Saliva Molecular Testing Bypassing RNA Extraction is Suitable for Monitoring and Diagnosing SARS-CoV-2 Infection in Children
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.17/4175 |
Resumo: | Background: Adults are being vaccinated against SARS-CoV-2 worldwide, but the longitudinal protection of these vaccines is uncertain, given the ongoing appearance of SARS-CoV-2 variants. Children remain largely unvaccinated and are susceptible to infection, with studies reporting that they actively transmit the virus even when asymptomatic, thus affecting the community. Methods: We investigated if saliva is an effective sample for detecting SARS-CoV-2 RNA and antibodies in children, and associated viral RNA levels to infectivity. For that, we used a saliva-based SARS-CoV-2 RT-qPCR test, preceded or not by RNA extraction, in 85 children aged 10 years and under, admitted to the hospital regardless of COVID-19 symptomatology. Amongst these, 29 (63.0%) presented at least one COVID-19 symptom, 46 (54.1%) were positive for SARS-CoV-2 infection, 28 (32.9%) were under the age of 1, and the mean (SD) age was 3.8 (3.4) years. Saliva samples were collected up to 48 h after a nasopharyngeal swab-RT-qPCR test. Results: In children aged 10 years and under, the sensitivity, specificity, and accuracy of saliva-RT-qPCR tests compared to NP swab-RT-qPCR were, respectively, 84.8% (71.8%-92.4%), 100% (91.0%-100%), and 91.8% (84.0%-96.6%) with RNA extraction, and 81.8% (68.0%-90.5%), 100% (91.0%-100%), and 90.4% (82.1%-95.0%) without RNA extraction. Rescue of infectious particles from saliva was limited to CT values below 26. In addition, we found significant IgM positive responses to SARS-CoV-2 in children positive for SARS-CoV-2 by NP swab and negative by saliva compared to other groups, indicating late infection onset (>7-10 days). Conclusions: Saliva is a suitable sample type for diagnosing children aged 10 years and under, including infants aged <1 year, even bypassing RNA extraction methods. Importantly, the detected viral RNA levels were significantly above the infectivity threshold in several samples. Further investigation is required to correlate SARS-CoV-2 RNA levels to viral transmission. |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Saliva Molecular Testing Bypassing RNA Extraction is Suitable for Monitoring and Diagnosing SARS-CoV-2 Infection in ChildrenSaliva molecular testingSARS-CoV-2/diagnosisChildHDE INF PEDBackground: Adults are being vaccinated against SARS-CoV-2 worldwide, but the longitudinal protection of these vaccines is uncertain, given the ongoing appearance of SARS-CoV-2 variants. Children remain largely unvaccinated and are susceptible to infection, with studies reporting that they actively transmit the virus even when asymptomatic, thus affecting the community. Methods: We investigated if saliva is an effective sample for detecting SARS-CoV-2 RNA and antibodies in children, and associated viral RNA levels to infectivity. For that, we used a saliva-based SARS-CoV-2 RT-qPCR test, preceded or not by RNA extraction, in 85 children aged 10 years and under, admitted to the hospital regardless of COVID-19 symptomatology. Amongst these, 29 (63.0%) presented at least one COVID-19 symptom, 46 (54.1%) were positive for SARS-CoV-2 infection, 28 (32.9%) were under the age of 1, and the mean (SD) age was 3.8 (3.4) years. Saliva samples were collected up to 48 h after a nasopharyngeal swab-RT-qPCR test. Results: In children aged 10 years and under, the sensitivity, specificity, and accuracy of saliva-RT-qPCR tests compared to NP swab-RT-qPCR were, respectively, 84.8% (71.8%-92.4%), 100% (91.0%-100%), and 91.8% (84.0%-96.6%) with RNA extraction, and 81.8% (68.0%-90.5%), 100% (91.0%-100%), and 90.4% (82.1%-95.0%) without RNA extraction. Rescue of infectious particles from saliva was limited to CT values below 26. In addition, we found significant IgM positive responses to SARS-CoV-2 in children positive for SARS-CoV-2 by NP swab and negative by saliva compared to other groups, indicating late infection onset (>7-10 days). Conclusions: Saliva is a suitable sample type for diagnosing children aged 10 years and under, including infants aged <1 year, even bypassing RNA extraction methods. Importantly, the detected viral RNA levels were significantly above the infectivity threshold in several samples. Further investigation is required to correlate SARS-CoV-2 RNA levels to viral transmission.Public Library of ScienceRepositório do Centro Hospitalar Universitário de Lisboa Central, EPEAlenquer, MMilheiro Silva, TAkpogheneta, OFerreira, FVale-Costa, SMedina-Lopes, MBatista, FGarcia, AMBarreto, VMPaulino, CCosta, JSobral, JDiniz-da-Costa, MLadeiro, SCorte-Real, RDelgado Alves, JLeite, RBDemengeot, JBrito, MJAmorim, MJ2022-07-29T15:03:17Z20222022-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/4175engPLoS One . 2022 Jun 15;17(6):e026838810.1371/journal.pone.0268388info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-10-28T10:30:18Zoai:repositorio.chlc.pt:10400.17/4175Portal AgregadorONGhttps://www.rcaap.pt/oai/openairemluisa.alvim@gmail.comopendoar:71602024-10-28T10:30:18Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Saliva Molecular Testing Bypassing RNA Extraction is Suitable for Monitoring and Diagnosing SARS-CoV-2 Infection in Children |
