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Fitness Ranking of Individual Mutants Drives Patterns of Epistatic Interactions in HIV-1
Fitness interactions between mutations, referred to as epistasis, can strongly impact evolution. For RNA viruses and retroviruses with their high mutation rates, epistasis may be particularly important to overcome fitness losses due to the accumulation of deleterious mutations and thus could influen...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069090/ https://www.ncbi.nlm.nih.gov/pubmed/21483787 http://dx.doi.org/10.1371/journal.pone.0018375 |
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author | Martínez, Javier P. Bocharov, Gennady Ignatovich, Anna Reiter, Jochen Dittmar, Matthias T. Wain-Hobson, Simon Meyerhans, Andreas |
author_facet | Martínez, Javier P. Bocharov, Gennady Ignatovich, Anna Reiter, Jochen Dittmar, Matthias T. Wain-Hobson, Simon Meyerhans, Andreas |
author_sort | Martínez, Javier P. |
collection | PubMed |
description | Fitness interactions between mutations, referred to as epistasis, can strongly impact evolution. For RNA viruses and retroviruses with their high mutation rates, epistasis may be particularly important to overcome fitness losses due to the accumulation of deleterious mutations and thus could influence the frequency of mutants in a viral population. As human immunodeficiency virus type 1 (HIV-1) resistance to azidothymidine (AZT) requires selection of sequential mutations, it is a good system to study the impact of epistasis. Here we present a thorough analysis of a classical AZT-resistance pathway (the 41–215 cluster) of HIV-1 variants by fitness measurements in single round infection assays covering physiological drug concentrations ex vivo. The sign and value of epistasis varied and did not predict the epistatic effect on the mutant frequency. This complex behavior is explained by the fitness ranking of the variants that strongly depends on environmental factors, i.e., the presence and absence of drugs and the host cells used. Although some interactions compensate fitness losses, the observed small effect on the relative mutant frequencies suggests that epistasis might be inefficient as a buffering mechanism for fitness losses in vivo. While the use of epistasis-based hypotheses to make general assumptions on the evolutionary dynamics of viral populations is appealing, our data caution their interpretation without further knowledge on the characteristics of the viral mutant spectrum under different environmental conditions. |
format | Text |
id | pubmed-3069090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30690902011-04-11 Fitness Ranking of Individual Mutants Drives Patterns of Epistatic Interactions in HIV-1 Martínez, Javier P. Bocharov, Gennady Ignatovich, Anna Reiter, Jochen Dittmar, Matthias T. Wain-Hobson, Simon Meyerhans, Andreas PLoS One Research Article Fitness interactions between mutations, referred to as epistasis, can strongly impact evolution. For RNA viruses and retroviruses with their high mutation rates, epistasis may be particularly important to overcome fitness losses due to the accumulation of deleterious mutations and thus could influence the frequency of mutants in a viral population. As human immunodeficiency virus type 1 (HIV-1) resistance to azidothymidine (AZT) requires selection of sequential mutations, it is a good system to study the impact of epistasis. Here we present a thorough analysis of a classical AZT-resistance pathway (the 41–215 cluster) of HIV-1 variants by fitness measurements in single round infection assays covering physiological drug concentrations ex vivo. The sign and value of epistasis varied and did not predict the epistatic effect on the mutant frequency. This complex behavior is explained by the fitness ranking of the variants that strongly depends on environmental factors, i.e., the presence and absence of drugs and the host cells used. Although some interactions compensate fitness losses, the observed small effect on the relative mutant frequencies suggests that epistasis might be inefficient as a buffering mechanism for fitness losses in vivo. While the use of epistasis-based hypotheses to make general assumptions on the evolutionary dynamics of viral populations is appealing, our data caution their interpretation without further knowledge on the characteristics of the viral mutant spectrum under different environmental conditions. Public Library of Science 2011-03-31 /pmc/articles/PMC3069090/ /pubmed/21483787 http://dx.doi.org/10.1371/journal.pone.0018375 Text en Martínez et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Martínez, Javier P. Bocharov, Gennady Ignatovich, Anna Reiter, Jochen Dittmar, Matthias T. Wain-Hobson, Simon Meyerhans, Andreas Fitness Ranking of Individual Mutants Drives Patterns of Epistatic Interactions in HIV-1 |
title | Fitness Ranking of Individual Mutants Drives Patterns of Epistatic Interactions in HIV-1 |
title_full | Fitness Ranking of Individual Mutants Drives Patterns of Epistatic Interactions in HIV-1 |
title_fullStr | Fitness Ranking of Individual Mutants Drives Patterns of Epistatic Interactions in HIV-1 |
title_full_unstemmed | Fitness Ranking of Individual Mutants Drives Patterns of Epistatic Interactions in HIV-1 |
title_short | Fitness Ranking of Individual Mutants Drives Patterns of Epistatic Interactions in HIV-1 |
title_sort | fitness ranking of individual mutants drives patterns of epistatic interactions in hiv-1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069090/ https://www.ncbi.nlm.nih.gov/pubmed/21483787 http://dx.doi.org/10.1371/journal.pone.0018375 |
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