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The influenza A virus genome packaging network — complex, flexible and yet unsolved
The genome of influenza A virus (IAV) consists of eight unique viral RNA segments. This genome organization allows genetic reassortment between co-infecting IAV strains, whereby new IAVs with altered genome segment compositions emerge. While it is known that reassortment events can create pandemic I...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458418/ https://www.ncbi.nlm.nih.gov/pubmed/35993811 http://dx.doi.org/10.1093/nar/gkac688 |
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author | Jakob, Celia Paul-Stansilaus, Rithu Schwemmle, Martin Marquet, Roland Bolte, Hardin |
author_facet | Jakob, Celia Paul-Stansilaus, Rithu Schwemmle, Martin Marquet, Roland Bolte, Hardin |
author_sort | Jakob, Celia |
collection | PubMed |
description | The genome of influenza A virus (IAV) consists of eight unique viral RNA segments. This genome organization allows genetic reassortment between co-infecting IAV strains, whereby new IAVs with altered genome segment compositions emerge. While it is known that reassortment events can create pandemic IAVs, it remains impossible to anticipate reassortment outcomes with pandemic prospects. Recent research indicates that reassortment is promoted by a viral genome packaging mechanism that delivers the eight genome segments as a supramolecular complex into the virus particle. This finding holds promise of predicting pandemic IAVs by understanding the intermolecular interactions governing this genome packaging mechanism. Here, we critically review the prevailing mechanistic model postulating that IAV genome packaging is orchestrated by a network of intersegmental RNA–RNA interactions. Although we find supporting evidence, including segment-specific packaging signals and experimentally proposed RNA–RNA interaction networks, this mechanistic model remains debatable due to a current shortage of functionally validated intersegmental RNA–RNA interactions. We speculate that identifying such functional intersegmental RNA–RNA contacts might be hampered by limitations of the utilized probing techniques and the inherent complexity of the genome packaging mechanism. Nevertheless, we anticipate that improved probing strategies combined with a mutagenesis-based validation could facilitate their discovery. |
format | Online Article Text |
id | pubmed-9458418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-94584182022-09-09 The influenza A virus genome packaging network — complex, flexible and yet unsolved Jakob, Celia Paul-Stansilaus, Rithu Schwemmle, Martin Marquet, Roland Bolte, Hardin Nucleic Acids Res Critical Reviews and Perspectives The genome of influenza A virus (IAV) consists of eight unique viral RNA segments. This genome organization allows genetic reassortment between co-infecting IAV strains, whereby new IAVs with altered genome segment compositions emerge. While it is known that reassortment events can create pandemic IAVs, it remains impossible to anticipate reassortment outcomes with pandemic prospects. Recent research indicates that reassortment is promoted by a viral genome packaging mechanism that delivers the eight genome segments as a supramolecular complex into the virus particle. This finding holds promise of predicting pandemic IAVs by understanding the intermolecular interactions governing this genome packaging mechanism. Here, we critically review the prevailing mechanistic model postulating that IAV genome packaging is orchestrated by a network of intersegmental RNA–RNA interactions. Although we find supporting evidence, including segment-specific packaging signals and experimentally proposed RNA–RNA interaction networks, this mechanistic model remains debatable due to a current shortage of functionally validated intersegmental RNA–RNA interactions. We speculate that identifying such functional intersegmental RNA–RNA contacts might be hampered by limitations of the utilized probing techniques and the inherent complexity of the genome packaging mechanism. Nevertheless, we anticipate that improved probing strategies combined with a mutagenesis-based validation could facilitate their discovery. Oxford University Press 2022-08-22 /pmc/articles/PMC9458418/ /pubmed/35993811 http://dx.doi.org/10.1093/nar/gkac688 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Critical Reviews and Perspectives Jakob, Celia Paul-Stansilaus, Rithu Schwemmle, Martin Marquet, Roland Bolte, Hardin The influenza A virus genome packaging network — complex, flexible and yet unsolved |
title | The influenza A virus genome packaging network — complex, flexible and yet unsolved |
title_full | The influenza A virus genome packaging network — complex, flexible and yet unsolved |
title_fullStr | The influenza A virus genome packaging network — complex, flexible and yet unsolved |
title_full_unstemmed | The influenza A virus genome packaging network — complex, flexible and yet unsolved |
title_short | The influenza A virus genome packaging network — complex, flexible and yet unsolved |
title_sort | influenza a virus genome packaging network — complex, flexible and yet unsolved |
topic | Critical Reviews and Perspectives |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458418/ https://www.ncbi.nlm.nih.gov/pubmed/35993811 http://dx.doi.org/10.1093/nar/gkac688 |
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