Cargando…
Ultra-Deep Sequencing of HIV-1 near Full-Length and Partial Proviral Genomes Reveals High Genetic Diversity among Brazilian Blood Donors
BACKGROUND: Here, we aimed to gain a comprehensive picture of the HIV-1 diversity in the northeast and southeast part of Brazil. To this end, a high-throughput sequencing-by-synthesis protocol and instrument were used to characterize the near full length (NFLG) and partial HIV-1 proviral genome in 2...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816342/ https://www.ncbi.nlm.nih.gov/pubmed/27031505 http://dx.doi.org/10.1371/journal.pone.0152499 |
_version_ | 1782424699908653056 |
---|---|
author | Pessôa, Rodrigo Loureiro, Paula Esther Lopes, Maria Carneiro-Proietti, Anna B. F. Sabino, Ester C Busch, Michael P. Sanabani, Sabri S |
author_facet | Pessôa, Rodrigo Loureiro, Paula Esther Lopes, Maria Carneiro-Proietti, Anna B. F. Sabino, Ester C Busch, Michael P. Sanabani, Sabri S |
author_sort | Pessôa, Rodrigo |
collection | PubMed |
description | BACKGROUND: Here, we aimed to gain a comprehensive picture of the HIV-1 diversity in the northeast and southeast part of Brazil. To this end, a high-throughput sequencing-by-synthesis protocol and instrument were used to characterize the near full length (NFLG) and partial HIV-1 proviral genome in 259 HIV-1 infected blood donors at four major blood centers in Brazil: Pro-Sangue foundation (São Paulo state (SP), n 51), Hemominas foundation (Minas Gerais state (MG), n 41), Hemope foundation (Recife state (PE), n 96) and Hemorio blood bank (Rio de Janeiro (RJ), n 70). MATERIALS AND METHODS: A total of 259 blood samples were obtained from 195 donors with long-standing infections and 64 donors with a lack of stage information. DNA was extracted from the peripheral blood mononuclear cells (PBMCs) to amplify the HIV-1 NFLGs from five overlapping fragments. The amplicons were molecularly bar-coded, pooled, and sequenced by Illumina paired-end protocol. RESULTS: Of the 259 samples studied, 208 (80%) NFLGs and 49 (18.8%) partial fragments were de novo assembled into contiguous sequences and successfully subtyped. Of these 257 samples, 183 (71.2%) were pure subtypes consisting of clade B (n = 167, 65%), C (n = 10, 3.9%), F1 (n = 4, 1.5%), and D (n = 2, 0.7%). Recombinant viruses were detected in 74 (28.8%) samples and consist of unique BF1 (n = 41, 15.9%), BC (n = 7, 2.7%), BCF1 (n = 4, 1.5%), CF1 and CDK (n = 1, 0.4%, each), CRF70_BF1 (n = 4, 1.5%), CRF71_BF1 (n = 12, 4.7%), and CRF72_BF1 (n = 4, 1.5%). Evidence of dual infection was detected in four patients coinfected with the same subtype (n = 3) and distinct subtype (n = 1). CONCLUSION: Based on this work, subtype B appears to be the prevalent subtype followed by a high proportion of intersubtype recombinants that appeared to be arising continually in this country. Our study represents the largest analysis of the viral NFLG ever undertaken worldwide and provides insights into the understanding the genesis of the HIV-1 epidemic in this particular area of South America and informs vaccine design and clinical trials. |
format | Online Article Text |
id | pubmed-4816342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48163422016-04-14 Ultra-Deep Sequencing of HIV-1 near Full-Length and Partial Proviral Genomes Reveals High Genetic Diversity among Brazilian Blood Donors Pessôa, Rodrigo Loureiro, Paula Esther Lopes, Maria Carneiro-Proietti, Anna B. F. Sabino, Ester C Busch, Michael P. Sanabani, Sabri S PLoS One Research Article BACKGROUND: Here, we aimed to gain a comprehensive picture of the HIV-1 diversity in the northeast and southeast part of Brazil. To this end, a high-throughput sequencing-by-synthesis protocol and instrument were used to characterize the near full length (NFLG) and partial HIV-1 proviral genome in 259 HIV-1 infected blood donors at four major blood centers in Brazil: Pro-Sangue foundation (São Paulo state (SP), n 51), Hemominas foundation (Minas Gerais state (MG), n 41), Hemope foundation (Recife state (PE), n 96) and Hemorio