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Molecular In-Depth on the Epidemiological Expansion of SARS-CoV-2 XBB.1.5

Since the beginning of the pandemic, the generation of new variants periodically recurs. The XBB.1.5 SARS-CoV-2 variant is one of the most recent. This research was aimed at verifying the potential hazard of this new subvariant. To achieve this objective, we performed a genome-based integrative appr...

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Autores principales: Scarpa, Fabio, Azzena, Ilenia, Locci, Chiara, Casu, Marco, Fiori, Pier Luigi, Ciccozzi, Alessandra, Angeletti, Silvia, Imperia, Elena, Giovanetti, Marta, Maruotti, Antonello, Borsetti, Alessandra, Cauda, Roberto, Cassone, Antonio, Via, Allegra, Pascarella, Stefano, Sanna, Daria, Ciccozzi, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142263/
https://www.ncbi.nlm.nih.gov/pubmed/37110335
http://dx.doi.org/10.3390/microorganisms11040912
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author Scarpa, Fabio
Azzena, Ilenia
Locci, Chiara
Casu, Marco
Fiori, Pier Luigi
Ciccozzi, Alessandra
Angeletti, Silvia
Imperia, Elena
Giovanetti, Marta
Maruotti, Antonello
Borsetti, Alessandra
Cauda, Roberto
Cassone, Antonio
Via, Allegra
Pascarella, Stefano
Sanna, Daria
Ciccozzi, Massimo
author_facet Scarpa, Fabio
Azzena, Ilenia
Locci, Chiara
Casu, Marco
Fiori, Pier Luigi
Ciccozzi, Alessandra
Angeletti, Silvia
Imperia, Elena
Giovanetti, Marta
Maruotti, Antonello
Borsetti, Alessandra
Cauda, Roberto
Cassone, Antonio
Via, Allegra
Pascarella, Stefano
Sanna, Daria
Ciccozzi, Massimo
author_sort Scarpa, Fabio
collection PubMed
description Since the beginning of the pandemic, the generation of new variants periodically recurs. The XBB.1.5 SARS-CoV-2 variant is one of the most recent. This research was aimed at verifying the potential hazard of this new subvariant. To achieve this objective, we performed a genome-based integrative approach, integrating results from genetic variability/phylodynamics with structural and immunoinformatic analyses to obtain as comprehensive a viewpoint as possible. The Bayesian Skyline Plot (BSP) shows that the viral population size reached the plateau phase on 24 November 2022, and the number of lineages peaked at the same time. The evolutionary rate is relatively low, amounting to 6.9 × 10(−4) subs/sites/years. The NTD domain is identical for XBB.1 and XBB.1.5 whereas their RBDs only differ for the mutations at position 486, where the Phe (in the original Wuhan) is replaced by a Ser in XBB and XBB.1, and by a Pro in XBB.1.5. The variant XBB.1.5 seems to spread more slowly than sub-variants that have caused concerns in 2022. The multidisciplinary molecular in-depth analyses on XBB.1.5 performed here does not provide evidence for a particularly high risk of viral expansion. Results indicate that XBB.1.5 does not possess features to become a new, global, public health threat. As of now, in its current molecular make-up, XBB.1.5 does not represent the most dangerous variant.
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spelling pubmed-101422632023-04-29 Molecular In-Depth on the Epidemiological Expansion of SARS-CoV-2 XBB.1.5 Scarpa, Fabio Azzena, Ilenia Locci, Chiara Casu, Marco Fiori, Pier Luigi Ciccozzi, Alessandra Angeletti, Silvia Imperia, Elena Giovanetti, Marta Maruotti, Antonello Borsetti, Alessandra Cauda, Roberto Cassone, Antonio Via, Allegra Pascarella, Stefano Sanna, Daria Ciccozzi, Massimo Microorganisms Article Since the beginning of the pandemic, the generation of new variants periodically recurs. The XBB.1.5 SARS-CoV-2 variant is one of the most recent. This research was aimed at verifying the potential hazard of this new subvariant. To achieve this objective, we performed a genome-based integrative approach, integrating results from genetic variability/phylodynamics with structural and immunoinformatic analyses to obtain as comprehensive a viewpoint as possible. The Bayesian Skyline Plot (BSP) shows that the viral population size reached the plateau phase on 24 November 2022, and the number of lineages peaked at the same time. The evolutionary rate is relatively low, amounting to 6.9 × 10(−4) subs/sites/years. The NTD domain is identical for XBB.1 and XBB.1.5 whereas their RBDs only differ for the mutations at position 486, where the Phe (in the original Wuhan) is replaced by a Ser in XBB and XBB.1, and by a Pro in XBB.1.5. The variant XBB.1.5 seems to spread more slowly than sub-variants that have caused concerns in 2022. The multidisciplinary molecular in-depth analyses on XBB.1.5 performed here does not provide evidence for a particularly high risk of viral expansion. Results indicate that XBB.1.5 does not possess features to become a new, global, public health threat. As of now, in its current molecular make-up, XBB.1.5 does not represent the most dangerous variant. MDPI 2023-03-31 /pmc/articles/PMC10142263/ /pubmed/37110335 http://dx.doi.org/10.3390/microorganisms11040912 Text en © 2023 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
Scarpa, Fabio
Azzena, Ilenia
Locci, Chiara
Casu, Marco
Fiori, Pier Luigi
Ciccozzi, Alessandra
Angeletti, Silvia
Imperia, Elena
Giovanetti, Marta
Maruotti, Antonello
Borsetti, Alessandra
Cauda, Roberto
Cassone, Antonio
Via, Allegra
Pascarella, Stefano
Sanna, Daria
Ciccozzi, Massimo
Molecular In-Depth on the Epidemiological Expansion of SARS-CoV-2 XBB.1.5
title Molecular In-Depth on the Epidemiological Expansion of SARS-CoV-2 XBB.1.5
title_full Molecular In-Depth on the Epidemiological Expansion of SARS-CoV-2 XBB.1.5
title_fullStr Molecular In-Depth on the Epidemiological Expansion of SARS-CoV-2 XBB.1.5
title_full_unstemmed Molecular In-Depth on the Epidemiological Expansion of SARS-CoV-2 XBB.1.5
title_short Molecular In-Depth on the Epidemiological Expansion of SARS-CoV-2 XBB.1.5
title_sort molecular in-depth on the epidemiological expansion of sars-cov-2 xbb.1.5
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142263/
https://www.ncbi.nlm.nih.gov/pubmed/37110335
http://dx.doi.org/10.3390/microorganisms11040912
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