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Surveillance of Severe Acute Respiratory Syndrome Coronavirus 2 and Variants Using Digital Droplet Polymerase Chain Reaction at a Large University and Healthcare System in California

BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants with different infectivity, transmission potential, and morbidity change the characteristics of local epidemics and affect vaccine effectiveness. As part of the University of Southern California COVID-19 Pandemic Resea...

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Autores principales: Stafylis, Chrysovalantis, Pernet, Olivier, Hernandez-Tamayo, Cassidy, Kovacs, Andrea, Emerson, Jane, Ward, Pamela M, Van Orman, Sarah, Gilliland, Frank, Conti, David, Weisenhaus, Maia, Ghanem-Uzqueda, Angie, Yepez, Daniel, Stellar, Sofia, Tadanki, Aditya P, Max, Jillian, Fottrell, Honour, Ong, Ethan, Navarro, Sabrina, Moses, Kaelyn, Akaolisa, Michael, Hosseini, Bijan, Sunesara, Shaleen, Wang, Yuzhu, Strum, Earl, Casagrande, Yolee, Arenas, Nathalie, Williams, Christopher, Thomas, Paul, Chu, Tara, Hu, Howard, Klausner, Jeffrey D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10117372/
https://www.ncbi.nlm.nih.gov/pubmed/37089777
http://dx.doi.org/10.1093/ofid/ofad147
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author Stafylis, Chrysovalantis
Pernet, Olivier
Hernandez-Tamayo, Cassidy
Kovacs, Andrea
Emerson, Jane
Ward, Pamela M
Van Orman, Sarah
Gilliland, Frank
Conti, David
Weisenhaus, Maia
Ghanem-Uzqueda, Angie
Yepez, Daniel
Stellar, Sofia
Tadanki, Aditya P
Max, Jillian
Fottrell, Honour
Ong, Ethan
Navarro, Sabrina
Moses, Kaelyn
Akaolisa, Michael
Hosseini, Bijan
Sunesara, Shaleen
Wang, Yuzhu
Strum, Earl
Casagrande, Yolee
Arenas, Nathalie
Williams, Christopher
Thomas, Paul
Chu, Tara
Hu, Howard
Klausner, Jeffrey D
author_facet Stafylis, Chrysovalantis
Pernet, Olivier
Hernandez-Tamayo, Cassidy
Kovacs, Andrea
Emerson, Jane
Ward, Pamela M
Van Orman, Sarah
Gilliland, Frank
Conti, David
Weisenhaus, Maia
Ghanem-Uzqueda, Angie
Yepez, Daniel
Stellar, Sofia
Tadanki, Aditya P
Max, Jillian
Fottrell, Honour
Ong, Ethan
Navarro, Sabrina
Moses, Kaelyn
Akaolisa, Michael
Hosseini, Bijan
Sunesara, Shaleen
Wang, Yuzhu
Strum, Earl
Casagrande, Yolee
Arenas, Nathalie
Williams, Christopher
Thomas, Paul
Chu, Tara
Hu, Howard
Klausner, Jeffrey D
author_sort Stafylis, Chrysovalantis
collection PubMed
description BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants with different infectivity, transmission potential, and morbidity change the characteristics of local epidemics and affect vaccine effectiveness. As part of the University of Southern California COVID-19 Pandemic Research Center's efforts to understand, control, and inform local community on coronavirus disease 2019 (COVID-19), we implemented a SARS-CoV-2 surveillance program among students, employees, and USC Keck Medical Center patients. We present the epidemiology and distribution of SARS-CoV-2 and its variants among the population. METHODS: We used digital droplet reverse-transcriptase polymerase chain reaction (PCR) to analyze in real-time remnant SARS-CoV-2 PCR-positive saliva specimens stored at the USC Keck Medicine laboratory between September 2020 and April 2022. Samples were tested for the original strain (A20) and 9 SARS-CoV-2 variants: α(B.1.1.7, Q.1–Q.8), β(B.1.351, B.1.351.2, B.1.351.3), γ(P.1, P.1.1, P.1.2), δ(B.1.617.2), δ+(or δ417N), ε(B.1.427 and B.1.429), η(B.1.525), λ(C.37) and ο(B.1.1.529, ΒΑ.1, BA.2). We reviewed deidentified health information from positive cases including demographics, history of COVID-19 (eg, symptoms, hospitalizations, and repeat infections), and COVID-19 vaccination status. RESULTS: We reviewed 1169 cases and determined the variant type of 482 specimens: 77 specimens were original strain, 119 “Delta”, 165 “Omicron”. The original strain was detected during the third and fourth quarters of 2020. The Delta variant appeared during the second quarter of 2021, whereas Omicron appeared in the fourth quarter of 2021. CONCLUSIONS: Prospectively tracking SARS-CoV-2 variants in a university population and a hospital system, utilizing a low-cost, high-throughput PCR assay, was feasible. Local variant monitoring remains important to inform prevention and control efforts among university and clinical settings.
