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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2013-09-01
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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 |
_version_ |
1725775683478618112 |