Cargando…

Development and evaluation of an enzyme-linked immunosorbent assay for detection of antibodies against the spike protein of SARS-coronavirus

BACKGROUND: Severe acute respiratory syndrome (SARS) is caused by infection with SARS-associated coronavirus (CoV). Amino acid residues 450–650 of the spike (S) glycoprotein of SARS-CoV (S450-650) contains dominant epitopes for anti-viral antibodies (Abs) in patient sera. OBJECTIVES: To develop and...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Jincun, Wang, Wei, Wang, Guang-Fa, Li, Yonghua, Zhuang, Hui, Xu, Xiaoyuan, Ren, Furong, Zhao, Zhendong, Gao, Xiao-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7108335/
https://www.ncbi.nlm.nih.gov/pubmed/15797360
http://dx.doi.org/10.1016/j.jcv.2004.09.024
_version_ 1783512790302982144
author Zhao, Jincun
Wang, Wei
Wang, Guang-Fa
Li, Yonghua
Zhuang, Hui
Xu, Xiaoyuan
Ren, Furong
Zhao, Zhendong
Gao, Xiao-Ming
author_facet Zhao, Jincun
Wang, Wei
Wang, Guang-Fa
Li, Yonghua
Zhuang, Hui
Xu, Xiaoyuan
Ren, Furong
Zhao, Zhendong
Gao, Xiao-Ming
author_sort Zhao, Jincun
collection PubMed
description BACKGROUND: Severe acute respiratory syndrome (SARS) is caused by infection with SARS-associated coronavirus (CoV). Amino acid residues 450–650 of the spike (S) glycoprotein of SARS-CoV (S450-650) contains dominant epitopes for anti-viral antibodies (Abs) in patient sera. OBJECTIVES: To develop and evaluate an ELISA system for detection of anti-S Abs in patient sera. STUDY DESIGN: Express recombinant S450-650 in E. Coli and evaluate the sensitivity and specificity of an ELISA system based on the S450-650 polypeptide. RESULTS: The S450-650-based ELISA detected IgG Abs in 41 out of 51 serum samples from 22 hospitalized patients with probable SARS, a result closely correlated with that obtained with a virus-based ELISA (r = 0.75, k = 0.8). Differential anti-S IgG responses were observed amongst SARS patients. Some of them produced anti-S Abs early during their infection, while others failed to make IgG Abs against the S450-650 polypeptide. None of the serum samples from 100 healthy blood donors was positive in the S450-650-based assay. CONCLUSION: The S450-650-based ELISA can detect anti-S IgG Abs with high sensitivity and specificity.
format Online
Article
Text
id pubmed-7108335
institution National Center for Biotechnology Information
language English
publishDate 2005
publisher Published by Elsevier B.V.
record_format MEDLINE/PubMed
spelling pubmed-71083352020-03-31 Development and evaluation of an enzyme-linked immunosorbent assay for detection of antibodies against the spike protein of SARS-coronavirus Zhao, Jincun Wang, Wei Wang, Guang-Fa Li, Yonghua Zhuang, Hui Xu, Xiaoyuan Ren, Furong Zhao, Zhendong Gao, Xiao-Ming J Clin Virol Article BACKGROUND: Severe acute respiratory syndrome (SARS) is caused by infection with SARS-associated coronavirus (CoV). Amino acid residues 450–650 of the spike (S) glycoprotein of SARS-CoV (S450-650) contains dominant epitopes for anti-viral antibodies (Abs) in patient sera. OBJECTIVES: To develop and evaluate an ELISA system for detection of anti-S Abs in patient sera. STUDY DESIGN: Express recombinant S450-650 in E. Coli and evaluate the sensitivity and specificity of an ELISA system based on the S450-650 polypeptide. RESULTS: The S450-650-based ELISA detected IgG Abs in 41 out of 51 serum samples from 22 hospitalized patients with probable SARS, a result closely correlated with that obtained with a virus-based ELISA (r = 0.75, k = 0.8). Differential anti-S IgG responses were observed amongst SARS patients. Some of them produced anti-S Abs early during their infection, while others failed to make IgG Abs against the S450-650 polypeptide. None of the serum samples from 100 healthy blood donors was positive in the S450-650-based assay. CONCLUSION: The S450-650-based ELISA can detect anti-S IgG Abs with high sensitivity and specificity. Published by Elsevier B.V. 2005-05 2004-11-23 /pmc/articles/PMC7108335/ /pubmed/15797360 http://dx.doi.org/10.1016/j.jcv.2004.09.024 Text en Copyright © 2004 Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Zhao, Jincun
Wang, Wei
Wang, Guang-Fa
Li, Yonghua
Zhuang, Hui
Xu, Xiaoyuan
Ren, Furong
Zhao, Zhendong
Gao, Xiao-Ming
Development and evaluation of an enzyme-linked immunosorbent assay for detection of antibodies against the spike protein of SARS-coronavirus
title Development and evaluation of an enzyme-linked immunosorbent assay for detection of antibodies against the spike protein of SARS-coronavirus
title_full Development and evaluation of an enzyme-linked immunosorbent assay for detection of antibodies against the spike protein of SARS-coronavirus
title_fullStr Development and evaluation of an enzyme-linked immunosorbent assay for detection of antibodies against the spike protein of SARS-coronavirus
title_full_unstemmed Development and evaluation of an enzyme-linked immunosorbent assay for detection of antibodies against the spike protein of SARS-coronavirus
title_short Development and evaluation of an enzyme-linked immunosorbent assay for detection of antibodies against the spike protein of SARS-coronavirus
title_sort development and evaluation of an enzyme-linked immunosorbent assay for detection of antibodies against the spike protein of sars-coronavirus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7108335/
https://www.ncbi.nlm.nih.gov/pubmed/15797360
http://dx.doi.org/10.1016/j.jcv.2004.09.024
work_keys_str_mv AT zhaojincun developmentandevaluationofanenzymelinkedimmunosorbentassayfordetectionofantibodiesagainstthespikeproteinofsarscoronavirus
AT wangwei developmentandevaluationofanenzymelinkedimmunosorbentassayfordetectionofantibodiesagainstthespikeproteinofsarscoronavirus
AT wangguangfa developmentandevaluationofanenzymelinkedimmunosorbentassayfordetectionofantibodiesagainstthespikeproteinofsarscoronavirus
AT liyonghua developmentandevaluationofanenzymelinkedimmunosorbentassayfordetectionofantibodiesagainstthespikeproteinofsarscoronavirus
AT zhuanghui developmentandevaluationofanenzymelinkedimmunosorbentassayfordetectionofantibodiesagainstthespikeproteinofsarscoronavirus
AT xuxiaoyuan developmentandevaluationofanenzymelinkedimmunosorbentassayfordetectionofantibodiesagainstthespikeproteinofsarscoronavirus
AT renfurong developmentandevaluationofanenzymelinkedimmunosorbentassayfordetectionofantibodiesagainstthespikeproteinofsarscoronavirus
AT zhaozhendong developmentandevaluationofanenzymelinkedimmunosorbentassayfordetectionofantibodiesagainstthespikeproteinofsarscoronavirus
AT gaoxiaoming developmentandevaluationofanenzymelinkedimmunosorbentassayfordetectionofantibodiesagainstthespikeproteinofsarscoronavirus