Concepts in disinfection of bacterial populations

Bacteria are responsible for a range of human diseases that are difficult to clear for a variety of reasons. Understanding the multilayered mechanisms that protect pathogens is of primary importance for developing effective treatments. Research over the past several decades has shown that bacteria can seek protected environments passively by avoiding deadly environments or actively by manipulating their phenotypic expression and gathering in structured biofilm communities. This article outlines the main tolerance mechanisms that have been studied and describes many of the mathematical models that indicate directions for new treatments. It is essential to understand that bacterial populations exploit a range of mechanisms to survive challenges and the mechanisms are often intertwined. This provides an opportunity for mathematical modeling to help provide insights into experiments that may uncouple particular mechanisms or optimize treatments.     

Language dynamics in finite populations

Any mechanism of language acquisition can only learn a restricted set of grammars. The human brain contains a mechanism for language acquisition which can learn a restricted set of grammars. The theory of this restricted set is universal grammar (UG). UG has to be sufficiently specific to induce linguistic coherence in a population. This phenomenon is known as "coherence threshold". Previously, we have calculated the coherence threshold for deterministic dynamics and infinitely large populations. Here, we extend the framework to stochastic processes and finite populations. If there is selection for communicative function (selective language dynamics), then the analytic results for infinite populations are excellent approximations for finite populations; as expected, finite populations need a slightly higher accuracy of language acquisition to maintain coherence. If there is no selection for communicative function (neutral language dynamics), then linguistic coherence is only possible for finite populations.     

On selection in finite populations

Journal of Mathematical Biology - Two major forces shaping evolution are drift and selection. The standard models of neutral drift—the Wright–Fisher (WF) and Moran processes—can...     

ESS-theory for finite populations

On the basis of some principles from the philosophy of science, the inadequacy of the ESS-theory as introduced by Maynard Smith and Price as a biological theory is discussed, and an improved ESS-theory for finite populations is presented which can adopt the ideas of the original formalism, although modified. Resulting are explicit conditions on the population sizes that ensure certain strategies to be evolutionarily stable.     

Fitness-dependent mutation rates in finite populations

Mutation rate may be condition dependent, whereby individuals in poor condition, perhaps from high mutation load, have higher mutation rates than individuals in good condition. Agrawal (J. Evol. Biol.15, 2002, 1004) explored the basic properties of fitness-dependent mutation rate (FDMR) in infinite populations and reported some heuristic results for finite populations. The key parameter governing how infinite populations evolve under FDMR is the curvature (k) of the relationship between fitness and mutation rate. We extend Agrawal's analysis to finite populations and consider dominance and epistasis. In finite populations, the probability of long-term existence depends on k. In sexual populations, positive curvature leads to low equilibrium mutation rate, whereas negative curvature results in high mutation rate. In asexual populations, negative curvature results in rapid extinction via 'mutational meltdown', whereas positive curvature sometimes allows persistence. We speculate that fitness-dependent mutation rate may provide the conditions for genetic architecture to diverge between sexual and asexual taxa.     

Evolutionary game dynamics in finite populations

We introduce a model of stochastic evolutionary game dynamics in finite populations which is similar to the familiar replicator dynamics for infinite populations. Our focus is on the conditions for selection favoring the invasion and/or fixation of new phenotypes. For infinite populations, there are three generic selection scenarios describing evolutionary game dynamics among two strategies. For finite populations, there are eight selection scenarios. For a fixed payoff matrix a number of these scenarios can occur for different population sizes. We discuss several examples with unexpected behavior.     

Multistage index selection in finite populations

Multistage selection with fixed proportions and selection indices based on covariates of the target variable is studied. Assuming a multivariate normal distribution before the selection, expressions are presented for the expectation and the variance of the target variable in the retained subpopulation. As the numerical evaluation for finite populations requires lengthy computations, some approximations using methods for infinite populations are proposed. Numerical illustrations are given for selections in up to three stages.     

Selection for mutational robustness in finite populations

We investigate the evolutionary dynamics of a finite population of RNA sequences replicating on a neutral network. Despite the lack of differential fitness between viable sequences, we observe typical properties of adaptive evolution, such as increase of mean fitness over time and punctuated-equilibrium transitions, after initial mutation-selection balance has been reached. We find that a product of population size and mutation rate of approximately 30 or larger is sufficient to generate selection pressure for mutational robustness, even if the population size is orders of magnitude smaller than the neutral network on which the population resides. Our results show that quasispecies effects and neutral drift can occur concurrently, and that the relative importance of each is determined by the product of population size and mutation rate.     

Stability properties of underdominance in finite subdivided populations

IN ISOLATED populations underdominance leads to bistable evolutionary dynamics: below a certain mutant allele frequency the wildtype succeeds. Above this point, the potentially underdominant mutant allele fixes. In subdivided populations with gene flow there can be stable states with coexistence of wildtypes and mutants: polymorphism can be maintained because of a migration-selection equilibrium, i.e., selection against rare recent immigrant alleles that tend to be heterozygous. We focus on the stochastic evolutionary dynamics of systems where demographic fluctuations in the coupled populations are the main source of internal noise. We discuss the influence of fitness, migration rate, and the relative sizes of two interacting populations on the mean extinction times of a group of potentially underdominant mutant alleles. We classify realistic initial conditions according to their impact on the stochastic extinction process. Even in small populations, where demographic fluctuations are large, stability properties predicted from deterministic dynamics show remarkable robustness. Fixation of the mutant allele becomes unlikely but the time to its extinction can be long.     

The distribution of lethal allelism in finite populations

It is shown that, under certain conditions, the distribution of lethal allelism in equilibrium populations is independent of the fitness of heterozygotes. For these conditions, an expression for the over-generation variance of allelism is given.