Cargando…

Analysis of SARS-CoV-2 variants from patient specimens in Nevada from October 2020 to August 2021

In early 2020, the emergence and spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in the human population quickly developed into a global pandemic. SARS-CoV-2 is the etiological agent of coronavirus disease 2019 (COVID-19) which has a broad range of respiratory illnesses. As th...

Descripción completa

Detalles Bibliográficos
Autores principales: Payen, Shannon Harger, Gorzalski, Andrew, Siao, Danielle Denise, Pandori, Mark, Verma, Subhash C., Rossetto, Cyprian C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier B.V. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10098042/
https://www.ncbi.nlm.nih.gov/pubmed/37059256
http://dx.doi.org/10.1016/j.meegid.2023.105434
_version_ 1785024707398991872
author Payen, Shannon Harger
Gorzalski, Andrew
Siao, Danielle Denise
Pandori, Mark
Verma, Subhash C.
Rossetto, Cyprian C.
author_facet Payen, Shannon Harger
Gorzalski, Andrew
Siao, Danielle Denise
Pandori, Mark
Verma, Subhash C.
Rossetto, Cyprian C.
author_sort Payen, Shannon Harger
collection PubMed
description In early 2020, the emergence and spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in the human population quickly developed into a global pandemic. SARS-CoV-2 is the etiological agent of coronavirus disease 2019 (COVID-19) which has a broad range of respiratory illnesses. As the virus circulates, it acquires nucleotide changes. These mutations are potentially due to the inherent differences in the selection pressures within the human population compared to the original zoonotic reservoir of SARS-CoV-2 and formerly naïve humans. The acquired mutations will most likely be neutral, but some may have implications for viral transmission, disease severity, and resistance to therapies or vaccines. This is a follow-up study from our early report (Hartley et al. J Genet Genomics. 01202021;48(1):40–51) which detected a rare variant (nsp12, RdRp P323F) circulating within Nevada in mid 2020 at high frequency. The primary goals of the current study were to determine the phylogenetic relationship of the SARS-CoV-2 genomes within Nevada and to determine if there are any unusual variants within Nevada compared to the current database of SARS-CoV-2 sequences. Whole genome sequencing and analysis of SARS-CoV-2 from 425 positively identified nasopharyngeal/nasal swab specimens were performed from October 2020 to August 2021 to determine any variants that could result in potential escape from current therapeutics. Our analysis focused on nucleotide mutations that generated amino acid variations in the viral Spike (S) protein, Receptor binding domain (RBD), and the RNA-dependent RNA-polymerase (RdRp) complex. The data indicate that SARS-CoV-2 sequences from Nevada did not contain any unusual variants that had not been previously reported. Additionally, we did not detect the previously identified the RdRp P323F variant in any of the samples. This suggests that the rare variant we detected before was only able to circulate because of the stay-at-home orders and semi-isolation experience during the early months of the pandemic. IMPORTANCE: SARS-COV-2 continues to circulate in the human population. In this study, SARS-CoV-2 positive nasopharyngeal/nasal swab samples were used for whole genome sequencing to determine the phylogenetic relationship of SARS-CoV-2 sequences within Nevada from October 2020 to August 2021. The resulting data is being added to a continually growing database of SARS-CoV-2 sequences that will be important for understanding the transmission and evolution of the virus as it spreads around the globe.
format Online
Article
Text
id pubmed-10098042
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher The Authors. Published by Elsevier B.V.
record_format MEDLINE/PubMed
