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A Rapid Zika Diagnostic Assay to Measure Neutralizing Antibodies in Patients
The potential association of microcephaly and other congenital abnormalities with Zika virus (ZIKV) infection during pregnancy underlines the critical need for a rapid and accurate diagnosis. Due to the short duration of ZIKV viremia in infected patients, a serologic assay that detects antibody resp...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360589/ https://www.ncbi.nlm.nih.gov/pubmed/28283425 http://dx.doi.org/10.1016/j.ebiom.2017.03.006 |
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author | Shan, Chao Xie, Xuping Ren, Ping Loeffelholz, Michael J. Yang, Yujiao Furuya, Andrea Dupuis, Alan P. Kramer, Laura D. Wong, Susan J. Shi, Pei-Yong |
author_facet | Shan, Chao Xie, Xuping Ren, Ping Loeffelholz, Michael J. Yang, Yujiao Furuya, Andrea Dupuis, Alan P. Kramer, Laura D. Wong, Susan J. Shi, Pei-Yong |
author_sort | Shan, Chao |
collection | PubMed |
description | The potential association of microcephaly and other congenital abnormalities with Zika virus (ZIKV) infection during pregnancy underlines the critical need for a rapid and accurate diagnosis. Due to the short duration of ZIKV viremia in infected patients, a serologic assay that detects antibody responses to viral infection plays an essential role in diagnosing patient specimens. The current serologic diagnosis of ZIKV infection relies heavily on the labor-intensive Plaque Reduction Neutralization Test (PRNT) that requires more than one-week turnaround time and represents a major bottleneck for patient diagnosis. To overcome this limitation, we have developed a high-throughput assay for ZIKV and dengue virus (DENV) diagnosis that can attain the “gold standard” of the current PRNT assay. The new assay is homogeneous and utilizes luciferase viruses to quantify the neutralizing antibody titers in a 96-well format. Using 91 human specimens, we showed that the reporter diagnostic assay has a higher dynamic range and maintains the relative specificity of the traditional PRNT assay. Besides the improvement of assay throughput, the reporter virus technology has also shortened the turnaround time to less than two days. Collectively, our results suggest that, along with the viral RT-PCR assay, the reporter virus-based serologic assay could be potentially used as the first-line test for clinical diagnosis of ZIKV infection as well as for vaccine clinical trials. |
format | Online Article Text |
id | pubmed-5360589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-53605892017-03-30 A Rapid Zika Diagnostic Assay to Measure Neutralizing Antibodies in Patients Shan, Chao Xie, Xuping Ren, Ping Loeffelholz, Michael J. Yang, Yujiao Furuya, Andrea Dupuis, Alan P. Kramer, Laura D. Wong, Susan J. Shi, Pei-Yong EBioMedicine Research Paper The potential association of microcephaly and other congenital abnormalities with Zika virus (ZIKV) infection during pregnancy underlines the critical need for a rapid and accurate diagnosis. Due to the short duration of ZIKV viremia in infected patients, a serologic assay that detects antibody responses to viral infection plays an essential role in diagnosing patient specimens. The current serologic diagnosis of ZIKV infection relies heavily on the labor-intensive Plaque Reduction Neutralization Test (PRNT) that requires more than one-week turnaround time and represents a major bottleneck for patient diagnosis. To overcome this limitation, we have developed a high-throughput assay for ZIKV and dengue virus (DENV) diagnosis that can attain the “gold standard” of the current PRNT assay. The new assay is homogeneous and utilizes luciferase viruses to quantify the neutralizing antibody titers in a 96-well format. Using 91 human specimens, we showed that the reporter diagnostic assay has a higher dynamic range and maintains the relative specificity of the traditional PRNT assay. Besides the improvement of assay throughput, the reporter virus technology has also shortened the turnaround time to less than two days. Collectively, our results suggest that, along with the viral RT-PCR assay, the reporter virus-based serologic assay could be potentially used as the first-line test for clinical diagnosis of ZIKV infection as well as for vaccine clinical trials. Elsevier 2017-03-04 /pmc/articles/PMC5360589/ /pubmed/28283425 http://dx.doi.org/10.1016/j.ebiom.2017.03.006 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Shan, Chao Xie, Xuping Ren, Ping Loeffelholz, Michael J. Yang, Yujiao Furuya, Andrea Dupuis, Alan P. Kramer, Laura D. Wong, Susan J. Shi, Pei-Yong A Rapid Zika Diagnostic Assay to Measure Neutralizing Antibodies in Patients |
title | A Rapid Zika Diagnostic Assay to Measure Neutralizing Antibodies in Patients |
title_full | A Rapid Zika Diagnostic Assay to Measure Neutralizing Antibodies in Patients |
title_fullStr | A Rapid Zika Diagnostic Assay to Measure Neutralizing Antibodies in Patients |
title_full_unstemmed | A Rapid Zika Diagnostic Assay to Measure Neutralizing Antibodies in Patients |
title_short | A Rapid Zika Diagnostic Assay to Measure Neutralizing Antibodies in Patients |
title_sort | rapid zika diagnostic assay to measure neutralizing antibodies in patients |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360589/ https://www.ncbi.nlm.nih.gov/pubmed/28283425 http://dx.doi.org/10.1016/j.ebiom.2017.03.006 |
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