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Saliva molecular testing bypassing RNA extraction is suitable for monitoring and diagnosing SARS-CoV-2 infection in children.
Alenquer, Marta; Milheiro Silva, Tiago; Akpogheneta, Onome; Ferreira, Filipe; Vale-Costa, Sílvia; Medina-Lopes, Mónica; Batista, Frederico; Garcia, Ana Margarida; Barreto, Vasco M; Paulino, Cathy; Costa, João; Sobral, João; Diniz-da-Costa, Maria; Ladeiro, Susana; Corte-Real, Rita; Delgado Alves, José; Leite, Ricardo B; Demengeot, Jocelyne; Rocha Brito, Maria João; Amorim, Maria João.
  • Alenquer M; Cell Biology of Viral Infection Lab, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
  • Milheiro Silva T; Pediatric Infectious Disease Unit, Hospital Dona Estefânia, Centro Hospitalar Universitário Lisboa Central, Lisboa, Portugal.
  • Akpogheneta O; Lymphocyte Physiology Lab, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
  • Ferreira F; Cell Biology of Viral Infection Lab, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
  • Vale-Costa S; Cell Biology of Viral Infection Lab, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
  • Medina-Lopes M; Cell Biology of Viral Infection Lab, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
  • Batista F; Department of Medicine 4, Hospital Prof Doutor Fernando Fonseca, Amadora, Portugal.
  • Garcia AM; Pediatric Infectious Disease Unit, Hospital Dona Estefânia, Centro Hospitalar Universitário Lisboa Central, Lisboa, Portugal.
  • Barreto VM; CEDOC NOVA, Centro de Estudos de Doenças Crónicas, Nova Medical School, Universidade Nova de Lisboa, Lisboa, Portugal.
  • Paulino C; Genomics Unit, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
  • Costa J; Genomics Unit, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
  • Sobral J; Genomics Unit, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
  • Diniz-da-Costa M; Genomics Unit, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
  • Ladeiro S; Genomics Unit, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
  • Corte-Real R; Molecular Biology Laboratory, Department of Clinical Pathology, Centro Hospitalar Universitário Lisboa Central, Lisboa, Portugal.
  • Delgado Alves J; Department of Medicine 4, Hospital Prof Doutor Fernando Fonseca, Amadora, Portugal.
  • Leite RB; CEDOC NOVA, Centro de Estudos de Doenças Crónicas, Nova Medical School, Universidade Nova de Lisboa, Lisboa, Portugal.
  • Demengeot J; Genomics Unit, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
  • Rocha Brito MJ; Lymphocyte Physiology Lab, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
  • Amorim MJ; Pediatric Infectious Disease Unit, Hospital Dona Estefânia, Centro Hospitalar Universitário Lisboa Central, Lisboa, Portugal.
PLoS One ; 17(6): e0268388, 2022.
Article in English | MEDLINE | ID: covidwho-1892317
ABSTRACT

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.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Diagnostic study / Experimental Studies / Prognostic study / Randomized controlled trials Topics: Long Covid / Vaccines / Variants Limits: Adult / Child / Humans Language: English Journal: PLoS One Journal subject: Science / Medicine Year: 2022 Document Type: Article Affiliation country: Journal.pone.0268388

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Diagnostic study / Experimental Studies / Prognostic study / Randomized controlled trials Topics: Long Covid / Vaccines / Variants Limits: Adult / Child / Humans Language: English Journal: PLoS One Journal subject: Science / Medicine Year: 2022 Document Type: Article Affiliation country: Journal.pone.0268388