» Articles » PMID: 12215495

Molecular Indetermination in the Transition to Error Catastrophe: Systematic Elimination of Lymphocytic Choriomeningitis Virus Through Mutagenesis Does Not Correlate Linearly with Large Increases in Mutant Spectrum Complexity

Overview
Specialty Science
Date 2002 Sep 7
PMID 12215495
Citations 59
Authors
Affiliations
Soon will be listed here.
Abstract

Studies with several RNA viruses have shown that enhanced mutagenesis resulted in decreases of infectivity or virus extinction, as predicted from virus entry into error catastrophe. Here we report that lymphocytic choriomeningitis virus, the prototype arenavirus, is extremely susceptible to extinction mutagenesis by the base analog 5-fluorouracil. Virus elimination was preceded by increases in complexity of the mutant spectra of treated populations. However, careful molecular comparison of the mutant spectra of several genomic segments suggests that the largest increases in mutation frequency do not predict virus extinction. Highly mutated viral genomes have escaped detection presumably because lymphocytic choriomeningitis virus replicates at or near the error threshold, and genomes in the transition toward error catastrophe may have an extremely short half-life and escape detection with state-of-the-art cloning and sequencing technologies.

Citing Articles

Current sampling and sequencing biases of Lassa mammarenavirus limit inference from phylogeography and molecular epidemiology in Lassa fever endemic regions.

Arruda L, Free H, Simons D, Ansumana R, Elton L, Haider N PLOS Glob Public Health. 2023; 3(11):e0002159.

PMID: 37939051 PMC: 10631635. DOI: 10.1371/journal.pgph.0002159.


Genetic diversity through social heterosis can increase virulence in RNA viral infections and cancer progression.

Ebrahimi S, Nonacs P R Soc Open Sci. 2021; 8(5):202219.

PMID: 34035948 PMC: 8097216. DOI: 10.1098/rsos.202219.


Quasispecies characteristic in "a" determinant region is a potential predictor for the risk of immunoprophylaxis failure of mother-to-child-transmission of sub-genotype C2 hepatitis B virus: a prospective nested case-control study.

Xiao Y, Sun K, Duan Z, Liu Z, Li Y, Yan L Gut. 2019; 69(5):933-941.

PMID: 31446427 PMC: 7229894. DOI: 10.1136/gutjnl-2019-318278.


Contribution of a Multifunctional Polymerase Region of Foot-and-Mouth Disease Virus to Lethal Mutagenesis.

de la Higuera I, Ferrer-Orta C, Moreno E, de Avila A, Soria M, Singh K J Virol. 2018; 92(20).

PMID: 30068642 PMC: 6158410. DOI: 10.1128/JVI.01119-18.


Extinction of Zika Virus and Usutu Virus by Lethal Mutagenesis Reveals Different Patterns of Sensitivity to Three Mutagenic Drugs.

Bassi M, Sempere R, Meyn P, Polacek C, Arias A Antimicrob Agents Chemother. 2018; 62(9).

PMID: 29914957 PMC: 6125542. DOI: 10.1128/AAC.00380-18.


References
1.
Drake J, Holland J . Mutation rates among RNA viruses. Proc Natl Acad Sci U S A. 1999; 96(24):13910-3. PMC: 24164. DOI: 10.1073/pnas.96.24.13910. View

2.
Loeb L, Essigmann J, Kazazi F, Zhang J, Rose K, Mullins J . Lethal mutagenesis of HIV with mutagenic nucleoside analogs. Proc Natl Acad Sci U S A. 1999; 96(4):1492-7. PMC: 15492. DOI: 10.1073/pnas.96.4.1492. View

3.
Loeb L, Mullins J . Lethal mutagenesis of HIV by mutagenic ribonucleoside analogs. AIDS Res Hum Retroviruses. 2000; 16(1):1-3. DOI: 10.1089/088922200309539. View

4.
Domingo E . Viruses at the edge of adaptation. Virology. 2000; 270(2):251-3. DOI: 10.1006/viro.2000.0320. View

5.
Sierra S, Davila M, Lowenstein P, Domingo E . Response of foot-and-mouth disease virus to increased mutagenesis: influence of viral load and fitness in loss of infectivity. J Virol. 2000; 74(18):8316-23. PMC: 116341. DOI: 10.1128/jvi.74.18.8316-8323.2000. View