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A universal microarray for detection of SARS coronavirus
Severe acute respiratory syndrome (SARS) is caused by the SARS coronavirus (SARS-CoV). There are many point mutations among SARS-CoV genome sequences. Previous studies suggested that the mutations are correlated closely with the SARS epidemic. It was found that the bases of six nucleotide positions...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112900/ https://www.ncbi.nlm.nih.gov/pubmed/15350733 http://dx.doi.org/10.1016/j.jviromet.2004.06.016 |
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author | Long, Wei-Hong Xiao, Hua-Sheng Gu, Xiao-Mei Zhang, Qing-Hua Yang, Hong-Jun Zhao, Guo-Ping Liu, Jian-Hua |
author_facet | Long, Wei-Hong Xiao, Hua-Sheng Gu, Xiao-Mei Zhang, Qing-Hua Yang, Hong-Jun Zhao, Guo-Ping Liu, Jian-Hua |
author_sort | Long, Wei-Hong |
collection | PubMed |
description | Severe acute respiratory syndrome (SARS) is caused by the SARS coronavirus (SARS-CoV). There are many point mutations among SARS-CoV genome sequences. Previous studies suggested that the mutations are correlated closely with the SARS epidemic. It was found that the bases of six nucleotide positions (nt9404, nt9479, nt19838, nt21721, nt22222 and nt27827) with high-mutation rate have an important relationship with the SARS epidemic. For viral detection as well as genotyping, a universal microarray system was developed that combines RT-PCR and ligase detection reaction (LDR). The Zip Codes attached covalently to a slide remain constant and their complementary Zip Codes (cZip Codes) can be used for tagging target sequence, making the microarrays universal. The discriminating oligonucleotides contain on the 5′ end “cZip Codes” that are used to direct LDR product to specific Zip Codes attached covalently to a slide. Since Zip Codes have no homology to either the target sequence or to other sequences in the genomes of both human host and SARS-CoV, there was no false signal due to mismatch hybridizations. 20 samples assayed with the universal microarray were confirmed by DNA sequencing, demonstrating that this microarray system is a promising diagnostic tool for detection and genotyping of the SARS-CoV. |
format | Online Article Text |
id | pubmed-7112900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71129002020-04-02 A universal microarray for detection of SARS coronavirus Long, Wei-Hong Xiao, Hua-Sheng Gu, Xiao-Mei Zhang, Qing-Hua Yang, Hong-Jun Zhao, Guo-Ping Liu, Jian-Hua J Virol Methods Article Severe acute respiratory syndrome (SARS) is caused by the SARS coronavirus (SARS-CoV). There are many point mutations among SARS-CoV genome sequences. Previous studies suggested that the mutations are correlated closely with the SARS epidemic. It was found that the bases of six nucleotide positions (nt9404, nt9479, nt19838, nt21721, nt22222 and nt27827) with high-mutation rate have an important relationship with the SARS epidemic. For viral detection as well as genotyping, a universal microarray system was developed that combines RT-PCR and ligase detection reaction (LDR). The Zip Codes attached covalently to a slide remain constant and their complementary Zip Codes (cZip Codes) can be used for tagging target sequence, making the microarrays universal. The discriminating oligonucleotides contain on the 5′ end “cZip Codes” that are used to direct LDR product to specific Zip Codes attached covalently to a slide. Since Zip Codes have no homology to either the target sequence or to other sequences in the genomes of both human host and SARS-CoV, there was no false signal due to mismatch hybridizations. 20 samples assayed with the universal microarray were confirmed by DNA sequencing, demonstrating that this microarray system is a promising diagnostic tool for detection and genotyping of the SARS-CoV. Elsevier B.V. 2004-10 2004-08-04 /pmc/articles/PMC7112900/ /pubmed/15350733 http://dx.doi.org/10.1016/j.jviromet.2004.06.016 Text en Copyright © 2004 Elsevier B.V. All rights reserved. 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 Long, Wei-Hong Xiao, Hua-Sheng Gu, Xiao-Mei Zhang, Qing-Hua Yang, Hong-Jun Zhao, Guo-Ping Liu, Jian-Hua A universal microarray for detection of SARS coronavirus |
title | A universal microarray for detection of SARS coronavirus |
title_full | A universal microarray for detection of SARS coronavirus |
title_fullStr | A universal microarray for detection of SARS coronavirus |
title_full_unstemmed | A universal microarray for detection of SARS coronavirus |
title_short | A universal microarray for detection of SARS coronavirus |
title_sort | universal microarray for detection of sars coronavirus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112900/ https://www.ncbi.nlm.nih.gov/pubmed/15350733 http://dx.doi.org/10.1016/j.jviromet.2004.06.016 |
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