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Nucleic acid sequence-based amplification methods to detect avian influenza virus
Infection of poultry with highly pathogenic avian influenza virus (AIV) can be devastating in terms of flock morbidity and mortality, economic loss, and social disruption. The causative agent is confined to certain isolates of influenza A virus subtypes H5 and H7. Due to the potential of direct tran...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111163/ https://www.ncbi.nlm.nih.gov/pubmed/14684165 http://dx.doi.org/10.1016/j.bbrc.2003.11.131 |
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author | Lau, Lok-Ting Banks, Jill Aherne, Rebecca Brown, Ian H. Dillon, Natalie Collins, Richard A. Chan, Ka-Yun Fung, Yin-Wan Wendy Xing, Jun Yu, Albert C.H. |
author_facet | Lau, Lok-Ting Banks, Jill Aherne, Rebecca Brown, Ian H. Dillon, Natalie Collins, Richard A. Chan, Ka-Yun Fung, Yin-Wan Wendy Xing, Jun Yu, Albert C.H. |
author_sort | Lau, Lok-Ting |
collection | PubMed |
description | Infection of poultry with highly pathogenic avian influenza virus (AIV) can be devastating in terms of flock morbidity and mortality, economic loss, and social disruption. The causative agent is confined to certain isolates of influenza A virus subtypes H5 and H7. Due to the potential of direct transfer of avian influenza to humans, continued research into rapid diagnostic tests for influenza is therefore necessary. A nucleic acid sequence-based amplification (NASBA) method was developed to detect a portion of the haemagglutinin gene of avian influenza A virus subtypes H5 and H7 irrespective of lineage. A further NASBA assay, based on the matrix gene, was able to detect examples of all known subtypes (H1–H15) of avian influenza virus. The entire nucleic acid isolation, amplification, and detection procedure was completed within 6 h. The dynamic range of the three AIV assays was five to seven orders of magnitude. The assays were sensitive and highly specific, with no cross-reactivity to phylogenetically or clinically relevant viruses. The results of the three AIV NASBA assays correlated with those obtained by viral culture in embryonated fowl’s eggs. |
format | Online Article Text |
id | pubmed-7111163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71111632020-04-02 Nucleic acid sequence-based amplification methods to detect avian influenza virus Lau, Lok-Ting Banks, Jill Aherne, Rebecca Brown, Ian H. Dillon, Natalie Collins, Richard A. Chan, Ka-Yun Fung, Yin-Wan Wendy Xing, Jun Yu, Albert C.H. Biochem Biophys Res Commun Article Infection of poultry with highly pathogenic avian influenza virus (AIV) can be devastating in terms of flock morbidity and mortality, economic loss, and social disruption. The causative agent is confined to certain isolates of influenza A virus subtypes H5 and H7. Due to the potential of direct transfer of avian influenza to humans, continued research into rapid diagnostic tests for influenza is therefore necessary. A nucleic acid sequence-based amplification (NASBA) method was developed to detect a portion of the haemagglutinin gene of avian influenza A virus subtypes H5 and H7 irrespective of lineage. A further NASBA assay, based on the matrix gene, was able to detect examples of all known subtypes (H1–H15) of avian influenza virus. The entire nucleic acid isolation, amplification, and detection procedure was completed within 6 h. The dynamic range of the three AIV assays was five to seven orders of magnitude. The assays were sensitive and highly specific, with no cross-reactivity to phylogenetically or clinically relevant viruses. The results of the three AIV NASBA assays correlated with those obtained by viral culture in embryonated fowl’s eggs. Elsevier Inc. 2004-01-09 2003-12-05 /pmc/articles/PMC7111163/ /pubmed/14684165 http://dx.doi.org/10.1016/j.bbrc.2003.11.131 Text en Copyright © 2003 Elsevier Inc. 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 Lau, Lok-Ting Banks, Jill Aherne, Rebecca Brown, Ian H. Dillon, Natalie Collins, Richard A. Chan, Ka-Yun Fung, Yin-Wan Wendy Xing, Jun Yu, Albert C.H. Nucleic acid sequence-based amplification methods to detect avian influenza virus |
title | Nucleic acid sequence-based amplification methods to detect avian influenza virus |
title_full | Nucleic acid sequence-based amplification methods to detect avian influenza virus |
title_fullStr | Nucleic acid sequence-based amplification methods to detect avian influenza virus |
title_full_unstemmed | Nucleic acid sequence-based amplification methods to detect avian influenza virus |
title_short | Nucleic acid sequence-based amplification methods to detect avian influenza virus |
title_sort | nucleic acid sequence-based amplification methods to detect avian influenza virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111163/ https://www.ncbi.nlm.nih.gov/pubmed/14684165 http://dx.doi.org/10.1016/j.bbrc.2003.11.131 |
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