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Performance of Saliva Samples for COVID-19 Diagnosis by Using the Allplex(TM) 2019-nCoV Assay Kit
Background: Although the nasopharyngeal swab (NPS) is the reference sampling method for the detection of SARS-Cov-2, it is not always possible to collect NPS in some patients. Saliva represents an interesting sampling method because it is less invasive and more convenient in patients with nasal or p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943474/ https://www.ncbi.nlm.nih.gov/pubmed/33718401 http://dx.doi.org/10.3389/fmed.2021.617399 |
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author | Tapia, Cecilia V. Marcia, Campos Ivone, Mora Nadia, Pozas Lesly, Morales Camila, Guzmán Valentina, Aguilera Paula, Ibarra Fabien, Magne |
author_facet | Tapia, Cecilia V. Marcia, Campos Ivone, Mora Nadia, Pozas Lesly, Morales Camila, Guzmán Valentina, Aguilera Paula, Ibarra Fabien, Magne |
author_sort | Tapia, Cecilia V. |
collection | PubMed |
description | Background: Although the nasopharyngeal swab (NPS) is the reference sampling method for the detection of SARS-Cov-2, it is not always possible to collect NPS in some patients. Saliva represents an interesting sampling method because it is less invasive and more convenient in patients with nasal or pharyngeal lesions. Objective: To compare the RT-qPCR test performances of saliva samples with nasal mid-turbinate swab (NMTS) and NPS samples in a cohort of ambulatory patients suspected of having COVID-19. Study Design: For each of the 112 enrolled patients, NPS, NMTS, and saliva samples were collected and tested for SARS-Cov-2 detection using three different target genes (RdRP, N and E genes) by RT-qPCR. Results: Among the positive samples (56/112), saliva samples showed a lower percentage of SARS-Cov-2 detection compared to NPS samples, (85.7 vs. 96.4%), while still a lower percentage was observed for NMTS samples (78.6%). In average, saliva samples showed higher Ct values for all tested target genes, compared to those from NPS and NMTS samples. Conclusions: By using the Allplex(TM) 2019-nCoV Assay Kit, saliva samples showed lower sensitivity for SARS CoV-2 compared to NPS samples; however, the not detected cases had lower viral burden in NPS samples (CT values >33) representing an interesting alternative sampling method in patients in which it is not possible to take a NPS sample. |
format | Online Article Text |
id | pubmed-7943474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79434742021-03-11 Performance of Saliva Samples for COVID-19 Diagnosis by Using the Allplex(TM) 2019-nCoV Assay Kit Tapia, Cecilia V. Marcia, Campos Ivone, Mora Nadia, Pozas Lesly, Morales Camila, Guzmán Valentina, Aguilera Paula, Ibarra Fabien, Magne Front Med (Lausanne) Medicine Background: Although the nasopharyngeal swab (NPS) is the reference sampling method for the detection of SARS-Cov-2, it is not always possible to collect NPS in some patients. Saliva represents an interesting sampling method because it is less invasive and more convenient in patients with nasal or pharyngeal lesions. Objective: To compare the RT-qPCR test performances of saliva samples with nasal mid-turbinate swab (NMTS) and NPS samples in a cohort of ambulatory patients suspected of having COVID-19. Study Design: For each of the 112 enrolled patients, NPS, NMTS, and saliva samples were collected and tested for SARS-Cov-2 detection using three different target genes (RdRP, N and E genes) by RT-qPCR. Results: Among the positive samples (56/112), saliva samples showed a lower percentage of SARS-Cov-2 detection compared to NPS samples, (85.7 vs. 96.4%), while still a lower percentage was observed for NMTS samples (78.6%). In average, saliva samples showed higher Ct values for all tested target genes, compared to those from NPS and NMTS samples. Conclusions: By using the Allplex(TM) 2019-nCoV Assay Kit, saliva samples showed lower sensitivity for SARS CoV-2 compared to NPS samples; however, the not detected cases had lower viral burden in NPS samples (CT values >33) representing an interesting alternative sampling method in patients in which it is not possible to take a NPS sample. Frontiers Media S.A. 2021-02-24 /pmc/articles/PMC7943474/ /pubmed/33718401 http://dx.doi.org/10.3389/fmed.2021.617399 Text en Copyright © 2021 Tapia, Marcia, Ivone, Nadia, Lesly, Camila, Valentina, Paula and Fabien. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Tapia, Cecilia V. Marcia, Campos Ivone, Mora Nadia, Pozas Lesly, Morales Camila, Guzmán Valentina, Aguilera Paula, Ibarra Fabien, Magne Performance of Saliva Samples for COVID-19 Diagnosis by Using the Allplex(TM) 2019-nCoV Assay Kit |
title | Performance of Saliva Samples for COVID-19 Diagnosis by Using the Allplex(TM) 2019-nCoV Assay Kit |
title_full | Performance of Saliva Samples for COVID-19 Diagnosis by Using the Allplex(TM) 2019-nCoV Assay Kit |
title_fullStr | Performance of Saliva Samples for COVID-19 Diagnosis by Using the Allplex(TM) 2019-nCoV Assay Kit |
title_full_unstemmed | Performance of Saliva Samples for COVID-19 Diagnosis by Using the Allplex(TM) 2019-nCoV Assay Kit |
title_short | Performance of Saliva Samples for COVID-19 Diagnosis by Using the Allplex(TM) 2019-nCoV Assay Kit |
title_sort | performance of saliva samples for covid-19 diagnosis by using the allplex(tm) 2019-ncov assay kit |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943474/ https://www.ncbi.nlm.nih.gov/pubmed/33718401 http://dx.doi.org/10.3389/fmed.2021.617399 |
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