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Alexander S. Bratus

Publications and source records attributed to Alexander S. Bratus.

17 recordsLinked to original sources

Mathematical Model of Evolution of Non-Degenerate Replicator Systems

We propose and analyse a mathematical model of evolutionary adaptation for non-degenerate (permanent) replicator systems, in which the fitness landscape matrix evolves on a slow timescale -- the evolutionary time -- while the species dynamics unfold on a fast timescale. Under a two-timescale separation justified by Tikhonov's theorem, the adaptation problem reduces to maximising the mean fitness at steady state over a convex admissible set of fitness landscape matrices. We derive a fitness variation formula and establish necessary and sufficient conditions for a fitness maximum, showing that the optimisation reduces at each step to a linear programming problem. The algorithm is applied to four canonical replicator systems: the hypercycle, the bi-hypercycle, the anthill system, and the RNA molecule network. In all cases the evolutionary process follows a universal three-phase pattern: an initial phase of fitness growth without equilibrium shift, during which purely altruistic replication gives way to mixed altruistic-selfish behaviour; a second phase of dominant species emergence; and a stabilisation phase analogous to the error catastrophe threshold in quasispecies models. A key consequence is that all evolved systems acquire resistance to parasitic species. We further prove that without non-degeneracy constraints the process leads to sequential species annihilation, with a provable spectral lower bound on fitness increase by dimension reduction.

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The Kolmogorov forward equation for a distributed model of regime-switching diffusions

For the regime-switching diffusion process with and without advection term we propose an integro-differential equation describing the densities of states continuously distributed over a segment. We demonstrate that there exists a constructive algorithm for solving the Cauchy problem. We then show that for some initial distributions of states, the solution can be found explicitly. We also discuss how a model with a discrete number of hidden states can be approximated by a model with continuously distributed states.

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A mathematical framework of consumer-resource dynamics: How to incorporate interactions between interactions in evolutionary process

A novel mathematical framework is proposed to describe the ecological and evolutionary consequences of consumer--resource interactions. Both the consumer and resource are assumed to consist of several (sub)species, which interact between themselves in addition to incorporating the deleterious effects of the consumer on the resource. Separating the ecological and evolutionary time scales, we allow our mathematical model to evolve, with the evolutionary steps chosen according to the (divergent) objective functions of the consumer and the resource. Numerical simulations show that the model, along with the expected outcomes of either consumer or resource winning the evolutionary battle, is capable of producing also the (quasi)stationary state of consumer--resource coexistence with monotone growth of both the consumer and resource fitnesses. Such stable states highlight the importance of the intra-population interactions, which, despite the opposite evolutionary goals of the consumer and the resource, lead to long term ecological stability.

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On a hypercycle equation with infinitely many members

A hypercycle equation with infinitely many types of macromolecules is formulated and studied both analytically and numerically. The resulting model is given by an integro-differential equation of the mixed type. Sufficient conditions for the existence, uniqueness, and non-negativity of solutions are formulated and proved. Analytical evidence is provided for the existence of non-uniform (with respect to the second variable) steady states. Finally, numerical simulations strongly indicate the existence of a stable nonlinear wave in the form of the wave train.

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Fitness landscape adaptation in open replicator systems with competition: application to cancer therapy

This study focuses on open quasispecies systems with competition and death flow, described by modified Eigen and Crow-Kimura models. We examine the evolutionary adaptation process as a reaction to changes in rates. One of the fundamental assumptions, which forms the basis of our mathematical model, is the existence of two different timescales: internal dynamics time and evolutionary time. The latter is much slower and exhibits significant adaptation events. These conditions allow us to represent the whole evolutionary process through a series of steady-state equations, where all the elements continuously depend on the evolutionary parameter.

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Food webs and the principle of evolutionary adaptation

A principle of evolutionary adaptation is applied to the Lotka--Volterra models, in particular to the food webs. We present a relatively simple computational algorithm of optimization with respect to a given criterion. This algorithm boils down to a sequence of easy to solve linear programming problems. As a criterion for the optimization we use the total weighted population size of the given community and an ecological fitness, which is an analogue of the potential energy in physics. We show by computational experiments that it is almost always possible to substantially increase the total weighed population size for an especially simple food web -- food chain; we also show that food chains are evolutionary unstable under the given optimization criteria and, if allowed, evolve into more complicated structures of food webs.

