Lack of detectable HIV-1 molecular evolution during suppressive antiretroviral therapy.

A better understanding of changes in HIV-1 population genetics with combination antiretroviral therapy (cART) is critical for designing eradication strategies. We therefore analyzed HIV-1 genetic variation and divergence in patients' plasma before cART, during suppression on cART, and after vir...

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Autores principales: Mary F Kearney, Jonathan Spindler, Wei Shao, Sloane Yu, Elizabeth M Anderson, Angeline O'Shea, Catherine Rehm, Carry Poethke, Nicholas Kovacs, John W Mellors, John M Coffin, Frank Maldarelli
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Publicado: Public Library of Science (PLoS) 2014
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Acceso en línea:https://doaj.org/article/5e79a5c84d0242e3801880d4e7d8f9e4
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spelling oai:doaj.org-article:5e79a5c84d0242e3801880d4e7d8f9e42021-11-18T06:06:49ZLack of detectable HIV-1 molecular evolution during suppressive antiretroviral therapy.1553-73661553-737410.1371/journal.ppat.1004010https://doaj.org/article/5e79a5c84d0242e3801880d4e7d8f9e42014-03-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24651464/?tool=EBIhttps://doaj.org/toc/1553-7366https://doaj.org/toc/1553-7374A better understanding of changes in HIV-1 population genetics with combination antiretroviral therapy (cART) is critical for designing eradication strategies. We therefore analyzed HIV-1 genetic variation and divergence in patients' plasma before cART, during suppression on cART, and after viral rebound. Single-genome sequences of plasma HIV-1 RNA were obtained from HIV-1 infected patients prior to cART (N = 14), during suppression on cART (N = 14) and/or after viral rebound following interruption of cART (N = 5). Intra-patient population diversity was measured by average pairwise difference (APD). Population structure was assessed by phylogenetic analyses and a test for panmixia. Measurements of intra-population diversity revealed no significant loss of overall genetic variation in patients treated for up to 15 years with cART. A test for panmixia, however, showed significant changes in population structure in 2/10 patients after short-term cART (<1 year) and in 7/10 patients after long-term cART (1-15 years). The changes consisted of diverse sets of viral variants prior to cART shifting to populations containing one or more genetically uniform subpopulations during cART. Despite these significant changes in population structure, rebound virus after long-term cART had little divergence from pretherapy virus, implicating long-lived cells infected before cART as the source for rebound virus. The appearance of genetically uniform virus populations and the lack of divergence after prolonged cART and cART interruption provide strong evidence that HIV-1 persists in long-lived cells infected before cART was initiated, that some of these infected cells may be capable of proliferation, and that on-going cycles of viral replication are not evident.Mary F KearneyJonathan SpindlerWei ShaoSloane YuElizabeth M AndersonAngeline O'SheaCatherine RehmCarry PoethkeNicholas KovacsJohn W MellorsJohn M CoffinFrank MaldarelliPublic Library of Science (PLoS)articleImmunologic diseases. AllergyRC581-607Biology (General)QH301-705.5ENPLoS Pathogens, Vol 10, Iss 3, p e1004010 (2014)
institution DOAJ
collection DOAJ
language EN
topic Immunologic diseases. Allergy
RC581-607
Biology (General)
QH301-705.5
spellingShingle Immunologic diseases. Allergy
RC581-607
Biology (General)
QH301-705.5
Mary F Kearney
Jonathan Spindler
Wei Shao
Sloane Yu
Elizabeth M Anderson
Angeline O'Shea
Catherine Rehm
Carry Poethke
Nicholas Kovacs
John W Mellors
John M Coffin
Frank Maldarelli
Lack of detectable HIV-1 molecular evolution during suppressive antiretroviral therapy.
description A better understanding of changes in HIV-1 population genetics with combination antiretroviral therapy (cART) is critical for designing eradication strategies. We therefore analyzed HIV-1 genetic variation and divergence in patients' plasma before cART, during suppression on cART, and after viral rebound. Single-genome sequences of plasma HIV-1 RNA were obtained from HIV-1 infected patients prior to cART (N = 14), during suppression on cART (N = 14) and/or after viral rebound following interruption of cART (N = 5). Intra-patient population diversity was measured by average pairwise difference (APD). Population structure was assessed by phylogenetic analyses and a test for panmixia. Measurements of intra-population diversity revealed no significant loss of overall genetic variation in patients treated for up to 15 years with cART. A test for panmixia, however, showed significant changes in population structure in 2/10 patients after short-term cART (<1 year) and in 7/10 patients after long-term cART (1-15 years). The changes consisted of diverse sets of viral variants prior to cART shifting to populations containing one or more genetically uniform subpopulations during cART. Despite these significant changes in population structure, rebound virus after long-term cART had little divergence from pretherapy virus, implicating long-lived cells infected before cART as the source for rebound virus. The appearance of genetically uniform virus populations and the lack of divergence after prolonged cART and cART interruption provide strong evidence that HIV-1 persists in long-lived cells infected before cART was initiated, that some of these infected cells may be capable of proliferation, and that on-going cycles of viral replication are not evident.
format article
author Mary F Kearney
Jonathan Spindler
Wei Shao
Sloane Yu
Elizabeth M Anderson
Angeline O'Shea
Catherine Rehm
Carry Poethke
Nicholas Kovacs
John W Mellors
John M Coffin
Frank Maldarelli
author_facet Mary F Kearney
Jonathan Spindler
Wei Shao
Sloane Yu
Elizabeth M Anderson
Angeline O'Shea
Catherine Rehm
Carry Poethke
Nicholas Kovacs
John W Mellors
John M Coffin
Frank Maldarelli
author_sort Mary F Kearney
title Lack of detectable HIV-1 molecular evolution during suppressive antiretroviral therapy.
title_short Lack of detectable HIV-1 molecular evolution during suppressive antiretroviral therapy.
title_full Lack of detectable HIV-1 molecular evolution during suppressive antiretroviral therapy.
title_fullStr Lack of detectable HIV-1 molecular evolution during suppressive antiretroviral therapy.
title_full_unstemmed Lack of detectable HIV-1 molecular evolution during suppressive antiretroviral therapy.
title_sort lack of detectable hiv-1 molecular evolution during suppressive antiretroviral therapy.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/5e79a5c84d0242e3801880d4e7d8f9e4
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