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Antigen concentration, viral load, and test performance for SARS-CoV-2 in multiple specimen types
The relationship between N-antigen concentration and viral load within and across different specimens guides the clinical performance of rapid diagnostic tests (RDT) in different uses. A prospective study was conducted in Porto Velho, Brazil, to investigate RDT performance in different specimen type...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10355390/ https://www.ncbi.nlm.nih.gov/pubmed/37467188 http://dx.doi.org/10.1371/journal.pone.0287814 |
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author | Golden, Allison Oliveira-Silva, Michelle Slater, Hannah Vieira, Alexia Martines Bansil, Pooja Gerth-Guyette, Emily Leader, Brandon T. Zobrist, Stephanie Braga Ferreira, Alan Kennedy Santos de Araujo, Erika Crhistina de Lucena Cruz, Catherine Duran Garbin, Eduardo Bizilj, Greg T. Carlson, Sean J. Sagalovsky, Mariana Pal, Sampa Gupta, Vin Wolansky, Leo Boyle, David S. Vieira Dall’Acqua, Deusilene Souza Naveca, Felipe Gomes do Nascimento, Valdinete Alves Villalobos Salcedo, Juan Miguel Drain, Paul K. Costa, Alexandre Dias Tavares Pereira, Dhélio Domingo, Gonzalo J. |
author_facet | Golden, Allison Oliveira-Silva, Michelle Slater, Hannah Vieira, Alexia Martines Bansil, Pooja Gerth-Guyette, Emily Leader, Brandon T. Zobrist, Stephanie Braga Ferreira, Alan Kennedy Santos de Araujo, Erika Crhistina de Lucena Cruz, Catherine Duran Garbin, Eduardo Bizilj, Greg T. Carlson, Sean J. Sagalovsky, Mariana Pal, Sampa Gupta, Vin Wolansky, Leo Boyle, David S. Vieira Dall’Acqua, Deusilene Souza Naveca, Felipe Gomes do Nascimento, Valdinete Alves Villalobos Salcedo, Juan Miguel Drain, Paul K. Costa, Alexandre Dias Tavares Pereira, Dhélio Domingo, Gonzalo J. |
author_sort | Golden, Allison |
collection | PubMed |
description | The relationship between N-antigen concentration and viral load within and across different specimens guides the clinical performance of rapid diagnostic tests (RDT) in different uses. A prospective study was conducted in Porto Velho, Brazil, to investigate RDT performance in different specimen types as a function of the correlation between antigen concentration and viral load. The study included 214 close contacts with recent exposures to confirmed cases, aged 12 years and older and with various levels of vaccination. Antigen concentration was measured in nasopharyngeal swab (NPS), anterior nares swab (ANS), and saliva specimens. Reverse transcriptase (RT)–PCR was conducted on the NPS and saliva specimens, and two RDTs were conducted on ANS and one RDT on saliva. Antigen concentration correlated well with viral load when measured in the same specimen type but not across specimen types. Antigen levels were higher in symptomatic cases compared to asymptomatic/oligosymptomatic cases and lower in saliva compared to NPS and ANS samples. Discordant results between the RDTs conducted on ANS and the RT-PCR on NPS were resolved by antigen concentration values. The analytical limit-of-detection of RDTs can be used to predict the performance of the tests in populations for which the antigen concentration is known. The antigen dynamics across different sample types observed in SARS-CoV-2 disease progression support use of RDTs with nasal samples. Given lower antigen concentrations in saliva, rapid testing using saliva is expected to require improved RDT analytical sensitivity to achieve clinical sensitivity similar to rapid testing of nasal samples. |
format | Online Article Text |