spelling pubmed-100980422023-04-13 Analysis of SARS-CoV-2 variants from patient specimens in Nevada from October 2020 to August 2021 Payen, Shannon Harger Gorzalski, Andrew Siao, Danielle Denise Pandori, Mark Verma, Subhash C. Rossetto, Cyprian C. Infect Genet Evol Article In early 2020, the emergence and spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in the human population quickly developed into a global pandemic. SARS-CoV-2 is the etiological agent of coronavirus disease 2019 (COVID-19) which has a broad range of respiratory illnesses. As the virus circulates, it acquires nucleotide changes. These mutations are potentially due to the inherent differences in the selection pressures within the human population compared to the original zoonotic reservoir of SARS-CoV-2 and formerly naïve humans. The acquired mutations will most likely be neutral, but some may have implications for viral transmission, disease severity, and resistance to therapies or vaccines. This is a follow-up study from our early report (Hartley et al. J Genet Genomics. 01202021;48(1):40–51) which detected a rare variant (nsp12, RdRp P323F) circulating within Nevada in mid 2020 at high frequency. The primary goals of the current study were to determine the phylogenetic relationship of the SARS-CoV-2 genomes within Nevada and to determine if there are any unusual variants within Nevada compared to the current database of SARS-CoV-2 sequences. Whole genome sequencing and analysis of SARS-CoV-2 from 425 positively identified nasopharyngeal/nasal swab specimens were performed from October 2020 to August 2021 to determine any variants that could result in potential escape from current therapeutics. Our analysis focused on nucleotide mutations that generated amino acid variations in the viral Spike (S) protein, Receptor binding domain (RBD), and the RNA-dependent RNA-polymerase (RdRp) complex. The data indicate that SARS-CoV-2 sequences from Nevada did not contain any unusual variants that had not been previously reported. Additionally, we did not detect the previously identified the RdRp P323F variant in any of the samples. This suggests that the rare variant we detected before was only able to circulate because of the stay-at-home orders and semi-isolation experience during the early months of the pandemic. IMPORTANCE: SARS-COV-2 continues to circulate in the human population. In this study, SARS-CoV-2 positive nasopharyngeal/nasal swab samples were used for whole genome sequencing to determine the phylogenetic relationship of SARS-CoV-2 sequences within Nevada from October 2020 to August 2021. The resulting data is being added to a continually growing database of SARS-CoV-2 sequences that will be important for understanding the transmission and evolution of the virus as it spreads around the globe. The Authors. Published by Elsevier B.V. 2023-07 2023-04-13 /pmc/articles/PMC10098042/ /pubmed/37059256 http://dx.doi.org/10.1016/j.meegid.2023.105434 Text en © 2023 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Payen, Shannon Harger
Gorzalski, Andrew
Siao, Danielle Denise
Pandori, Mark
Verma, Subhash C.
Rossetto, Cyprian C.
Analysis of SARS-CoV-2 variants from patient specimens in Nevada from October 2020 to August 2021
title Analysis of SARS-CoV-2 variants from patient specimens in Nevada from October 2020 to August 2021
title_full Analysis of SARS-CoV-2 variants from patient specimens in Nevada from October 2020 to August 2021
title_fullStr Analysis of SARS-CoV-2 variants from patient specimens in Nevada from October 2020 to August 2021
title_full_unstemmed Analysis of SARS-CoV-2 variants from patient specimens in Nevada from October 2020 to August 2021
title_short Analysis of SARS-CoV-2 variants from patient specimens in Nevada from October 2020 to August 2021
title_sort analysis of sars-cov-2 variants from patient specimens in nevada from october 2020 to august 2021
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10098042/
https://www.ncbi.nlm.nih.gov/pubmed/37059256
http://dx.doi.org/10.1016/j.meegid.2023.105434
work_keys_str_mv AT payenshannonharger analysisofsarscov2variantsfrompatientspecimensinnevadafromoctober2020toaugust2021
AT gorzalskiandrew analysisofsarscov2variantsfrompatientspecimensinnevadafromoctober2020toaugust2021
AT siaodanielledenise analysisofsarscov2variantsfrompatientspecimensinnevadafromoctober2020toaugust2021
AT pandorimark analysisofsarscov2variantsfrompatientspecimensinnevadafromoctober2020toaugust2021
AT vermasubhashc analysisofsarscov2variantsfrompatientspecimensinnevadafromoctober2020toaugust2021
AT rossettocyprianc analysisofsarscov2variantsfrompatientspecimensinnevadafromoctober2020toaugust2021