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spelling pubmed-101173722023-04-21 Surveillance of Severe Acute Respiratory Syndrome Coronavirus 2 and Variants Using Digital Droplet Polymerase Chain Reaction at a Large University and Healthcare System in California Stafylis, Chrysovalantis Pernet, Olivier Hernandez-Tamayo, Cassidy Kovacs, Andrea Emerson, Jane Ward, Pamela M Van Orman, Sarah Gilliland, Frank Conti, David Weisenhaus, Maia Ghanem-Uzqueda, Angie Yepez, Daniel Stellar, Sofia Tadanki, Aditya P Max, Jillian Fottrell, Honour Ong, Ethan Navarro, Sabrina Moses, Kaelyn Akaolisa, Michael Hosseini, Bijan Sunesara, Shaleen Wang, Yuzhu Strum, Earl Casagrande, Yolee Arenas, Nathalie Williams, Christopher Thomas, Paul Chu, Tara Hu, Howard Klausner, Jeffrey D Open Forum Infect Dis Major Article BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants with different infectivity, transmission potential, and morbidity change the characteristics of local epidemics and affect vaccine effectiveness. As part of the University of Southern California COVID-19 Pandemic Research Center's efforts to understand, control, and inform local community on coronavirus disease 2019 (COVID-19), we implemented a SARS-CoV-2 surveillance program among students, employees, and USC Keck Medical Center patients. We present the epidemiology and distribution of SARS-CoV-2 and its variants among the population. METHODS: We used digital droplet reverse-transcriptase polymerase chain reaction (PCR) to analyze in real-time remnant SARS-CoV-2 PCR-positive saliva specimens stored at the USC Keck Medicine laboratory between September 2020 and April 2022. Samples were tested for the original strain (A20) and 9 SARS-CoV-2 variants: α(B.1.1.7, Q.1–Q.8), β(B.1.351, B.1.351.2, B.1.351.3), γ(P.1, P.1.1, P.1.2), δ(B.1.617.2), δ+(or δ417N), ε(B.1.427 and B.1.429), η(B.1.525), λ(C.37) and ο(B.1.1.529, ΒΑ.1, BA.2). We reviewed deidentified health information from positive cases including demographics, history of COVID-19 (eg, symptoms, hospitalizations, and repeat infections), and COVID-19 vaccination status. RESULTS: We reviewed 1169 cases and determined the variant type of 482 specimens: 77 specimens were original strain, 119 “Delta”, 165 “Omicron”. The original strain was detected during the third and fourth quarters of 2020. The Delta variant appeared during the second quarter of 2021, whereas Omicron appeared in the fourth quarter of 2021. CONCLUSIONS: Prospectively tracking SARS-CoV-2 variants in a university population and a hospital system, utilizing a low-cost, high-throughput PCR assay, was feasible. Local variant monitoring remains important to inform prevention and control efforts among university and clinical settings. Oxford University Press 2023-03-18 /pmc/articles/PMC10117372/ /pubmed/37089777 http://dx.doi.org/10.1093/ofid/ofad147 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://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 (https://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 Major Article
Stafylis, Chrysovalantis
Pernet, Olivier
Hernandez-Tamayo, Cassidy
Kovacs, Andrea
Emerson, Jane
Ward, Pamela M
Van Orman, Sarah
Gilliland, Frank
Conti, David
Weisenhaus, Maia
Ghanem-Uzqueda, Angie
Yepez, Daniel
Stellar, Sofia
Tadanki, Aditya P
Max, Jillian
Fottrell, Honour
Ong, Ethan
Navarro, Sabrina
Moses, Kaelyn
Akaolisa, Michael
Hosseini, Bijan
Sunesara, Shaleen
Wang, Yuzhu
Strum, Earl
Casagrande, Yolee
Arenas, Nathalie
Williams, Christopher
Thomas, Paul
Chu, Tara
Hu, Howard
Klausner, Jeffrey D
Surveillance of Severe Acute Respiratory Syndrome Coronavirus 2 and Variants Using Digital Droplet Polymerase Chain Reaction at a Large University and Healthcare System in California
title Surveillance of Severe Acute Respiratory Syndrome Coronavirus 2 and Variants Using Digital Droplet Polymerase Chain Reaction at a Large University and Healthcare System in California
title_full Surveillance of Severe Acute Respiratory Syndrome Coronavirus 2 and Variants Using Digital Droplet Polymerase Chain Reaction at a Large University and Healthcare System in California
title_fullStr Surveillance of Severe Acute Respiratory Syndrome Coronavirus 2 and Variants Using Digital Droplet Polymerase Chain Reaction at a Large University and Healthcare System in California
title_full_unstemmed Surveillance of Severe Acute Respiratory Syndrome Coronavirus 2 and Variants Using Digital Droplet Polymerase Chain Reaction at a Large University and Healthcare System in California
title_short Surveillance of Severe Acute Respiratory Syndrome Coronavirus 2 and Variants Using Digital Droplet Polymerase Chain Reaction at a Large University and Healthcare System in California
title_sort surveillance of severe acute respiratory syndrome coronavirus 2 and variants using digital droplet polymerase chain reaction at a large university and healthcare system in california
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10117372/
https://www.ncbi.nlm.nih.gov/pubmed/37089777
http://dx.doi.org/10.1093/ofid/ofad147
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