Cargando…

Development of immunoglobulin G enzyme-linked immunosorbent assay for the serodiagnosis of severe acute respiratory syndrome

Severe acute respiratory syndrome (SARS) is an emerging infectious disease caused by a novel SARS-associated coronavirus (SARS-CoV). The clinical characteristics are high fever, rapidly progressive diffuse pneumonitis and respiratory distress. It is highly infectious through intimate contact or dire...

Descripción completa

Detalles Bibliográficos
Autores principales: Shao, Pei-Lan, Hsueh, Po-Ren, Chang, Luan-Yin, Lu, Chun-Yi, Kao, Chuan-Liang, Chiang, Yu-Ping, Huang, Hsiang-Yi, Huang, Fu-Yuan, Lee, Chin-Yun, Chang, Lung-Ji, Wu, T.-C., Huang, Li-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kluwer Academic Publishers 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088774/
https://www.ncbi.nlm.nih.gov/pubmed/15864739
http://dx.doi.org/10.1007/s11373-004-8184-6
_version_ 1783509608874115072
author Shao, Pei-Lan
Hsueh, Po-Ren
Chang, Luan-Yin
Lu, Chun-Yi
Kao, Chuan-Liang
Chiang, Yu-Ping
Huang, Hsiang-Yi
Huang, Fu-Yuan
Lee, Chin-Yun
Chang, Lung-Ji
Wu, T.-C.
Huang, Li-Min
author_facet Shao, Pei-Lan
Hsueh, Po-Ren
Chang, Luan-Yin
Lu, Chun-Yi
Kao, Chuan-Liang
Chiang, Yu-Ping
Huang, Hsiang-Yi
Huang, Fu-Yuan
Lee, Chin-Yun
Chang, Lung-Ji
Wu, T.-C.
Huang, Li-Min
author_sort Shao, Pei-Lan
collection PubMed
description Severe acute respiratory syndrome (SARS) is an emerging infectious disease caused by a novel SARS-associated coronavirus (SARS-CoV). The clinical characteristics are high fever, rapidly progressive diffuse pneumonitis and respiratory distress. It is highly infectious through intimate contact or direct contact with infectious body fluids. Outbreaks within communities and hospitals have been reported. Development of rapid and reliable diagnostic tools is urgently needed. We developed an immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA), using whole virus antigen of SARS-CoV. Eighty-six serum samples collected from patients who were hospitalized for other causes were examined to determine the cut-off O.D. value. The cut-off O.D. value was defined as 0.175 by calculating the mean O.D. value of the 86 sera plus 3 standard deviations. To determine the sensitivity and specificity of the ELISA, 56 positive sera and 204 negative sera were tested. The sensitivity was 96.4% and the specificity was 100%. The results suggest that the IgG ELISA using whole virus antigen of SARS-CoV has a high sensitivity and specificity in detecting SARS IgG antibodies. This IgG ELISA is a powerful tool for serodiagnosis of SARS.
format Online
Article
Text
id pubmed-7088774
institution National Center for Biotechnology Information
language English
publishDate 2005
publisher Kluwer Academic Publishers
record_format MEDLINE/PubMed
spelling pubmed-70887742020-03-23 Development of immunoglobulin G enzyme-linked immunosorbent assay for the serodiagnosis of severe acute respiratory syndrome Shao, Pei-Lan Hsueh, Po-Ren Chang, Luan-Yin Lu, Chun-Yi Kao, Chuan-Liang Chiang, Yu-Ping Huang, Hsiang-Yi Huang, Fu-Yuan Lee, Chin-Yun Chang, Lung-Ji Wu, T.-C. Huang, Li-Min J Biomed Sci Article Severe acute respiratory syndrome (SARS) is an emerging infectious disease caused by a novel SARS-associated coronavirus (SARS-CoV). The clinical characteristics are high fever, rapidly progressive diffuse pneumonitis and respiratory distress. It is highly infectious through intimate contact or direct contact with infectious body fluids. Outbreaks within communities and hospitals have been reported. Development of rapid and reliable diagnostic tools is urgently needed. We developed an immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA), using