» Articles » PMID: 28416661

Single-cell Analysis of HIV-1 Transcriptional Activity Reveals Expression of Proviruses in Expanded Clones During ART

Overview
Specialty Science
Date 2017 Apr 19
PMID 28416661
Citations 103
Authors
Affiliations
Soon will be listed here.
Abstract

Little is known about the fraction of human immunodeficiency virus type 1 (HIV-1) proviruses that express unspliced viral RNA in vivo or about the levels of HIV RNA expression within single infected cells. We developed a sensitive cell-associated HIV RNA and DNA single-genome sequencing (CARD-SGS) method to investigate fractional proviral expression of HIV RNA (1.3-kb fragment of p6, protease, and reverse transcriptase) and the levels of HIV RNA in single HIV-infected cells from blood samples obtained from individuals with viremia or individuals on long-term suppressive antiretroviral therapy (ART). Spiking experiments show that the CARD-SGS method can detect a single cell expressing HIV RNA. Applying CARD-SGS to blood mononuclear cells in six samples from four HIV-infected donors (one with viremia and not on ART and three with viremia suppressed on ART) revealed that an average of 7% of proviruses (range: 2-18%) expressed HIV RNA. Levels of expression varied from one to 62 HIV RNA molecules per cell (median of 1). CARD-SGS also revealed the frequent expression of identical HIV RNA sequences across multiple single cells and across multiple time points in donors on suppressive ART consistent with constitutive expression of HIV RNA in infected cell clones. Defective proviruses were found to express HIV RNA at levels similar to those proviruses that had no obvious defects. CARD-SGS is a useful tool to characterize fractional proviral expression in single infected cells that persist despite ART and to assess the impact of experimental interventions on proviral populations and their expression.

Citing Articles

Inhibition of TIGIT on NK cells improves their cytotoxicity and HIV reservoir eradication potential.

Wang Y, Li Y, Chen J, Guo C, Yu X, Zhang Z mBio. 2025; 16(3):e0322624.

PMID: 39918313 PMC: 11898710. DOI: 10.1128/mbio.03226-24.


The persistent pool of HIV-1-infected cells is formed episodically during untreated infection.

Council O, Tyers L, Moeser M, Sondgeroth A, Spielvogel E, Richardson B J Virol. 2024; 99(2):e0097924.

PMID: 39723838 PMC: 11852786. DOI: 10.1128/jvi.00979-24.


Cognate antigen engagement induces HIV-1 expression in latently infected CD4 T cells from people on long-term antiretroviral therapy.

Moskovljevic M, Dragoni F, Board N, Wu F, Lai J, Zhang H Immunity. 2024; 57(12):2928-2944.e6.

PMID: 39612916 PMC: 11896817. DOI: 10.1016/j.immuni.2024.11.002.


Distinguishable topology of the task-evoked functional genome networks in HIV-1 reservoirs.

Wisniewski J, Wiecek K, Ali H, Pyrc K, Kula-Pacurar A, Wagner M iScience. 2024; 27(11):111222.

PMID: 39559761 PMC: 11570469. DOI: 10.1016/j.isci.2024.111222.


HIV-1 latency reversal agent boosting is not limited by opioid use.

Lilie T, Bouzy J, Asundi A, Taylor J, Roche S, Olson A JCI Insight. 2024; 9(22).

PMID: 39470739 PMC: 11601940. DOI: 10.1172/jci.insight.185480.


References
1.
Rothenberger M, Keele B, Wietgrefe S, Fletcher C, Beilman G, Chipman J . Large number of rebounding/founder HIV variants emerge from multifocal infection in lymphatic tissues after treatment interruption. Proc Natl Acad Sci U S A. 2015; 112(10):E1126-34. PMC: 4364237. DOI: 10.1073/pnas.1414926112. View

2.
Besson G, Lalama C, Bosch R, Gandhi R, Bedison M, Aga E . HIV-1 DNA decay dynamics in blood during more than a decade of suppressive antiretroviral therapy. Clin Infect Dis. 2014; 59(9):1312-21. PMC: 4200019. DOI: 10.1093/cid/ciu585. View

3.
Lau J, Levy D, Wodarz D . Contribution of HIV-1 genomes that do not integrate to the basic reproductive ratio of the virus. J Theor Biol. 2014; 367:222-229. PMC: 4361409. DOI: 10.1016/j.jtbi.2014.12.004. View

4.
Althaus C, Joos B, Perelson A, Gunthard H . Quantifying the turnover of transcriptional subclasses of HIV-1-infected cells. PLoS Comput Biol. 2014; 10(10):e1003871. PMC: 4207463. DOI: 10.1371/journal.pcbi.1003871. View

5.
Kearney M, Wiegand A, Shao W, Coffin J, Mellors J, Lederman M . Origin of Rebound Plasma HIV Includes Cells with Identical Proviruses That Are Transcriptionally Active before Stopping of Antiretroviral Therapy. J Virol. 2015; 90(3):1369-76. PMC: 4719635. DOI: 10.1128/JVI.02139-15. View