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High Multiplicity Infection by HIV-1 in Men Who Have Sex with Men
Elucidating virus-host interactions responsible for HIV-1 transmission is important for advancing HIV-1 prevention strategies. To this end, single genome amplification (SGA) and sequencing of HIV-1 within the context of a model of random virus evolution has made possible for the first time an unambi...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2869329/ https://www.ncbi.nlm.nih.gov/pubmed/20485520 http://dx.doi.org/10.1371/journal.ppat.1000890 |
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author | Li, Hui Bar, Katharine J. Wang, Shuyi Decker, Julie M. Chen, Yalu Sun, Chuanxi Salazar-Gonzalez, Jesus F. Salazar, Maria G. Learn, Gerald H. Morgan, Charity J. Schumacher, Joseph E. Hraber, Peter Giorgi, Elena E. Bhattacharya, Tanmoy Korber, Bette T. Perelson, Alan S. Eron, Joseph J. Cohen, Myron S. Hicks, Charles B. Haynes, Barton F. Markowitz, Martin Keele, Brandon F. Hahn, Beatrice H. Shaw, George M. |
author_facet | Li, Hui Bar, Katharine J. Wang, Shuyi Decker, Julie M. Chen, Yalu Sun, Chuanxi Salazar-Gonzalez, Jesus F. Salazar, Maria G. Learn, Gerald H. Morgan, Charity J. Schumacher, Joseph E. Hraber, Peter Giorgi, Elena E. Bhattacharya, Tanmoy Korber, Bette T. Perelson, Alan S. Eron, Joseph J. Cohen, Myron S. Hicks, Charles B. Haynes, Barton F. Markowitz, Martin Keele, Brandon F. Hahn, Beatrice H. Shaw, George M. |
author_sort | Li, Hui |
collection | PubMed |
description | Elucidating virus-host interactions responsible for HIV-1 transmission is important for advancing HIV-1 prevention strategies. To this end, single genome amplification (SGA) and sequencing of HIV-1 within the context of a model of random virus evolution has made possible for the first time an unambiguous identification of transmitted/founder viruses and a precise estimation of their numbers. Here, we applied this approach to HIV-1 env analyses in a cohort of acutely infected men who have sex with men (MSM) and found that a high proportion (10 of 28; 36%) had been productively infected by more than one virus. In subjects with multivariant transmission, the minimum number of transmitted viruses ranged from 2 to 10 with viral recombination leading to rapid and extensive genetic shuffling among virus lineages. A combined analysis of these results, together with recently published findings based on identical SGA methods in largely heterosexual (HSX) cohorts, revealed a significantly higher frequency of multivariant transmission in MSM than in HSX [19 of 50 subjects (38%) versus 34 of 175 subjects (19%); Fisher's exact p = 0.008]. To further evaluate the SGA strategy for identifying transmitted/founder viruses, we analyzed 239 overlapping 5′ and 3′ half genome or env-only sequences from plasma viral RNA (vRNA) and blood mononuclear cell DNA in an MSM subject who had a particularly well-documented virus exposure history 3–6 days before symptom onset and 14–17 days before peak plasma viremia (47,600,000 vRNA molecules/ml). All 239 sequences coalesced to a single transmitted/founder virus genome in a time frame consistent with the clinical history, and a molecular clone of this genome encoded replication competent virus in accord with model predictions. Higher multiplicity of HIV-1 infection in MSM compared with HSX is consistent with the demonstrably higher epidemiological risk of virus acquisition in MSM and could indicate a greater challenge for HIV-1 vaccines than previously recognized. |
format | Text |
id | pubmed-2869329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-28693292010-05-19 High Multiplicity Infection by HIV-1 in Men Who Have Sex with Men Li, Hui Bar, Katharine J. Wang, Shuyi Decker, Julie M. Chen, Yalu Sun, Chuanxi Salazar-Gonzalez, Jesus F. Salazar, Maria G. Learn, Gerald H. Morgan, Charity J. Schumacher, Joseph E. Hraber, Peter Giorgi, Elena E. Bhattacharya, Tanmoy Korber, Bette T. Perelson, Alan S. Eron, Joseph J. Cohen, Myron S. Hicks, Charles B. Haynes, Barton F. Markowitz, Martin Keele, Brandon F. Hahn, Beatrice H. Shaw, George M. PLoS Pathog Research Article Elucidating virus-host interactions responsible for HIV-1 transmission is important for advancing HIV-1 prevention strategies. To this end, single genome amplification (SGA) and sequencing of HIV-1 within the context of a model of random virus evolution has made possible for the first time an unambiguous identification of transmitted/founder viruses and a precise estimation of their numbers. Here, we applied this approach to HIV-1 env analyses in a cohort of acutely infected men who have sex with men (MSM) and found that a high proportion (10 of 28; 36%) had been productively infected by more than one virus. In subjects with multivariant transmission, the minimum number of transmitted viruses ranged from 2 to 10 with viral recombination leading to rapid and extensive genetic shuffling among virus lineages. A combined analysis of these results, together with recently published findings based on identical SGA methods in largely heterosexual (HSX) cohorts, revealed a significantly higher frequency of multivariant transmission in MSM than in HSX [19 of 50 subjects (38%) versus 34 of 175 subjects (19%); Fisher's exact p = 0.008]. To further evaluate the SGA strategy for identifying transmitted/founder viruses, we analyzed 239 overlapping 5′ and 3′ half genome or env-only sequences from plasma viral RNA (vRNA) and blood mononuclear cell DNA in an MSM subject who had a particularly well-documented virus exposure history 3–6 days before symptom onset and 14–17 days before peak plasma viremia (47,600,000 vRNA molecules/ml). All 239 sequences coalesced to a single transmitted/founder virus genome in a time frame consistent with the clinical history, and a molecular clone of this genome encoded replication competent virus in accord with model predictions. Higher multiplicity of HIV-1 infection in MSM compared with HSX is consistent with the demonstrably higher epidemiological risk of virus acquisition in MSM and could indicate a greater challenge for HIV-1 vaccines than previously recognized. Public Library of Science 2010-05-13 /pmc/articles/PMC2869329/ /pubmed/20485520 http://dx.doi.org/10.1371/journal.ppat.1000890 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Li, Hui Bar, Katharine J. Wang, Shuyi Decker, Julie M. Chen, Yalu Sun, Chuanxi Salazar-Gonzalez, Jesus F. Salazar, Maria G. Learn, Gerald H. Morgan, Charity J. Schumacher, Joseph E. Hraber, Peter Giorgi, Elena E. Bhattacharya, Tanmoy Korber, Bette T. Perelson, Alan S. Eron, Joseph J. Cohen, Myron S. Hicks, Charles B. Haynes, Barton F. Markowitz, Martin Keele, Brandon F. Hahn, Beatrice H. Shaw, George M. High Multiplicity Infection by HIV-1 in Men Who Have Sex with Men |
title | High Multiplicity Infection by HIV-1 in Men Who Have Sex with Men |
title_full | High Multiplicity Infection by HIV-1 in Men Who Have Sex with Men |
title_fullStr | High Multiplicity Infection by HIV-1 in Men Who Have Sex with Men |
title_full_unstemmed | High Multiplicity Infection by HIV-1 in Men Who Have Sex with Men |
title_short | High Multiplicity Infection by HIV-1 in Men Who Have Sex with Men |
title_sort | high multiplicity infection by hiv-1 in men who have sex with men |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2869329/ https://www.ncbi.nlm.nih.gov/pubmed/20485520 http://dx.doi.org/10.1371/journal.ppat.1000890 |
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