Molecular Architecture of Early Dissemination and Massive Second Wave of the SARS-CoV-2 Virus in a Major Metropolitan Area

ABSTRACT We sequenced the genomes of 5,085 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) strains causing two coronavirus disease 2019 (COVID-19) disease waves in metropolitan Houston, TX, an ethnically diverse region with 7 million residents. The genomes were from viruses recovered in...

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Autores principales: S. Wesley Long, Randall J. Olsen, Paul A. Christensen, David W. Bernard, James J. Davis, Maulik Shukla, Marcus Nguyen, Matthew Ojeda Saavedra, Prasanti Yerramilli, Layne Pruitt, Sishir Subedi, Hung-Che Kuo, Heather Hendrickson, Ghazaleh Eskandari, Hoang A. T. Nguyen, J. Hunter Long, Muthiah Kumaraswami, Jule Goike, Daniel Boutz, Jimmy Gollihar, Jason S. McLellan, Chia-Wei Chou, Kamyab Javanmardi, Ilya J. Finkelstein, James M. Musser
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Publicado: American Society for Microbiology 2020
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spelling oai:doaj.org-article:9f1850b41a7e45ea80ff416602d5d71c2021-11-15T15:55:44ZMolecular Architecture of Early Dissemination and Massive Second Wave of the SARS-CoV-2 Virus in a Major Metropolitan Area10.1128/mBio.02707-202150-7511https://doaj.org/article/9f1850b41a7e45ea80ff416602d5d71c2020-12-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.02707-20https://doaj.org/toc/2150-7511ABSTRACT We sequenced the genomes of 5,085 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) strains causing two coronavirus disease 2019 (COVID-19) disease waves in metropolitan Houston, TX, an ethnically diverse region with 7 million residents. The genomes were from viruses recovered in the earliest recognized phase of the pandemic in Houston and from viruses recovered in an ongoing massive second wave of infections. The virus was originally introduced into Houston many times independently. Virtually all strains in the second wave have a Gly614 amino acid replacement in the spike protein, a polymorphism that has been linked to increased transmission and infectivity. Patients infected with the Gly614 variant strains had significantly higher virus loads in the nasopharynx on initial diagnosis. We found little evidence of a significant relationship between virus genotype and altered virulence, stressing the linkage between disease severity, underlying medical conditions, and host genetics. Some regions of the spike protein—the primary target of global vaccine efforts—are replete with amino acid replacements, perhaps indicating the action of selection. We exploited the genomic data to generate defined single amino acid replacements in the receptor binding domain of spike protein that, importantly, produced decreased recognition by the neutralizing monoclonal antibody CR3022. Our report represents the first analysis of the molecular architecture of SARS-CoV-2 in two infection waves in a major metropolitan region. The findings will help us to understand the origin, composition, and trajectory of future infection waves and the potential effect of the host immune response and therapeutic maneuvers on SARS-CoV-2 evolution. IMPORTANCE There is concern about second and subsequent waves of COVID-19 caused by the SARS-CoV-2 coronavirus occurring in communities globally that had an initial disease wave. Metropolitan Houston, TX, with a population of 7 million, is experiencing a massive second disease wave that began in late May 2020. To understand SARS-CoV-2 molecular population genomic architecture and evolution and the relationship between virus genotypes and patient features, we sequenced the genomes of 5,085 SARS-CoV-2 strains from these two waves. Our report provides the first molecular characterization of SARS-CoV-2 strains causing two distinct COVID-19 disease waves.S. Wesley LongRandall J. OlsenPaul A. ChristensenDavid W. BernardJames J. DavisMaulik ShuklaMarcus NguyenMatthew Ojeda SaavedraPrasanti YerramilliLayne PruittSishir SubediHung-Che KuoHeather HendricksonGhazaleh EskandariHoang A. T. NguyenJ. Hunter LongMuthiah KumaraswamiJule GoikeDaniel BoutzJimmy GolliharJason S. McLellanChia-Wei ChouKamyab JavanmardiIlya J. FinkelsteinJames M. MusserAmerican Society for MicrobiologyarticleSARS-CoV-2COVID-19 diseasegenome sequencingmolecular population genomicsevolutionCOVID-19MicrobiologyQR1-502ENmBio, Vol 11, Iss 6 (2020)
institution DOAJ
collection DOAJ
language EN
topic SARS-CoV-2
COVID-19 disease
genome sequencing
molecular population genomics
evolution
COVID-19
Microbiology
QR1-502
spellingShingle SARS-CoV-2
COVID-19 disease
genome sequencing
molecular population genomics
evolution
COVID-19
Microbiology
QR1-502
S. Wesley Long
Randall J. Olsen
