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Viro-fluidics: Real-time analysis of virus production kinetics at the single-cell level

Real-time visualization and quantification of viruses released by a cell are crucial to further decipher infection processes. Kinetics studies at the single-cell level will circumvent the limitations of bulk assays with asynchronous virus replication. We have implemented a “viro-fluidic” method, whi...

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Autores principales: Eid, Joëlle, Socol, Marius, Naillon, Antoine, Feuillard, Jérôme, Ciandrini, Luca, Margeat, Emmanuel, Charlot, Benoit, Mougel, Marylène
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680794/
https://www.ncbi.nlm.nih.gov/pubmed/36425325
http://dx.doi.org/10.1016/j.bpr.2022.100068
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author Eid, Joëlle
Socol, Marius
Naillon, Antoine
Feuillard, Jérôme
Ciandrini, Luca
Margeat, Emmanuel
Charlot, Benoit
Mougel, Marylène
author_facet Eid, Joëlle
Socol, Marius
Naillon, Antoine
Feuillard, Jérôme
Ciandrini, Luca
Margeat, Emmanuel
Charlot, Benoit
Mougel, Marylène
author_sort Eid, Joëlle
collection PubMed
description Real-time visualization and quantification of viruses released by a cell are crucial to further decipher infection processes. Kinetics studies at the single-cell level will circumvent the limitations of bulk assays with asynchronous virus replication. We have implemented a “viro-fluidic” method, which combines microfluidics and virology at single-cell and single-virus resolutions. As an experimental model, we used standard cell lines producing fluorescent HIV-like particles (VLPs). First, to scale the strategy to the single-cell level, we validated a sensitive flow virometry system to detect VLPs in low concentration samples (≥10(4) VLPs/mL). Then, this system was coupled to a single-cell trapping device to monitor in real-time the VLPs released, one at a time, from single cells under cell culture conditions. Our results revealed an average production rate of 50 VLPs/h/cell similar to the rate estimated for the same cells grown in population. Thus, the virus-producing capacities of the trapped cells were preserved and its real-time monitoring was accurate. Moreover, single-cell analysis revealed a release of VLPs with stochastic bursts with typical time intervals of few minutes, revealing the existence of limiting step(s) in the virus biogenesis process. Our tools can be applied to other pathogens or to extracellular vesicles to elucidate the dissemination mechanisms of these biological nanoparticles.
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spelling pubmed-96807942022-11-23 Viro-fluidics: Real-time analysis of virus production kinetics at the single-cell level Eid, Joëlle Socol, Marius Naillon, Antoine Feuillard, Jérôme Ciandrini, Luca Margeat, Emmanuel Charlot, Benoit Mougel, Marylène Biophys Rep (N Y) Article Real-time visualization and quantification of viruses released by a cell are crucial to further decipher infection processes. Kinetics studies at the single-cell level will circumvent the limitations of bulk assays with asynchronous virus replication. We have implemented a “viro-fluidic” method, which combines microfluidics and virology at single-cell and single-virus resolutions. As an experimental model, we used standard cell lines producing fluorescent HIV-like particles (VLPs). First, to scale the strategy to the single-cell level, we validated a sensitive flow virometry system to detect VLPs in low concentration samples (≥10(4) VLPs/mL). Then, this system was coupled to a single-cell trapping device to monitor in real-time the VLPs released, one at a time, from single cells under cell culture conditions. Our results revealed an average production rate of 50 VLPs/h/cell similar to the rate estimated for the same cells grown in population. Thus, the virus-producing capacities of the trapped cells were preserved and its real-time monitoring was accurate. Moreover, single-cell analysis revealed a release of VLPs with stochastic bursts with typical time intervals of few minutes, revealing the existence of limiting step(s) in the virus biogenesis process. Our tools can be applied to other pathogens or to extracellular vesicles to elucidate the dissemination mechanisms of these biological nanoparticles. Elsevier 2022-08-11 /pmc/articles/PMC9680794/ /pubmed/36425325 http://dx.doi.org/10.1016/j.bpr.2022.100068 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Eid, Joëlle
Socol, Marius
Naillon, Antoine
Feuillard, Jérôme
Ciandrini, Luca
Margeat, Emmanuel
Charlot, Benoit
Mougel, Marylène
Viro-fluidics: Real-time analysis of virus production kinetics at the single-cell level
title Viro-fluidics: Real-time analysis of virus production kinetics at the single-cell level
title_full Viro-fluidics: Real-time analysis of virus production kinetics at the single-cell level
title_fullStr Viro-fluidics: Real-time analysis of virus production kinetics at the single-cell level
title_full_unstemmed Viro-fluidics: Real-time analysis of virus production kinetics at the single-cell level
title_short Viro-fluidics: Real-time analysis of virus production kinetics at the single-cell level
title_sort viro-fluidics: real-time analysis of virus production kinetics at the single-cell level
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680794/
https://www.ncbi.nlm.nih.gov/pubmed/36425325
http://dx.doi.org/10.1016/j.bpr.2022.100068
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