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A sensitive and specific antigen detection assay for Middle East respiratory syndrome coronavirus

Since its emergence in 2012, more than 900 laboratory-confirmed cases of Middle East respiratory syndrome (MERS) have been reported with a fatality rate of more than 30%. However, no antigen detection assay for commercial use is available for diagnosis. In this study, the full-length nucleocapsid pr...

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Autores principales: Chen, Yixin, Chan, Kwok-Hung, Kang, Yahong, Chen, Honglin, Luk, Hayes KH, Poon, Rosana WS, Chan, Jasper FW, Yuen, Kwok-Yung, Xia, Ningshao, Lau, Susanna KP, Woo, Patrick CY
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4575394/
https://www.ncbi.nlm.nih.gov/pubmed/26421268
http://dx.doi.org/10.1038/emi.2015.26
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author Chen, Yixin
Chan, Kwok-Hung
Kang, Yahong
Chen, Honglin
Luk, Hayes KH
Poon, Rosana WS
Chan, Jasper FW
Yuen, Kwok-Yung
Xia, Ningshao
Lau, Susanna KP
Woo, Patrick CY
author_facet Chen, Yixin
Chan, Kwok-Hung
Kang, Yahong
Chen, Honglin
Luk, Hayes KH
Poon, Rosana WS
Chan, Jasper FW
Yuen, Kwok-Yung
Xia, Ningshao
Lau, Susanna KP
Woo, Patrick CY
author_sort Chen, Yixin
collection PubMed
description Since its emergence in 2012, more than 900 laboratory-confirmed cases of Middle East respiratory syndrome (MERS) have been reported with a fatality rate of more than 30%. However, no antigen detection assay for commercial use is available for diagnosis. In this study, the full-length nucleocapsid protein (NP) gene of MERS coronavirus (MERS-CoV) was cloned and expressed in Escherichia coli. A MERS-CoV NP capture enzyme-linked immunosorbent assay (ELISA) using two MERS-CoV-NP-specific monoclonal antibodies (MAbs) generated was developed. The ELISA was evaluated using 129 nasopharyngeal aspirates (NPAs) positive for various respiratory viruses and simulated positive NPAs by adding serial dilutions of MERS-CoV. Using a cutoff OD of 0.19, all 129 NPAs positive for respiratory viruses showed very low OD, with a specificity of 100%. For the two simulated MERS-CoV-positive NPAs with serial dilutions of live MERS-CoV, all samples with ≥10 50% tissue culture infective dose (TCID(50))/0.1 mL showed positive results. For the 10 additional NPAs with 20 and 200 TCID(50)/0.1 mL of live MERS-CoV added, all were positive. A highly sensitive and specific MAbs-based antigen capture ELISA has been developed for MERS. This sensitive and specific antigen capture ELISA should be useful for detection of MERS-CoV in human and dromedaries and in field studies.
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spelling pubmed-45753942015-09-29 A sensitive and specific antigen detection assay for Middle East respiratory syndrome coronavirus Chen, Yixin Chan, Kwok-Hung Kang, Yahong Chen, Honglin Luk, Hayes KH Poon, Rosana WS Chan, Jasper FW Yuen, Kwok-Yung Xia, Ningshao Lau, Susanna KP Woo, Patrick CY Emerg Microbes Infect Original Article Since its emergence in 2012, more than 900 laboratory-confirmed cases of Middle East respiratory syndrome (MERS) have been reported with a fatality rate of more than 30%. However, no antigen detection assay for commercial use is available for diagnosis. In this study, the full-length nucleocapsid protein (NP) gene of MERS coronavirus (MERS-CoV) was cloned and expressed in Escherichia coli. A MERS-CoV NP capture enzyme-linked immunosorbent assay (ELISA) using two MERS-CoV-NP-specific monoclonal antibodies (MAbs) generated was developed. The ELISA was evaluated using 129 nasopharyngeal aspirates (NPAs) positive for various respiratory viruses and simulated positive NPAs by adding serial dilutions of MERS-CoV. Using a cutoff OD of 0.19, all 129 NPAs positive for respiratory viruses showed very low OD, with a specificity of 100%. For the two simulated MERS-CoV-positive NPAs with serial dilutions of live MERS-CoV, all samples with ≥10 50% tissue culture infective dose (TCID(50))/0.1 mL showed positive results. For the 10 additional NPAs with 20 and 200 TCID(50)/0.1 mL of live MERS-CoV added, all were positive. A highly sensitive and specific MAbs-based antigen capture ELISA has been developed for MERS. This sensitive and specific antigen capture ELISA should be useful for detection of MERS-CoV in human and dromedaries and in field studies. Nature Publishing Group 2015-04 2015-04-22 /pmc/articles/PMC4575394/ /pubmed/26421268 http://dx.doi.org/10.1038/emi.2015.26 Text en Copyright © 2015 Shanghai Shangyixun Cultural Communication Co., Ltd http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permissing from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Original Article
Chen, Yixin
Chan, Kwok-Hung
Kang, Yahong
Chen, Honglin
Luk, Hayes KH
Poon, Rosana WS
Chan, Jasper FW
Yuen, Kwok-Yung
Xia, Ningshao
Lau, Susanna KP
Woo, Patrick CY
A sensitive and specific antigen detection assay for Middle East respiratory syndrome coronavirus
title A sensitive and specific antigen detection assay for Middle East respiratory syndrome coronavirus
title_full A sensitive and specific antigen detection assay for Middle East respiratory syndrome coronavirus
title_fullStr A sensitive and specific antigen detection assay for Middle East respiratory syndrome coronavirus
title_full_unstemmed A sensitive and specific antigen detection assay for Middle East respiratory syndrome coronavirus
title_short A sensitive and specific antigen detection assay for Middle East respiratory syndrome coronavirus
title_sort sensitive and specific antigen detection assay for middle east respiratory syndrome coronavirus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4575394/
https://www.ncbi.nlm.nih.gov/pubmed/26421268
http://dx.doi.org/10.1038/emi.2015.26
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