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An infectious bat-derived chimeric influenza virus harbouring the entry machinery of an influenza A virus
In 2012, the complete genomic sequence of a new and potentially harmful influenza A-like virus from bats (H17N10) was identified. However, infectious influenza virus was neither isolated from infected bats nor reconstituted, impeding further characterization of this virus. Here we show the generatio...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533278/ https://www.ncbi.nlm.nih.gov/pubmed/25055345 http://dx.doi.org/10.1038/ncomms5448 |
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author | Juozapaitis, Mindaugas Aguiar Moreira, Étori Mena, Ignacio Giese, Sebastian Riegger, David Pohlmann, Anne Höper, Dirk Zimmer, Gert Beer, Martin García-Sastre, Adolfo Schwemmle, Martin |
author_facet | Juozapaitis, Mindaugas Aguiar Moreira, Étori Mena, Ignacio Giese, Sebastian Riegger, David Pohlmann, Anne Höper, Dirk Zimmer, Gert Beer, Martin García-Sastre, Adolfo Schwemmle, Martin |
author_sort | Juozapaitis, Mindaugas |
collection | PubMed |
description | In 2012, the complete genomic sequence of a new and potentially harmful influenza A-like virus from bats (H17N10) was identified. However, infectious influenza virus was neither isolated from infected bats nor reconstituted, impeding further characterization of this virus. Here we show the generation of an infectious chimeric virus containing six out of the eight bat virus genes, with the remaining two genes encoding the haemagglutinin and neuraminidase proteins of a prototypic influenza A virus. This engineered virus replicates well in a broad range of mammalian cell cultures, human primary airway epithelial cells and mice, but poorly in avian cells and chicken embryos without further adaptation. Importantly, the bat chimeric virus is unable to reassort with other influenza A viruses. Although our data do not exclude the possibility of zoonotic transmission of bat influenza viruses into the human population, they indicate that multiple barriers exist that makes this an unlikely event. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/ncomms5448) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5533278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55332782017-07-28 An infectious bat-derived chimeric influenza virus harbouring the entry machinery of an influenza A virus Juozapaitis, Mindaugas Aguiar Moreira, Étori Mena, Ignacio Giese, Sebastian Riegger, David Pohlmann, Anne Höper, Dirk Zimmer, Gert Beer, Martin García-Sastre, Adolfo Schwemmle, Martin Nat Commun Article In 2012, the complete genomic sequence of a new and potentially harmful influenza A-like virus from bats (H17N10) was identified. However, infectious influenza virus was neither isolated from infected bats nor reconstituted, impeding further characterization of this virus. Here we show the generation of an infectious chimeric virus containing six out of the eight bat virus genes, with the remaining two genes encoding the haemagglutinin and neuraminidase proteins of a prototypic influenza A virus. This engineered virus replicates well in a broad range of mammalian cell cultures, human primary airway epithelial cells and mice, but poorly in avian cells and chicken embryos without further adaptation. Importantly, the bat chimeric virus is unable to reassort with other influenza A viruses. Although our data do not exclude the possibility of zoonotic transmission of bat influenza viruses into the human population, they indicate that multiple barriers exist that makes this an unlikely event. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/ncomms5448) contains supplementary material, which is available to authorized users. Nature Publishing Group UK 2014-07-23 /pmc/articles/PMC5533278/ /pubmed/25055345 http://dx.doi.org/10.1038/ncomms5448 Text en © Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 2014 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Juozapaitis, Mindaugas Aguiar Moreira, Étori Mena, Ignacio Giese, Sebastian Riegger, David Pohlmann, Anne Höper, Dirk Zimmer, Gert Beer, Martin García-Sastre, Adolfo Schwemmle, Martin An infectious bat-derived chimeric influenza virus harbouring the entry machinery of an influenza A virus |
title | An infectious bat-derived chimeric influenza virus harbouring the entry machinery of an influenza A virus |
title_full | An infectious bat-derived chimeric influenza virus harbouring the entry machinery of an influenza A virus |
title_fullStr | An infectious bat-derived chimeric influenza virus harbouring the entry machinery of an influenza A virus |
title_full_unstemmed | An infectious bat-derived chimeric influenza virus harbouring the entry machinery of an influenza A virus |
title_short | An infectious bat-derived chimeric influenza virus harbouring the entry machinery of an influenza A virus |
title_sort | infectious bat-derived chimeric influenza virus harbouring the entry machinery of an influenza a virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533278/ https://www.ncbi.nlm.nih.gov/pubmed/25055345 http://dx.doi.org/10.1038/ncomms5448 |
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