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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.
Afiliação
  • Golden A; Diagnostics, PATH, Seattle, Washington, United States of America.
  • Oliveira-Silva M; Centro de Pesquisa em Medicina Tropical (CEPEM), Porto Velho, Rondônia, Brazil.
  • Slater H; Diagnostics, PATH, Seattle, Washington, United States of America.
  • Vieira AM; Centro de Pesquisa em Medicina Tropical (CEPEM), Porto Velho, Rondônia, Brazil.
  • Bansil P; Diagnostics, PATH, Seattle, Washington, United States of America.
  • Gerth-Guyette E; Diagnostics, PATH, Seattle, Washington, United States of America.
  • Leader BT; Diagnostics, PATH, Seattle, Washington, United States of America.
  • Zobrist S; Diagnostics, PATH, Seattle, Washington, United States of America.
  • Braga Ferreira AK; Centro de Pesquisa em Medicina Tropical (CEPEM), Porto Velho, Rondônia, Brazil.
  • Santos de Araujo EC; Centro de Pesquisa em Medicina Tropical (CEPEM), Porto Velho, Rondônia, Brazil.
  • de Lucena Cruz CD; Centro de Pesquisa em Medicina Tropical (CEPEM), Porto Velho, Rondônia, Brazil.
  • Garbin E; Centro de Pesquisa em Medicina Tropical (CEPEM), Porto Velho, Rondônia, Brazil.
  • Bizilj GT; Diagnostics, PATH, Seattle, Washington, United States of America.
  • Carlson SJ; Diagnostics, PATH, Seattle, Washington, United States of America.
  • Sagalovsky M; Diagnostics, PATH, Seattle, Washington, United States of America.
  • Pal S; Diagnostics, PATH, Seattle, Washington, United States of America.
  • Gupta V; Amazon.com, Seattle, Washington, United States of America.
  • Wolansky L; Pandemic Prevention Institute, The Rockefeller Foundation, New York City, New York, United States of America.
  • Boyle DS; Diagnostics, PATH, Seattle, Washington, United States of America.
  • Vieira Dall'Acqua DS; Fundação Oswaldo Cruz (FIOCRUZ), Porto Velho, Rondônia, Brazil.
  • Naveca FG; Instituto Leônidas e Maria Deane (ILMD), Fundação Oswaldo Cruz (FIOCRUZ), Manaus, Amazonas, Brazil.
  • do Nascimento VA; Instituto Leônidas e Maria Deane (ILMD), Fundação Oswaldo Cruz (FIOCRUZ), Manaus, Amazonas, Brazil.
  • Villalobos Salcedo JM; Fundação Oswaldo Cruz (FIOCRUZ), Porto Velho, Rondônia, Brazil.
  • Drain PK; Department of Global Health, University of Washington, Seattle, Washington, United States of America.
  • Costa ADT; Department of Medicine, University of Washington, Seattle, Washington, United States of America.
  • Pereira D; Instituto Carlos Chagas (ICC), Fundação Oswaldo Cruz (FIOCRUZ), Curitiba, Paraná, Brazil.
  • Domingo GJ; Centro de Pesquisa em Medicina Tropical (CEPEM), Porto Velho, Rondônia, Brazil.
PLoS One ; 18(7): e0287814, 2023.
Article em En | MEDLINE | ID: mdl-37467188
ABSTRACT
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: SARS-CoV-2 / COVID-19 Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: SARS-CoV-2 / COVID-19 Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article