Transmission selects for HIV-1 strains of intermediate virulence: a modelling approach.

Recent data shows that HIV-1 is characterised by variation in viral virulence factors that is heritable between infections, which suggests that viral virulence can be naturally selected at the population level. A trade-off between transmissibility and duration of infection appears to favour viruses...

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Main Authors: George Shirreff, Lorenzo Pellis, Oliver Laeyendecker, Christophe Fraser
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-10-01
Series:PLoS Computational Biology
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22022243/?tool=EBI
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spelling doaj-254947274cf74bfe92b83f53b61d506a2021-04-21T15:09:57ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582011-10-01710e100218510.1371/journal.pcbi.1002185Transmission selects for HIV-1 strains of intermediate virulence: a modelling approach.George ShirreffLorenzo PellisOliver LaeyendeckerChristophe FraserRecent data shows that HIV-1 is characterised by variation in viral virulence factors that is heritable between infections, which suggests that viral virulence can be naturally selected at the population level. A trade-off between transmissibility and duration of infection appears to favour viruses of intermediate virulence. We developed a mathematical model to simulate the dynamics of putative viral genotypes that differ in their virulence. As a proxy for virulence, we use set-point viral load (SPVL), which is the steady density of viral particles in blood during asymptomatic infection. Mutation, the dependency of survival and transmissibility on SPVL, and host effects were incorporated into the model. The model was fitted to data to estimate unknown parameters, and was found to fit existing data well. The maximum likelihood estimates of the parameters produced a model in which SPVL converged from any initial conditions to observed values within 100-150 years of first emergence of HIV-1. We estimated the 1) host effect and 2) the extent to which the viral virulence genotype mutates from one infection to the next, and found a trade-off between these two parameters in explaining the variation in SPVL. The model confirms that evolution of virulence towards intermediate levels is sufficiently rapid for it to have happened in the early stages of the HIV epidemic, and confirms that existing viral loads are nearly optimal given the assumed constraints on evolution. The model provides a useful framework under which to examine the future evolution of HIV-1 virulence.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22022243/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author George Shirreff
Lorenzo Pellis
Oliver Laeyendecker
Christophe Fraser
spellingShingle George Shirreff
Lorenzo Pellis
Oliver Laeyendecker
Christophe Fraser
Transmission selects for HIV-1 strains of intermediate virulence: a modelling approach.
PLoS Computational Biology
author_facet George Shirreff
Lorenzo Pellis
Oliver Laeyendecker
Christophe Fraser
author_sort George Shirreff
title Transmission selects for HIV-1 strains of intermediate virulence: a modelling approach.
title_short Transmission selects for HIV-1 strains of intermediate virulence: a modelling approach.
title_full Transmission selects for HIV-1 strains of intermediate virulence: a modelling approach.
title_fullStr Transmission selects for HIV-1 strains of intermediate virulence: a modelling approach.
title_full_unstemmed Transmission selects for HIV-1 strains of intermediate virulence: a modelling approach.
title_sort transmission selects for hiv-1 strains of intermediate virulence: a modelling approach.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2011-10-01
description Recent data shows that HIV-1 is characterised by variation in viral virulence factors that is heritable between infections, which suggests that viral virulence can be naturally selected at the population level. A trade-off between transmissibility and duration of infection appears to favour viruses of intermediate virulence. We developed a mathematical model to simulate the dynamics of putative viral genotypes that differ in their virulence. As a proxy for virulence, we use set-point viral load (SPVL), which is the steady density of viral particles in blood during asymptomatic infection. Mutation, the dependency of survival and transmissibility on SPVL, and host effects were incorporated into the model. The model was fitted to data to estimate unknown parameters, and was found to fit existing data well. The maximum likelihood estimates of the parameters produced a model in which SPVL converged from any initial conditions to observed values within 100-150 years of first emergence of HIV-1. We estimated the 1) host effect and 2) the extent to which the viral virulence genotype mutates from one infection to the next, and found a trade-off between these two parameters in explaining the variation in SPVL. The model confirms that evolution of virulence towards intermediate levels is sufficiently rapid for it to have happened in the early stages of the HIV epidemic, and confirms that existing viral loads are nearly optimal given the assumed constraints on evolution. The model provides a useful framework under which to examine the future evolution of HIV-1 virulence.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22022243/?tool=EBI
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