id | pubmed-10355390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-103553902023-07-20 Antigen concentration, viral load, and test performance for SARS-CoV-2 in multiple specimen types Golden, Allison Oliveira-Silva, Michelle Slater, Hannah Vieira, Alexia Martines Bansil, Pooja Gerth-Guyette, Emily Leader, Brandon T. Zobrist, Stephanie Braga Ferreira, Alan Kennedy Santos de Araujo, Erika Crhistina de Lucena Cruz, Catherine Duran Garbin, Eduardo Bizilj, Greg T. Carlson, Sean J. Sagalovsky, Mariana Pal, Sampa Gupta, Vin Wolansky, Leo Boyle, David S. Vieira Dall’Acqua, Deusilene Souza Naveca, Felipe Gomes do Nascimento, Valdinete Alves Villalobos Salcedo, Juan Miguel Drain, Paul K. Costa, Alexandre Dias Tavares Pereira, Dhélio Domingo, Gonzalo J. PLoS One Research Article The relationship between N-antigen concentration and viral load within and across different specimens guides the clinical performance of rapid diagnostic tests (RDT) in different uses. A prospective study was conducted in Porto Velho, Brazil, to investigate RDT performance in different specimen types as a function of the correlation between antigen concentration and viral load. The study included 214 close contacts with recent exposures to confirmed cases, aged 12 years and older and with various levels of vaccination. Antigen concentration was measured in nasopharyngeal swab (NPS), anterior nares swab (ANS), and saliva specimens. Reverse transcriptase (RT)–PCR was conducted on the NPS and saliva specimens, and two RDTs were conducted on ANS and one RDT on saliva. Antigen concentration correlated well with viral load when measured in the same specimen type but not across specimen types. Antigen levels were higher in symptomatic cases compared to asymptomatic/oligosymptomatic cases and lower in saliva compared to NPS and ANS samples. Discordant results between the RDTs conducted on ANS and the RT-PCR on NPS were resolved by antigen concentration values. The analytical limit-of-detection of RDTs can be used to predict the performance of the tests in populations for which the antigen concentration is known. The antigen dynamics across different sample types observed in SARS-CoV-2 disease progression support use of RDTs with nasal samples. Given lower antigen concentrations in saliva, rapid testing using saliva is expected to require improved RDT analytical sensitivity to achieve clinical sensitivity similar to rapid testing of nasal samples. Public Library of Science 2023-07-19 /pmc/articles/PMC10355390/ /pubmed/37467188 http://dx.doi.org/10.1371/journal.pone.0287814 Text en © 2023 Golden et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Golden, Allison Oliveira-Silva, Michelle Slater, Hannah Vieira, Alexia Martines Bansil, Pooja Gerth-Guyette, Emily Leader, Brandon T. Zobrist, Stephanie Braga Ferreira, Alan Kennedy Santos de Araujo, Erika Crhistina de Lucena Cruz, Catherine Duran Garbin, Eduardo Bizilj, Greg T. Carlson, Sean J. Sagalovsky, Mariana Pal, Sampa Gupta, Vin Wolansky, Leo Boyle, David S. Vieira Dall’Acqua, Deusilene Souza Naveca, Felipe Gomes do Nascimento, Valdinete Alves Villalobos Salcedo, Juan Miguel Drain, Paul K. Costa, Alexandre Dias Tavares Pereira, Dhélio Domingo, Gonzalo J. Antigen concentration, viral load, and test performance for SARS-CoV-2 in multiple specimen types |
title | Antigen concentration, viral load, and test performance for SARS-CoV-2 in multiple specimen types |
title_full | Antigen concentration, viral load, and test performance for SARS-CoV-2 in multiple specimen types |
title_fullStr | Antigen concentration, viral load, and test performance for SARS-CoV-2 in multiple specimen types |
title_full_unstemmed | Antigen concentration, viral load, and test performance for SARS-CoV-2 in multiple specimen types |
title_short | Antigen concentration, viral load, and test performance for SARS-CoV-2 in multiple specimen types |
title_sort | antigen concentration, viral load, and test performance for sars-cov-2 in multiple specimen types |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10355390/ https://www.ncbi.nlm.nih.gov/pubmed/37467188 http://dx.doi.org/10.1371/journal.pone.0287814 |
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