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The Emergence of H7N7 Highly Pathogenic Avian Influenza Virus from Low Pathogenicity Avian Influenza Virus Using an in ovo Embryo Culture Model
Outbreaks of highly pathogenic avian influenza virus (HPAIV) often result in the infection of millions of poultry, causing up to 100% mortality. HPAIV has been shown to emerge from low pathogenicity avian influenza virus (LPAIV) in field outbreaks. Direct evidence for the emergence of H7N7 HPAIV fro...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7552004/ https://www.ncbi.nlm.nih.gov/pubmed/32839404 http://dx.doi.org/10.3390/v12090920 |
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author | Seekings, Amanda H. Howard, Wendy A. Nuñéz, Alejandro Slomka, Marek J. Banyard, Ashley C. Hicks, Daniel Ellis, Richard J. Nuñéz-García, Javier Hartgroves, Lorian C. Barclay, Wendy S. Banks, Jill Brown, Ian H. |
author_facet | Seekings, Amanda H. Howard, Wendy A. Nuñéz, Alejandro Slomka, Marek J. Banyard, Ashley C. Hicks, Daniel Ellis, Richard J. Nuñéz-García, Javier Hartgroves, Lorian C. Barclay, Wendy S. Banks, Jill Brown, Ian H. |
author_sort | Seekings, Amanda H. |
collection | PubMed |
description | Outbreaks of highly pathogenic avian influenza virus (HPAIV) often result in the infection of millions of poultry, causing up to 100% mortality. HPAIV has been shown to emerge from low pathogenicity avian influenza virus (LPAIV) in field outbreaks. Direct evidence for the emergence of H7N7 HPAIV from a LPAIV precursor with a rare di-basic cleavage site (DBCS) was identified in the UK in 2008. The DBCS contained an additional basic amino acid compared to commonly circulating LPAIVs that harbor a single-basic amino acid at the cleavage site (SBCS). Using reverse genetics, outbreak HPAIVs were rescued with a DBCS (H7N7(DB)), as seen in the LPAIV precursor or an SBCS representative of common H7 LPAIVs (H7N7(SB)). Passage of H7N7(DB) in chicken embryo tissues showed spontaneous evolution to a HPAIV. In contrast, deep sequencing of extracts from embryo tissues in which H7N7(SB) was serially passaged showed retention of the LPAIV genotype. Thus, in chicken embryos, an H7N7 virus containing a DBCS appears naturally unstable, enabling rapid evolution to HPAIV. Evaluation in embryo tissue presents a useful approach to study AIV evolution and allows a laboratory-based dissection of molecular mechanisms behind the emergence of HPAIV. |
format | Online Article Text |
id | pubmed-7552004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75520042020-10-14 The Emergence of H7N7 Highly Pathogenic Avian Influenza Virus from Low Pathogenicity Avian Influenza Virus Using an in ovo Embryo Culture Model Seekings, Amanda H. Howard, Wendy A. Nuñéz, Alejandro Slomka, Marek J. Banyard, Ashley C. Hicks, Daniel Ellis, Richard J. Nuñéz-García, Javier Hartgroves, Lorian C. Barclay, Wendy S. Banks, Jill Brown, Ian H. Viruses Article Outbreaks of highly pathogenic avian influenza virus (HPAIV) often result in the infection of millions of poultry, causing up to 100% mortality. HPAIV has been shown to emerge from low pathogenicity avian influenza virus (LPAIV) in field outbreaks. Direct evidence for the emergence of H7N7 HPAIV from a LPAIV precursor with a rare di-basic cleavage site (DBCS) was identified in the UK in 2008. The DBCS contained an additional basic amino acid compared to commonly circulating LPAIVs that harbor a single-basic amino acid at the cleavage site (SBCS). Using reverse genetics, outbreak HPAIVs were rescued with a DBCS (H7N7(DB)), as seen in the LPAIV precursor or an SBCS representative of common H7 LPAIVs (H7N7(SB)). Passage of H7N7(DB) in chicken embryo tissues showed spontaneous evolution to a HPAIV. In contrast, deep sequencing of extracts from embryo tissues in which H7N7(SB) was serially passaged showed retention of the LPAIV genotype. Thus, in chicken embryos, an H7N7 virus containing a DBCS appears naturally unstable, enabling rapid evolution to HPAIV. Evaluation in embryo tissue presents a useful approach to study AIV evolution and allows a laboratory-based dissection of molecular mechanisms behind the emergence of HPAIV. MDPI 2020-08-21 /pmc/articles/PMC7552004/ /pubmed/32839404 http://dx.doi.org/10.3390/v12090920 Text en © 2020 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 Seekings, Amanda H. Howard, Wendy A. Nuñéz, Alejandro Slomka, Marek J. Banyard, Ashley C. Hicks, Daniel Ellis, Richard J. Nuñéz-García, Javier Hartgroves, Lorian C. Barclay, Wendy S. Banks, Jill Brown, Ian H. The Emergence of H7N7 Highly Pathogenic Avian Influenza Virus from Low Pathogenicity Avian Influenza Virus Using an in ovo Embryo Culture Model |
title | The Emergence of H7N7 Highly Pathogenic Avian Influenza Virus from Low Pathogenicity Avian Influenza Virus Using an in ovo Embryo Culture Model |
title_full | The Emergence of H7N7 Highly Pathogenic Avian Influenza Virus from Low Pathogenicity Avian Influenza Virus Using an in ovo Embryo Culture Model |
title_fullStr | The Emergence of H7N7 Highly Pathogenic Avian Influenza Virus from Low Pathogenicity Avian Influenza Virus Using an in ovo Embryo Culture Model |
title_full_unstemmed | The Emergence of H7N7 Highly Pathogenic Avian Influenza Virus from Low Pathogenicity Avian Influenza Virus Using an in ovo Embryo Culture Model |
title_short | The Emergence of H7N7 Highly Pathogenic Avian Influenza Virus from Low Pathogenicity Avian Influenza Virus Using an in ovo Embryo Culture Model |
title_sort | emergence of h7n7 highly pathogenic avian influenza virus from low pathogenicity avian influenza virus using an in ovo embryo culture model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7552004/ https://www.ncbi.nlm.nih.gov/pubmed/32839404 http://dx.doi.org/10.3390/v12090920 |
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