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HIV-1 integrase polymorphisms are associated with prior antiretroviral drug exposure
In a recent summary of integrase sequences, primary integrase inhibitor mutations were rare. In a review of integrase inhibitor-naïve Australian HIV-1 sequences, primary mutations were not identified, although the accessory mutation G140S was detected. A link with previous antiretroviral therapy, in...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2649883/ https://www.ncbi.nlm.nih.gov/pubmed/19203393 http://dx.doi.org/10.1186/1742-4690-6-12 |
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author | van Hal, Sebastiaan J Herring, Belinda Deris, Zaquan Wang, Bin Saksena, Nitin K Dwyer, Dominic E |
author_facet | van Hal, Sebastiaan J Herring, Belinda Deris, Zaquan Wang, Bin Saksena, Nitin K Dwyer, Dominic E |
author_sort | van Hal, Sebastiaan J |
collection | PubMed |
description | In a recent summary of integrase sequences, primary integrase inhibitor mutations were rare. In a review of integrase inhibitor-naïve Australian HIV-1 sequences, primary mutations were not identified, although the accessory mutation G140S was detected. A link with previous antiretroviral therapy, intra-subtype B divergence across the integrase gene and transmission of integrase polymorphisms were also noted. Based on these findings, we would recommend ongoing surveillance of integrase mutations, and integrase region sequencing for patients prior to commencement of integrase inhibitors. |
format | Text |
id | pubmed-2649883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26498832009-03-03 HIV-1 integrase polymorphisms are associated with prior antiretroviral drug exposure van Hal, Sebastiaan J Herring, Belinda Deris, Zaquan Wang, Bin Saksena, Nitin K Dwyer, Dominic E Retrovirology Correspondence In a recent summary of integrase sequences, primary integrase inhibitor mutations were rare. In a review of integrase inhibitor-naïve Australian HIV-1 sequences, primary mutations were not identified, although the accessory mutation G140S was detected. A link with previous antiretroviral therapy, intra-subtype B divergence across the integrase gene and transmission of integrase polymorphisms were also noted. Based on these findings, we would recommend ongoing surveillance of integrase mutations, and integrase region sequencing for patients prior to commencement of integrase inhibitors. BioMed Central 2009-02-09 /pmc/articles/PMC2649883/ /pubmed/19203393 http://dx.doi.org/10.1186/1742-4690-6-12 Text en Copyright © 2009 van Hal et al; 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 | Correspondence van Hal, Sebastiaan J Herring, Belinda Deris, Zaquan Wang, Bin Saksena, Nitin K Dwyer, Dominic E HIV-1 integrase polymorphisms are associated with prior antiretroviral drug exposure |
title | HIV-1 integrase polymorphisms are associated with prior antiretroviral drug exposure |
title_full | HIV-1 integrase polymorphisms are associated with prior antiretroviral drug exposure |
title_fullStr | HIV-1 integrase polymorphisms are associated with prior antiretroviral drug exposure |
title_full_unstemmed | HIV-1 integrase polymorphisms are associated with prior antiretroviral drug exposure |
title_short | HIV-1 integrase polymorphisms are associated with prior antiretroviral drug exposure |
title_sort | hiv-1 integrase polymorphisms are associated with prior antiretroviral drug exposure |
topic | Correspondence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2649883/ https://www.ncbi.nlm.nih.gov/pubmed/19203393 http://dx.doi.org/10.1186/1742-4690-6-12 |
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