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Deep Sequencing Reveals Central Nervous System Compartmentalization in Multiple Transmitted/Founder Virus Acute HIV-1 Infection.

Authors :
Tovanabutra S
Sirijatuphat R
Pham PT
Bonar L
Harbolick EA
Bose M
Song H
Chang D
Oropeza C
O'Sullivan AM
Balinang J
Kroon E
Colby DJ
Sacdalan C
Hellmuth J
Chan P
Prueksakaew P
Pinyakorn S
Jagodzinski LL
Sutthichom D
Pattamaswin S
de Souza M
Gramzinski RA
Kim JH
Michael NL
Robb ML
Phanuphak N
Ananworanich J
Valcour V
Kijak GH
Sanders-Buell E
Spudich S
Source :
Cells [Cells] 2019 Aug 15; Vol. 8 (8). Date of Electronic Publication: 2019 Aug 15.
Publication Year :
2019

Abstract

HIV-1 disseminates to a broad range of tissue compartments during acute HIV-1 infection (AHI). The central nervous system (CNS) can serve as an early and persistent site of viral replication, which poses a potential challenge for HIV-1 remission strategies that target the HIV reservoir. CNS compartmentalization is a key feature of HIV-1 neuropathogenesis. Thus far, the timing of how early CNS compartmentalization develops after infection is unknown. We examined whether HIV-1 transmitted/founder (T/F) viruses differ between CNS and blood during AHI using single-genome sequencing of envelope gene and further examined subregions in pol and env using next-generation sequencing in paired plasma and cerebrospinal fluid (CSF) from 18 individuals. Different proportions of mostly minor variants were found in six of the eight multiple T/F-infected individuals, indicating enrichment of some variants in CSF that may lead to significant compartmentalization in the later stages of infection. This study provides evidence for the first time that HIV-1 compartmentalization in the CNS can occur within days of HIV-1 exposure in multiple T/F infections. Further understanding of factors that determine enrichment of T/F variants in the CNS, as well as potential long-term implications of these findings for persistence of HIV-1 reservoirs and neurological impairment in HIV, is needed.

Details

Language :
English
ISSN :
2073-4409
Volume :
8
Issue :
8
Database :
MEDLINE
Journal :
Cells
Publication Type :
Academic Journal
Accession number :
31443253
Full Text :
https://doi.org/10.3390/cells8080902