ArticlePloS one2011
Quasispecies spatial models for RNA viruses with different replication modes and infection strategies.
Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
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Who cites it
14 citing papers in PubMed.
- Synergistic antiviral effects of structure-guided peptides and a mutagenic base analog on SARS-CoV-2 replication.Antimicrobial agents and chemotherapy · 2026Article
- Quasispecies theory and emerging viruses: challenges and applications.Npj viruses · 2024Review
- Evolutionary Dynamics of Accelerated Antiviral Resistance Development in Hypermutator Herpesvirus.Molecular biology and evolution · 2024Article
- Decay of HCoV-OC43 infectivity is lower in cell debris-containing media than in fresh culture media.microPublication biology · 2024Article
- Rescuing eGFP-Tagged Canine Distemper Virus for 40 Serial Passages Separately in Ribavirin- and Non-Treated Cells: Comparative Analysis of Viral Mutation Profiles.Frontiers in cellular and infection microbiology · 2021Article
- Noise-induced bistability in the quasi-neutral coexistence of viral RNAs under different replication modes.Journal of the Royal Society, Interface · 2018Article
- Mechanisms of viral mutation.Cellular and molecular life sciences : CMLS · 2016Review
- Delayed lysis confers resistance to the nucleoside analogue 5-fluorouracil and alleviates mutation accumulation in the single-stranded DNA bacteriophage ϕX174.Journal of virology · 2014Article
- Variability in mutational fitness effects prevents full lethal transitions in large quasispecies populations.Scientific reports · 2014Article
- Realistic three dimensional fitness landscapes generated by self organizing maps for the analysis of experimental HIV-1 evolution.PloS one · 2014Article
- Determining the cellular diversity of hepatitis C virus quasispecies by single-cell viral sequencing.Journal of virology · 2013Article
- Genomic mutation rates that neutralize adaptive evolution and natural selection.Journal of the Royal Society, Interface · 2013Article
- Viral population dynamics and virulence thresholds.Current opinion in microbiology · 2012Review
- Viral quasispecies evolution.Microbiology and molecular biology reviews : MMBR · 2012Review
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Empirical observations and theoretical studies suggest that viruses may use different replication strategies to amplify their genomes, which impact the dynamics of mutation accumulation in viral populations and therefore, their fitness and virulence. Similarly, during natural infections, viruses replicate and infect cells that are rarely in suspension but spatially organized. Surprisingly, most quasispecies models of virus replication have ignored these two phenomena. In order to study these two viral characteristics, we have developed stochastic cellular automata models that simulate two different modes of replication (geometric vs stamping machine) for quasispecies replicating and spreading on a two-dimensional space. Furthermore, we explored these two replication models considering epistatic fitness landscapes (antagonistic vs synergistic) and different scenarios for cell-to-cell spread, one with free superinfection and another with superinfection inhibition. We found that the master sequences for populations replicating geometrically and with antagonistic fitness effects vanished at low critical mutation rates. By contrast, the highest critical mutation rate was observed for populations replicating geometrically but with a synergistic fitness landscape. Our simulations also showed that for stamping machine replication and antagonistic epistasis, a combination that appears to be common among plant viruses, populations further increased their robustness by inhibiting superinfection. We have also shown that the mode of replication strongly influenced the linkage between viral loci, which rapidly reached linkage equilibrium at increasing mutations for geometric replication. We also found that the strategy that minimized the time required to spread over the whole space was the stamping machine with antagonistic epistasis among mutations. Finally, our simulations revealed that the multiplicity of infection fluctuated but generically increased along time.
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