Cargando…

FRET-Based Detection and Quantification of HIV-1 Virion Maturation

HIV-1 infectivity is achieved through virion maturation. Virus particles undergo structural changes via cleavage of the Gag polyprotein mediated by the viral protease, causing the transition from an uninfectious to an infectious status. The majority of proviruses in people living with HIV-1 treated...

Descripción completa

Detalles Bibliográficos
Autores principales: Sarca, Anamaria D., Sardo, Luca, Fukuda, Hirofumi, Matsui, Hiroyuki, Shirakawa, Kotaro, Horikawa, Kazuki, Takaori-Kondo, Akifumi, Izumi, Taisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985248/
https://www.ncbi.nlm.nih.gov/pubmed/33767685
http://dx.doi.org/10.3389/fmicb.2021.647452
_version_ 1783668204477874176
author Sarca, Anamaria D.
Sardo, Luca
Fukuda, Hirofumi
Matsui, Hiroyuki
Shirakawa, Kotaro
Horikawa, Kazuki
Takaori-Kondo, Akifumi
Izumi, Taisuke
author_facet Sarca, Anamaria D.
Sardo, Luca
Fukuda, Hirofumi
Matsui, Hiroyuki
Shirakawa, Kotaro
Horikawa, Kazuki
Takaori-Kondo, Akifumi
Izumi, Taisuke
author_sort Sarca, Anamaria D.
collection PubMed
description HIV-1 infectivity is achieved through virion maturation. Virus particles undergo structural changes via cleavage of the Gag polyprotein mediated by the viral protease, causing the transition from an uninfectious to an infectious status. The majority of proviruses in people living with HIV-1 treated with combination antiretroviral therapy are defective with large internal deletions. Defective proviral DNA frequently preserves intact sequences capable of expressing viral structural proteins to form virus-like particles whose maturation status is an important factor for chronic antigen-mediated immune stimulation and inflammation. Thus, novel methods to study the maturation capability of defective virus particles are needed to characterize their immunogenicity. To build a quantitative tool to study virion maturation in vitro, we developed a novel single virion visualization technique based on fluorescence resonance energy transfer (FRET). We inserted an optimized intramolecular CFP-YPF FRET donor-acceptor pair bridged with an HIV-1 protease cleavage sequence between the Gag MA-CA domains. This system allowed us to microscopically distinguish mature and immature virions via their FRET signal when the FRET donor and acceptor proteins were separated by the viral protease during maturation. We found that approximately 80% of the FRET labeled virus particles were mature with equivalent infectivity to wild type. The proportion of immature virions was increased by treatment of virus producer cells with a protease inhibitor in a dose-dependent manner, which corresponded to a relative decrease in infectivity. Potential areas of application for this tool are assessing maturation efficiency in different cell type settings of intact or deficient proviral DNA integrated cells. We believe that this FRET-based single-virion imaging platform will facilitate estimating the impact on the immune system of both extracellular intact and defective viruses by quantifying the Gag maturation status.
format Online
Article
Text
id pubmed-7985248
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-79852482021-03-24 FRET-Based Detection and Quantification of HIV-1 Virion Maturation Sarca, Anamaria D. Sardo, Luca Fukuda, Hirofumi Matsui, Hiroyuki Shirakawa, Kotaro Horikawa, Kazuki Takaori-Kondo, Akifumi Izumi, Taisuke Front Microbiol Microbiology HIV-1 infectivity is achieved through virion maturation. Virus particles undergo structural changes via cleavage of the Gag polyprotein mediated by the viral protease, causing the transition from an uninfectious to an infectious status. The majority of proviruses in people living with HIV-1 treated with combination antiretroviral therapy are defective with large internal deletions. Defective proviral DNA frequently preserves intact sequences capable of expressing viral structural proteins to form virus-like particles whose maturation status is an important factor for chronic antigen-mediated immune stimulation and inflammation. Thus, novel methods to study the maturation capability of defective virus particles are needed to characterize their immunogenicity. To build a quantitative tool to study virion maturation in vitro, we developed a novel single virion visualization technique based on fluorescence resonance energy transfer (FRET). We inserted an optimized intramolecular CFP-YPF FRET donor-acceptor pair bridged with an HIV-1 protease cleavage sequence between the Gag MA-CA domains. This system allowed us to microscopically distinguish mature and immature virions via their FRET signal when the FRET donor and acceptor proteins were separated by the viral protease during maturation. We found that approximately 80% of the FRET labeled virus particles were mature with equivalent infectivity to wild type. The proportion of immature virions was increased by treatment of virus producer cells with a protease inhibitor in a dose-dependent manner, which corresponded to a relative decrease in infectivity. Potential areas of application for this tool are assessing maturation efficiency in different cell type settings of intact or deficient proviral DNA integrated cells. We believe that this FRET-based single-virion imaging platform will facilitate estimating the impact on the immune system of both extracellular intact and defective viruses by quantifying the Gag maturation status. Frontiers Media S.A. 2021-03-09 /pmc/articles/PMC7985248/ /pubmed/33767685 http://dx.doi.org/10.3389/fmicb.2021.647452 Text en Copyright © 2021 Sarca, Sardo, Fukuda, Matsui, Shirakawa, Horikawa, Takaori-Kondo and Izumi. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Sarca, Anamaria D.
Sardo, Luca
Fukuda, Hirofumi
Matsui, Hiroyuki
Shirakawa, Kotaro
Horikawa, Kazuki
Takaori-Kondo, Akifumi
Izumi, Taisuke
FRET-Based Detection and Quantification of HIV-1 Virion Maturation
title FRET-Based Detection and Quantification of HIV-1 Virion Maturation
title_full FRET-Based Detection and Quantification of HIV-1 Virion Maturation
title_fullStr FRET-Based Detection and Quantification of HIV-1 Virion Maturation
title_full_unstemmed FRET-Based Detection and Quantification of HIV-1 Virion Maturation
title_short FRET-Based Detection and Quantification of HIV-1 Virion Maturation
title_sort fret-based detection and quantification of hiv-1 virion maturation
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985248/
https://www.ncbi.nlm.nih.gov/pubmed/33767685
http://dx.doi.org/10.3389/fmicb.2021.647452
work_keys_str_mv AT sarcaanamariad fretbaseddetectionandquantificationofhiv1virionmaturation
AT sardoluca fretbaseddetectionandquantificationofhiv1virionmaturation
AT fukudahirofumi fretbaseddetectionandquantificationofhiv1virionmaturation
AT matsuihiroyuki fretbaseddetectionandquantificationofhiv1virionmaturation
AT shirakawakotaro fretbaseddetectionandquantificationofhiv1virionmaturation
AT horikawakazuki fretbaseddetectionandquantificationofhiv1virionmaturation
AT takaorikondoakifumi fretbaseddetectionandquantificationofhiv1virionmaturation
AT izumitaisuke fretbaseddetectionandquantificationofhiv1virionmaturation