whole virus antigen of SARS-CoV. Eighty-six serum samples collected from patients who were hospitalized for other causes were examined to determine the cut-off O.D. value. The cut-off O.D. value was defined as 0.175 by calculating the mean O.D. value of the 86 sera plus 3 standard deviations. To determine the sensitivity and specificity of the ELISA, 56 positive sera and 204 negative sera were tested. The sensitivity was 96.4% and the specificity was 100%. The results suggest that the IgG ELISA using whole virus antigen of SARS-CoV has a high sensitivity and specificity in detecting SARS IgG antibodies. This IgG ELISA is a powerful tool for serodiagnosis of SARS. Kluwer Academic Publishers 2005-02-04 2005-01 /pmc/articles/PMC7088774/ /pubmed/15864739 http://dx.doi.org/10.1007/s11373-004-8184-6 Text en © National Science Council, Taipei 2005 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Shao, Pei-Lan
Hsueh, Po-Ren
Chang, Luan-Yin
Lu, Chun-Yi
Kao, Chuan-Liang
Chiang, Yu-Ping
Huang, Hsiang-Yi
Huang, Fu-Yuan
Lee, Chin-Yun
Chang, Lung-Ji
Wu, T.-C.
Huang, Li-Min
Development of immunoglobulin G enzyme-linked immunosorbent assay for the serodiagnosis of severe acute respiratory syndrome
title Development of immunoglobulin G enzyme-linked immunosorbent assay for the serodiagnosis of severe acute respiratory syndrome
title_full Development of immunoglobulin G enzyme-linked immunosorbent assay for the serodiagnosis of severe acute respiratory syndrome
title_fullStr Development of immunoglobulin G enzyme-linked immunosorbent assay for the serodiagnosis of severe acute respiratory syndrome
title_full_unstemmed Development of immunoglobulin G enzyme-linked immunosorbent assay for the serodiagnosis of severe acute respiratory syndrome
title_short Development of immunoglobulin G enzyme-linked immunosorbent assay for the serodiagnosis of severe acute respiratory syndrome
title_sort development of immunoglobulin g enzyme-linked immunosorbent assay for the serodiagnosis of severe acute respiratory syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088774/
https://www.ncbi.nlm.nih.gov/pubmed/15864739
http://dx.doi.org/10.1007/s11373-004-8184-6
work_keys_str_mv AT shaopeilan developmentofimmunoglobulingenzymelinkedimmunosorbentassayfortheserodiagnosisofsevereacuterespiratorysyndrome
AT hsuehporen developmentofimmunoglobulingenzymelinkedimmunosorbentassayfortheserodiagnosisofsevereacuterespiratorysyndrome
AT changluanyin developmentofimmunoglobulingenzymelinkedimmunosorbentassayfortheserodiagnosisofsevereacuterespiratorysyndrome
AT luchunyi developmentofimmunoglobulingenzymelinkedimmunosorbentassayfortheserodiagnosisofsevereacuterespiratorysyndrome
AT kaochuanliang developmentofimmunoglobulingenzymelinkedimmunosorbentassayfortheserodiagnosisofsevereacuterespiratorysyndrome
AT chiangyuping developmentofimmunoglobulingenzymelinkedimmunosorbentassayfortheserodiagnosisofsevereacuterespiratorysyndrome
AT huanghsiangyi developmentofimmunoglobulingenzymelinkedimmunosorbentassayfortheserodiagnosisofsevereacuterespiratorysyndrome
AT huangfuyuan developmentofimmunoglobulingenzymelinkedimmunosorbentassayfortheserodiagnosisofsevereacuterespiratorysyndrome
AT leechinyun developmentofimmunoglobulingenzymelinkedimmunosorbentassayfortheserodiagnosisofsevereacuterespiratorysyndrome
AT changlungji developmentofimmunoglobulingenzymelinkedimmunosorbentassayfortheserodiagnosisofsevereacuterespiratorysyndrome
AT wutc developmentofimmunoglobulingenzymelinkedimmunosorbentassayfortheserodiagnosisofsevereacuterespiratorysyndrome
AT huanglimin developmentofimmunoglobulingenzymelinkedimmunosorbentassayfortheserodiagnosisofsevereacuterespiratorysyndrome