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Hermsen, R.

Publications and source records attributed to Hermsen, R..

10 recordsLinked to original sources

Fluid-Derived Lattices for Unbiased Modeling of Bacterial Colony Growth

Bacterial colonies can form a wide variety of shapes and structures based on ambient and internal conditions. To help understand the mechanisms that determine the structure of and the diversity within these colonies, various numerical modeling techniques have been applied. The most commonly used ones are continuum models, agent-based models, and lattice models. Continuum models are usually computationally fast, but disregard information at the level of the individual, which can be crucial to understanding diversity in a colony. Agent-based models resolve local details to a greater level, but are computationally costly. Lattice-based approaches strike a balance between these two limiting cases. However, this is known to come at the price of introducing undesirable artifacts into the structure of the colonies. For instance, square lattices tend to produce square colonies even where an isotropic shape is expected. Here, we aim to overcome these limitations and therefore study lattice-induced orientational symmetry in a class of hybrid numerical methods that combine aspects of lattice-based and continuum descriptions. We characterize these artifacts and show that they can be circumvented through the use of a disordered lattice which derives from an unstructured fluid. The main advantage of this approach is that the lattice itself does not imbue the colony with a preferential directionality. We demonstrate that our implementation enables the study of colony growth involving millions of individuals within hours of computation time on an ordinary desktop computer, while retaining many of the desirable features of agent-based models. Furthermore, our method can be readily adapted for a wide range of applications, opening up new avenues for studying the formation of colonies with diverse shapes and complex internal interactions. Author summaryBacterial colonies develop highly diverse shapes, ranging from branches to disks and concentric rings. These structures are important because they affect competition between bacteria and evolution in the population. To study the origins and consequences of bacterial colony structures, computational models have been used to great success. However, to speed up simulations, many such models approximate continuous space using regular lattices even though this is known to cause artifacts in the resulting colony shapes. To address this, we explored the use of disordered lattices. We compared two methods from the literature for perturbing a square reference lattice. In some cases, these appeared to work, yet, when the distance between lattice sites, the contact area between cells, and the size of the cells were incorporated into the model, the symmetries of the square reference lattice reappeared. We therefore came up with a method that uses the structure of a dense fluid of disks to generate a disordered lattice. This fluid-derived lattice did not impose undesirable orientational symmetries in any of the models that we tested. Lastly, we show that our approach is very efficient, enabling the simulation of bacterial populations containing millions of individuals on a regular desktop computer.

biophysics↗

The interplay between metabolic stochasticity and regulation in single E. coli cells

Metabolism is inherently stochastic at the cellular level. Whether cells actively regulate processes in response to these random internal variations is a fundamental problem that remains unaddressed, yet critical to understanding biological homeostasis. Here, we show that in E. coli cells, expression of the main catabolic enzymes is continuously adjusted in response to metabolic fluctuations under constant external conditions. This noise feedback is performed by the cAMP-CRP system, which controls transcription of the catabolic enzymes by modulating concentrations of the second messenger cAMP upon changes in metabolite abundance. Using time-lapse microscopy, genetic constructs that selectively disable cAMP-CRP noise feedback, and mathematical modelling, we show how fluctuations circulate through this hybrid metabolic-genetic network at sub cell-cycle timescales. This circulation of stochastic fluctuations is explained by four distinct noise propagation modes, one of which describes the continuous cAMP-CRP regulation. The model successfully predicts how noise circulation is impacted by C-sector under and over-expression. The results raise the question whether the cAMP-CRP system, as well as other metabolic regulation mechanisms, have evolved to manage internal metabolic fluctuations in addition to external growth conditions. We conjecture that second messengers may broadly function to control metabolic stochasticity and achieve cellular homeostasis.

systems biology↗

Multiscale selection in spatially structured populations

The spatial structure of natural populations is key to many of their evolutionary processes. Formal theories analysing the interplay between natural selection and spatial structure have mostly focused on populations divided into distinct, non-overlapping groups. Most populations, however, are not structured in this way, but rather (self-)organise into dynamic patterns unfolding at various spatial scales. Here, we present a mathematical framework that quantifies how patterns and processes at different spatial scales contribute to natural selection in such populations. To that end, we define the Local Selection Differential (LSD): a measure of the selection acting on a trait within a given local environment. Based on the LSD, natural selection in a population can be decomposed into two parts: the contribution of local selection, acting within local environments, and the contribution of interlocal selection, acting among them. Varying the size of the local environments subsequently allows one to measure the contribution of each length scale. To illustrate the use of this new multiscale selection framework, we apply it to two simulation models of the evolution of traits known to be affected by spatial population structure: altruism and pathogen transmissibility. In both models, the spatial decomposition of selection reveals that local and interlocal selection can have opposite signs, thus providing a mathematically rigorous underpinning to intuitive explanations of how processes at different spatial scales may compete. It furthermore identifies which length scales--and hence which patterns--are relevant for natural selection. The multiscale selection framework can thus be used to address complex questions on evolution in spatially structured populations.

