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Virologic features of SARS-CoV-2 infection in children
BACKGROUND: Data on pediatric COVID-19 has lagged behind adults throughout the pandemic. An understanding of SARS-CoV-2 viral dynamics in children would enable data-driven public health guidance. METHODS: Respiratory swabs were collected from children with COVID-19. Viral load was quantified by RT-P...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8193793/ https://www.ncbi.nlm.nih.gov/pubmed/34124714 http://dx.doi.org/10.1101/2021.05.30.21258086 |
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author | Yonker, Lael M. Boucau, Julie Regan, James Choudhary, Manish C. Burns, Madeleine D. Young, Nicola Farkas, Eva J. Davis, Jameson P. Moschovis, Peter P. Kinane, T. Bernard Fasano, Alessio Neilan, Anne M. Li, Jonathan Z. Barczak, Amy K. |
author_facet | Yonker, Lael M. Boucau, Julie Regan, James Choudhary, Manish C. Burns, Madeleine D. Young, Nicola Farkas, Eva J. Davis, Jameson P. Moschovis, Peter P. Kinane, T. Bernard Fasano, Alessio Neilan, Anne M. Li, Jonathan Z. Barczak, Amy K. |
author_sort | Yonker, Lael M. |
collection | PubMed |
description | BACKGROUND: Data on pediatric COVID-19 has lagged behind adults throughout the pandemic. An understanding of SARS-CoV-2 viral dynamics in children would enable data-driven public health guidance. METHODS: Respiratory swabs were collected from children with COVID-19. Viral load was quantified by RT-PCR; viral culture was assessed by direct observation of cytopathic effects and semiquantitative viral titers. Correlations with age, symptom duration, and disease severity were analyzed. SARS-CoV-2 whole genome sequences were compared with contemporaneous sequences. RESULTS: 110 children with COVID-19 (median age 10 years, range 2 weeks-21 years) were included in this study. Age did not impact SARS-CoV-2 viral load. Children were most infectious within the first five days of illness, and severe disease did not correlate with increased viral loads. Pediatric SARS-CoV-2 sequences were representative of those in the community and novel variants were identified. CONCLUSIONS: Symptomatic and asymptomatic children can carry high quantities of live, replicating SARS-CoV-2, creating a potential reservoir for transmission and evolution of genetic variants. As guidance around social distancing and masking evolves following vaccine uptake in older populations, a clear understanding of SARS-CoV-2 infection dynamics in children is critical for rational development of public health policies and vaccination strategies to mitigate the impact of COVID-19. |
format | Online Article Text |
id | pubmed-8193793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-81937932021-06-12 Virologic features of SARS-CoV-2 infection in children Yonker, Lael M. Boucau, Julie Regan, James Choudhary, Manish C. Burns, Madeleine D. Young, Nicola Farkas, Eva J. Davis, Jameson P. Moschovis, Peter P. Kinane, T. Bernard Fasano, Alessio Neilan, Anne M. Li, Jonathan Z. Barczak, Amy K. medRxiv Article BACKGROUND: Data on pediatric COVID-19 has lagged behind adults throughout the pandemic. An understanding of SARS-CoV-2 viral dynamics in children would enable data-driven public health guidance. METHODS: Respiratory swabs were collected from children with COVID-19. Viral load was quantified by RT-PCR; viral culture was assessed by direct observation of cytopathic effects and semiquantitative viral titers. Correlations with age, symptom duration, and disease severity were analyzed. SARS-CoV-2 whole genome sequences were compared with contemporaneous sequences. RESULTS: 110 children with COVID-19 (median age 10 years, range 2 weeks-21 years) were included in this study. Age did not impact SARS-CoV-2 viral load. Children were most infectious within the first five days of illness, and severe disease did not correlate with increased viral loads. Pediatric SARS-CoV-2 sequences were representative of those in the community and novel variants were identified. CONCLUSIONS: Symptomatic and asymptomatic children can carry high quantities of live, replicating SARS-CoV-2, creating a potential reservoir for transmission and evolution of genetic variants. As guidance around social distancing and masking evolves following vaccine uptake in older populations, a clear understanding of SARS-CoV-2 infection dynamics in children is critical for rational development of public health policies and vaccination strategies to mitigate the impact of COVID-19. Cold Spring Harbor Laboratory 2021-08-17 /pmc/articles/PMC8193793/ /pubmed/34124714 http://dx.doi.org/10.1101/2021.05.30.21258086 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Yonker, Lael M. Boucau, Julie Regan, James Choudhary, Manish C. Burns, Madeleine D. Young, Nicola Farkas, Eva J. Davis, Jameson P. Moschovis, Peter P. Kinane, T. Bernard Fasano, Alessio Neilan, Anne M. Li, Jonathan Z. Barczak, Amy K. Virologic features of SARS-CoV-2 infection in children |
title | Virologic features of SARS-CoV-2 infection in children |
title_full | Virologic features of SARS-CoV-2 infection in children |
title_fullStr | Virologic features of SARS-CoV-2 infection in children |
title_full_unstemmed | Virologic features of SARS-CoV-2 infection in children |
title_short | Virologic features of SARS-CoV-2 infection in children |
title_sort | virologic features of sars-cov-2 infection in children |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8193793/ https://www.ncbi.nlm.nih.gov/pubmed/34124714 http://dx.doi.org/10.1101/2021.05.30.21258086 |
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