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516. SARS-CoV-2 Exhibits Clade-specific Differences in Nasopharyngeal Viral Loads
BACKGROUND: The rapid spread of SARS-CoV-2, the causative agent of Coronavirus disease 2019 (COVID-19), has been accompanied by the emergence of distinct viral clades, although their clinical significance has yet to be fully elucidated. While whole genome sequencing efforts have identified viral div...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776718/ http://dx.doi.org/10.1093/ofid/ofaa439.710 |
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author | Nam, Hannah Lorenzo-Redondo, Ramon Roberts, Scott C Simons, Lacy Achenbach, Chad Hauser, Alan R Ison, Michael G Hultquist, Judd F Ozer, Egon A |
author_facet | Nam, Hannah Lorenzo-Redondo, Ramon Roberts, Scott C Simons, Lacy Achenbach, Chad Hauser, Alan R Ison, Michael G Hultquist, Judd F Ozer, Egon A |
author_sort | Nam, Hannah |
collection | PubMed |
description | BACKGROUND: The rapid spread of SARS-CoV-2, the causative agent of Coronavirus disease 2019 (COVID-19), has been accompanied by the emergence of distinct viral clades, although their clinical significance has yet to be fully elucidated. While whole genome sequencing efforts have identified viral diversity over time, less is known about the clinical significance of this diversity. This study assessed the nasopharyngeal viral loads within patients over time to determine if these changes affect clinical parameters. METHODS: Samples were collected from patients presenting to Northwestern Memorial Hospital in Chicago, IL with a positive SARS-CoV-2 RT-PCR from nasopharyngeal swabs. Cycle threshold (Ct) values less than 35 were considered positive, and whole genome sequencing was performed by reverse transcription, multiplex PCR, and Nanopore sequencing. Phylogenetic analysis was conducted on sequenced isolates and compared with publicly available global sequences. Sequence characteristics and viral loads were correlated with each clade. RESULTS: 177 samples were analyzed from March 14, 2020, through May 1, 2020. Most of the sequences (92.6%) clustered in three main clades [Figure 1]. Clade IDs were ordered by relative abundance as Clades 1 (n=122, 68.9%), 2 (n=34, 19.2%), and 3 (n=8, 4.5%). Over this time, Clade 1 viruses have been increasing in incidence across the USA and globally while Clade 2 viruses were uniquely predominant in Illinois with limited global distribution. Ct values were compared across clades [Figure 2]. Significantly lower average Ct values (higher viral loads) were observed in Clade 1 relative to both Clade 2 (p=0.0002) and Clade 3 (p=0.0011). These findings were independent of time from symptom onset to specimen collection. Phylogenetic Analysis of SARS-CoV-2 Isolates with Number of Clades and Clade Distribution [Image: see text] Associations Between Viral Clade and Ct Value [Image: see text] CONCLUSION: These data suggest that SARS-CoV-2 genotype may impact viral load in the upper airways. It remains to be determined whether this difference in clades may impact transmission potential and overall viral spread. Further longitudinal studies with more specimens and associated clinical data are needed. DISCLOSURES: Michael G. Ison, MD MS, AlloVir (Consultant) |
format | Online Article Text |
id | pubmed-7776718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-77767182021-01-07 516. SARS-CoV-2 Exhibits Clade-specific Differences in Nasopharyngeal Viral Loads Nam, Hannah Lorenzo-Redondo, Ramon Roberts, Scott C Simons, Lacy Achenbach, Chad Hauser, Alan R Ison, Michael G Hultquist, Judd F Ozer, Egon A Open Forum Infect Dis Poster Abstracts BACKGROUND: The rapid spread of SARS-CoV-2, the causative agent of Coronavirus disease 2019 (COVID-19), has been accompanied by the emergence of distinct viral clades, although their clinical significance has yet to be fully elucidated. While whole genome sequencing efforts have identified viral diversity over time, less is known about the clinical significance of this diversity. This study assessed the nasopharyngeal viral loads within patients over time to determine if these changes affect clinical parameters. METHODS: Samples were collected from patients presenting to Northwestern Memorial Hospital in Chicago, IL with a positive SARS-CoV-2 RT-PCR from nasopharyngeal swabs. Cycle threshold (Ct) values less than 35 were considered positive, and whole genome sequencing was performed by reverse transcription, multiplex PCR, and Nanopore sequencing. Phylogenetic analysis was conducted on sequenced isolates and compared with publicly available global sequences. Sequence characteristics and viral loads were correlated with each clade. RESULTS: 177 samples were analyzed from March 14, 2020, through May 1, 2020. Most of the sequences (92.6%) clustered in three main clades [Figure 1]. Clade IDs were ordered by relative abundance as Clades 1 (n=122, 68.9%), 2 (n=34, 19.2%), and 3 (n=8, 4.5%). Over this time, Clade 1 viruses have been increasing in incidence across the USA and globally while Clade 2 viruses were uniquely predominant in Illinois with limited global distribution. Ct values were compared across clades [Figure 2]. Significantly lower average Ct values (higher viral loads) were observed in Clade 1 relative to both Clade 2 (p=0.0002) and Clade 3 (p=0.0011). These findings were independent of time from symptom onset to specimen collection. Phylogenetic Analysis of SARS-CoV-2 Isolates with Number of Clades and Clade Distribution [Image: see text] Associations Between Viral Clade and Ct Value [Image: see text] CONCLUSION: These data suggest that SARS-CoV-2 genotype may impact viral load in the upper airways. It remains to be determined whether this difference in clades may impact transmission potential and overall viral spread. Further longitudinal studies with more specimens and associated clinical data are needed. DISCLOSURES: Michael G. Ison, MD MS, AlloVir (Consultant) Oxford University Press 2020-12-31 /pmc/articles/PMC7776718/ http://dx.doi.org/10.1093/ofid/ofaa439.710 Text en © The Author 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Poster Abstracts Nam, Hannah Lorenzo-Redondo, Ramon Roberts, Scott C Simons, Lacy Achenbach, Chad Hauser, Alan R Ison, Michael G Hultquist, Judd F Ozer, Egon A 516. SARS-CoV-2 Exhibits Clade-specific Differences in Nasopharyngeal Viral Loads |
title | 516. SARS-CoV-2 Exhibits Clade-specific Differences in Nasopharyngeal Viral Loads |
title_full | 516. SARS-CoV-2 Exhibits Clade-specific Differences in Nasopharyngeal Viral Loads |
title_fullStr | 516. SARS-CoV-2 Exhibits Clade-specific Differences in Nasopharyngeal Viral Loads |
title_full_unstemmed | 516. SARS-CoV-2 Exhibits Clade-specific Differences in Nasopharyngeal Viral Loads |
title_short | 516. SARS-CoV-2 Exhibits Clade-specific Differences in Nasopharyngeal Viral Loads |
title_sort | 516. sars-cov-2 exhibits clade-specific differences in nasopharyngeal viral loads |
topic | Poster Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776718/ http://dx.doi.org/10.1093/ofid/ofaa439.710 |
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