Saliva for molecular detection of SARS‐CoV‐2 in pre‐school and school‐age children
SARS‐CoV‐2 diagnosis is a cornerstone for the management of coronavirus disease 2019 (COVID‐19). Numerous studies have assessed saliva performance over nasopharyngeal sampling (NPS), but data in young children are still rare. We explored saliva performance for SARS‐CoV‐2 detection by RT‐PCR accordin...
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Published in | Environmental microbiology Vol. 24; no. 10; pp. 4725 - 4737 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken, USA
John Wiley & Sons, Inc
01.10.2022
Wiley Subscription Services, Inc Society for Applied Microbiology and Wiley-Blackwell |
Series | Thematic Issue on Pathogen and Antimicrobial Resistance Ecology |
Subjects | |
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Abstract | SARS‐CoV‐2 diagnosis is a cornerstone for the management of coronavirus disease 2019 (COVID‐19). Numerous studies have assessed saliva performance over nasopharyngeal sampling (NPS), but data in young children are still rare. We explored saliva performance for SARS‐CoV‐2 detection by RT‐PCR according to the time interval from initial symptoms or patient serological status. We collected 509 NPS and saliva paired samples at initial diagnosis from 166 children under 12 years of age (including 57 children under 6), 106 between 12 and 17, and 237 adults. In children under 12, overall detection rate for SARS‐CoV‐2 was comparable in saliva and NPS, with an overall agreement of 89.8%. Saliva sensitivity was significantly lower than that of NPS (77.1% compared to 95.8%) in pre‐school and school‐age children but regained 96% when considering seronegative children only. This pattern was also observed to a lesser degree in adolescents but not in adults. Sensitivity of saliva was independent of symptoms, in contrary to NPS, whose sensitivity decreased significantly in asymptomatic subjects. Performance of saliva is excellent in children under 12 at early stages of infection. This reinforces saliva as a collection method for early and unbiased SARS‐CoV‐2 detection and a less invasive alternative for young children. |
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AbstractList | SARS‐CoV‐2 diagnosis is a cornerstone for the management of coronavirus disease 2019 (COVID‐19). Numerous studies have assessed saliva performance over nasopharyngeal sampling (NPS), but data in young children are still rare. We explored saliva performance for SARS‐CoV‐2 detection by RT‐PCR according to the time interval from initial symptoms or patient serological status. We collected 509 NPS and saliva paired samples at initial diagnosis from 166 children under 12 years of age (including 57 children under 6), 106 between 12 and 17, and 237 adults. In children under 12, overall detection rate for SARS‐CoV‐2 was comparable in saliva and NPS, with an overall agreement of 89.8%. Saliva sensitivity was significantly lower than that of NPS (77.1% compared to 95.8%) in pre‐school and school‐age children but regained 96% when considering seronegative children only. This pattern was also observed to a lesser degree in adolescents but not in adults. Sensitivity of saliva was independent of symptoms, in contrary to NPS, whose sensitivity decreased significantly in asymptomatic subjects. Performance of saliva is excellent in children under 12 at early stages of infection. This reinforces saliva as a collection method for early and unbiased SARS‐CoV‐2 detection and a less invasive alternative for young children. SARS-CoV-2 diagnosis is a cornerstone for the management of coronavirus disease 2019 (COVID-19). Numerous studies have assessed saliva performance over nasopharyngeal sampling (NPS), but data in young children are still rare. We explored saliva performance for SARS-CoV-2 detection by RT-PCR according to the time interval from initial symptoms or patient serological status. We collected 509 NPS and saliva paired samples at initial diagnosis from 166 children under 12 years of age (including 57 children under 6), 106 between 12 and 17, and 237 adults. In children under 12, overall detection rate for SARS-CoV-2 was comparable in saliva and NPS, with an overall agreement of 89.8%. Saliva sensitivity was significantly lower than that of NPS (77.1% compared to 95.8%) in pre-school and school-age children but regained 96% when considering seronegative children only. This pattern was also observed to a lesser degree in adolescents but not in adults. Sensitivity of saliva was independent of symptoms, in contrary to NPS, whose sensitivity decreased significantly in asymptomatic subjects. Performance of saliva is excellent in children under 12 at early stages of infection. This reinforces saliva as a collection method for early and unbiased SARS-CoV-2 detection and a less invasive alternative for young children.SARS-CoV-2 diagnosis is a cornerstone for the management of coronavirus disease 2019 (COVID-19). Numerous studies have assessed saliva performance over nasopharyngeal sampling (NPS), but data in young children are still rare. We explored saliva performance for SARS-CoV-2 detection by RT-PCR according to the time interval from initial symptoms or patient serological status. We collected 509 NPS and saliva paired samples at initial diagnosis from 166 children under 12 years of age (including 57 children under 6), 106 between 12 and 17, and 237 adults. In children under 12, overall detection rate for SARS-CoV-2 was comparable in saliva and NPS, with an overall agreement of 89.8%. Saliva sensitivity was significantly lower than that of NPS (77.1% compared to 95.8%) in pre-school and school-age children but regained 96% when considering seronegative children only. This pattern was also observed to a lesser degree in adolescents but not in adults. Sensitivity of saliva was independent of symptoms, in contrary to NPS, whose sensitivity decreased significantly in asymptomatic subjects. Performance of saliva is excellent in children under 12 at early stages of infection. This reinforces saliva as a collection method for early and unbiased SARS-CoV-2 detection and a less invasive alternative for young children. |
