Inferring HIV escape rates from multi-locus genotype data

Cytotoxic T-lymphocytes (CTLs) recognize viral protein fragments displayed by major histocompatibility complex (MHC) molecules on the surface of virally infected cells and generate an anti-viral response that can kill the infected cells. Virus variants whose protein fragments are not efficiently pre...

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Main Authors: Taylor A Kessinger, Alan S Perelson, Richard A Neher
Format: Article
Language:English
Published: Frontiers Media S.A. 2013-09-01
Series:Frontiers in Immunology
Subjects:
HIV
Online Access:http://journal.frontiersin.org/Journal/10.3389/fimmu.2013.00252/full
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spelling doaj-344307837ca940fc9894b24eded652ba2020-11-24T22:20:21ZengFrontiers Media S.A.Frontiers in Immunology1664-32242013-09-01410.3389/fimmu.2013.0025257551Inferring HIV escape rates from multi-locus genotype dataTaylor A Kessinger0Alan S Perelson1Richard A Neher2Max Planck Institute for Developmental BiologyLos Alamos National LaboratoryMax Planck Institute for Developmental BiologyCytotoxic T-lymphocytes (CTLs) recognize viral protein fragments displayed by major histocompatibility complex (MHC) molecules on the surface of virally infected cells and generate an anti-viral response that can kill the infected cells. Virus variants whose protein fragments are not efficiently presented on infected cells or whose fragments are presented but not recognized by CTLs therefore have a competitive advantage and spread rapidly through the population. We present a method that allows a more robust estimation of these escape rates from serially sampled sequence data. The proposed method accounts for competition between multiple escapes by explicitly modeling the accumulation of escape mutations and the stochastic effects of rare multiple mutants. Applying our method to serially sampled HIV sequence data, we estimate rates of HIV escape that are substantially larger than those previously reported. The method can be extended to complex escapes that require compensatory mutations. We expect our method to be applicable in other contexts such as cancer evolution where time series data is also available.http://journal.frontiersin.org/Journal/10.3389/fimmu.2013.00252/fullHIVcytotoxic T lymphocytesviral dynamicsselection coefficientCTL escapeHIV evolution
collection DOAJ
language English
format Article
sources DOAJ
author Taylor A Kessinger
Alan S Perelson
Richard A Neher
spellingShingle Taylor A Kessinger
Alan S Perelson
Richard A Neher
Inferring HIV escape rates from multi-locus genotype data
Frontiers in Immunology
HIV
cytotoxic T lymphocytes
viral dynamics
selection coefficient
CTL escape
HIV evolution
author_facet Taylor A Kessinger
Alan S Perelson
Richard A Neher
author_sort Taylor A Kessinger
title Inferring HIV escape rates from multi-locus genotype data
title_short Inferring HIV escape rates from multi-locus genotype data
title_full Inferring HIV escape rates from multi-locus genotype data
title_fullStr Inferring HIV escape rates from multi-locus genotype data
title_full_unstemmed Inferring HIV escape rates from multi-locus genotype data
title_sort inferring hiv escape rates from multi-locus genotype data
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2013-09-01
description Cytotoxic T-lymphocytes (CTLs) recognize viral protein fragments displayed by major histocompatibility complex (MHC) molecules on the surface of virally infected cells and generate an anti-viral response that can kill the infected cells. Virus variants whose protein fragments are not efficiently presented on infected cells or whose fragments are presented but not recognized by CTLs therefore have a competitive advantage and spread rapidly through the population. We present a method that allows a more robust estimation of these escape rates from serially sampled sequence data. The proposed method accounts for competition between multiple escapes by explicitly modeling the accumulation of escape mutations and the stochastic effects of rare multiple mutants. Applying our method to serially sampled HIV sequence data, we estimate rates of HIV escape that are substantially larger than those previously reported. The method can be extended to complex escapes that require compensatory mutations. We expect our method to be applicable in other contexts such as cancer evolution where time series data is also available.
topic HIV
cytotoxic T lymphocytes
viral dynamics
selection coefficient
CTL escape
HIV evolution
url http://journal.frontiersin.org/Journal/10.3389/fimmu.2013.00252/full
work_keys_str_mv AT taylorakessinger inferringhivescaperatesfrommultilocusgenotypedata
AT alansperelson inferringhivescaperatesfrommultilocusgenotypedata
AT richardaneher inferringhivescaperatesfrommultilocusgenotypedata
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