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Open Quasispecies Systems: New Approach to Evolutionary Adaptation

Consider a mathematical model of evolutionary adaptation of fitness landscape and mutation matrix as a reaction to population changes. As a basis, we use an open quasispecies model, which is modified to include explicit death flow. We assume that evolutionary parameters of mutation and selection processes vary in a way to maximize the mean fitness of the system. From this standpoint, Fisher's theorem of natural selection is being rethought and discussed. Another assumption is that system dynamics has two significant timescales. According to our central hypothesis, major evolutionary transitions happen in the steady-state of the corresponding dynamical system, so the evolutionary time is much slower than the one of internal dynamics. For the specific cases of quasispecies systems, we show how our premises form the fitness landscape adaptation process.

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Open Quasispecies Models: Stability, Optimization, and Distributed Extension

We suggest a natural approach that leads to a modification of classical quasispecies models and incorporates the possibility of population extinction in addition to growth. The resulting modified models are called open. Their essential properties, regarding in particular equilibrium behavior, are investigated both analytically and numerically. The hallmarks of the quasispecies dynamics, viz. the heterogeneous quasispecies distribution itself and the error threshold phenomenon, can be observed in our models, along with extinction. In order to demonstrate the flexibility of the introduced framework, we study the inverse problem of fitness allocation under the biologically motivated criterion of steady-state fitness maximization. Having in mind the complexity of numerical investigation of high-dimensional quasispecies problems and the fact that the actual number of genotypes or alleles involved in a studied process can be extremely large, we also build continuous-time distributed open quasispecies models. The obtained results may serve as an initial step to developing mathematical models that involve directed therapy against various pathogens.

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Rigorous mathematical analysis of the quasispecies model: From Manfred Eigen to the recent developments

We review the major progress in the rigorous analysis of the classical quasispecies model that usually comes in two related but different forms: the Eigen model and the Crow--Kimura model. The model itself was formulated almost 50 years ago, and in its stationary form represents an easy to formulate eigenvalue problem. Notwithstanding the simplicity of the problem statement, we still lack full understanding of the behavior of the mean population fitness and the quasispecies distribution for an arbitrary fitness landscape. Our main goal in this review is two-fold: First, to highlight a number of impressive mathematical results, including some of the recent ones, which pertain to the mathematical development of the quasispecies theory. Second, to emphasize that, despite these 50 years of vigorous research, there are still very natural both biological and mathematical questions that remain to be addressed within the quasispecies framework. Our hope is that at least some of the approaches we review in this text can be of help for anyone embarking on further analysis of the quasispecies model.

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Adaptive Fitness Landscape for Replicator Systems: To Maximize or not to Maximize

Sewall Wright's adaptive landscape metaphor penetrates a significant part of evolutionary thinking. Supplemented with Fisher's fundamental theorem of natural selection and Kimura's maximum principle, it provides a unifying and intuitive representation of the evolutionary process under the influence of natural selection as the hill climbing on the surface of mean population fitness. On the other hand, it is also well known that for many more or less realistic mathematical models this picture is a sever misrepresentation of what actually occurs. Therefore, we are faced with two questions. First, it is important to identify the cases in which adaptive landscape metaphor actually holds exactly in the models, that is, to identify the conditions under which system's dynamics coincides with the process of searching for a (local) fitness maximum. Second, even if the mean fitness is not maximized in the process of evolution, it is still important to understand the structure of the mean fitness manifold and see the implications of this structure on the system's dynamics. Using as a basic model the classical replicator equation, in this note we attempt to answer these two questions and illustrate our results with simple well studied systems.

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Solutions with a bounded support promote permanence of a distributed replicator equation

The now classical replicator equation describes a wide variety of biological phenomena, including those in theoretical genetics, evolutionary game theory, or in the theories of the origin of life. Among other questions, the permanence of the replicator equation is well studied in the local, well-mixed case. Inasmuch as the spatial heterogeneities are key to understanding the species coexistence at least in some cases, it is important to supplement the classical theory of the non-distributed replicator equation with a spatially explicit framework. One possible approach, motivated by the porous medium equation, is introduced. It is shown that the solutions to the spatially heterogeneous replicator equation may evolve to equilibrium states that have a bounded support, and, moreover, that these solutions are of paramount importance for the overall system permanence, which is shown to be a more commonplace phenomenon for the spatially explicit equation if compared with the local model.

