Designing and expression of novel recombinant fusion protein for efficient antigen screening of SARS-CoV-2.

IF 3.5 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY AMB Express Pub Date : 2024-07-11 DOI:10.1186/s13568-024-01719-y
G Vinaya Chandu Vidyasagar, P V Janardhan Reddy, M Md Ghouse, T C Venkateswarulu, P B Kavi Kishor, Prashanth Suravajhala, Rathnagiri Polavarapu
{"title":"Designing and expression of novel recombinant fusion protein for efficient antigen screening of SARS-CoV-2.","authors":"G Vinaya Chandu Vidyasagar, P V Janardhan Reddy, M Md Ghouse, T C Venkateswarulu, P B Kavi Kishor, Prashanth Suravajhala, Rathnagiri Polavarapu","doi":"10.1186/s13568-024-01719-y","DOIUrl":null,"url":null,"abstract":"<p><p>Corona virus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), claimed millions globally. After the report of the first incidence of the virus, variants emerged with each posing a unique threat than its predecessors. Though many advanced diagnostic assays like real-time PCR are available for screening of SARS-CoV-2, their applications are being hindered because of accessibility and cost. With the advent of rapid assays for antigenic screening of SARS-CoV-2 made diagnostics far easy as the assays are rapid, cost-effective and can be used at point-of-care settings. In the present study, a fusion construct was made utilising highly immunogenic B cell epitopes from the three important structural proteins of SARS-CoV-2. The protein was expressed; purified capture mAbs generated and rapid antigen assay was developed. Eight hundred and forty nasopharyngeal swab samples were screened for the evaluation of the developed assay which showed 37.14% positivity, 96.51% and 100% sensitivity and specificity respectively. The assay developed was supposed to identify SARS-CoV-2 wild-type as well as variants of concern and variants of importance in real-time conditions.</p>","PeriodicalId":7537,"journal":{"name":"AMB Express","volume":null,"pages":null},"PeriodicalIF":3.5000,"publicationDate":"2024-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11239635/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"AMB Express","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1186/s13568-024-01719-y","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Corona virus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), claimed millions globally. After the report of the first incidence of the virus, variants emerged with each posing a unique threat than its predecessors. Though many advanced diagnostic assays like real-time PCR are available for screening of SARS-CoV-2, their applications are being hindered because of accessibility and cost. With the advent of rapid assays for antigenic screening of SARS-CoV-2 made diagnostics far easy as the assays are rapid, cost-effective and can be used at point-of-care settings. In the present study, a fusion construct was made utilising highly immunogenic B cell epitopes from the three important structural proteins of SARS-CoV-2. The protein was expressed; purified capture mAbs generated and rapid antigen assay was developed. Eight hundred and forty nasopharyngeal swab samples were screened for the evaluation of the developed assay which showed 37.14% positivity, 96.51% and 100% sensitivity and specificity respectively. The assay developed was supposed to identify SARS-CoV-2 wild-type as well as variants of concern and variants of importance in real-time conditions.

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
设计和表达新型重组融合蛋白,用于高效筛选 SARS-CoV-2 抗原。
由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起的 2019 年科罗娜病毒病(COVID-19)大流行夺走了全球数百万人的生命。在报告了该病毒的首次发病后,又出现了一些变种,每种变种都比其前身构成了独特的威胁。尽管有许多先进的诊断方法(如实时 PCR)可用于筛查 SARS-CoV-2 病毒,但它们的应用却因可及性和成本问题而受到阻碍。随着用于 SARS-CoV-2 抗原筛选的快速检测方法的出现,诊断变得容易多了,因为这些检测方法快速、成本效益高,而且可在护理点环境中使用。本研究利用 SARS-CoV-2 三个重要结构蛋白中的高免疫原性 B 细胞表位制作了一个融合构建体。对蛋白进行了表达,生成了纯化的捕获 mAbs,并开发了快速抗原检测方法。对 840 份鼻咽拭子样本进行了筛选,以评估所开发的检测方法,结果显示阳性率为 37.14%,灵敏度和特异性分别为 96.51% 和 100%。所开发的检测方法可在实时条件下识别 SARS-CoV-2 野生型以及令人担忧的变种和重要变种。
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
AMB Express
AMB Express BIOTECHNOLOGY & APPLIED MICROBIOLOGY-
CiteScore
7.20
自引率
2.70%
发文量
141
审稿时长
13 weeks
期刊介绍: AMB Express is a high quality journal that brings together research in the area of Applied and Industrial Microbiology with a particular interest in ''White Biotechnology'' and ''Red Biotechnology''. The emphasis is on processes employing microorganisms, eukaryotic cell cultures or enzymes for the biosynthesis, transformation and degradation of compounds. This includes fine and bulk chemicals, polymeric compounds and enzymes or other proteins. Downstream processes are also considered. Integrated processes combining biochemical and chemical processes are also published.
期刊最新文献
Compatibility and antimicrobial activity of silver nanoparticles synthesized using Lycopersicon esculentum peels. Scaling up production of cephalosporin C by Acremonium chrysogenum W42-I in a fermenter using submerged fermentation. Nano selenium in broiler feeding: physiological roles and nutritional effects. Crotalaria madurensis flavonol glycosides' antibacterial activity against Staphylococcus aureus. In vitro antibacterial activity of photoactivated flavonoid glycosides against Acinetobacter baumannii.
×
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