evolutionary biology↗

Emergent multilevel selection in a simple spatial model of the evolution of altruism

Theories on the evolutionary origins of altruistic behavior have a long history and have become a canonical part of the theory of evolution. Nevertheless, the mechanisms that allow altruism to appear and persist are still incompletely understood. It is well known, however, that the spatial structure of populations is an important determinant. In both theoretical and experimental studies, much attention has been devoted to populations that are subdivided into discrete groups. Such studies typically imposed the structure and dynamics of the groups by hand. Here, we instead present a simple individual-based model in which altruistic organisms spontaneously self-organize into spatially separated colonies that themselves reproduce by binary fission and hence behave as Darwinian entities in their own right. Using software to automatically track the rise and fall of colonies, we are able to apply formal theory on multilevel selection and thus quantify the within- and among-group dynamics. This reveals that individual colonies inevitably succumb to defectors in a within-colony "tragedy of the commons". Even so, altruism persists in the population because more altruistic colonies reproduce more frequently and drive less altruistic ones to extinction. Evidently, the colonies promote the selection of altruism but in turn depend on altruism for their existence; the selection of altruism hence involves a kind of evolutionary bootstrapping. The emergence of the colonies also depends crucially on the length scales of motility, altruism, and competition. This reconfirms the general relevance of these scales for social evolution, but also stresses that their impact can only be understood fully in the light of the emergent eco-evolutionary spatial patterns. The results also suggest that emergent spatial population patterns can function as a starting point for transitions of individuality.

evolutionary biology↗

Abundant proteins contribute strongly to noise in the growth rate of optimally growing bacteria

In bacterial cells, protein expression is a highly stochastic process. At the same time, physiological variables such as the cellular growth rate also fluctuate significantly. A common intuition is that, due to their relatively high noise amplitudes, proteins with a low mean expression level are the most important causes of these fluctuations on a larger, physiological scale. Noise in highly expressed proteins, whose stochastic fluctuations are relatively small, is often ignored. In this work, we challenge this intuition by developing a theory that predicts the contribution of a proteins expression noise to the noise in the instantaneous, cellular growth rate. Using mathematical analysis, we decomposed the contribution of each protein into two factors: the noise amplitude of the protein, and the sensitivity of the growth rate to fluctuations in that proteins concentration. Next, we incorporated evolution, which has shaped the mean abundances of growth-related proteins to optimise the growth rate, causing protein abundances, but also cellular sensitivities to be non-random. We show that in cells that grow optimally fast, the growth rate is most sensitive to fluctuations in highly abundant proteins. This causes such proteins to overall contribute strongly to the noise in the growth-rate, despite their low noise levels. The results are confirmed in a stochastic toy model of cellular growth.

evolutionary biology↗

Long identical sequences found in multiple bacterial genomes reveal frequent and widespread exchange of genetic material between distant species.

Horizontal transfer of genomic elements is an essential force that shapes microbial genome evolution. Horizontal Gene Transfer (HGT) occurs via various mechanisms and has been studied in detail for a variety of systems. However, a coarse-grained, global picture of HGT in the microbial world is still missing. One reason is the difficulty to process large amounts of genomic microbial data to find and characterise HGT events, especially for highly distant organisms. Here, we exploit the fact that HGT between distant species creates long identical DNA sequences in genomes of distant species, which can be found efficiently using alignment-free methods. We analysed over 90 000 bacterial genomes and thus identified over 100 000 events of HGT. We further developed a mathematical model to analyse the statistical properties of those long exact matches and thus estimate the transfer rate between any pair of taxa. Our results demonstrate that long-distance gene exchange (across phyla) is very frequent, as more than 8% of the bacterial genomes analysed have been involved in at least one such event. Finally, we confirm that the function of the transferred sequences strongly impact the transfer rate, as we observe a 3.5 order of magnitude variation between the most and the least transferred categories. Overall, we provide a unique view of horizontal transfer across the bacterial tree of life, illuminating a fundamental process driving bacterial evolution.