Author | Benoist, Gregoire Quartier, Pierre Galeotti, Caroline Delaunay‐Moisan, Agnes Rifai, Mahmoud Basmaci, Romain Werf, Sylvie Moltrecht, Brigitte Gajdos, Vincent Behillil, Sylvie Berthaud, Romain Maurin, Caroline Morelle, Guillaume Savetier‐Leroy, Catherine Briand, Nelly Lorrot, Mathie Lorenzi, Michelle Sermet‐Gaudelus, Isabelle Leruez‐Ville, Marianne Guilleminot, Tiffany Padavia, Faheemah M'Sakni, Zakary Pontual, Loic Bader‐Meunier, Brigitte Semeraro, Michaela Elenga, Narcisse Crespin, Matis Bouazza, Naim |
AuthorAffiliation | 13 Centre de Référence des Virus émergents. Institut Pasteur France 14 Service de Pédiatrie Générale Hôpital Jean Verdier, Assistance Publique Hôpitaux de Paris, Université Sorbonne Paris Nord France 1 Université Paris‐Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC) Gif‐sur‐Yvette France 7 Service de Pédiatrie Générale, Hôpital Louis Mourier Assistance Publique Hôpitaux de Paris France 11 Centre de Références Maladies Rares Mucoviscidose et Maladies Apparentées CHU Necker Enfants Malades, Assistance Publique Hôpitaux de Paris Paris 75015 France 9 Service de Pédiatrie Générale Hôpital Antoine Beclère, Assistance Publique Hôpitaux de Paris France 10 Service de Pédiatrie Générale Hôpital Armand Trousseau, Assistance Publique Hôpitaux de Paris France 5 Reference centre for Rheumatic, AutoImmune and Systemic Diseases in Children (RAISE), Imagine Institute,Inserm U 1163 Paris France 15 Service de Pédiatrie Générale Centre Hospitalier de Cayenne Andrée Rosemon France 3 Unité de |
AuthorAffiliation_xml | – name: 4 Department of Paediatric Hematology‐Immunology and Rheumatology Necker‐Enfants Malades Hospital, AP‐HP Paris France – name: 12 Ministère de l'Education Nationale Médecine Scolaire France – name: 7 Service de Pédiatrie Générale, Hôpital Louis Mourier Assistance Publique Hôpitaux de Paris France – name: 15 Service de Pédiatrie Générale Centre Hospitalier de Cayenne Andrée Rosemon France – name: 9 Service de Pédiatrie Générale Hôpital Antoine Beclère, Assistance Publique Hôpitaux de Paris France – name: 1 Université Paris‐Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC) Gif‐sur‐Yvette France – name: 14 Service de Pédiatrie Générale Hôpital Jean Verdier, Assistance Publique Hôpitaux de Paris, Université Sorbonne Paris Nord France – name: 3 Unité de Recherche Clinique‐Centre Investigation Clinique, Hôpital Necker‐Enfants Malades, Assistance Publique Hôpitaux de Paris France – name: 10 Service de Pédiatrie Générale Hôpital Armand Trousseau, Assistance Publique Hôpitaux de Paris France – name: 13 Centre de Référence des Virus émergents. Institut Pasteur France – name: 6 Service de Pédiatrie Générale, Hôpital Kremlin Bicêtre Assistance Publique Hôpitaux de Paris France – name: 2 Virology Laboratory Hospital Necker‐Enfants‐Malades, Assistance Publique Hôpitaux de Paris UMR 7328 Imagine Paris Cité Paris France – name: 5 Reference centre for Rheumatic, AutoImmune and Systemic Diseases in Children (RAISE), Imagine Institute,Inserm U 1163 Paris France – name: 17 European Reference Network for Rare Respiratory Diseases Belgium – name: 16 Institut Necker Enfants Malades, INSERM UMR‐SU1151, Université Paris Cité France – name: 8 Service de Pédiatrie Générale Hôpital Ambroise Paré, Assistance Publique Hôpitaux de Paris France – name: 11 Centre de Références Maladies Rares Mucoviscidose et Maladies Apparentées CHU Necker Enfants Malades, Assistance Publique Hôpitaux de Paris Paris 75015 France |
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Notes | Funding information Brigitte Moltrecht, Sylvie van der Werf, Marianne Leruez‐Ville, and Isabelle Sermet‐Gaudelus are co‐last authors. Assistance Publique ‐ Hôpitaux de Paris, Grant/Award Number: Code projet: APHP200467/N° IDRCB: 2020‐A00999; Ministry of Health ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 PMCID: PMC9538513 Funding information Assistance Publique ‐ Hôpitaux de Paris, Grant/Award Number: Code projet: APHP200467/N° IDRCB: 2020‐A00999; Ministry of Health |
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Snippet | SARS‐CoV‐2 diagnosis is a cornerstone for the management of coronavirus disease 2019 (COVID‐19). Numerous studies have assessed saliva performance over... SARS-CoV-2 diagnosis is a cornerstone for the management of coronavirus disease 2019 (COVID-19). Numerous studies have assessed saliva performance over... |
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SubjectTerms | Adolescents Adults Age Children Coronaviruses COVID-19 COVID-19 infection Detection Diagnosis Life Sciences microbiology Nucleotide sequence patients Research Paper Research Papers Saliva Sensitivity Severe acute respiratory syndrome Severe acute respiratory syndrome coronavirus 2 Signs and symptoms Symptoms Viral diseases |
Title | Saliva for molecular detection of SARS‐CoV‐2 in pre‐school and school‐age children |
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