blood bank (Rio de Janeiro (RJ), n 70). MATERIALS AND METHODS: A total of 259 blood samples were obtained from 195 donors with long-standing infections and 64 donors with a lack of stage information. DNA was extracted from the peripheral blood mononuclear cells (PBMCs) to amplify the HIV-1 NFLGs from five overlapping fragments. The amplicons were molecularly bar-coded, pooled, and sequenced by Illumina paired-end protocol. RESULTS: Of the 259 samples studied, 208 (80%) NFLGs and 49 (18.8%) partial fragments were de novo assembled into contiguous sequences and successfully subtyped. Of these 257 samples, 183 (71.2%) were pure subtypes consisting of clade B (n = 167, 65%), C (n = 10, 3.9%), F1 (n = 4, 1.5%), and D (n = 2, 0.7%). Recombinant viruses were detected in 74 (28.8%) samples and consist of unique BF1 (n = 41, 15.9%), BC (n = 7, 2.7%), BCF1 (n = 4, 1.5%), CF1 and CDK (n = 1, 0.4%, each), CRF70_BF1 (n = 4, 1.5%), CRF71_BF1 (n = 12, 4.7%), and CRF72_BF1 (n = 4, 1.5%). Evidence of dual infection was detected in four patients coinfected with the same subtype (n = 3) and distinct subtype (n = 1). CONCLUSION: Based on this work, subtype B appears to be the prevalent subtype followed by a high proportion of intersubtype recombinants that appeared to be arising continually in this country. Our study represents the largest analysis of the viral NFLG ever undertaken worldwide and provides insights into the understanding the genesis of the HIV-1 epidemic in this particular area of South America and informs vaccine design and clinical trials. Public Library of Science 2016-03-31 /pmc/articles/PMC4816342/ /pubmed/27031505 http://dx.doi.org/10.1371/journal.pone.0152499 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Pessôa, Rodrigo Loureiro, Paula Esther Lopes, Maria Carneiro-Proietti, Anna B. F. Sabino, Ester C Busch, Michael P. Sanabani, Sabri S Ultra-Deep Sequencing of HIV-1 near Full-Length and Partial Proviral Genomes Reveals High Genetic Diversity among Brazilian Blood Donors |
title | Ultra-Deep Sequencing of HIV-1 near Full-Length and Partial Proviral Genomes Reveals High Genetic Diversity among Brazilian Blood Donors |
title_full | Ultra-Deep Sequencing of HIV-1 near Full-Length and Partial Proviral Genomes Reveals High Genetic Diversity among Brazilian Blood Donors |
title_fullStr | Ultra-Deep Sequencing of HIV-1 near Full-Length and Partial Proviral Genomes Reveals High Genetic Diversity among Brazilian Blood Donors |
title_full_unstemmed | Ultra-Deep Sequencing of HIV-1 near Full-Length and Partial Proviral Genomes Reveals High Genetic Diversity among Brazilian Blood Donors |
title_short | Ultra-Deep Sequencing of HIV-1 near Full-Length and Partial Proviral Genomes Reveals High Genetic Diversity among Brazilian Blood Donors |
title_sort | ultra-deep sequencing of hiv-1 near full-length and partial proviral genomes reveals high genetic diversity among brazilian blood donors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816342/ https://www.ncbi.nlm.nih.gov/pubmed/27031505 http://dx.doi.org/10.1371/journal.pone.0152499 |
work_keys_str_mv | AT pessoarodrigo ultradeepsequencingofhiv1nearfulllengthandpartialproviralgenomesrevealshighgeneticdiversityamongbrazilianblooddonors AT loureiropaula ultradeepsequencingofhiv1nearfulllengthandpartialproviralgenomesrevealshighgeneticdiversityamongbrazilianblooddonors AT estherlopesmaria ultradeepsequencingofhiv1nearfulllengthandpartialproviralgenomesrevealshighgeneticdiversityamongbrazilianblooddonors AT carneiroproiettiannabf ultradeepsequencingofhiv1nearfulllengthandpartialproviralgenomesrevealshighgeneticdiversityamongbrazilianblooddonors AT sabinoesterc ultradeepsequencingofhiv1nearfulllengthandpartialproviralgenomesrevealshighgeneticdiversityamongbrazilianblooddonors AT buschmichaelp ultradeepsequencingofhiv1nearfulllengthandpartialproviralgenomesrevealshighgeneticdiversityamongbrazilianblooddonors AT sanabanisabris ultradeepsequencingofhiv1nearfulllengthandpartialproviralgenomesrevealshighgeneticdiversityamongbrazilianblooddonors |