bioinformatics↗

How repeated outbreaks drive the evolution of bacteriophage communication: Insights from a mathematical model

Communication based on small signalling molecules is widespread among bacteria. Recently, such communication was also described in bacteriophages. Upon infection of a host cell, temperate phages of the Bacillus subtilis-infecting SPbeta group induce the secretion of a phage-encoded signalling peptide, which is used to inform the lysis-lysogeny decision in subsequent infections: the phages produce new virions and lyse their host cell when the signal concentration is low, but favour a latent infection strategy, lysogenising the host cell, when the signal concentration is high. Here, we present a mathematical model to study the ecological and evolutionary dynamics of such viral communication. We show that a communication strategy in which phages use the lytic cycle early in an outbreak (when susceptible host cells are abundant) but switch to the lysogenic cycle later (when susceptible cells become scarce) is favoured over a bet-hedging strategy in which cells are lysogenised with constant probability. However, such phage communication can evolve only if phage-bacteria populations are regularly perturbed away from their equilibrium state, so that acute outbreaks of phage infections in pools of susceptible cells continue to occur. Our model then predicts the selection of phages that switch infection strategy when half of the available susceptible cells have been infected.

evolutionary biology↗

The naive T-cell receptor repertoire has an extremely broad distribution of clone sizes

The human naive T-cell receptor (TCR) repertoire is extremely diverse and accurately estimating its distribution is challenging. We address this challenge by combining a quantitative sequencing protocol of TCRA and TCRB sequences with computational modelling. We observed the vast majority of TCR chains only once in our samples, confirming the enormous diversity of the naive repertoire. However, a substantial number of sequences were observed multiple times within samples, and we demonstrated that this is due to expression by many cells in the naive pool. We reason that and {beta} chains are frequently observed due to a combination of selective processes and summation over multiple clones expressing these chains. We test the contribution of both mechanisms by predicting samples from phenomenological and mechanistically modelled repertoire distributions. By comparing these with sequencing data, we show that frequently observed chains are likely to be derived from multiple clones. Still, a neutral model of T-cell homeostasis cannot account for the observed distributions. We conclude that the data are only compatible with distributions of many small clones in combination with a sufficient number of very large naive T-cell clones, the latter most likely as a result of peripheral selection.

immunology↗

Noise propagation in an integrated model of bacterial gene expression and growth

In bacterial cells, gene expression, metabolism, and growth are highly interdependent and tightly coordinated. As a result, stochastic fluctuations in expression levels and instantaneous growth rate show intricate cross-correlations. These correlations are shaped by feedback loops, trade-offs and constraints acting at the cellular level; therefore a quantitative understanding requires an integrated approach. To that end, we here present a mathematical model describing a cell that contains multiple proteins that are each expressed stochastically and jointly limit the growth rate. Conversely, metabolism and growth affect protein synthesis and dilution. Thus, expression noise originating in one gene propagates to metabolism, growth, and the expression of all other genes. Nevertheless, under a small-noise approximation many statistical quantities can be calculated analytically. We identify several routes of noise propagation, illustrate their origins and scaling, and establish important connections between noise propagation and the field of metabolic control analysis. We then present a many-protein model containing > 1000 proteins parameterized by previously measured abundance data and demonstrate that the predicted cross-correlations between gene expression and growth rate are in broad agreement with published measurements.

systems biology↗

Effects of DNA oxidation on the evolution of genomes

Oxidation of DNA increases its mutation rate, causing otherwise rare G [->] T transversions during DNA replication. Here we use a comparative genomic approach to assess the importance of DNA oxidation for the evolution of genomic sequences. To do so, we study the mutational spectrum of Gn-tracks on various timescales, ranging from one human generation to the divergence between primates, and compare it to the properties of guanines oxidation known from experimental and computational studies. Our results suggest that, in short Gn tracks (n [≤] 3), oxidation does not dominate the mutagenesis of guanines, except in cancerous tumors, especially in lungs. However, we consistently find that the G [->] T transversion rate is elevated by an order of magnitude in long Gn tracks (n {gtrsim} 6). In such long Gn-tracks, G [->] T substitutions in fact dominate the mutational spectrum, suggesting that long Gn tracks are oxidized more frequently and/or repaired less efficiently.

evolutionary biology↗