4.6 Review

Transition between stochastic evolution and deterministic evolution in the presence of selection: General theory and application to virology

Journal

MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS
Volume 65, Issue 1, Pages 151-+

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/MMBR.65.1.151-185.2001

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Funding

  1. NCI NIH HHS [R35CA44385] Funding Source: Medline
  2. NIAID NIH HHS [1K25AI01811, K25 AI001811] Funding Source: Medline

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We present here a self-contained analytic review of the role of stochastic factors acting on a vines population. We develop a simple one-locus, two-allele model of a haploid population of constant size including the factors of random drift, purifying selection, and random mutation. We consider different virological experiments: accumulation and reversion of deleterious mutations, competition between mutant and wild-type viruses, gene fixation, mutation frequencies at the steady state, divergence of two populations split from one population, and genetic turnover within a single population. In the first part of the review, we present all principal results in qualitative terms and illustrate them with examples obtained by computer simulation. In the second part we derive the results formally from a diffusion equation of the Wright-Fisher type and boundary conditions, all derived from the first principles for the virus population model. We show that the leading factors and observable behavior of evolution differ significantly in three broad intervals of population size, N. The neutral limit is reached when N is smaller than the inverse selection coefficient When N is larger than the inverse mutation rate per base, selection dominates and evolution is almost deterministic. If the selection coefficient is much larger than the mutation rare, there exists a broad interval of population sizes, in which weakly diverse populations are almost neutral while highly diverse populations are controlled by selection pressure. We discuss in detail the application of our results to human immunodeficiency virus population in vivo, sampling effects, and limitations of the model.

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