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Comparative transmissibility of SARS-CoV-2 variants Delta and Alpha in New England, USA
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Delta variant quickly rose to dominance in mid-2021, displacing other variants, including Alpha. Studies using data from the United Kingdom and India estimated that Delta was 40–80% more transmissible than Alpha, allowing Delta to beco...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8509091/ https://www.ncbi.nlm.nih.gov/pubmed/34642698 http://dx.doi.org/10.1101/2021.10.06.21264641 |
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author | Earnest, Rebecca Uddin, Rockib Matluk, Nicholas Renzette, Nicholas Siddle, Katherine J. Loreth, Christine Adams, Gordon Tomkins-Tinch, Christopher H. Petrone, Mary E. Rothman, Jessica E. Breban, Mallery I. Koch, Robert Tobias Billig, Kendall Fauver, Joseph R. Vogels, Chantal B.F. Turbett, Sarah Bilguvar, Kaya De Kumar, Bony Landry, Marie L. Peaper, David R. Kelly, Kevin Omerza, Greg Grieser, Heather Meak, Sim Martha, John Dewey, Hannah H. Kales, Susan Berenzy, Daniel Carpenter-Azevedo, Kristin King, Ewa Huard, Richard C. Smole, Sandra C. Brown, Catherine M. Fink, Timelia Lang, Andrew S. Gallagher, Glen R. Sabeti, Pardis C. Gabriel, Stacey MacInnis, Bronwyn L. Tewhey, Ryan Adams, Mark D. Park, Daniel J. Lemieux, Jacob E. Grubaugh, Nathan D. |
author_facet | Earnest, Rebecca Uddin, Rockib Matluk, Nicholas Renzette, Nicholas Siddle, Katherine J. Loreth, Christine Adams, Gordon Tomkins-Tinch, Christopher H. Petrone, Mary E. Rothman, Jessica E. Breban, Mallery I. Koch, Robert Tobias Billig, Kendall Fauver, Joseph R. Vogels, Chantal B.F. Turbett, Sarah Bilguvar, Kaya De Kumar, Bony Landry, Marie L. Peaper, David R. Kelly, Kevin Omerza, Greg Grieser, Heather Meak, Sim Martha, John Dewey, Hannah H. Kales, Susan Berenzy, Daniel Carpenter-Azevedo, Kristin King, Ewa Huard, Richard C. Smole, Sandra C. Brown, Catherine M. Fink, Timelia Lang, Andrew S. Gallagher, Glen R. Sabeti, Pardis C. Gabriel, Stacey MacInnis, Bronwyn L. Tewhey, Ryan Adams, Mark D. Park, Daniel J. Lemieux, Jacob E. Grubaugh, Nathan D. |
author_sort | Earnest, Rebecca |
collection | PubMed |
description | The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Delta variant quickly rose to dominance in mid-2021, displacing other variants, including Alpha. Studies using data from the United Kingdom and India estimated that Delta was 40–80% more transmissible than Alpha, allowing Delta to become the globally dominant variant. However, it was unclear if the ostensible difference in relative transmissibility was due mostly to innate properties of Delta’s infectiousness or differences in the study populations. To investigate, we formed a partnership with SARS-CoV-2 genomic surveillance programs from all six New England US states. By comparing logistic growth rates, we found that Delta emerged 37–163% faster than Alpha in early 2021 (37% Massachusetts, 75% New Hampshire, 95% Maine, 98% Rhode Island, 151% Connecticut, and 163% Vermont). We next computed variant-specific effective reproductive numbers and estimated that Delta was 58–120% more transmissible than Alpha across New England (58% New Hampshire, 68% Massachusetts, 76% Connecticut, 85% Rhode Island, 98% Maine, and 120% Vermont). Finally, using RT-PCR data, we estimated that Delta infections generate on average ~6 times more viral RNA copies per mL than Alpha infections. Overall, our evidence indicates that Delta’s enhanced transmissibility could be attributed to its innate ability to increase infectiousness, but its epidemiological dynamics may vary depending on the underlying immunity and behavior of distinct populations. |
format | Online Article Text |
