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Central Nervous System Compartmentalization of HIV-1 Subtype C Variants Early and Late in Infection in Young Children

HIV-1 subtype B replication in the CNS can occur in CD4+ T cells or macrophages/microglia in adults. However, little is known about CNS infection in children or the ability of subtype C HIV-1 to evolve macrophage-tropic variants. In this study, we examined HIV-1 variants in ART-naïve children aged t...

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Autores principales: Sturdevant, Christa Buckheit, Dow, Anna, Jabara, Cassandra B., Joseph, Sarah B., Schnell, Gretja, Takamune, Nobutoki, Mallewa, Macpherson, Heyderman, Robert S., Van Rie, Annelies, Swanstrom, Ronald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531524/
https://www.ncbi.nlm.nih.gov/pubmed/23300446
http://dx.doi.org/10.1371/journal.ppat.1003094
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author Sturdevant, Christa Buckheit
Dow, Anna
Jabara, Cassandra B.
Joseph, Sarah B.
Schnell, Gretja
Takamune, Nobutoki
Mallewa, Macpherson
Heyderman, Robert S.
Van Rie, Annelies
Swanstrom, Ronald
author_facet Sturdevant, Christa Buckheit
Dow, Anna
Jabara, Cassandra B.
Joseph, Sarah B.
Schnell, Gretja
Takamune, Nobutoki
Mallewa, Macpherson
Heyderman, Robert S.
Van Rie, Annelies
Swanstrom, Ronald
author_sort Sturdevant, Christa Buckheit
collection PubMed
description HIV-1 subtype B replication in the CNS can occur in CD4+ T cells or macrophages/microglia in adults. However, little is known about CNS infection in children or the ability of subtype C HIV-1 to evolve macrophage-tropic variants. In this study, we examined HIV-1 variants in ART-naïve children aged three years or younger to determine viral genotypes and phenotypes associated with HIV-1 subtype C pediatric CNS infection. We examined HIV-1 subtype C populations in blood and CSF of 43 Malawian children with neurodevelopmental delay or acute neurological symptoms. Using single genome amplification (SGA) and phylogenetic analysis of the full-length env gene, we defined four states: equilibrated virus in blood and CSF (n = 20, 47%), intermediate compartmentalization (n = 11, 25%), and two distinct types of compartmentalized CSF virus (n = 12, 28%). Older age and a higher CSF/blood viral load ratio were associated with compartmentalization, consistent with independent replication in the CNS. Cell tropism was assessed using pseudotyped reporter viruses to enter a cell line on which CD4 and CCR5 receptor expression can be differentially induced. In a subset of compartmentalized cases (n = 2, 17%), the CNS virus was able to infect cells with low CD4 surface expression, a hallmark of macrophage-tropic viruses, and intermediate compartmentalization early was associated with an intermediate CD4 entry phenotype. Transmission of multiple variants was observed for 5 children; in several cases, one variant was sequestered within the CNS, consistent with early stochastic colonization of the CNS by virus. Thus we hypothesize two pathways to compartmentalization: early stochastic sequestration in the CNS of one of multiple variants transmitted from mother to child, and emergence of compartmentalized variants later in infection, on average at age 13.5 months, and becoming fully apparent in the CSF by age 18 months. Overall, compartmentalized viral replication in the CNS occurred in half of children by year three.
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spelling pubmed-35315242013-01-08 Central Nervous System Compartmentalization of HIV-1 Subtype C Variants Early and Late in Infection in Young Children Sturdevant, Christa Buckheit Dow, Anna Jabara, Cassandra B. Joseph, Sarah B. Schnell, Gretja Takamune, Nobutoki Mallewa, Macpherson Heyderman, Robert S. Van Rie, Annelies Swanstrom, Ronald PLoS Pathog Research Article HIV-1 subtype B replication in the CNS can occur in CD4+ T cells or macrophages/microglia in adults. However, little is known about CNS infection in children or the ability of subtype C HIV-1 to evolve macrophage-tropic variants. In this study, we examined HIV-1 variants in ART-naïve children aged three years or younger to determine viral genotypes and phenotypes associated with HIV-1 subtype C pediatric CNS infection. We examined HIV-1 subtype C populations in blood and CSF of 43 Malawian children with neurodevelopmental delay or acute neurological symptoms. Using single genome amplification (SGA) and phylogenetic analysis of the full-length env gene, we defined four states: equilibrated virus in blood and CSF (n = 20, 47%), intermediate compartmentalization (n = 11, 25%), and two distinct types of compartmentalized CSF virus (n = 12, 28%). Older age and a higher CSF/blood viral load ratio were associated with compartmentalization, consistent with independent replication in the CNS. Cell tropism was assessed using pseudotyped reporter viruses to enter a cell line on which CD4 and CCR5 receptor expression can be differentially induced. In a subset of compartmentalized cases (n = 2, 17%), the CNS virus was able to infect cells with low CD4 surface expression, a hallmark of macrophage-tropic viruses, and intermediate compartmentalization early was associated with an intermediate CD4 entry phenotype. Transmission of multiple variants was observed for 5 children; in several cases, one variant was sequestered within the CNS, consistent with early stochastic colonization of the CNS by virus. Thus we hypothesize two pathways to compartmentalization: early stochastic sequestration in the CNS of one of multiple variants transmitted from mother to child, and emergence of compartmentalized variants later in infection, on average at age 13.5 months, and becoming fully apparent in the CSF by age 18 months. Overall, compartmentalized viral replication in the CNS occurred in half of children by year three. Public Library of Science 2012-12-27 /pmc/articles/PMC3531524/ /pubmed/23300446 http://dx.doi.org/10.1371/journal.ppat.1003094 Text en © 2012 Sturdevant et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Sturdevant, Christa Buckheit
Dow, Anna
Jabara, Cassandra B.
Joseph, Sarah B.
Schnell, Gretja
Takamune, Nobutoki
Mallewa, Macpherson
Heyderman, Robert S.
Van Rie, Annelies
Swanstrom, Ronald
Central Nervous System Compartmentalization of HIV-1 Subtype C Variants Early and Late in Infection in Young Children
title Central Nervous System Compartmentalization of HIV-1 Subtype C Variants Early and Late in Infection in Young Children
title_full Central Nervous System Compartmentalization of HIV-1 Subtype C Variants Early and Late in Infection in Young Children
title_fullStr Central Nervous System Compartmentalization of HIV-1 Subtype C Variants Early and Late in Infection in Young Children
title_full_unstemmed Central Nervous System Compartmentalization of HIV-1 Subtype C Variants Early and Late in Infection in Young Children
title_short Central Nervous System Compartmentalization of HIV-1 Subtype C Variants Early and Late in Infection in Young Children
title_sort central nervous system compartmentalization of hiv-1 subtype c variants early and late in infection in young children
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531524/
https://www.ncbi.nlm.nih.gov/pubmed/23300446
http://dx.doi.org/10.1371/journal.ppat.1003094
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