Literature DB >> 26210988

Theories of Lethal Mutagenesis: From Error Catastrophe to Lethal Defection.

Héctor Tejero1,2, Francisco Montero3, Juan Carlos Nuño4.   

Abstract

RNA viruses get extinct in a process called lethal mutagenesis when subjected to an increase in their mutation rate, for instance, by the action of mutagenic drugs. Several approaches have been proposed to understand this phenomenon. The extinction of RNA viruses by increased mutational pressure was inspired by the concept of the error threshold. The now classic quasispecies model predicts the existence of a limit to the mutation rate beyond which the genetic information of the wild type could not be efficiently transmitted to the next generation. This limit was called the error threshold, and for mutation rates larger than this threshold, the quasispecies was said to enter into error catastrophe. This transition has been assumed to foster the extinction of the whole population. Alternative explanations of lethal mutagenesis have been proposed recently. In the first place, a distinction is made between the error threshold and the extinction threshold, the mutation rate beyond which a population gets extinct. Extinction is explained from the effect the mutation rate has, throughout the mutational load, on the reproductive ability of the whole population. Secondly, lethal defection takes also into account the effect of interactions within mutant spectra, which have been shown to be determinant for the understanding the extinction of RNA virus due to an augmented mutational pressure. Nonetheless, some relevant issues concerning lethal mutagenesis are not completely understood yet, as so survival of the flattest, i.e. the development of resistance to lethal mutagenesis by evolving towards mutationally more robust regions of sequence space, or sublethal mutagenesis, i.e., the increase of the mutation rate below the extinction threshold which may boost the adaptability of RNA virus, increasing their ability to develop resistance to drugs (including mutagens). A better design of antiviral therapies will still require an improvement of our knowledge about lethal mutagenesis.

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Year:  2016        PMID: 26210988     DOI: 10.1007/82_2015_463

Source DB:  PubMed          Journal:  Curr Top Microbiol Immunol        ISSN: 0070-217X            Impact factor:   4.291


  12 in total

Review 1.  Emergency Services of Viral RNAs: Repair and Remodeling.

Authors:  Vadim I Agol; Anatoly P Gmyl
Journal:  Microbiol Mol Biol Rev       Date:  2018-03-14       Impact factor: 11.056

2.  β-d-N 4-Hydroxycytidine Is a Potent Anti-alphavirus Compound That Induces a High Level of Mutations in the Viral Genome.

Authors:  Nadya Urakova; Valeriya Kuznetsova; David K Crossman; Arpine Sokratian; David B Guthrie; Alexander A Kolykhalov; Mark A Lockwood; Michael G Natchus; Michael R Crowley; George R Painter; Elena I Frolova; Ilya Frolov
Journal:  J Virol       Date:  2018-01-17       Impact factor: 5.103

Review 3.  Quasispecies and virus.

Authors:  Esteban Domingo; Celia Perales
Journal:  Eur Biophys J       Date:  2018-02-03       Impact factor: 1.733

4.  Synergistic lethal mutagenesis of hepatitis C virus.

Authors:  Isabel Gallego; María Eugenia Soria; Josep Gregori; Ana I de Ávila; Carlos García-Crespo; Elena Moreno; Ignacio Gadea; Jaime Esteban; Ricardo Fernández-Roblas; Juan Ignacio Esteban; Jordi Gómez; Josep Quer; Esteban Domingo; Celia Perales
Journal:  Antimicrob Agents Chemother       Date:  2019-09-30       Impact factor: 5.191

Review 5.  The Potential of Purinergic Signaling to Thwart Viruses Including SARS-CoV-2.

Authors:  Davide Ferrari; Michele Rubini; Jorge S Burns
Journal:  Front Immunol       Date:  2022-06-17       Impact factor: 8.786

6.  Molecular and Functional Bases of Selection against a Mutation Bias in an RNA Virus.

Authors:  Ignacio de la Higuera; Cristina Ferrer-Orta; Ana I de Ávila; Celia Perales; Macarena Sierra; Kamalendra Singh; Stefan G Sarafianos; Yves Dehouck; Ugo Bastolla; Nuria Verdaguer; Esteban Domingo
Journal:  Genome Biol Evol       Date:  2017-05-01       Impact factor: 3.416

Review 7.  Nucleoside analogues for the treatment of coronavirus infections.

Authors:  Andrea J Pruijssers; Mark R Denison
Journal:  Curr Opin Virol       Date:  2019-05-21       Impact factor: 7.090

8.  Small-Molecule Antiviral β-d-N 4-Hydroxycytidine Inhibits a Proofreading-Intact Coronavirus with a High Genetic Barrier to Resistance.

Authors:  Maria L Agostini; Andrea J Pruijssers; James D Chappell; Jennifer Gribble; Xiaotao Lu; Erica L Andres; Gregory R Bluemling; Mark A Lockwood; Timothy P Sheahan; Amy C Sims; Michael G Natchus; Manohar Saindane; Alexander A Kolykhalov; George R Painter; Ralph S Baric; Mark R Denison
Journal:  J Virol       Date:  2019-11-26       Impact factor: 5.103

Review 9.  Mutagenic Effects of Ribavirin on Hepatitis E Virus-Viral Extinction versus Selection of Fitness-Enhancing Mutations.

Authors:  Daniel Todt; Stephanie Walter; Richard J P Brown; Eike Steinmann
Journal:  Viruses       Date:  2016-10-13       Impact factor: 5.048

10.  Viral quasispecies.

Authors:  Esteban Domingo; Celia Perales
Journal:  PLoS Genet       Date:  2019-10-17       Impact factor: 5.917

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