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Incorporation of the influenza A virus NA segment into virions does not require cognate non-coding sequences
For each influenza virus genome segment, the coding sequence is flanked by non-coding (NC) regions comprising shared, conserved sequences and specific, non-conserved sequences. The latter and adjacent parts of the coding sequence are involved in genome packaging, but the precise role of the non-cons...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5327478/ https://www.ncbi.nlm.nih.gov/pubmed/28240311 http://dx.doi.org/10.1038/srep43462 |
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author | Crescenzo-Chaigne, Bernadette Barbezange, Cyril V. S. Léandri, Stéphane Roquin, Camille Berthault, Camille van der Werf, Sylvie |
author_facet | Crescenzo-Chaigne, Bernadette Barbezange, Cyril V. S. Léandri, Stéphane Roquin, Camille Berthault, Camille van der Werf, Sylvie |
author_sort | Crescenzo-Chaigne, Bernadette |
collection | PubMed |
description | For each influenza virus genome segment, the coding sequence is flanked by non-coding (NC) regions comprising shared, conserved sequences and specific, non-conserved sequences. The latter and adjacent parts of the coding sequence are involved in genome packaging, but the precise role of the non-conserved NC sequences is still unclear. The aim of this study is to better understand the role of the non-conserved non-coding sequences in the incorporation of the viral segments into virions. The NA-segment NC sequences were systematically replaced by those of the seven other segments. Recombinant viruses harbouring two segments with identical NC sequences were successfully rescued. Virus growth kinetics and serial passages were performed, and incorporation of the viral segments was tested by real-time RT-PCR. An initial virus growth deficiency correlated to a specific defect in NA segment incorporation. Upon serial passages, growth properties were restored. Sequencing revealed that the replacing 5′NC sequence length drove the type of mutations obtained. With sequences longer than the original, point mutations in the coding region with or without substitutions in the 3′NC region were detected. With shorter sequences, insertions were observed in the 5′NC region. Restoration of viral fitness was linked to restoration of the NA segment incorporation. |
format | Online Article Text |
id | pubmed-5327478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53274782017-03-03 Incorporation of the influenza A virus NA segment into virions does not require cognate non-coding sequences Crescenzo-Chaigne, Bernadette Barbezange, Cyril V. S. Léandri, Stéphane Roquin, Camille Berthault, Camille van der Werf, Sylvie Sci Rep Article For each influenza virus genome segment, the coding sequence is flanked by non-coding (NC) regions comprising shared, conserved sequences and specific, non-conserved sequences. The latter and adjacent parts of the coding sequence are involved in genome packaging, but the precise role of the non-conserved NC sequences is still unclear. The aim of this study is to better understand the role of the non-conserved non-coding sequences in the incorporation of the viral segments into virions. The NA-segment NC sequences were systematically replaced by those of the seven other segments. Recombinant viruses harbouring two segments with identical NC sequences were successfully rescued. Virus growth kinetics and serial passages were performed, and incorporation of the viral segments was tested by real-time RT-PCR. An initial virus growth deficiency correlated to a specific defect in NA segment incorporation. Upon serial passages, growth properties were restored. Sequencing revealed that the replacing 5′NC sequence length drove the type of mutations obtained. With sequences longer than the original, point mutations in the coding region with or without substitutions in the 3′NC region were detected. With shorter sequences, insertions were observed in the 5′NC region. Restoration of viral fitness was linked to restoration of the NA segment incorporation. Nature Publishing Group 2017-02-27 /pmc/articles/PMC5327478/ /pubmed/28240311 http://dx.doi.org/10.1038/srep43462 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Crescenzo-Chaigne, Bernadette Barbezange, Cyril V. S. Léandri, Stéphane Roquin, Camille Berthault, Camille van der Werf, Sylvie Incorporation of the influenza A virus NA segment into virions does not require cognate non-coding sequences |
title | Incorporation of the influenza A virus NA segment into virions does not require cognate non-coding sequences |
title_full | Incorporation of the influenza A virus NA segment into virions does not require cognate non-coding sequences |
title_fullStr | Incorporation of the influenza A virus NA segment into virions does not require cognate non-coding sequences |
title_full_unstemmed | Incorporation of the influenza A virus NA segment into virions does not require cognate non-coding sequences |
title_short | Incorporation of the influenza A virus NA segment into virions does not require cognate non-coding sequences |
title_sort | incorporation of the influenza a virus na segment into virions does not require cognate non-coding sequences |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5327478/ https://www.ncbi.nlm.nih.gov/pubmed/28240311 http://dx.doi.org/10.1038/srep43462 |
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