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Characterization of Mouse Monoclonal Antibodies Against the HA of A(H7N9) Influenza Virus

Many cases of human infection with the H7N9 virus have been detected in China since 2013. H7N9 viruses are maintained in chickens and are transmitted to humans at live bird markets. During circulation in birds, H7N9 viruses have accumulated amino acid substitutions in their hemagglutinin (HA), which...

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Autores principales: Ito, Mutsumi, Yamayoshi, Seiya, Murakami, Kazushi, Saito, Kenji, Motojima, Atsuo, Nakaishi, Kazunari, Kawaoka, Yoshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410113/
https://www.ncbi.nlm.nih.gov/pubmed/30754701
http://dx.doi.org/10.3390/v11020149
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author Ito, Mutsumi
Yamayoshi, Seiya
Murakami, Kazushi
Saito, Kenji
Motojima, Atsuo
Nakaishi, Kazunari
Kawaoka, Yoshihiro
author_facet Ito, Mutsumi
Yamayoshi, Seiya
Murakami, Kazushi
Saito, Kenji
Motojima, Atsuo
Nakaishi, Kazunari
Kawaoka, Yoshihiro
author_sort Ito, Mutsumi
collection PubMed
description Many cases of human infection with the H7N9 virus have been detected in China since 2013. H7N9 viruses are maintained in chickens and are transmitted to humans at live bird markets. During circulation in birds, H7N9 viruses have accumulated amino acid substitutions in their hemagglutinin (HA), which resulted in an antigenically change in the recent H7N9 viruses. Here, we characterized 46 mouse monoclonal antibodies against the HA of the prototype strain. 16 H7-HA-specific monoclonal antibodies (mAbs) possessed hemagglutination inhibition (HI) and neutralization activities by recognizing the major antigenic site A; four other H7-HA-specific clones also showed HI and neutralizing activities via recognition of the major antigenic sites A and D; seven mAbs that reacted with several HA subtypes and possibly recognized the HA stem partially protected mice from lethal infection with prototype H7N9 virus; and the remaining 19 mAbs had neither HI nor neutralization activity. All human H7N9 viruses tested showed a similar neutralization sensitivity to the first group of 16 mAbs, whereas human H7N9 viruses isolated in 2016–2017 were not neutralized by a second group of 4 mAbs. These results suggest that amino acid substitutions at the epitope of the second mAb group appear to be involved in the antigenic drift of the H7N9 viruses. Further analysis is required to fully understand the antigenic change in H7N9 viruses.
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spelling pubmed-64101132019-04-01 Characterization of Mouse Monoclonal Antibodies Against the HA of A(H7N9) Influenza Virus Ito, Mutsumi Yamayoshi, Seiya Murakami, Kazushi Saito, Kenji Motojima, Atsuo Nakaishi, Kazunari Kawaoka, Yoshihiro Viruses Article Many cases of human infection with the H7N9 virus have been detected in China since 2013. H7N9 viruses are maintained in chickens and are transmitted to humans at live bird markets. During circulation in birds, H7N9 viruses have accumulated amino acid substitutions in their hemagglutinin (HA), which resulted in an antigenically change in the recent H7N9 viruses. Here, we characterized 46 mouse monoclonal antibodies against the HA of the prototype strain. 16 H7-HA-specific monoclonal antibodies (mAbs) possessed hemagglutination inhibition (HI) and neutralization activities by recognizing the major antigenic site A; four other H7-HA-specific clones also showed HI and neutralizing activities via recognition of the major antigenic sites A and D; seven mAbs that reacted with several HA subtypes and possibly recognized the HA stem partially protected mice from lethal infection with prototype H7N9 virus; and the remaining 19 mAbs had neither HI nor neutralization activity. All human H7N9 viruses tested showed a similar neutralization sensitivity to the first group of 16 mAbs, whereas human H7N9 viruses isolated in 2016–2017 were not neutralized by a second group of 4 mAbs. These results suggest that amino acid substitutions at the epitope of the second mAb group appear to be involved in the antigenic drift of the H7N9 viruses. Further analysis is required to fully understand the antigenic change in H7N9 viruses. MDPI 2019-02-11 /pmc/articles/PMC6410113/ /pubmed/30754701 http://dx.doi.org/10.3390/v11020149 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ito, Mutsumi
Yamayoshi, Seiya
Murakami, Kazushi
Saito, Kenji
Motojima, Atsuo
Nakaishi, Kazunari
Kawaoka, Yoshihiro
Characterization of Mouse Monoclonal Antibodies Against the HA of A(H7N9) Influenza Virus
title Characterization of Mouse Monoclonal Antibodies Against the HA of A(H7N9) Influenza Virus
title_full Characterization of Mouse Monoclonal Antibodies Against the HA of A(H7N9) Influenza Virus
title_fullStr Characterization of Mouse Monoclonal Antibodies Against the HA of A(H7N9) Influenza Virus
title_full_unstemmed Characterization of Mouse Monoclonal Antibodies Against the HA of A(H7N9) Influenza Virus
title_short Characterization of Mouse Monoclonal Antibodies Against the HA of A(H7N9) Influenza Virus
title_sort characterization of mouse monoclonal antibodies against the ha of a(h7n9) influenza virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410113/
https://www.ncbi.nlm.nih.gov/pubmed/30754701
http://dx.doi.org/10.3390/v11020149
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