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The CpG dinucleotide content of the HIV-1 envelope gene may predict disease progression

The clinical course of HIV-1 varies greatly among infected individuals. Despite extensive research, virus factors associated with slow-progression remain poorly understood. Identification of unique HIV-1 genomic signatures linked to slow-progression remains elusive. We investigated CpG dinucleotide...

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Autores principales: Wasson, Mishi Kaushal, Borkakoti, Jayanta, Kumar, Amit, Biswas, Banhi, Vivekanandan, Perumal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557942/
https://www.ncbi.nlm.nih.gov/pubmed/28811638
http://dx.doi.org/10.1038/s41598-017-08716-1
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author Wasson, Mishi Kaushal
Borkakoti, Jayanta
Kumar, Amit
Biswas, Banhi
Vivekanandan, Perumal
author_facet Wasson, Mishi Kaushal
Borkakoti, Jayanta
Kumar, Amit
Biswas, Banhi
Vivekanandan, Perumal
author_sort Wasson, Mishi Kaushal
collection PubMed
description The clinical course of HIV-1 varies greatly among infected individuals. Despite extensive research, virus factors associated with slow-progression remain poorly understood. Identification of unique HIV-1 genomic signatures linked to slow-progression remains elusive. We investigated CpG dinucleotide content in HIV-1 envelope gene as a potential virus factor in disease progression. We analysed 1808 HIV-1 envelope gene sequences from three independent longitudinal studies; this included 1280 sequences from twelve typical-progressors and 528 sequences from six slow-progressors. Relative abundance of CpG dinucleotides and relative synonymous codon usage (RSCU) for CpG-containing codons among HIV-1 envelope gene sequences from typical-progressors and slow-progressors were analysed. HIV-1 envelope gene sequences from slow-progressors have high-CpG dinucleotide content and increased number of CpG-containing codons as compared to typical-progressors. Our findings suggest that observed differences in CpG-content between typical-progressors and slow-progressors is not explained by differences in the mononucleotide content. Our results also highlight that the high-CpG content in HIV-1 envelope gene from slow-progressors is observed immediately after seroconversion. Thus CpG dinucleotide content of HIV-1 envelope gene is a potential virus-related factor that is linked to disease progression. The CpG dinucleotide content of HIV-1 envelope gene may help predict HIV-1 disease progression at early stages after seroconversion.
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spelling pubmed-55579422017-08-16 The CpG dinucleotide content of the HIV-1 envelope gene may predict disease progression Wasson, Mishi Kaushal Borkakoti, Jayanta Kumar, Amit Biswas, Banhi Vivekanandan, Perumal Sci Rep Article The clinical course of HIV-1 varies greatly among infected individuals. Despite extensive research, virus factors associated with slow-progression remain poorly understood. Identification of unique HIV-1 genomic signatures linked to slow-progression remains elusive. We investigated CpG dinucleotide content in HIV-1 envelope gene as a potential virus factor in disease progression. We analysed 1808 HIV-1 envelope gene sequences from three independent longitudinal studies; this included 1280 sequences from twelve typical-progressors and 528 sequences from six slow-progressors. Relative abundance of CpG dinucleotides and relative synonymous codon usage (RSCU) for CpG-containing codons among HIV-1 envelope gene sequences from typical-progressors and slow-progressors were analysed. HIV-1 envelope gene sequences from slow-progressors have high-CpG dinucleotide content and increased number of CpG-containing codons as compared to typical-progressors. Our findings suggest that observed differences in CpG-content between typical-progressors and slow-progressors is not explained by differences in the mononucleotide content. Our results also highlight that the high-CpG content in HIV-1 envelope gene from slow-progressors is observed immediately after seroconversion. Thus CpG dinucleotide content of HIV-1 envelope gene is a potential virus-related factor that is linked to disease progression. The CpG dinucleotide content of HIV-1 envelope gene may help predict HIV-1 disease progression at early stages after seroconversion. Nature Publishing Group UK 2017-08-15 /pmc/articles/PMC5557942/ /pubmed/28811638 http://dx.doi.org/10.1038/s41598-017-08716-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wasson, Mishi Kaushal
Borkakoti, Jayanta
Kumar, Amit
Biswas, Banhi
Vivekanandan, Perumal
The CpG dinucleotide content of the HIV-1 envelope gene may predict disease progression
title The CpG dinucleotide content of the HIV-1 envelope gene may predict disease progression
title_full The CpG dinucleotide content of the HIV-1 envelope gene may predict disease progression
title_fullStr The CpG dinucleotide content of the HIV-1 envelope gene may predict disease progression
title_full_unstemmed The CpG dinucleotide content of the HIV-1 envelope gene may predict disease progression
title_short The CpG dinucleotide content of the HIV-1 envelope gene may predict disease progression
title_sort cpg dinucleotide content of the hiv-1 envelope gene may predict disease progression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557942/
https://www.ncbi.nlm.nih.gov/pubmed/28811638
http://dx.doi.org/10.1038/s41598-017-08716-1
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