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Systemic and Intestinal Viral Reservoirs in CD4+ T Cell Subsets in Primary SIV Infection

The HIV reservoir size in target CD4+ T cells during primary infection remains unknown. Here, we sorted peripheral and intestinal CD4+ T cells and quantified the levels of cell-associated SIV RNA and DNA in rhesus macaques within days of SIVmac251 inoculation. As a major target cell of HIV/SIV, CD4+...

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Autores principales: Wang, Xiaolei, Ziani, Widade, Veazey, Ronald S., Xu, Huanbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704255/
https://www.ncbi.nlm.nih.gov/pubmed/34960667
http://dx.doi.org/10.3390/v13122398
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author Wang, Xiaolei
Ziani, Widade
Veazey, Ronald S.
Xu, Huanbin
author_facet Wang, Xiaolei
Ziani, Widade
Veazey, Ronald S.
Xu, Huanbin
author_sort Wang, Xiaolei
collection PubMed
description The HIV reservoir size in target CD4+ T cells during primary infection remains unknown. Here, we sorted peripheral and intestinal CD4+ T cells and quantified the levels of cell-associated SIV RNA and DNA in rhesus macaques within days of SIVmac251 inoculation. As a major target cell of HIV/SIV, CD4+ T cells in both tissues contained a large amount of SIV RNA and DNA at day 8–13 post-SIV infection, in which productive SIV RNA highly correlated with the levels of cell-associated SIV DNA. Memory CD4+ T cells had much higher viral RNA and DNA than naïve subsets, yet memory CD4+ T cells co-expressing CCR5 had no significant reservoir size compared with those that were CCR5-negative in blood and intestine. Collectively, memory CD4+ T cells appear to be the major targets for primary infection, and viral reservoirs are equally distributed in systemic and lymphoid compartments in acutely SIV-infected macaques.
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spelling pubmed-87042552021-12-25 Systemic and Intestinal Viral Reservoirs in CD4+ T Cell Subsets in Primary SIV Infection Wang, Xiaolei Ziani, Widade Veazey, Ronald S. Xu, Huanbin Viruses Article The HIV reservoir size in target CD4+ T cells during primary infection remains unknown. Here, we sorted peripheral and intestinal CD4+ T cells and quantified the levels of cell-associated SIV RNA and DNA in rhesus macaques within days of SIVmac251 inoculation. As a major target cell of HIV/SIV, CD4+ T cells in both tissues contained a large amount of SIV RNA and DNA at day 8–13 post-SIV infection, in which productive SIV RNA highly correlated with the levels of cell-associated SIV DNA. Memory CD4+ T cells had much higher viral RNA and DNA than naïve subsets, yet memory CD4+ T cells co-expressing CCR5 had no significant reservoir size compared with those that were CCR5-negative in blood and intestine. Collectively, memory CD4+ T cells appear to be the major targets for primary infection, and viral reservoirs are equally distributed in systemic and lymphoid compartments in acutely SIV-infected macaques. MDPI 2021-11-30 /pmc/articles/PMC8704255/ /pubmed/34960667 http://dx.doi.org/10.3390/v13122398 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wang, Xiaolei
Ziani, Widade
Veazey, Ronald S.
Xu, Huanbin
Systemic and Intestinal Viral Reservoirs in CD4+ T Cell Subsets in Primary SIV Infection
title Systemic and Intestinal Viral Reservoirs in CD4+ T Cell Subsets in Primary SIV Infection
title_full Systemic and Intestinal Viral Reservoirs in CD4+ T Cell Subsets in Primary SIV Infection
title_fullStr Systemic and Intestinal Viral Reservoirs in CD4+ T Cell Subsets in Primary SIV Infection
title_full_unstemmed Systemic and Intestinal Viral Reservoirs in CD4+ T Cell Subsets in Primary SIV Infection
title_short Systemic and Intestinal Viral Reservoirs in CD4+ T Cell Subsets in Primary SIV Infection
title_sort systemic and intestinal viral reservoirs in cd4+ t cell subsets in primary siv infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704255/
https://www.ncbi.nlm.nih.gov/pubmed/34960667
http://dx.doi.org/10.3390/v13122398
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