id | pubmed-8509091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-85090912021-10-13 Comparative transmissibility of SARS-CoV-2 variants Delta and Alpha in New England, USA Earnest, Rebecca Uddin, Rockib Matluk, Nicholas Renzette, Nicholas Siddle, Katherine J. Loreth, Christine Adams, Gordon Tomkins-Tinch, Christopher H. Petrone, Mary E. Rothman, Jessica E. Breban, Mallery I. Koch, Robert Tobias Billig, Kendall Fauver, Joseph R. Vogels, Chantal B.F. Turbett, Sarah Bilguvar, Kaya De Kumar, Bony Landry, Marie L. Peaper, David R. Kelly, Kevin Omerza, Greg Grieser, Heather Meak, Sim Martha, John Dewey, Hannah H. Kales, Susan Berenzy, Daniel Carpenter-Azevedo, Kristin King, Ewa Huard, Richard C. Smole, Sandra C. Brown, Catherine M. Fink, Timelia Lang, Andrew S. Gallagher, Glen R. Sabeti, Pardis C. Gabriel, Stacey MacInnis, Bronwyn L. Tewhey, Ryan Adams, Mark D. Park, Daniel J. Lemieux, Jacob E. Grubaugh, Nathan D. medRxiv Article The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Delta variant quickly rose to dominance in mid-2021, displacing other variants, including Alpha. Studies using data from the United Kingdom and India estimated that Delta was 40–80% more transmissible than Alpha, allowing Delta to become the globally dominant variant. However, it was unclear if the ostensible difference in relative transmissibility was due mostly to innate properties of Delta’s infectiousness or differences in the study populations. To investigate, we formed a partnership with SARS-CoV-2 genomic surveillance programs from all six New England US states. By comparing logistic growth rates, we found that Delta emerged 37–163% faster than Alpha in early 2021 (37% Massachusetts, 75% New Hampshire, 95% Maine, 98% Rhode Island, 151% Connecticut, and 163% Vermont). We next computed variant-specific effective reproductive numbers and estimated that Delta was 58–120% more transmissible than Alpha across New England (58% New Hampshire, 68% Massachusetts, 76% Connecticut, 85% Rhode Island, 98% Maine, and 120% Vermont). Finally, using RT-PCR data, we estimated that Delta infections generate on average ~6 times more viral RNA copies per mL than Alpha infections. Overall, our evidence indicates that Delta’s enhanced transmissibility could be attributed to its innate ability to increase infectiousness, but its epidemiological dynamics may vary depending on the underlying immunity and behavior of distinct populations. Cold Spring Harbor Laboratory 2021-10-07 /pmc/articles/PMC8509091/ /pubmed/34642698 http://dx.doi.org/10.1101/2021.10.06.21264641 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Earnest, Rebecca Uddin, Rockib Matluk, Nicholas Renzette, Nicholas Siddle, Katherine J. Loreth, Christine Adams, Gordon Tomkins-Tinch, Christopher H. Petrone, Mary E. Rothman, Jessica E. Breban, Mallery I. Koch, Robert Tobias Billig, Kendall Fauver, Joseph R. Vogels, Chantal B.F. Turbett, Sarah Bilguvar, Kaya De Kumar, Bony Landry, Marie L. Peaper, David R. Kelly, Kevin Omerza, Greg Grieser, Heather Meak, Sim Martha, John Dewey, Hannah H. Kales, Susan Berenzy, Daniel Carpenter-Azevedo, Kristin King, Ewa Huard, Richard C. Smole, Sandra C. Brown, Catherine M. Fink, Timelia Lang, Andrew S. Gallagher, Glen R. Sabeti, Pardis C. Gabriel, Stacey MacInnis, Bronwyn L. Tewhey, Ryan Adams, Mark D. Park, Daniel J. Lemieux, Jacob E. Grubaugh, Nathan D. Comparative transmissibility of SARS-CoV-2 variants Delta and Alpha in New England, USA |
title | Comparative transmissibility of SARS-CoV-2 variants Delta and Alpha in New England, USA |
title_full | Comparative transmissibility of SARS-CoV-2 variants Delta and Alpha in New England, USA |
title_fullStr | Comparative transmissibility of SARS-CoV-2 variants Delta and Alpha in New England, USA |
title_full_unstemmed | Comparative transmissibility of SARS-CoV-2 variants Delta and Alpha in New England, USA |
title_short | Comparative transmissibility of SARS-CoV-2 variants Delta and Alpha in New England, USA |
title_sort | comparative transmissibility of sars-cov-2 variants delta and alpha in new england, usa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8509091/ https://www.ncbi.nlm.nih.gov/pubmed/34642698 http://dx.doi.org/10.1101/2021.10.06.21264641 |
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