Quasispecies Theory and the Behavior of RNA Viruses
Top Cited Papers
Open Access
- 22 July 2010
- journal article
- review article
- Published by Public Library of Science (PLoS) in PLoS Pathogens
- Vol. 6 (7) , e1001005
- https://doi.org/10.1371/journal.ppat.1001005
Abstract
A large number of medically important viruses, including HIV, hepatitis C virus, and influenza, have RNA genomes. These viruses replicate with extremely high mutation rates and exhibit significant genetic diversity. This diversity allows a viral population to rapidly adapt to dynamic environments and evolve resistance to vaccines and antiviral drugs. For the last 30 years, quasispecies theory has provided a population-based framework for understanding RNA viral evolution. A quasispecies is a cloud of diverse variants that are genetically linked through mutation, interact cooperatively on a functional level, and collectively contribute to the characteristics of the population. Many predictions of quasispecies theory run counter to traditional views of microbial behavior and evolution and have profound implications for our understanding of viral disease. Here, we discuss basic principles of quasispecies theory and describe its relevance for our understanding of viral fitness, virulence, and antiviral therapeutic strategy.Keywords
This publication has 88 references indexed in Scilit:
- Mutational robustness can facilitate adaptationNature, 2010
- Fitness and its role in evolutionary geneticsNature Reviews Genetics, 2009
- Emergence of a Novel Swine-Origin Influenza A (H1N1) Virus in HumansNew England Journal of Medicine, 2009
- Ultra‐Deep Pyrosequencing of Hepatitis B Virus Quasispecies from Nucleoside and Nucleotide Reverse‐Transcriptase Inhibitor (NRTI)–Treated Patients and NRTI‐Naive PatientsThe Journal of Infectious Diseases, 2009
- APOBEC proteins and intrinsic resistance to HIV-1 infectionPhilosophical Transactions Of The Royal Society B-Biological Sciences, 2008
- Cytidine deamination induced HIV-1 drug resistanceProceedings of the National Academy of Sciences, 2008
- Sequence editing by Apolipoprotein B RNA-editing catalytic component-B and epidemiological surveillance of transmitted HIV-1 drug resistanceAIDS, 2008
- Avian Influenza A (H5N1) Infection in HumansNew England Journal of Medicine, 2005
- Broad antiretroviral defence by human APOBEC3G through lethal editing of nascent reverse transcriptsNature, 2003
- Isolation of a human gene that inhibits HIV-1 infection and is suppressed by the viral Vif proteinNature, 2002