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Serial evolutionary networks of within-patient HIV-1 sequences reveal patterns of evolution of X4 strains
BACKGROUND: The HIV virus is known for its ability to exploit numerous genetic and evolutionary mechanisms to ensure its proliferation, among them, high replication, mutation and recombination rates. Sliding MinPD, a recently introduced computational method [1], was used to investigate the patterns...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2709891/ https://www.ncbi.nlm.nih.gov/pubmed/19531207 http://dx.doi.org/10.1186/1752-0509-3-62 |
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author | Buendia, Patricia Narasimhan, Giri |
author_facet | Buendia, Patricia Narasimhan, Giri |
author_sort | Buendia, Patricia |
collection | PubMed |
description | BACKGROUND: The HIV virus is known for its ability to exploit numerous genetic and evolutionary mechanisms to ensure its proliferation, among them, high replication, mutation and recombination rates. Sliding MinPD, a recently introduced computational method [1], was used to investigate the patterns of evolution of serially-sampled HIV-1 sequence data from eight patients with a special focus on the emergence of X4 strains. Unlike other phylogenetic methods, Sliding MinPD combines distance-based inference with a nonparametric bootstrap procedure and automated recombination detection to reconstruct the evolutionary history of longitudinal sequence data. We present serial evolutionary networks as a longitudinal representation of the mutational pathways of a viral population in a within-host environment. The longitudinal representation of the evolutionary networks was complemented with charts of clinical markers to facilitate correlation analysis between pertinent clinical information and the evolutionary relationships. RESULTS: Analysis based on the predicted networks suggests the following:: significantly stronger recombination signals (p = 0.003) for the inferred ancestors of the X4 strains, recombination events between different lineages and recombination events between putative reservoir virus and those from a later population, an early star-like topology observed for four of the patients who died of AIDS. A significantly higher number of recombinants were predicted at sampling points that corresponded to peaks in the viral load levels (p = 0.0042). CONCLUSION: Our results indicate that serial evolutionary networks of HIV sequences enable systematic statistical analysis of the implicit relations embedded in the topology of the structure and can greatly facilitate identification of patterns of evolution that can lead to specific hypotheses and new insights. The conclusions of applying our method to empirical HIV data support the conventional wisdom of the new generation HIV treatments, that in order to keep the virus in check, viral loads need to be suppressed to almost undetectable levels. |
format | Text |
id | pubmed-2709891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27098912009-07-14 Serial evolutionary networks of within-patient HIV-1 sequences reveal patterns of evolution of X4 strains Buendia, Patricia Narasimhan, Giri BMC Syst Biol Research Article BACKGROUND: The HIV virus is known for its ability to exploit numerous genetic and evolutionary mechanisms to ensure its proliferation, among them, high replication, mutation and recombination rates. Sliding MinPD, a recently introduced computational method [1], was used to investigate the patterns of evolution of serially-sampled HIV-1 sequence data from eight patients with a special focus on the emergence of X4 strains. Unlike other phylogenetic methods, Sliding MinPD combines distance-based inference with a nonparametric bootstrap procedure and automated recombination detection to reconstruct the evolutionary history of longitudinal sequence data. We present serial evolutionary networks as a longitudinal representation of the mutational pathways of a viral population in a within-host environment. The longitudinal representation of the evolutionary networks was complemented with charts of clinical markers to facilitate correlation analysis between pertinent clinical information and the evolutionary relationships. RESULTS: Analysis based on the predicted networks suggests the following:: significantly stronger recombination signals (p = 0.003) for the inferred ancestors of the X4 strains, recombination events between different lineages and recombination events between putative reservoir virus and those from a later population, an early star-like topology observed for four of the patients who died of AIDS. A significantly higher number of recombinants were predicted at sampling points that corresponded to peaks in the viral load levels (p = 0.0042). CONCLUSION: Our results indicate that serial evolutionary networks of HIV sequences enable systematic statistical analysis of the implicit relations embedded in the topology of the structure and can greatly facilitate identification of patterns of evolution that can lead to specific hypotheses and new insights. The conclusions of applying our method to empirical HIV data support the conventional wisdom of the new generation HIV treatments, that in order to keep the virus in check, viral loads need to be suppressed to almost undetectable levels. BioMed Central 2009-06-16 /pmc/articles/PMC2709891/ /pubmed/19531207 http://dx.doi.org/10.1186/1752-0509-3-62 Text en Copyright © 2009 Buendia and Narasimhan; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Buendia, Patricia Narasimhan, Giri Serial evolutionary networks of within-patient HIV-1 sequences reveal patterns of evolution of X4 strains |
title | Serial evolutionary networks of within-patient HIV-1 sequences reveal patterns of evolution of X4 strains |
title_full | Serial evolutionary networks of within-patient HIV-1 sequences reveal patterns of evolution of X4 strains |
title_fullStr | Serial evolutionary networks of within-patient HIV-1 sequences reveal patterns of evolution of X4 strains |
title_full_unstemmed | Serial evolutionary networks of within-patient HIV-1 sequences reveal patterns of evolution of X4 strains |
title_short | Serial evolutionary networks of within-patient HIV-1 sequences reveal patterns of evolution of X4 strains |
title_sort | serial evolutionary networks of within-patient hiv-1 sequences reveal patterns of evolution of x4 strains |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2709891/ https://www.ncbi.nlm.nih.gov/pubmed/19531207 http://dx.doi.org/10.1186/1752-0509-3-62 |
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