Cargando…
Reproducible breath metabolite changes in children with SARS-CoV-2 infection
SARS-CoV-2 infection is diagnosed through detection of specific viral nucleic acid or antigens from respiratory samples. These techniques are relatively expensive, slow, and susceptible to false-negative results. A rapid non-invasive method to detect infection would be highly advantageous. Compellin...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7743102/ https://www.ncbi.nlm.nih.gov/pubmed/33330891 http://dx.doi.org/10.1101/2020.12.04.20230755 |
_version_ | 1783624138408067072 |
---|---|
author | Berna, Amalia Z. Akaho, Elikplim H. Harris, Rebecca M. Congdon, Morgan Korn, Emilie Neher, Samuel M’Farrej, Mirna Burns, Julianne John, Audrey R. Odom |
author_facet | Berna, Amalia Z. Akaho, Elikplim H. Harris, Rebecca M. Congdon, Morgan Korn, Emilie Neher, Samuel M’Farrej, Mirna Burns, Julianne John, Audrey R. Odom |
author_sort | Berna, Amalia Z. |
collection | PubMed |
description | SARS-CoV-2 infection is diagnosed through detection of specific viral nucleic acid or antigens from respiratory samples. These techniques are relatively expensive, slow, and susceptible to false-negative results. A rapid non-invasive method to detect infection would be highly advantageous. Compelling evidence from canine biosensors and studies of adults with COVID-19 suggests that infection reproducibly alters human volatile organic compounds (VOCs) profiles. To determine whether pediatric infection is associated with VOC changes, we enrolled SARS-CoV-2-infected and -uninfected children admitted to a major pediatric academic medical center. Breath samples were collected from children and analyzed through state-of-the-art GCxGC-ToFMS. Isolated features included 84 targeted VOCs. Candidate biomarkers that were correlated with infection status were subsequently validated in a second, independent cohort of children. We thus find that six volatile organic compounds are significantly and reproducibly increased in the breath of SARS-CoV-2-infected children. Three aldehydes (octanal, nonanal, and heptanal) drew special attention, as aldehydes are also elevated in the breath of adults with COVID-19. Together, these biomarkers demonstrate high accuracy for distinguishing pediatric SARS-CoV-2 infection and support the ongoing development of novel breath-based diagnostics. |
format | Online Article Text |
id | pubmed-7743102 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-77431022020-12-17 Reproducible breath metabolite changes in children with SARS-CoV-2 infection Berna, Amalia Z. Akaho, Elikplim H. Harris, Rebecca M. Congdon, Morgan Korn, Emilie Neher, Samuel M’Farrej, Mirna Burns, Julianne John, Audrey R. Odom medRxiv Article SARS-CoV-2 infection is diagnosed through detection of specific viral nucleic acid or antigens from respiratory samples. These techniques are relatively expensive, slow, and susceptible to false-negative results. A rapid non-invasive method to detect infection would be highly advantageous. Compelling evidence from canine biosensors and studies of adults with COVID-19 suggests that infection reproducibly alters human volatile organic compounds (VOCs) profiles. To determine whether pediatric infection is associated with VOC changes, we enrolled SARS-CoV-2-infected and -uninfected children admitted to a major pediatric academic medical center. Breath samples were collected from children and analyzed through state-of-the-art GCxGC-ToFMS. Isolated features included 84 targeted VOCs. Candidate biomarkers that were correlated with infection status were subsequently validated in a second, independent cohort of children. We thus find that six volatile organic compounds are significantly and reproducibly increased in the breath of SARS-CoV-2-infected children. Three aldehydes (octanal, nonanal, and heptanal) drew special attention, as aldehydes are also elevated in the breath of adults with COVID-19. Together, these biomarkers demonstrate high accuracy for distinguishing pediatric SARS-CoV-2 infection and support the ongoing development of novel breath-based diagnostics. Cold Spring Harbor Laboratory 2021-05-07 /pmc/articles/PMC7743102/ /pubmed/33330891 http://dx.doi.org/10.1101/2020.12.04.20230755 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Berna, Amalia Z. Akaho, Elikplim H. Harris, Rebecca M. Congdon, Morgan Korn, Emilie Neher, Samuel M’Farrej, Mirna Burns, Julianne John, Audrey R. Odom Reproducible breath metabolite changes in children with SARS-CoV-2 infection |
title | Reproducible breath metabolite changes in children with SARS-CoV-2 infection |
title_full | Reproducible breath metabolite changes in children with SARS-CoV-2 infection |
title_fullStr | Reproducible breath metabolite changes in children with SARS-CoV-2 infection |
title_full_unstemmed | Reproducible breath metabolite changes in children with SARS-CoV-2 infection |
title_short | Reproducible breath metabolite changes in children with SARS-CoV-2 infection |
title_sort | reproducible breath metabolite changes in children with sars-cov-2 infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7743102/ https://www.ncbi.nlm.nih.gov/pubmed/33330891 http://dx.doi.org/10.1101/2020.12.04.20230755 |
work_keys_str_mv | AT bernaamaliaz reproduciblebreathmetabolitechangesinchildrenwithsarscov2infection AT akahoelikplimh reproduciblebreathmetabolitechangesinchildrenwithsarscov2infection AT harrisrebeccam reproduciblebreathmetabolitechangesinchildrenwithsarscov2infection AT congdonmorgan reproduciblebreathmetabolitechangesinchildrenwithsarscov2infection AT kornemilie reproduciblebreathmetabolitechangesinchildrenwithsarscov2infection AT nehersamuel reproduciblebreathmetabolitechangesinchildrenwithsarscov2infection AT mfarrejmirna reproduciblebreathmetabolitechangesinchildrenwithsarscov2infection AT burnsjulianne reproduciblebreathmetabolitechangesinchildrenwithsarscov2infection AT johnaudreyrodom reproduciblebreathmetabolitechangesinchildrenwithsarscov2infection |