Cargando…

A Generalized Entropy Measure of Within-Host Viral Diversity for Identifying Recent HIV-1 Infections

There is a need for incidence assays that accurately estimate HIV incidence based on cross-sectional specimens. Viral diversity-based assays have shown promises but are not particularly accurate. We hypothesize that certain viral genetic regions are more predictive of recent infection than others an...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Julia Wei, Patterson-Lomba, Oscar, Novitsky, Vladimir, Pagano, Marcello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620842/
https://www.ncbi.nlm.nih.gov/pubmed/26496342
http://dx.doi.org/10.1097/MD.0000000000001865
_version_ 1782397367118462976
author Wu, Julia Wei
Patterson-Lomba, Oscar
Novitsky, Vladimir
Pagano, Marcello
author_facet Wu, Julia Wei
Patterson-Lomba, Oscar
Novitsky, Vladimir
Pagano, Marcello
author_sort Wu, Julia Wei
collection PubMed
description There is a need for incidence assays that accurately estimate HIV incidence based on cross-sectional specimens. Viral diversity-based assays have shown promises but are not particularly accurate. We hypothesize that certain viral genetic regions are more predictive of recent infection than others and aim to improve assay accuracy by using classification algorithms that focus on highly informative regions (HIRs). We analyzed HIV gag sequences from a cohort in Botswana. Forty-two subjects newly infected by HIV-1 Subtype C were followed through 500 days post-seroconversion. Using sliding window analysis, we screened for genetic regions within gag that best differentiate recent versus chronic infections. We used both nonparametric and parametric approaches to evaluate the discriminatory abilities of sequence regions. Segmented Shannon Entropy measures of HIRs were aggregated to develop generalized entropy measures to improve prediction of recency. Using logistic regression as the basis for our classification algorithm, we evaluated the predictive power of these novel biomarkers and compared them with recently reported viral diversity measures using area under the curve (AUC) analysis. Change of diversity over time varied across different sequence regions within gag. We identified the top 50% of the most informative regions by both nonparametric and parametric approaches. In both cases, HIRs were in more variable regions of gag and less likely in the p24 coding region. Entropy measures based on HIRs outperformed previously reported viral-diversity-based biomarkers. These methods are better suited for population-level estimation of HIV recency. The patterns of diversification of certain regions within the gag gene are more predictive of recency of infection than others. We expect this result to apply in other HIV genetic regions as well. Focusing on these informative regions, our generalized entropy measure of viral diversity demonstrates the potential for improving accuracy when identifying recent HIV-1 infections.
format Online
Article
Text
id pubmed-4620842
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Wolters Kluwer Health
record_format MEDLINE/PubMed
spelling pubmed-46208422015-10-27 A Generalized Entropy Measure of Within-Host Viral Diversity for Identifying Recent HIV-1 Infections Wu, Julia Wei Patterson-Lomba, Oscar Novitsky, Vladimir Pagano, Marcello Medicine (Baltimore) 4850 There is a need for incidence assays that accurately estimate HIV incidence based on cross-sectional specimens. Viral diversity-based assays have shown promises but are not particularly accurate. We hypothesize that certain viral genetic regions are more predictive of recent infection than others and aim to improve assay accuracy by using classification algorithms that focus on highly informative regions (HIRs). We analyzed HIV gag sequences from a cohort in Botswana. Forty-two subjects newly infected by HIV-1 Subtype C were followed through 500 days post-seroconversion. Using sliding window analysis, we screened for genetic regions within gag that best differentiate recent versus chronic infections. We used both nonparametric and parametric approaches to evaluate the discriminatory abilities of sequence regions. Segmented Shannon Entropy measures of HIRs were aggregated to develop generalized entropy measures to improve prediction of recency. Using logistic regression as the basis for our classification algorithm, we evaluated the predictive power of these novel biomarkers and compared them with recently reported viral diversity measures using area under the curve (AUC) analysis. Change of diversity over time varied across different sequence regions within gag. We identified the top 50% of the most informative regions by both nonparametric and parametric approaches. In both cases, HIRs were in more variable regions of gag and less likely in the p24 coding region. Entropy measures based on HIRs outperformed previously reported viral-diversity-based biomarkers. These methods are better suited for population-level estimation of HIV recency. The patterns of diversification of certain regions within the gag gene are more predictive of recency of infection than others. We expect this result to apply in other HIV genetic regions as well. Focusing on these informative regions, our generalized entropy measure of viral diversity demonstrates the potential for improving accuracy when identifying recent HIV-1 infections. Wolters Kluwer Health 2015-10-23 /pmc/articles/PMC4620842/ /pubmed/26496342 http://dx.doi.org/10.1097/MD.0000000000001865 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle 4850
Wu, Julia Wei
Patterson-Lomba, Oscar
Novitsky, Vladimir
Pagano, Marcello
A Generalized Entropy Measure of Within-Host Viral Diversity for Identifying Recent HIV-1 Infections
title A Generalized Entropy Measure of Within-Host Viral Diversity for Identifying Recent HIV-1 Infections
title_full A Generalized Entropy Measure of Within-Host Viral Diversity for Identifying Recent HIV-1 Infections
title_fullStr A Generalized Entropy Measure of Within-Host Viral Diversity for Identifying Recent HIV-1 Infections
title_full_unstemmed A Generalized Entropy Measure of Within-Host Viral Diversity for Identifying Recent HIV-1 Infections
title_short A Generalized Entropy Measure of Within-Host Viral Diversity for Identifying Recent HIV-1 Infections
title_sort generalized entropy measure of within-host viral diversity for identifying recent hiv-1 infections
topic 4850
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620842/
https://www.ncbi.nlm.nih.gov/pubmed/26496342
http://dx.doi.org/10.1097/MD.0000000000001865
work_keys_str_mv AT wujuliawei ageneralizedentropymeasureofwithinhostviraldiversityforidentifyingrecenthiv1infections
AT pattersonlombaoscar ageneralizedentropymeasureofwithinhostviraldiversityforidentifyingrecenthiv1infections
AT novitskyvladimir ageneralizedentropymeasureofwithinhostviraldiversityforidentifyingrecenthiv1infections
AT paganomarcello ageneralizedentropymeasureofwithinhostviraldiversityforidentifyingrecenthiv1infections
AT wujuliawei generalizedentropymeasureofwithinhostviraldiversityforidentifyingrecenthiv1infections
AT pattersonlombaoscar generalizedentropymeasureofwithinhostviraldiversityforidentifyingrecenthiv1infections
AT novitskyvladimir generalizedentropymeasureofwithinhostviraldiversityforidentifyingrecenthiv1infections
AT paganomarcello generalizedentropymeasureofwithinhostviraldiversityforidentifyingrecenthiv1infections