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Linear algebra of the permutation invariant Crow-Kimura model of prebiotic evolution

A particular case of the famous quasispecies model - the Crow-Kimura model with a permutation invariant fitness landscape - is investigated. Using the fact that the mutation matrix in the case of a permutation invariant fitness landscape has a special tridiagonal form, a change of the basis is suggested such that in the new coordinates a number of analytical results can be obtained. In particular, using the eigenvectors of the mutation matrix as the new basis, we show that the quasispecies distribution approaches a binomial one and give simple estimates for the speed of convergence. Another consequence of the suggested approach is a parametric solution to the system of equations determining the quasispecies. Using this parametric solution we show that our approach leads to exact asymptotic results in some cases, which are not covered by the existing methods. In particular, we are able to present not only the limit behavior of the leading eigenvalue (mean population fitness), but also the exact formulas for the limit quasispecies eigenvector for special cases. For instance, this eigenvector has a geometric distribution in the case of the classical single peaked fitness landscape. On the biological side, we propose a mathematical definition, based on the closeness of the quasispecies to the binomial distribution, which can be used as an operational definition of the notorious error threshold. Using this definition, we suggest two approximate formulas to estimate the critical mutation rate after which the quasispecies delocalization occurs.

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Asymptotic behavior of spatially distributed replicator systems

The question of biological stability (permanence) of a replicator reaction-diffusion system is considered. Sufficient conditions of biological stability are found. It is proved that there are situations when biologically unstable non-distributed replicator system becomes biologically stable in the distributed case. Numerical examples illustrate analytical findings. This manuscript is a continuation of arXiv:1308.5631.

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On the behavior of the leading eigenvalue of Eigen's evolutionary matrices

We study general properties of the leading eigenvalue $\overline{w}(q)$ of Eigen's evolutionary matrices depending on the probability $q$ of faithful reproduction. This is a linear algebra problem that has various applications in theoretical biology, including such diverse fields as the origin of life, evolution of cancer progression, and virus evolution. We present the exact expressions for $\overline{w}(q),\overline{w}'(q),\overline{w}''(q)$ for $q=0,0.5,1$ and prove that the absolute minimum of $\overline{w}(q)$, which always exists, belongs to the interval $[0,0.5]$. For the specific case of a single peaked landscape we also find lower and upper bounds on $\overline{w}(q)$, which are used to estimate the critical mutation rate, after which the distribution of the types of individuals in the population becomes almost uniform. This estimate is used as a starting point to conjecture another estimate, valid for any fitness landscape, and which is checked by numerical calculations. The last estimate stresses the fact that the inverse dependence of the critical mutation rate on the sequence length is not a generally valid fact. Therefore, the discussions of the error threshold applied to biological systems must take this fact into account.

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On diffusive stability of Eigen's quasispecies model

Eigen's quasispecies system with explicit space and global regulation is considered. Limit behavior and stability of the system in a functional space under perturbations of a diffusion matrix with nonnegative spectrum are investigated. It is proven that if the diffusion matrix has only positive eigenvalues then the solutions of the distributed system converge to the equilibrium solution of the corresponding local dynamical system. These results imply that the error threshold does not change if the spatial interactions under the principle of global regulation are taken into account.

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Replicator equations and space

A reaction--diffusion replicator equation is studied. A novel method to apply the principle of global regulation is used to write down the model with explicit spatial structure. Properties of stationary solutions together with their stability are analyzed analytically, and relationships between stability of the rest points of the non-distributed replicator equation and distributed system are shown. A numerical example is given to show that the spatial variable in this particular model promotes the system's permanence.

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On the reaction-diffusion replicator systems: Spatial patterns and asymptotic behavior

The replicator equation is ubiquitous for many areas of mathematical biology. One of major shortcomings of this equation is that it does not allow for an explicit spatial structure. Here we review analytical approaches to include spatial variables to the system. We also provide a concise exposition of the results concerning the appearance of spatial patterns in replicator reaction-diffusion systems.

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