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Generation and characterisation of monoclonal antibodies against influenza virus A, subtype H5N1

The emergence of highly pathogenic avian influenza A virus (HPAIV) subtype H5N1 in 1997 has since resulted in large outbreaks in poultry and in transmission from poultry to humans, mostly in southeast Asia, but also in several European countries. Effective diagnosis and control measures are essentia...

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Autores principales: Linke, Sonja, Neubauer, Katrin, Dorner, Martin B., Dorner, Brigitte G., Pauli, Georg, Schweiger, Brunhilde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185612/
https://www.ncbi.nlm.nih.gov/pubmed/21549148
http://dx.doi.org/10.1016/j.jviromet.2011.04.025
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author Linke, Sonja
Neubauer, Katrin
Dorner, Martin B.
Dorner, Brigitte G.
Pauli, Georg
Schweiger, Brunhilde
author_facet Linke, Sonja
Neubauer, Katrin
Dorner, Martin B.
Dorner, Brigitte G.
Pauli, Georg
Schweiger, Brunhilde
author_sort Linke, Sonja
collection PubMed
description The emergence of highly pathogenic avian influenza A virus (HPAIV) subtype H5N1 in 1997 has since resulted in large outbreaks in poultry and in transmission from poultry to humans, mostly in southeast Asia, but also in several European countries. Effective diagnosis and control measures are essential for the management of HPAIV infections. To develop a rapid diagnostic test, a panel of murine monoclonal antibodies (mAbs) against influenza virus A subtype H5 was generated. Eleven mAbs were produced and characterised according to their reactivity by indirect and sandwich ELISA and western blotting against different H5 subtypes representing past and viruses currently circulating. Ten out of 11 mAbs reacted strongly with the haemagglutinin (HA) protein of H5 viruses, whereas one mAb reacted with the M1 protein. Targeted HA protein epitopes seemed to be conformational. One hybridoma clone binds to a linear epitope of the M1 protein. One specific mAb reacts with HPAIV H5 in the immunofluorescence test, and two antibodies neutralised H5 viruses. On the basis of the results, the set of seven mAbs is appropriate for developing diagnostic tests. With the generated mAbs, a sandwich ELISA was developed recognising all H5N1 strains tested but no other influenza viruses. With this ELISA, as little as 0.005 HA units or 0.1 ng/ml H5N1 was detected, surpassing other ELISA tests. The novel reagents have the potential to improve significantly available rapid antigen detection systems.
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spelling pubmed-71856122020-04-28 Generation and characterisation of monoclonal antibodies against influenza virus A, subtype H5N1 Linke, Sonja Neubauer, Katrin Dorner, Martin B. Dorner, Brigitte G. Pauli, Georg Schweiger, Brunhilde J Virol Methods Article The emergence of highly pathogenic avian influenza A virus (HPAIV) subtype H5N1 in 1997 has since resulted in large outbreaks in poultry and in transmission from poultry to humans, mostly in southeast Asia, but also in several European countries. Effective diagnosis and control measures are essential for the management of HPAIV infections. To develop a rapid diagnostic test, a panel of murine monoclonal antibodies (mAbs) against influenza virus A subtype H5 was generated. Eleven mAbs were produced and characterised according to their reactivity by indirect and sandwich ELISA and western blotting against different H5 subtypes representing past and viruses currently circulating. Ten out of 11 mAbs reacted strongly with the haemagglutinin (HA) protein of H5 viruses, whereas one mAb reacted with the M1 protein. Targeted HA protein epitopes seemed to be conformational. One hybridoma clone binds to a linear epitope of the M1 protein. One specific mAb reacts with HPAIV H5 in the immunofluorescence test, and two antibodies neutralised H5 viruses. On the basis of the results, the set of seven mAbs is appropriate for developing diagnostic tests. With the generated mAbs, a sandwich ELISA was developed recognising all H5N1 strains tested but no other influenza viruses. With this ELISA, as little as 0.005 HA units or 0.1 ng/ml H5N1 was detected, surpassing other ELISA tests. The novel reagents have the potential to improve significantly available rapid antigen detection systems. Elsevier B.V. 2011-07 2011-04-28 /pmc/articles/PMC7185612/ /pubmed/21549148 http://dx.doi.org/10.1016/j.jviromet.2011.04.025 Text en Copyright © 2011 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
Linke, Sonja
Neubauer, Katrin
Dorner, Martin B.
Dorner, Brigitte G.
Pauli, Georg
Schweiger, Brunhilde
Generation and characterisation of monoclonal antibodies against influenza virus A, subtype H5N1
title Generation and characterisation of monoclonal antibodies against influenza virus A, subtype H5N1
title_full Generation and characterisation of monoclonal antibodies against influenza virus A, subtype H5N1
title_fullStr Generation and characterisation of monoclonal antibodies against influenza virus A, subtype H5N1
title_full_unstemmed Generation and characterisation of monoclonal antibodies against influenza virus A, subtype H5N1
title_short Generation and characterisation of monoclonal antibodies against influenza virus A, subtype H5N1
title_sort generation and characterisation of monoclonal antibodies against influenza virus a, subtype h5n1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185612/
https://www.ncbi.nlm.nih.gov/pubmed/21549148
http://dx.doi.org/10.1016/j.jviromet.2011.04.025
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