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Trajectory of Growth of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants in Houston, Texas, January through May 2021, Based on 12,476 Genome Sequences

Certain genetic variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are of substantial concern because they may be more transmissible or detrimentally alter the pandemic course and disease features in individual patients. SARS-CoV-2 genome sequences from 12,476 patients in the H...

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Autores principales: Olsen, Randall J., Christensen, Paul A., Long, S. Wesley, Subedi, Sishir, Hodjat, Parsa, Olson, Robert, Nguyen, Marcus, Davis, James J., Yerramilli, Prasanti, Saavedra, Matthew O., Pruitt, Layne, Reppond, Kristina, Shyer, Madison N., Cambric, Jessica, Gadd, Ryan, Thakur, Rashi M., Batajoo, Akanksha, Finkelstein, Ilya J., Gollihar, Jimmy, Musser, James M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Investigative Pathology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299152/
https://www.ncbi.nlm.nih.gov/pubmed/34303698
http://dx.doi.org/10.1016/j.ajpath.2021.07.002
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author Olsen, Randall J.
Christensen, Paul A.
Long, S. Wesley
Subedi, Sishir
Hodjat, Parsa
Olson, Robert
Nguyen, Marcus
Davis, James J.
Yerramilli, Prasanti
Saavedra, Matthew O.
Pruitt, Layne
Reppond, Kristina
Shyer, Madison N.
Cambric, Jessica
Gadd, Ryan
Thakur, Rashi M.
Batajoo, Akanksha
Finkelstein, Ilya J.
Gollihar, Jimmy
Musser, James M.
author_facet Olsen, Randall J.
Christensen, Paul A.
Long, S. Wesley
Subedi, Sishir
Hodjat, Parsa
Olson, Robert
Nguyen, Marcus
Davis, James J.
Yerramilli, Prasanti
Saavedra, Matthew O.
Pruitt, Layne
Reppond, Kristina
Shyer, Madison N.
Cambric, Jessica
Gadd, Ryan
Thakur, Rashi M.
Batajoo, Akanksha
Finkelstein, Ilya J.
Gollihar, Jimmy
Musser, James M.
author_sort Olsen, Randall J.
collection PubMed
description Certain genetic variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are of substantial concern because they may be more transmissible or detrimentally alter the pandemic course and disease features in individual patients. SARS-CoV-2 genome sequences from 12,476 patients in the Houston Methodist health care system diagnosed from January 1 through May 31, 2021 are reported here. Prevalence of the B.1.1.7 (Alpha) variant increased rapidly and caused 63% to 90% of new cases in the latter half of May. Eleven B.1.1.7 genomes had an E484K replacement in spike protein, a change also identified in other SARS-CoV-2 lineages. Compared with non–B.1.1.7-infected patients, individuals with B.1.1.7 had a significantly lower cycle threshold (a proxy for higher virus load) and significantly higher hospitalization rate. Other variants [eg, B.1.429 and B.1.427 (Epsilon), P.1 (Gamma), P.2 (Zeta), and R.1] also increased rapidly, although the magnitude was less than that in B.1.1.7. Twenty-two patients infected with B.1.617.1 (Kappa) or B.1.617.2 (Delta) variants had a high rate of hospitalization. Breakthrough cases (n = 207) in fully vaccinated patients were caused by a heterogeneous array of virus genotypes, including many not currently designated variants of interest or concern. In the aggregate, this study delineates the trajectory of SARS-CoV-2 variants circulating in a major metropolitan area, documents B.1.1.7 as the major cause of new cases in Houston, TX, and heralds the arrival of B.1.617 variants in the metroplex.
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spelling pubmed-82991522021-07-23 Trajectory of Growth of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants in Houston, Texas, January through May 2021, Based on 12,476 Genome Sequences Olsen, Randall J. Christensen, Paul A. Long, S. Wesley Subedi, Sishir Hodjat, Parsa Olson, Robert Nguyen, Marcus Davis, James J. Yerramilli, Prasanti Saavedra, Matthew O. Pruitt, Layne Reppond, Kristina Shyer, Madison N. Cambric, Jessica Gadd, Ryan Thakur, Rashi M. Batajoo, Akanksha Finkelstein, Ilya J. Gollihar, Jimmy Musser, James M. Am J Pathol Regular Article Certain genetic variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are of substantial concern because they may be more transmissible or detrimentally alter the pandemic course and disease features in individual patients. SARS-CoV-2 genome sequences from 12,476 patients in the Houston Methodist health care system diagnosed from January 1 through May 31, 2021 are reported here. Prevalence of the B.1.1.7 (Alpha) variant increased rapidly and caused 63% to 90% of new cases in the latter half of May. Eleven B.1.1.7 genomes had an E484K replacement in spike protein, a change also identified in other SARS-CoV-2 lineages. Compared with non–B.1.1.7-infected patients, individuals with B.1.1.7 had a significantly lower cycle threshold (a proxy for higher virus load) and significantly higher hospitalization rate. Other variants [eg, B.1.429 and B.1.427 (Epsilon), P.1 (Gamma), P.2 (Zeta), and R.1] also increased rapidly, although the magnitude was less than that in B.1.1.7. Twenty-two patients infected with B.1.617.1 (Kappa) or B.1.617.2 (Delta) variants had a high rate of hospitalization. Breakthrough cases (n = 207) in fully vaccinated patients were caused by a heterogeneous array of virus genotypes, including many not currently designated variants of interest or concern. In the aggregate, this study delineates the trajectory of SARS-CoV-2 variants circulating in a major metropolitan area, documents B.1.1.7 as the major cause of new cases in Houston, TX, and heralds the arrival of B.1.617 variants in the metroplex. American Society for Investigative Pathology 2021-10 /pmc/articles/PMC8299152/ /pubmed/34303698 http://dx.doi.org/10.1016/j.ajpath.2021.07.002 Text en © 2021 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.
spellingShingle Regular Article
Olsen, Randall J.
Christensen, Paul A.
Long, S. Wesley
Subedi, Sishir
Hodjat, Parsa
Olson, Robert
Nguyen, Marcus
Davis, James J.
Yerramilli, Prasanti
Saavedra, Matthew O.
Pruitt, Layne
Reppond, Kristina
Shyer, Madison N.
Cambric, Jessica
Gadd, Ryan
Thakur, Rashi M.
Batajoo, Akanksha
Finkelstein, Ilya J.
Gollihar, Jimmy
Musser, James M.
Trajectory of Growth of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants in Houston, Texas, January through May 2021, Based on 12,476 Genome Sequences
title Trajectory of Growth of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants in Houston, Texas, January through May 2021, Based on 12,476 Genome Sequences
title_full Trajectory of Growth of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants in Houston, Texas, January through May 2021, Based on 12,476 Genome Sequences
title_fullStr Trajectory of Growth of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants in Houston, Texas, January through May 2021, Based on 12,476 Genome Sequences
title_full_unstemmed Trajectory of Growth of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants in Houston, Texas, January through May 2021, Based on 12,476 Genome Sequences
title_short Trajectory of Growth of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants in Houston, Texas, January through May 2021, Based on 12,476 Genome Sequences
title_sort trajectory of growth of severe acute respiratory syndrome coronavirus 2 (sars-cov-2) variants in houston, texas, january through may 2021, based on 12,476 genome sequences
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299152/
https://www.ncbi.nlm.nih.gov/pubmed/34303698
http://dx.doi.org/10.1016/j.ajpath.2021.07.002
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