Transient antiretroviral therapy selecting for common HIV-1 mutations substantially accelerates the appearance of rare mutations

<p>Abstract</p> <p>Background</p> <p>Highly selective antiretroviral (ARV) regimens such as single dose nevirapine (NVP) used for prevention of mother to child transmission (PMTCT) in resource-limited settings produce transient increases in otherwise marginal subpopulat...

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Main Authors: Shiri Tinevimbo, Welte Alex
Format: Article
Language:English
Published: BMC 2008-11-01
Series:Theoretical Biology and Medical Modelling
Online Access:http://www.tbiomed.com/content/5/1/25
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spelling doaj-353438464d794450ba0772f8664dd4692020-11-25T01:38:28ZengBMCTheoretical Biology and Medical Modelling1742-46822008-11-01512510.1186/1742-4682-5-25Transient antiretroviral therapy selecting for common HIV-1 mutations substantially accelerates the appearance of rare mutationsShiri TinevimboWelte Alex<p>Abstract</p> <p>Background</p> <p>Highly selective antiretroviral (ARV) regimens such as single dose nevirapine (NVP) used for prevention of mother to child transmission (PMTCT) in resource-limited settings produce transient increases in otherwise marginal subpopulations of cells infected by mutant genomes. The longer term implications for accumulation of further resistance mutations are not fully understood.</p> <p>Methods</p> <p>We develop a new strain-differentiated hybrid deterministic-stochastic population dynamic type model of healthy and infected cells. We explore how the transient increase in a population of cells transcribed with a common mutation (modelled deterministically), which occurs in response to a short course of monotherapy, has an impact on the risk of appearance of rarer, higher-order, therapy-defeating mutations (modelled stochastically).</p> <p>Results</p> <p>Scenarios with a transient of a magnitude and duration such as is known to occur under NVP monotherapy exhibit significantly accelerated viral evolution compared to no-treatment scenarios. We identify a possibly important new biological timescale; namely, the duration of persistence, after a seminal mutation, of a sub-population of cells bearing the new mutant gene, and we show how increased persistence leads to an increased probability that a rare mutant will be present at the moment at which a new treatment regimen is initiated.</p> <p>Conclusion</p> <p>Even transient increases in subpopulations of common mutants are associated with accelerated appearance of further rarer mutations. Experimental data on the persistence of small subpopulations of rare mutants, in unfavourable environments, should be sought, as this affects the risk of subverting later regimens.</p> http://www.tbiomed.com/content/5/1/25
collection DOAJ
language English
format Article
sources DOAJ
author Shiri Tinevimbo
Welte Alex
spellingShingle Shiri Tinevimbo
Welte Alex
Transient antiretroviral therapy selecting for common HIV-1 mutations substantially accelerates the appearance of rare mutations
Theoretical Biology and Medical Modelling
author_facet Shiri Tinevimbo
Welte Alex
author_sort Shiri Tinevimbo
title Transient antiretroviral therapy selecting for common HIV-1 mutations substantially accelerates the appearance of rare mutations
title_short Transient antiretroviral therapy selecting for common HIV-1 mutations substantially accelerates the appearance of rare mutations
title_full Transient antiretroviral therapy selecting for common HIV-1 mutations substantially accelerates the appearance of rare mutations
title_fullStr Transient antiretroviral therapy selecting for common HIV-1 mutations substantially accelerates the appearance of rare mutations
title_full_unstemmed Transient antiretroviral therapy selecting for common HIV-1 mutations substantially accelerates the appearance of rare mutations
title_sort transient antiretroviral therapy selecting for common hiv-1 mutations substantially accelerates the appearance of rare mutations
publisher BMC
series Theoretical Biology and Medical Modelling
issn 1742-4682
publishDate 2008-11-01
description <p>Abstract</p> <p>Background</p> <p>Highly selective antiretroviral (ARV) regimens such as single dose nevirapine (NVP) used for prevention of mother to child transmission (PMTCT) in resource-limited settings produce transient increases in otherwise marginal subpopulations of cells infected by mutant genomes. The longer term implications for accumulation of further resistance mutations are not fully understood.</p> <p>Methods</p> <p>We develop a new strain-differentiated hybrid deterministic-stochastic population dynamic type model of healthy and infected cells. We explore how the transient increase in a population of cells transcribed with a common mutation (modelled deterministically), which occurs in response to a short course of monotherapy, has an impact on the risk of appearance of rarer, higher-order, therapy-defeating mutations (modelled stochastically).</p> <p>Results</p> <p>Scenarios with a transient of a magnitude and duration such as is known to occur under NVP monotherapy exhibit significantly accelerated viral evolution compared to no-treatment scenarios. We identify a possibly important new biological timescale; namely, the duration of persistence, after a seminal mutation, of a sub-population of cells bearing the new mutant gene, and we show how increased persistence leads to an increased probability that a rare mutant will be present at the moment at which a new treatment regimen is initiated.</p> <p>Conclusion</p> <p>Even transient increases in subpopulations of common mutants are associated with accelerated appearance of further rarer mutations. Experimental data on the persistence of small subpopulations of rare mutants, in unfavourable environments, should be sought, as this affects the risk of subverting later regimens.</p>
url http://www.tbiomed.com/content/5/1/25
work_keys_str_mv AT shiritinevimbo transientantiretroviraltherapyselectingforcommonhiv1mutationssubstantiallyacceleratestheappearanceofraremutations
AT weltealex transientantiretroviraltherapyselectingforcommonhiv1mutationssubstantiallyacceleratestheappearanceofraremutations
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