title |
Saliva Molecular Testing Bypassing RNA Extraction is Suitable for Monitoring and Diagnosing SARS-CoV-2 Infection in Children |
spellingShingle |
Saliva Molecular Testing Bypassing RNA Extraction is Suitable for Monitoring and Diagnosing SARS-CoV-2 Infection in Children Alenquer, M Saliva molecular testing SARS-CoV-2/diagnosis Child HDE INF PED |
title_short |
Saliva Molecular Testing Bypassing RNA Extraction is Suitable for Monitoring and Diagnosing SARS-CoV-2 Infection in Children |
title_full |
Saliva Molecular Testing Bypassing RNA Extraction is Suitable for Monitoring and Diagnosing SARS-CoV-2 Infection in Children |
title_fullStr |
Saliva Molecular Testing Bypassing RNA Extraction is Suitable for Monitoring and Diagnosing SARS-CoV-2 Infection in Children |
title_full_unstemmed |
Saliva Molecular Testing Bypassing RNA Extraction is Suitable for Monitoring and Diagnosing SARS-CoV-2 Infection in Children |
title_sort |
Saliva Molecular Testing Bypassing RNA Extraction is Suitable for Monitoring and Diagnosing SARS-CoV-2 Infection in Children |
author |
Alenquer, M |
author_facet |
Alenquer, M Milheiro Silva, T Akpogheneta, O Ferreira, F Vale-Costa, S Medina-Lopes, M Batista, F Garcia, AM Barreto, VM Paulino, C Costa, J Sobral, J Diniz-da-Costa, M Ladeiro, S Corte-Real, R Delgado Alves, J Leite, RB Demengeot, J Brito, MJ Amorim, MJ |
author_role |
author |
author2 |
Milheiro Silva, T Akpogheneta, O Ferreira, F Vale-Costa, S Medina-Lopes, M Batista, F Garcia, AM Barreto, VM Paulino, C Costa, J Sobral, J Diniz-da-Costa, M Ladeiro, S Corte-Real, R Delgado Alves, J Leite, RB Demengeot, J Brito, MJ Amorim, MJ |
author2_role |
author author author author author author author author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE |
dc.contributor.author.fl_str_mv |
Alenquer, M Milheiro Silva, T Akpogheneta, O Ferreira, F Vale-Costa, S Medina-Lopes, M Batista, F Garcia, AM Barreto, VM Paulino, C Costa, J Sobral, J Diniz-da-Costa, M Ladeiro, S Corte-Real, R Delgado Alves, J Leite, RB Demengeot, J Brito, MJ Amorim, MJ |
dc.subject.por.fl_str_mv |
Saliva molecular testing SARS-CoV-2/diagnosis Child HDE INF PED |
topic |
Saliva molecular testing SARS-CoV-2/diagnosis Child HDE INF PED |
description |
Background: Adults are being vaccinated against SARS-CoV-2 worldwide, but the longitudinal protection of these vaccines is uncertain, given the ongoing appearance of SARS-CoV-2 variants. Children remain largely unvaccinated and are susceptible to infection, with studies reporting that they actively transmit the virus even when asymptomatic, thus affecting the community. Methods: We investigated if saliva is an effective sample for detecting SARS-CoV-2 RNA and antibodies in children, and associated viral RNA levels to infectivity. For that, we used a saliva-based SARS-CoV-2 RT-qPCR test, preceded or not by RNA extraction, in 85 children aged 10 years and under, admitted to the hospital regardless of COVID-19 symptomatology. Amongst these, 29 (63.0%) presented at least one COVID-19 symptom, 46 (54.1%) were positive for SARS-CoV-2 infection, 28 (32.9%) were under the age of 1, and the mean (SD) age was 3.8 (3.4) years. Saliva samples were collected up to 48 h after a nasopharyngeal swab-RT-qPCR test. Results: In children aged 10 years and under, the sensitivity, specificity, and accuracy of saliva-RT-qPCR tests compared to NP swab-RT-qPCR were, respectively, 84.8% (71.8%-92.4%), 100% (91.0%-100%), and 91.8% (84.0%-96.6%) with RNA extraction, and 81.8% (68.0%-90.5%), 100% (91.0%-100%), and 90.4% (82.1%-95.0%) without RNA extraction. Rescue of infectious particles from saliva was limited to CT values below 26. In addition, we found significant IgM positive responses to SARS-CoV-2 in children positive for SARS-CoV-2 by NP swab and negative by saliva compared to other groups, indicating late infection onset (>7-10 days). Conclusions: Saliva is a suitable sample type for diagnosing children aged 10 years and under, including infants aged <1 year, even bypassing RNA extraction methods. Importantly, the detected viral RNA levels were significantly above the infectivity threshold in several samples. Further investigation is required to correlate SARS-CoV-2 RNA levels to viral transmission. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-07-29T15:03:17Z 2022 2022-01-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.17/4175 |
url |
http://hdl.handle.net/10400.17/4175 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
PLoS One . 2022 Jun 15;17(6):e0268388 10.1371/journal.pone.0268388 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Public Library of Science |
publisher.none.fl_str_mv |
Public Library of Science |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
mluisa.alvim@gmail.com |
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1817548657450287104 |