Mutation induced extinction in finite populations: lethal mutagenesis and lethal isolation.

Reproduction is inherently risky, in part because genomic replication can introduce new mutations that are usually deleterious toward fitness. This risk is especially severe for organisms whose genomes replicate "semi-conservatively," e.g. viruses and bacteria, where no master copy of the...

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Main Authors: C Scott Wylie, Eugene I Shakhnovich
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC3410861?pdf=render
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author C Scott Wylie
Eugene I Shakhnovich
author_facet C Scott Wylie
Eugene I Shakhnovich
author_sort C Scott Wylie
collection DOAJ
description Reproduction is inherently risky, in part because genomic replication can introduce new mutations that are usually deleterious toward fitness. This risk is especially severe for organisms whose genomes replicate "semi-conservatively," e.g. viruses and bacteria, where no master copy of the genome is preserved. Lethal mutagenesis refers to extinction of populations due to an unbearably high mutation rate (U), and is important both theoretically and clinically, where drugs can extinguish pathogens by increasing their mutation rate. Previous theoretical models of lethal mutagenesis assume infinite population size (N). However, in addition to high U, small N can accelerate extinction by strengthening genetic drift and relaxing selection. Here, we examine how the time until extinction depends jointly on N and U. We first analytically compute the mean time until extinction (τ) in a simplistic model where all mutations are either lethal or neutral. The solution motivates the definition of two distinct regimes: a survival phase and an extinction phase, which differ dramatically in both how τ scales with N and in the coefficient of variation in time until extinction. Next, we perform stochastic population-genetics simulations on a realistic fitness landscape that both (i) features an epistatic distribution of fitness effects that agrees with experimental data on viruses and (ii) is based on the biophysics of protein folding. More specifically, we assume that mutations inflict fitness penalties proportional to the extent that they unfold proteins. We find that decreasing N can cause phase transition-like behavior from survival to extinction, which motivates the concept of "lethal isolation." Furthermore, we find that lethal mutagenesis and lethal isolation interact synergistically, which may have clinical implications for treating infections. Broadly, we conclude that stably folded proteins are only possible in ecological settings that support sufficiently large populations.
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spelling doaj.art-9ee31c85d5b5474aa9b3d8e2f61906c02022-12-21T18:37:21ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582012-01-0188e100260910.1371/journal.pcbi.1002609Mutation induced extinction in finite populations: lethal mutagenesis and lethal isolation.C Scott WylieEugene I ShakhnovichReproduction is inherently risky, in part because genomic replication can introduce new mutations that are usually deleterious toward fitness. This risk is especially severe for organisms whose genomes replicate "semi-conservatively," e.g. viruses and bacteria, where no master copy of the genome is preserved. Lethal mutagenesis refers to extinction of populations due to an unbearably high mutation rate (U), and is important both theoretically and clinically, where drugs can extinguish pathogens by increasing their mutation rate. Previous theoretical models of lethal mutagenesis assume infinite population size (N). However, in addition to high U, small N can accelerate extinction by strengthening genetic drift and relaxing selection. Here, we examine how the time until extinction depends jointly on N and U. We first analytically compute the mean time until extinction (τ) in a simplistic model where all mutations are either lethal or neutral. The solution motivates the definition of two distinct regimes: a survival phase and an extinction phase, which differ dramatically in both how τ scales with N and in the coefficient of variation in time until extinction. Next, we perform stochastic population-genetics simulations on a realistic fitness landscape that both (i) features an epistatic distribution of fitness effects that agrees with experimental data on viruses and (ii) is based on the biophysics of protein folding. More specifically, we assume that mutations inflict fitness penalties proportional to the extent that they unfold proteins. We find that decreasing N can cause phase transition-like behavior from survival to extinction, which motivates the concept of "lethal isolation." Furthermore, we find that lethal mutagenesis and lethal isolation interact synergistically, which may have clinical implications for treating infections. Broadly, we conclude that stably folded proteins are only possible in ecological settings that support sufficiently large populations.http://europepmc.org/articles/PMC3410861?pdf=render
spellingShingle C Scott Wylie
Eugene I Shakhnovich
Mutation induced extinction in finite populations: lethal mutagenesis and lethal isolation.
PLoS Computational Biology
title Mutation induced extinction in finite populations: lethal mutagenesis and lethal isolation.
title_full Mutation induced extinction in finite populations: lethal mutagenesis and lethal isolation.
title_fullStr Mutation induced extinction in finite populations: lethal mutagenesis and lethal isolation.
title_full_unstemmed Mutation induced extinction in finite populations: lethal mutagenesis and lethal isolation.
title_short Mutation induced extinction in finite populations: lethal mutagenesis and lethal isolation.
title_sort mutation induced extinction in finite populations lethal mutagenesis and lethal isolation
url http://europepmc.org/articles/PMC3410861?pdf=render
work_keys_str_mv AT cscottwylie mutationinducedextinctioninfinitepopulationslethalmutagenesisandlethalisolation
AT eugeneishakhnovich mutationinducedextinctioninfinitepopulationslethalmutagenesisandlethalisolation