Impedance-based method for the quantification of infectious SARS-CoV-2

IF 1.6 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Journal of virological methods Pub Date : 2025-04-01 Epub Date: 2025-01-23 DOI:10.1016/j.jviromet.2025.115110
Audrey Fraisse , Laurent Guillier , Christophe Cordevant , Sophie Le Poder , Sylvie Perelle , Sandra Martin-Latil
{"title":"Impedance-based method for the quantification of infectious SARS-CoV-2","authors":"Audrey Fraisse ,&nbsp;Laurent Guillier ,&nbsp;Christophe Cordevant ,&nbsp;Sophie Le Poder ,&nbsp;Sylvie Perelle ,&nbsp;Sandra Martin-Latil","doi":"10.1016/j.jviromet.2025.115110","DOIUrl":null,"url":null,"abstract":"<div><div>Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the etiologic agent involved in the coronavirus disease 2019 (COVID-19) pandemic. The development of infectious titration methods is crucial to provide data for a better understanding of transmission routes, as well as to validate the efficacy of inactivation treatments. Nevertheless, the low-throughput analytical capacity of traditional methods may be a limiting factor for a large screening of samples.</div><div>The aim of the study was to develop a Real-Time Cell Analysis (RTCA) assay based on the measurement of cell impedance to quantify infectious SARS-CoV-2. The kinetics of cell impedance showed a virus-specific Cell Index (CI) drop. This enabled the correlation between viral concentrations and time at which a 50 % drop in CI values was observed (tCI<sub>50</sub>), with establishment of a standard curve. In parallel, the improved Spearman and Kärber method was used to quantify infectious titer since the virus-induced CI drop is correlated to the Cytopathic Effect. The estimated uncertainty was respectively 0.57, 0.36, and 0.26 log<sub>10</sub> with 4, 8, and 16 wells per dilution.</div><div>Thus, the RTCA assay is a powerful tool with a greatly simplified workflow for effective risk assessment in the field of food and environmental virology.</div></div>","PeriodicalId":17663,"journal":{"name":"Journal of virological methods","volume":"333 ","pages":"Article 115110"},"PeriodicalIF":1.6000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of virological methods","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0166093425000035","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/23 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the etiologic agent involved in the coronavirus disease 2019 (COVID-19) pandemic. The development of infectious titration methods is crucial to provide data for a better understanding of transmission routes, as well as to validate the efficacy of inactivation treatments. Nevertheless, the low-throughput analytical capacity of traditional methods may be a limiting factor for a large screening of samples.
The aim of the study was to develop a Real-Time Cell Analysis (RTCA) assay based on the measurement of cell impedance to quantify infectious SARS-CoV-2. The kinetics of cell impedance showed a virus-specific Cell Index (CI) drop. This enabled the correlation between viral concentrations and time at which a 50 % drop in CI values was observed (tCI50), with establishment of a standard curve. In parallel, the improved Spearman and Kärber method was used to quantify infectious titer since the virus-induced CI drop is correlated to the Cytopathic Effect. The estimated uncertainty was respectively 0.57, 0.36, and 0.26 log10 with 4, 8, and 16 wells per dilution.
Thus, the RTCA assay is a powerful tool with a greatly simplified workflow for effective risk assessment in the field of food and environmental virology.
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
基于阻抗的传染性SARS-CoV-2定量方法
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)是2019年冠状病毒病(COVID-19)大流行的病原。发展感染滴定方法对于提供数据以更好地了解传播途径以及验证灭活治疗的有效性至关重要。然而,传统方法的低通量分析能力可能是大量筛选样品的限制因素。该研究的目的是开发一种基于细胞阻抗测量的实时细胞分析(RTCA)方法,以量化传染性SARS-CoV-2。细胞阻抗动力学显示病毒特异性细胞指数(CI)下降。这使得病毒浓度与观察到CI值下降50%的时间(tCI50)之间存在相关性,并建立了标准曲线。同时,由于病毒诱导的CI下降与细胞病变效应相关,因此采用改进的Spearman和Kärber方法定量感染滴度。每次稀释4、8和16个孔时,估计不确定度分别为0.57、0.36和0.26 log10。因此,在食品和环境病毒学领域,RTCA检测是一个强大的工具,它大大简化了工作流程,可以进行有效的风险评估。
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
CiteScore
5.80
自引率
0.00%
发文量
209
审稿时长
41 days
期刊介绍: The Journal of Virological Methods focuses on original, high quality research papers that describe novel and comprehensively tested methods which enhance human, animal, plant, bacterial or environmental virology and prions research and discovery. The methods may include, but not limited to, the study of: Viral components and morphology- Virus isolation, propagation and development of viral vectors- Viral pathogenesis, oncogenesis, vaccines and antivirals- Virus replication, host-pathogen interactions and responses- Virus transmission, prevention, control and treatment- Viral metagenomics and virome- Virus ecology, adaption and evolution- Applied virology such as nanotechnology- Viral diagnosis with novelty and comprehensive evaluation. We seek articles, systematic reviews, meta-analyses and laboratory protocols that include comprehensive technical details with statistical confirmations that provide validations against current best practice, international standards or quality assurance programs and which advance knowledge in virology leading to improved medical, veterinary or agricultural practices and management.
期刊最新文献
PEG-8000 precipitation as a rapid method for enrichment and purification of feline calicivirus Transfer factor from REV-challenged chicken spleens enhances protection against reticuloendotheliosis virus infection in chicks Detection of jeilongvirus circulation in Finnish urban rat populations by a novel pan-jeilong-RT-qPCR Rethinking classical swine fever virus phylogenetics: NS3 Outperforms traditional gene markers Rapid and sensitive SYBR Green-based RT-qPCR assays for the detection and quantification of mink coronavirus
×
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:604180095
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