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

IF 2.4 Q3 BIOPHYSICS Biophysical reports Pub Date : 2022-08-11 eCollection Date: 2022-09-14 DOI:10.1016/j.bpr.2022.100068
Joëlle Eid, Marius Socol, Antoine Naillon, Jérôme Feuillard, Luca Ciandrini, Emmanuel Margeat, Benoit Charlot, Marylène Mougel
{"title":"Viro-fluidics: Real-time analysis of virus production kinetics at the single-cell level.","authors":"Joëlle Eid,&nbsp;Marius Socol,&nbsp;Antoine Naillon,&nbsp;Jérôme Feuillard,&nbsp;Luca Ciandrini,&nbsp;Emmanuel Margeat,&nbsp;Benoit Charlot,&nbsp;Marylène Mougel","doi":"10.1016/j.bpr.2022.100068","DOIUrl":null,"url":null,"abstract":"<p><p>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<sup>4</sup> 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.</p>","PeriodicalId":72402,"journal":{"name":"Biophysical reports","volume":null,"pages":null},"PeriodicalIF":2.4000,"publicationDate":"2022-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/32/b5/main.PMC9680794.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biophysical reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.bpr.2022.100068","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/9/14 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0

Abstract

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 (≥104 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.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
病毒流体学:在单细胞水平上实时分析病毒产生动力学。
细胞释放的病毒的实时可视化和定量对进一步破译感染过程至关重要。在单细胞水平上的动力学研究将绕过异步病毒复制的批量分析的局限性。我们已经实现了一种“病毒流控”方法,它结合了单细胞和单病毒分辨率的微流体学和病毒学。作为实验模型,我们使用产生荧光hiv样颗粒(VLPs)的标准细胞系。首先,为了将该策略扩展到单细胞水平,我们验证了一种灵敏的流动病毒学系统,以检测低浓度样品(≥104 VLPs/mL)中的VLPs。然后,将该系统与单细胞捕获装置耦合,以实时监测在细胞培养条件下单细胞一次释放一个VLPs。我们的结果显示,平均产量为50 VLPs/h/细胞,与在群体中生长的相同细胞的估计速度相似。因此,保留了捕获细胞的产病毒能力,并对其进行了准确的实时监测。此外,单细胞分析显示,VLPs以随机爆发的方式释放,典型的时间间隔为几分钟,这表明在病毒生物发生过程中存在限制步骤。我们的工具可以应用于其他病原体或细胞外囊泡,以阐明这些生物纳米颗粒的传播机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Biophysical reports
Biophysical reports Biophysics
CiteScore
2.40
自引率
0.00%
发文量
0
审稿时长
75 days
期刊最新文献
Development of a digital amplifier system for cut-open oocyte electrophysiology. Structural studies of the human α1 glycine receptor via site-specific chemical cross-linking coupled with mass spectrometry. Expression level of cardiac ryanodine receptors dictates properties of Ca2+-induced Ca2+ release. Nonlinear classifiers for wet-neuromorphic computing using gene regulatory neural network. Magnetic field platform for experiments on well-mixed and spatially structured microbial populations.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1