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Local occurrence and fast spread of B.1.1.7 lineage: A glimpse into Friuli Venezia Giulia
In-depth study of the entire SARS-CoV-2 genome has uncovered many mutations, which have replaced the lineage that characterized the first wave of infections all around the world. In December 2020, the outbreak of variant of concern (VOC) 202012/01 (lineage B.1.1.7) in the United Kingdom defined a tu...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8670677/ https://www.ncbi.nlm.nih.gov/pubmed/34905574 http://dx.doi.org/10.1371/journal.pone.0261229 |
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author | Mio, Catia Dal Secco, Chiara Marzinotto, Stefania Bruno, Claudio Pimpo, Santa Betto, Elena Bertoni, Martina Pipan, Corrado Sozio, Emanuela Tascini, Carlo Damante, Giuseppe Curcio, Francesco |
author_facet | Mio, Catia Dal Secco, Chiara Marzinotto, Stefania Bruno, Claudio Pimpo, Santa Betto, Elena Bertoni, Martina Pipan, Corrado Sozio, Emanuela Tascini, Carlo Damante, Giuseppe Curcio, Francesco |
author_sort | Mio, Catia |
collection | PubMed |
description | In-depth study of the entire SARS-CoV-2 genome has uncovered many mutations, which have replaced the lineage that characterized the first wave of infections all around the world. In December 2020, the outbreak of variant of concern (VOC) 202012/01 (lineage B.1.1.7) in the United Kingdom defined a turning point during the pandemic, immediately posing a worldwide threat on the Covid-19 vaccination campaign. Here, we reported the evolution of B.1.1.7 lineage-related infections, analyzing samples collected from January 1(st) 2021, until April 15(th) 2021, in Friuli Venezia Giulia, a northeastern region of Italy. A cohort of 1508 nasopharyngeal swabs was analyzed by High Resolution Melting (HRM) and 479 randomly selected samples underwent Next Generation Sequencing analysis (NGS), uncovering a steady and continuous accumulation of B.1.1.7 lineage-related specimens, joined by sporadic cases of other known lineages (i.e. harboring the Spike glycoprotein p.E484K mutation). All the SARS-CoV-2 genome has been analyzed in order to highlight all the rare mutations that may eventually result in a new variant of interest. This work suggests that a thorough monitoring of the SARS-CoV-2 genome by NGS is essential to contain any new variant that could jeopardize all the efforts that have been made so far to resolve the emergence of the pandemic. |
format | Online Article Text |
id | pubmed-8670677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-86706772021-12-15 Local occurrence and fast spread of B.1.1.7 lineage: A glimpse into Friuli Venezia Giulia Mio, Catia Dal Secco, Chiara Marzinotto, Stefania Bruno, Claudio Pimpo, Santa Betto, Elena Bertoni, Martina Pipan, Corrado Sozio, Emanuela Tascini, Carlo Damante, Giuseppe Curcio, Francesco PLoS One Research Article In-depth study of the entire SARS-CoV-2 genome has uncovered many mutations, which have replaced the lineage that characterized the first wave of infections all around the world. In December 2020, the outbreak of variant of concern (VOC) 202012/01 (lineage B.1.1.7) in the United Kingdom defined a turning point during the pandemic, immediately posing a worldwide threat on the Covid-19 vaccination campaign. Here, we reported the evolution of B.1.1.7 lineage-related infections, analyzing samples collected from January 1(st) 2021, until April 15(th) 2021, in Friuli Venezia Giulia, a northeastern region of Italy. A cohort of 1508 nasopharyngeal swabs was analyzed by High Resolution Melting (HRM) and 479 randomly selected samples underwent Next Generation Sequencing analysis (NGS), uncovering a steady and continuous accumulation of B.1.1.7 lineage-related specimens, joined by sporadic cases of other known lineages (i.e. harboring the Spike glycoprotein p.E484K mutation). All the SARS-CoV-2 genome has been analyzed in order to highlight all the rare mutations that may eventually result in a new variant of interest. This work suggests that a thorough monitoring of the SARS-CoV-2 genome by NGS is essential to contain any new variant that could jeopardize all the efforts that have been made so far to resolve the emergence of the pandemic. Public Library of Science 2021-12-14 /pmc/articles/PMC8670677/ /pubmed/34905574 http://dx.doi.org/10.1371/journal.pone.0261229 Text en © 2021 Mio et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Mio, Catia Dal Secco, Chiara Marzinotto, Stefania Bruno, Claudio Pimpo, Santa Betto, Elena Bertoni, Martina Pipan, Corrado Sozio, Emanuela Tascini, Carlo Damante, Giuseppe Curcio, Francesco Local occurrence and fast spread of B.1.1.7 lineage: A glimpse into Friuli Venezia Giulia |
title | Local occurrence and fast spread of B.1.1.7 lineage: A glimpse into Friuli Venezia Giulia |
title_full | Local occurrence and fast spread of B.1.1.7 lineage: A glimpse into Friuli Venezia Giulia |
title_fullStr | Local occurrence and fast spread of B.1.1.7 lineage: A glimpse into Friuli Venezia Giulia |
title_full_unstemmed | Local occurrence and fast spread of B.1.1.7 lineage: A glimpse into Friuli Venezia Giulia |
title_short | Local occurrence and fast spread of B.1.1.7 lineage: A glimpse into Friuli Venezia Giulia |
title_sort | local occurrence and fast spread of b.1.1.7 lineage: a glimpse into friuli venezia giulia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8670677/ https://www.ncbi.nlm.nih.gov/pubmed/34905574 http://dx.doi.org/10.1371/journal.pone.0261229 |
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