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HIV-1 DNA sequence diversity and evolution during acute subtype C infection

Little is known about the genotypic make-up of HIV-1 DNA genomes during the earliest stages of HIV-1 infection. Here, we use near-full-length, single genome next-generation sequencing to longitudinally genotype and quantify subtype C HIV-1 DNA in four women identified during acute HIV-1 infection in...

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Autores principales: Lee, Guinevere Q., Reddy, Kavidha, Einkauf, Kevin B., Gounder, Kamini, Chevalier, Joshua M., Dong, Krista L., Walker, Bruce D., Yu, Xu G., Ndung’u, Thumbi, Lichterfeld, Mathias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6588551/
https://www.ncbi.nlm.nih.gov/pubmed/31227699
http://dx.doi.org/10.1038/s41467-019-10659-2
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author Lee, Guinevere Q.
Reddy, Kavidha
Einkauf, Kevin B.
Gounder, Kamini
Chevalier, Joshua M.
Dong, Krista L.
Walker, Bruce D.
Yu, Xu G.
Ndung’u, Thumbi
Lichterfeld, Mathias
author_facet Lee, Guinevere Q.
Reddy, Kavidha
Einkauf, Kevin B.
Gounder, Kamini
Chevalier, Joshua M.
Dong, Krista L.
Walker, Bruce D.
Yu, Xu G.
Ndung’u, Thumbi
Lichterfeld, Mathias
author_sort Lee, Guinevere Q.
collection PubMed
description Little is known about the genotypic make-up of HIV-1 DNA genomes during the earliest stages of HIV-1 infection. Here, we use near-full-length, single genome next-generation sequencing to longitudinally genotype and quantify subtype C HIV-1 DNA in four women identified during acute HIV-1 infection in Durban, South Africa, through twice-weekly screening of high-risk participants. In contrast to chronically HIV-1-infected patients, we found that at the earliest phases of infection in these four participants, the majority of viral DNA genomes are intact, lack APOBEC-3G/F-associated hypermutations, have limited genome truncations, and over one year show little indication of cytotoxic T cell-driven immune selections. Viral sequence divergence during acute infection is predominantly fueled by single-base substitutions and is limited by treatment initiation during the earliest stages of disease. Our observations provide rare longitudinal insights of HIV-1 DNA sequence profiles during the first year of infection to inform future HIV cure research.
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spelling pubmed-65885512019-06-25 HIV-1 DNA sequence diversity and evolution during acute subtype C infection Lee, Guinevere Q. Reddy, Kavidha Einkauf, Kevin B. Gounder, Kamini Chevalier, Joshua M. Dong, Krista L. Walker, Bruce D. Yu, Xu G. Ndung’u, Thumbi Lichterfeld, Mathias Nat Commun Article Little is known about the genotypic make-up of HIV-1 DNA genomes during the earliest stages of HIV-1 infection. Here, we use near-full-length, single genome next-generation sequencing to longitudinally genotype and quantify subtype C HIV-1 DNA in four women identified during acute HIV-1 infection in Durban, South Africa, through twice-weekly screening of high-risk participants. In contrast to chronically HIV-1-infected patients, we found that at the earliest phases of infection in these four participants, the majority of viral DNA genomes are intact, lack APOBEC-3G/F-associated hypermutations, have limited genome truncations, and over one year show little indication of cytotoxic T cell-driven immune selections. Viral sequence divergence during acute infection is predominantly fueled by single-base substitutions and is limited by treatment initiation during the earliest stages of disease. Our observations provide rare longitudinal insights of HIV-1 DNA sequence profiles during the first year of infection to inform future HIV cure research. Nature Publishing Group UK 2019-06-21 /pmc/articles/PMC6588551/ /pubmed/31227699 http://dx.doi.org/10.1038/s41467-019-10659-2 Text en © The Author(s) 2019 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
Lee, Guinevere Q.
Reddy, Kavidha
Einkauf, Kevin B.
Gounder, Kamini
Chevalier, Joshua M.
Dong, Krista L.
Walker, Bruce D.
Yu, Xu G.
Ndung’u, Thumbi
Lichterfeld, Mathias
HIV-1 DNA sequence diversity and evolution during acute subtype C infection
title HIV-1 DNA sequence diversity and evolution during acute subtype C infection
title_full HIV-1 DNA sequence diversity and evolution during acute subtype C infection
title_fullStr HIV-1 DNA sequence diversity and evolution during acute subtype C infection
title_full_unstemmed HIV-1 DNA sequence diversity and evolution during acute subtype C infection
title_short HIV-1 DNA sequence diversity and evolution during acute subtype C infection
title_sort hiv-1 dna sequence diversity and evolution during acute subtype c infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6588551/
https://www.ncbi.nlm.nih.gov/pubmed/31227699
http://dx.doi.org/10.1038/s41467-019-10659-2
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