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Secondary Structure of Influenza A Virus Genomic Segment 8 RNA Folded in a Cellular Environment
Influenza A virus (IAV) is a member of the single-stranded RNA (ssRNA) family of viruses. The most recent global pandemic caused by the SARS-CoV-2 virus has shown the major threat that RNA viruses can pose to humanity. In comparison, influenza has an even higher pandemic potential as a result of its...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8910647/ https://www.ncbi.nlm.nih.gov/pubmed/35269600 http://dx.doi.org/10.3390/ijms23052452 |
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author | Szutkowska, Barbara Wieczorek, Klaudia Kierzek, Ryszard Zmora, Pawel Peterson, Jake M. Moss, Walter N. Mathews, David H. Kierzek, Elzbieta |
author_facet | Szutkowska, Barbara Wieczorek, Klaudia Kierzek, Ryszard Zmora, Pawel Peterson, Jake M. Moss, Walter N. Mathews, David H. Kierzek, Elzbieta |
author_sort | Szutkowska, Barbara |
collection | PubMed |
description | Influenza A virus (IAV) is a member of the single-stranded RNA (ssRNA) family of viruses. The most recent global pandemic caused by the SARS-CoV-2 virus has shown the major threat that RNA viruses can pose to humanity. In comparison, influenza has an even higher pandemic potential as a result of its high rate of mutations within its relatively short (<13 kbp) genome, as well as its capability to undergo genetic reassortment. In light of this threat, and the fact that RNA structure is connected to a broad range of known biological functions, deeper investigation of viral RNA (vRNA) structures is of high interest. Here, for the first time, we propose a secondary structure for segment 8 vRNA (vRNA8) of A/California/04/2009 (H1N1) formed in the presence of cellular and viral components. This structure shows similarities with prior in vitro experiments. Additionally, we determined the location of several well-defined, conserved structural motifs of vRNA8 within IAV strains with possible functionality. These RNA motifs appear to fold independently of regional nucleoprotein (NP)-binding affinity, but a low or uneven distribution of NP in each motif region is noted. This research also highlights several accessible sites for oligonucleotide tools and small molecules in vRNA8 in a cellular environment that might be a target for influenza A virus inhibition on the RNA level. |
format | Online Article Text |
id | pubmed-8910647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89106472022-03-11 Secondary Structure of Influenza A Virus Genomic Segment 8 RNA Folded in a Cellular Environment Szutkowska, Barbara Wieczorek, Klaudia Kierzek, Ryszard Zmora, Pawel Peterson, Jake M. Moss, Walter N. Mathews, David H. Kierzek, Elzbieta Int J Mol Sci Article Influenza A virus (IAV) is a member of the single-stranded RNA (ssRNA) family of viruses. The most recent global pandemic caused by the SARS-CoV-2 virus has shown the major threat that RNA viruses can pose to humanity. In comparison, influenza has an even higher pandemic potential as a result of its high rate of mutations within its relatively short (<13 kbp) genome, as well as its capability to undergo genetic reassortment. In light of this threat, and the fact that RNA structure is connected to a broad range of known biological functions, deeper investigation of viral RNA (vRNA) structures is of high interest. Here, for the first time, we propose a secondary structure for segment 8 vRNA (vRNA8) of A/California/04/2009 (H1N1) formed in the presence of cellular and viral components. This structure shows similarities with prior in vitro experiments. Additionally, we determined the location of several well-defined, conserved structural motifs of vRNA8 within IAV strains with possible functionality. These RNA motifs appear to fold independently of regional nucleoprotein (NP)-binding affinity, but a low or uneven distribution of NP in each motif region is noted. This research also highlights several accessible sites for oligonucleotide tools and small molecules in vRNA8 in a cellular environment that might be a target for influenza A virus inhibition on the RNA level. MDPI 2022-02-23 /pmc/articles/PMC8910647/ /pubmed/35269600 http://dx.doi.org/10.3390/ijms23052452 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Szutkowska, Barbara Wieczorek, Klaudia Kierzek, Ryszard Zmora, Pawel Peterson, Jake M. Moss, Walter N. Mathews, David H. Kierzek, Elzbieta Secondary Structure of Influenza A Virus Genomic Segment 8 RNA Folded in a Cellular Environment |
title | Secondary Structure of Influenza A Virus Genomic Segment 8 RNA Folded in a Cellular Environment |
title_full | Secondary Structure of Influenza A Virus Genomic Segment 8 RNA Folded in a Cellular Environment |
title_fullStr | Secondary Structure of Influenza A Virus Genomic Segment 8 RNA Folded in a Cellular Environment |
title_full_unstemmed | Secondary Structure of Influenza A Virus Genomic Segment 8 RNA Folded in a Cellular Environment |
title_short | Secondary Structure of Influenza A Virus Genomic Segment 8 RNA Folded in a Cellular Environment |
title_sort | secondary structure of influenza a virus genomic segment 8 rna folded in a cellular environment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8910647/ https://www.ncbi.nlm.nih.gov/pubmed/35269600 http://dx.doi.org/10.3390/ijms23052452 |
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