Paul A. Christensen
David W. Bernard
James J. Davis
Maulik Shukla
Marcus Nguyen
Matthew Ojeda Saavedra
Prasanti Yerramilli
Layne Pruitt
Sishir Subedi
Hung-Che Kuo
Heather Hendrickson
Ghazaleh Eskandari
Hoang A. T. Nguyen
J. Hunter Long
Muthiah Kumaraswami
Jule Goike
Daniel Boutz
Jimmy Gollihar
Jason S. McLellan
Chia-Wei Chou
Kamyab Javanmardi
Ilya J. Finkelstein
James M. Musser
Molecular Architecture of Early Dissemination and Massive Second Wave of the SARS-CoV-2 Virus in a Major Metropolitan Area
description ABSTRACT We sequenced the genomes of 5,085 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) strains causing two coronavirus disease 2019 (COVID-19) disease waves in metropolitan Houston, TX, an ethnically diverse region with 7 million residents. The genomes were from viruses recovered in the earliest recognized phase of the pandemic in Houston and from viruses recovered in an ongoing massive second wave of infections. The virus was originally introduced into Houston many times independently. Virtually all strains in the second wave have a Gly614 amino acid replacement in the spike protein, a polymorphism that has been linked to increased transmission and infectivity. Patients infected with the Gly614 variant strains had significantly higher virus loads in the nasopharynx on initial diagnosis. We found little evidence of a significant relationship between virus genotype and altered virulence, stressing the linkage between disease severity, underlying medical conditions, and host genetics. Some regions of the spike protein—the primary target of global vaccine efforts—are replete with amino acid replacements, perhaps indicating the action of selection. We exploited the genomic data to generate defined single amino acid replacements in the receptor binding domain of spike protein that, importantly, produced decreased recognition by the neutralizing monoclonal antibody CR3022. Our report represents the first analysis of the molecular architecture of SARS-CoV-2 in two infection waves in a major metropolitan region. The findings will help us to understand the origin, composition, and trajectory of future infection waves and the potential effect of the host immune response and therapeutic maneuvers on SARS-CoV-2 evolution. IMPORTANCE There is concern about second and subsequent waves of COVID-19 caused by the SARS-CoV-2 coronavirus occurring in communities globally that had an initial disease wave. Metropolitan Houston, TX, with a population of 7 million, is experiencing a massive second disease wave that began in late May 2020. To understand SARS-CoV-2 molecular population genomic architecture and evolution and the relationship between virus genotypes and patient features, we sequenced the genomes of 5,085 SARS-CoV-2 strains from these two waves. Our report provides the first molecular characterization of SARS-CoV-2 strains causing two distinct COVID-19 disease waves.
format article
author S. Wesley Long
Randall J. Olsen
Paul A. Christensen
David W. Bernard
James J. Davis
Maulik Shukla
Marcus Nguyen
Matthew Ojeda Saavedra
Prasanti Yerramilli
Layne Pruitt
Sishir Subedi
Hung-Che Kuo
Heather Hendrickson
Ghazaleh Eskandari
Hoang A. T. Nguyen
J. Hunter Long
Muthiah Kumaraswami
Jule Goike
Daniel Boutz
Jimmy Gollihar
Jason S. McLellan
Chia-Wei Chou
Kamyab Javanmardi
Ilya J. Finkelstein
James M. Musser
author_facet S. Wesley Long
Randall J. Olsen
Paul A. Christensen
David W. Bernard
James J. Davis
Maulik Shukla
Marcus Nguyen
Matthew Ojeda Saavedra
Prasanti Yerramilli
Layne Pruitt
Sishir Subedi
Hung-Che Kuo
Heather Hendrickson
Ghazaleh Eskandari
Hoang A. T. Nguyen
J. Hunter Long
Muthiah Kumaraswami
Jule Goike
Daniel Boutz
Jimmy Gollihar
Jason S. McLellan
Chia-Wei Chou
Kamyab Javanmardi
Ilya J. Finkelstein
James M. Musser
author_sort S. Wesley Long
title Molecular Architecture of Early Dissemination and Massive Second Wave of the SARS-CoV-2 Virus in a Major Metropolitan Area
title_short Molecular Architecture of Early Dissemination and Massive Second Wave of the SARS-CoV-2 Virus in a Major Metropolitan Area
title_full Molecular Architecture of Early Dissemination and Massive Second Wave of the SARS-CoV-2 Virus in a Major Metropolitan Area
title_fullStr Molecular Architecture of Early Dissemination and Massive Second Wave of the SARS-CoV-2 Virus in a Major Metropolitan Area
title_full_unstemmed Molecular Architecture of Early Dissemination and Massive Second Wave of the SARS-CoV-2 Virus in a Major Metropolitan Area
title_sort molecular architecture of early dissemination and massive second wave of the sars-cov-2 virus in a major metropolitan area
publisher American Society for Microbiology
publishDate 2020
url https://doaj.org/article/9f1850b41a7e45ea80ff416602d5d71c
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