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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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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 |
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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 |
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