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Tracking Changes in SARS-CoV-2 Spike: Evidence that D614G Increases Infectivity of the COVID-19 Virus
A SARS-CoV-2 variant carrying the Spike protein amino acid change D614G has become the most prevalent form in the global pandemic. Dynamic tracking of variant frequencies revealed a recurrent pattern of G614 increase at multiple geographic levels: national, regional, and municipal. The shift occurre...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332439/ https://www.ncbi.nlm.nih.gov/pubmed/32697968 http://dx.doi.org/10.1016/j.cell.2020.06.043 |
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author | Korber, Bette Fischer, Will M. Gnanakaran, Sandrasegaram Yoon, Hyejin Theiler, James Abfalterer, Werner Hengartner, Nick Giorgi, Elena E. Bhattacharya, Tanmoy Foley, Brian Hastie, Kathryn M. Parker, Matthew D. Partridge, David G. Evans, Cariad M. Freeman, Timothy M. de Silva, Thushan I. McDanal, Charlene Perez, Lautaro G. Tang, Haili Moon-Walker, Alex Whelan, Sean P. LaBranche, Celia C. Saphire, Erica O. Montefiori, David C. |
author_facet | Korber, Bette Fischer, Will M. Gnanakaran, Sandrasegaram Yoon, Hyejin Theiler, James Abfalterer, Werner Hengartner, Nick Giorgi, Elena E. Bhattacharya, Tanmoy Foley, Brian Hastie, Kathryn M. Parker, Matthew D. Partridge, David G. Evans, Cariad M. Freeman, Timothy M. de Silva, Thushan I. McDanal, Charlene Perez, Lautaro G. Tang, Haili Moon-Walker, Alex Whelan, Sean P. LaBranche, Celia C. Saphire, Erica O. Montefiori, David C. |
author_sort | Korber, Bette |
collection | PubMed |
description | A SARS-CoV-2 variant carrying the Spike protein amino acid change D614G has become the most prevalent form in the global pandemic. Dynamic tracking of variant frequencies revealed a recurrent pattern of G614 increase at multiple geographic levels: national, regional, and municipal. The shift occurred even in local epidemics where the original D614 form was well established prior to introduction of the G614 variant. The consistency of this pattern was highly statistically significant, suggesting that the G614 variant may have a fitness advantage. We found that the G614 variant grows to a higher titer as pseudotyped virions. In infected individuals, G614 is associated with lower RT-PCR cycle thresholds, suggestive of higher upper respiratory tract viral loads, but not with increased disease severity. These findings illuminate changes important for a mechanistic understanding of the virus and support continuing surveillance of Spike mutations to aid with development of immunological interventions. |
format | Online Article Text |
id | pubmed-7332439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-73324392020-07-06 Tracking Changes in SARS-CoV-2 Spike: Evidence that D614G Increases Infectivity of the COVID-19 Virus Korber, Bette Fischer, Will M. Gnanakaran, Sandrasegaram Yoon, Hyejin Theiler, James Abfalterer, Werner Hengartner, Nick Giorgi, Elena E. Bhattacharya, Tanmoy Foley, Brian Hastie, Kathryn M. Parker, Matthew D. Partridge, David G. Evans, Cariad M. Freeman, Timothy M. de Silva, Thushan I. McDanal, Charlene Perez, Lautaro G. Tang, Haili Moon-Walker, Alex Whelan, Sean P. LaBranche, Celia C. Saphire, Erica O. Montefiori, David C. Cell Article A SARS-CoV-2 variant carrying the Spike protein amino acid change D614G has become the most prevalent form in the global pandemic. Dynamic tracking of variant frequencies revealed a recurrent pattern of G614 increase at multiple geographic levels: national, regional, and municipal. The shift occurred even in local epidemics where the original D614 form was well established prior to introduction of the G614 variant. The consistency of this pattern was highly statistically significant, suggesting that the G614 variant may have a fitness advantage. We found that the G614 variant grows to a higher titer as pseudotyped virions. In infected individuals, G614 is associated with lower RT-PCR cycle thresholds, suggestive of higher upper respiratory tract viral loads, but not with increased disease severity. These findings illuminate changes important for a mechanistic understanding of the virus and support continuing surveillance of Spike mutations to aid with development of immunological interventions. Cell Press 2020-08-20 /pmc/articles/PMC7332439/ /pubmed/32697968 http://dx.doi.org/10.1016/j.cell.2020.06.043 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Korber, Bette Fischer, Will M. Gnanakaran, Sandrasegaram Yoon, Hyejin Theiler, James Abfalterer, Werner Hengartner, Nick Giorgi, Elena E. Bhattacharya, Tanmoy Foley, Brian Hastie, Kathryn M. Parker, Matthew D. Partridge, David G. Evans, Cariad M. Freeman, Timothy M. de Silva, Thushan I. McDanal, Charlene Perez, Lautaro G. Tang, Haili Moon-Walker, Alex Whelan, Sean P. LaBranche, Celia C. Saphire, Erica O. Montefiori, David C. Tracking Changes in SARS-CoV-2 Spike: Evidence that D614G Increases Infectivity of the COVID-19 Virus |
title | Tracking Changes in SARS-CoV-2 Spike: Evidence that D614G Increases Infectivity of the COVID-19 Virus |
title_full | Tracking Changes in SARS-CoV-2 Spike: Evidence that D614G Increases Infectivity of the COVID-19 Virus |
title_fullStr | Tracking Changes in SARS-CoV-2 Spike: Evidence that D614G Increases Infectivity of the COVID-19 Virus |
title_full_unstemmed | Tracking Changes in SARS-CoV-2 Spike: Evidence that D614G Increases Infectivity of the COVID-19 Virus |
title_short | Tracking Changes in SARS-CoV-2 Spike: Evidence that D614G Increases Infectivity of the COVID-19 Virus |
title_sort | tracking changes in sars-cov-2 spike: evidence that d614g increases infectivity of the covid-19 virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332439/ https://www.ncbi.nlm.nih.gov/pubmed/32697968 http://dx.doi.org/10.1016/j.cell.2020.06.043 |
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