-documented in both the macro- and microscopic world, has yet to be connected to processes shaping spatially structured microbial populations and communities. Pursuing this analogy from solid state physics further we generated different degrees of randomness in the patchconnecting ecological corridor widths within a microfabricated microfluidics landscape, we found that a critical level of randomness leads to a qualitative transition in the fluctuation scaling of an Escherichia coli metapopulation. That induced randomness leads to such a result is neither expected experimentally nor completely understood theoretically. Nevertheless, these results bring a landscape perspective to Taylor’s law and the desire to connect this phenomena to ecological processes. Furthermore, bridging Taylor’s Law with other ecological scaling laws is an ongoing effort in the field of macroecology and one which we think would benefit from collaborations between theoreticians and experimental cell biophysics techniques like the one implemented here. Finally, given the unique perspective of this collaborative effort between cell biophysics and theoretical ecology, we conclude this thesis with a review of the literature in the field. Primarily, we focus on the necessary theoretical ecology needed for cell biophysicists to interpret their experimental results. In particular, we review landmark experimental cell biophysics discoveries from the past 15 years ranging from single-cell, population and community/biofilm studies, as well as following-up with newer findings all of which we discuss from an ecological viewpoint. | |
| dc.description.version | 2021-10-02 | |
| dc.format.extent | 189 páginas | |
| dc.fuente.origen | Autoarchivo | |
| dc.identifier.doi | 10.7764/tesisUC/BIO/59531 | |
| dc.identifier.uri | https://doi.org/10.7764/tesisUC/BIO/59531 | |
| dc.identifier.uri | https://repositorio.uc.cl/handle/11534/59531 | |
| dc.information.autoruc | Facultad de Ciencias Biológicas ; Keymer, Juan E. ; 0000-0001-6566-3778 ; 93580 | |
| dc.information.autoruc | Facultad de Ciencias Biológicas ; Wetherington, Miles T. ; S/I ; 1031040 | |
| dc.language.iso | en | |
| dc.nota.acceso | Contenido completo | |
| dc.rights | acceso abierto | |
| dc.subject.ddc | 579.17 | |
| dc.subject.dewey | Biología | es_ES |
| dc.subject.other | Ecología microbiana - Investigaciones - Chile | es_ES |
| dc.title | The spatial ecology of microbes | es_ES |
| dc.type | tesis doctoral | |
| sipa.codpersvinculados | 93580 | |
| sipa.codpersvinculados | 1031040 |