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Efficient Detection of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) from Exhaled Breath
Severe acute respiratory syndrome–coronavirus 2 (SARS-CoV-2) is transmitted through airborne particles in exhaled breath, causing severe respiratory disease, coronavirus disease–2019 (COVID-19), in some patients. Samples for SARS-CoV-2 testing are typically collected by nasopharyngeal swab, with the...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Investigative Pathology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8480135/ https://www.ncbi.nlm.nih.gov/pubmed/34600137 http://dx.doi.org/10.1016/j.jmoldx.2021.09.005 |
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author | Duan, Chaorui Buerer, Luke Wang, Jing Kaplan, Samuel Sabalewski, Gavin Jay, Gregory D. Monaghan, Sean F. Arena, Andrea E. Fairbrother, William G. |
author_facet | Duan, Chaorui Buerer, Luke Wang, Jing Kaplan, Samuel Sabalewski, Gavin Jay, Gregory D. Monaghan, Sean F. Arena, Andrea E. Fairbrother, William G. |
author_sort | Duan, Chaorui |
collection | PubMed |
description | Severe acute respiratory syndrome–coronavirus 2 (SARS-CoV-2) is transmitted through airborne particles in exhaled breath, causing severe respiratory disease, coronavirus disease–2019 (COVID-19), in some patients. Samples for SARS-CoV-2 testing are typically collected by nasopharyngeal swab, with the virus detected by PCR; however, patients can test positive for 3 months after infection. Without the capacity to assay SARS-CoV-2 in breath, it is not possible to understand the risk for transmission from infected individuals. To detect virus in breath, the Bubbler—a breathalyzer that reverse-transcribes RNA from SARS-CoV-2 particles into a sample-specific barcoded cDNA—was developed. In a study of 70 hospitalized patients, the Bubbler was both more predictive of lower respiratory tract involvement (abnormal chest X-ray) and less invasive than alternatives. Samples tested using the Bubbler were threefold more enriched for SARS-CoV-2 RNA than were samples from tongue swabs, implying that virus particles were being directly sampled. The barcode-enabled Bubbler was used for simultaneous diagnosis in large batches of pooled samples at a lower limit of detection of 334 genomic copies per sample. Diagnosis by sequencing can provide additional information, such as viral load and strain identity. The Bubbler was configured to sample nucleic acids in water droplets circulating in air, demonstrating its potential in environmental monitoring and the protective effect of adequate ventilation. |
format | Online Article Text |
id | pubmed-8480135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Investigative Pathology |
record_format | MEDLINE/PubMed |
spelling | pubmed-84801352021-09-30 Efficient Detection of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) from Exhaled Breath Duan, Chaorui Buerer, Luke Wang, Jing Kaplan, Samuel Sabalewski, Gavin Jay, Gregory D. Monaghan, Sean F. Arena, Andrea E. Fairbrother, William G. J Mol Diagn Regular Article Severe acute respiratory syndrome–coronavirus 2 (SARS-CoV-2) is transmitted through airborne particles in exhaled breath, causing severe respiratory disease, coronavirus disease–2019 (COVID-19), in some patients. Samples for SARS-CoV-2 testing are typically collected by nasopharyngeal swab, with the virus detected by PCR; however, patients can test positive for 3 months after infection. Without the capacity to assay SARS-CoV-2 in breath, it is not possible to understand the risk for transmission from infected individuals. To detect virus in breath, the Bubbler—a breathalyzer that reverse-transcribes RNA from SARS-CoV-2 particles into a sample-specific barcoded cDNA—was developed. In a study of 70 hospitalized patients, the Bubbler was both more predictive of lower respiratory tract involvement (abnormal chest X-ray) and less invasive than alternatives. Samples tested using the Bubbler were threefold more enriched for SARS-CoV-2 RNA than were samples from tongue swabs, implying that virus particles were being directly sampled. The barcode-enabled Bubbler was used for simultaneous diagnosis in large batches of pooled samples at a lower limit of detection of 334 genomic copies per sample. Diagnosis by sequencing can provide additional information, such as viral load and strain identity. The Bubbler was configured to sample nucleic acids in water droplets circulating in air, demonstrating its potential in environmental monitoring and the protective effect of adequate ventilation. American Society for Investigative Pathology 2021-12 /pmc/articles/PMC8480135/ /pubmed/34600137 http://dx.doi.org/10.1016/j.jmoldx.2021.09.005 Text en © 2021 Association for Molecular Pathology and American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved. |
spellingShingle | Regular Article Duan, Chaorui Buerer, Luke Wang, Jing Kaplan, Samuel Sabalewski, Gavin Jay, Gregory D. Monaghan, Sean F. Arena, Andrea E. Fairbrother, William G. Efficient Detection of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) from Exhaled Breath |
title | Efficient Detection of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) from Exhaled Breath |
title_full | Efficient Detection of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) from Exhaled Breath |
title_fullStr | Efficient Detection of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) from Exhaled Breath |
title_full_unstemmed | Efficient Detection of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) from Exhaled Breath |
title_short | Efficient Detection of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) from Exhaled Breath |
title_sort | efficient detection of severe acute respiratory syndrome coronavirus 2 (sars-cov-2) from exhaled breath |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8480135/ https://www.ncbi.nlm.nih.gov/pubmed/34600137 http://dx.doi.org/10.1016/j.jmoldx.2021.09.005 |
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