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SARS-CoV-2 RNA detected in blood products from patients with COVID-19 is not associated with infectious virus
Background: Laboratory diagnosis of SARS-CoV-2 infection (the cause of COVID-19) uses PCR to detect viral RNA (vRNA) in respiratory samples. SARS-CoV-2 RNA has also been detected in other sample types, but there is limited understanding of the clinical or laboratory significance of its detection in...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689603/ https://www.ncbi.nlm.nih.gov/pubmed/33283055 http://dx.doi.org/10.12688/wellcomeopenres.16002.2 |
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author | Andersson, Monique I. Arancibia-Carcamo, Carolina V. Auckland, Kathryn Baillie, J. Kenneth Barnes, Eleanor Beneke, Tom Bibi, Sagida Brooks, Tim Carroll, Miles Crook, Derrick Dingle, Kate Dold, Christina Downs, Louise O. Dunn, Laura Eyre, David W. Gilbert Jaramillo, Javier Harvala, Heli Hoosdally, Sarah Ijaz, Samreen James, Tim James, William Jeffery, Katie Justice, Anita Klenerman, Paul Knight, Julian C. Knight, Michael Liu, Xu Lumley, Sheila F. Matthews, Philippa C. McNaughton, Anna L. Mentzer, Alexander J. Mongkolsapaya, Juthathip Oakley, Sarah Oliveira, Marta S. Peto, Timothy Ploeg, Rutger J. Ratcliff, Jeremy Robbins, Melanie J. Roberts, David J. Rudkin, Justine Russell, Rebecca A. Screaton, Gavin Semple, Malcolm G. Skelly, Donal Simmonds, Peter Stoesser, Nicole Turtle, Lance Wareing, Susan Zambon, Maria |
author_facet | Andersson, Monique I. Arancibia-Carcamo, Carolina V. Auckland, Kathryn Baillie, J. Kenneth Barnes, Eleanor Beneke, Tom Bibi, Sagida Brooks, Tim Carroll, Miles Crook, Derrick Dingle, Kate Dold, Christina Downs, Louise O. Dunn, Laura Eyre, David W. Gilbert Jaramillo, Javier Harvala, Heli Hoosdally, Sarah Ijaz, Samreen James, Tim James, William Jeffery, Katie Justice, Anita Klenerman, Paul Knight, Julian C. Knight, Michael Liu, Xu Lumley, Sheila F. Matthews, Philippa C. McNaughton, Anna L. Mentzer, Alexander J. Mongkolsapaya, Juthathip Oakley, Sarah Oliveira, Marta S. Peto, Timothy Ploeg, Rutger J. Ratcliff, Jeremy Robbins, Melanie J. Roberts, David J. Rudkin, Justine Russell, Rebecca A. Screaton, Gavin Semple, Malcolm G. Skelly, Donal Simmonds, Peter Stoesser, Nicole Turtle, Lance Wareing, Susan Zambon, Maria |
author_sort | Andersson, Monique I. |
collection | PubMed |
description | Background: Laboratory diagnosis of SARS-CoV-2 infection (the cause of COVID-19) uses PCR to detect viral RNA (vRNA) in respiratory samples. SARS-CoV-2 RNA has also been detected in other sample types, but there is limited understanding of the clinical or laboratory significance of its detection in blood. Methods: We undertook a systematic literature review to assimilate the evidence for the frequency of vRNA in blood, and to identify associated clinical characteristics. We performed RT-PCR in serum samples from a UK clinical cohort of acute and convalescent COVID-19 cases (n=212), together with convalescent plasma samples collected by NHS Blood and Transplant (NHSBT) (n=462 additional samples). To determine whether PCR-positive blood samples could pose an infection risk, we attempted virus isolation from a subset of RNA-positive samples. Results: We identified 28 relevant studies, reporting SARS-CoV-2 RNA in 0-76% of blood samples; pooled estimate 10% (95%CI 5-18%). Among serum samples from our clinical cohort, 27/212 (12.7%) had SARS-CoV-2 RNA detected by RT-PCR. RNA detection occurred in samples up to day 20 post symptom onset, and was associated with more severe disease (multivariable odds ratio 7.5). Across all samples collected ≥28 days post symptom onset, 0/494 (0%, 95%CI 0-0.7%) had vRNA detected. Among our PCR-positive samples, cycle threshold (ct) values were high (range 33.5-44.8), suggesting low vRNA copy numbers. PCR-positive sera inoculated into cell culture did not produce any cytopathic effect or yield an increase in detectable SARS-CoV-2 RNA. There was a relationship between RT-PCR negativity and the presence of total SARS-CoV-2 antibody (p=0.02). Conclusions: vRNA was detectable at low viral loads in a minority of serum samples collected in acute infection, but was not associated with infectious SARS-CoV-2 (within the limitations of the assays used). This work helps to inform biosafety precautions for handling blood products from patients with current or previous COVID-19. |
format | Online Article Text |
id | pubmed-7689603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-76896032020-12-04 SARS-CoV-2 RNA detected in blood products from patients with COVID-19 is not associated with infectious virus Andersson, Monique I. Arancibia-Carcamo, Carolina V. Auckland, Kathryn Baillie, J. Kenneth Barnes, Eleanor Beneke, Tom Bibi, Sagida Brooks, Tim Carroll, Miles Crook, Derrick Dingle, Kate Dold, Christina Downs, Louise O. Dunn, Laura Eyre, David W. Gilbert Jaramillo, Javier Harvala, Heli Hoosdally, Sarah Ijaz, Samreen James, Tim James, William Jeffery, Katie Justice, Anita Klenerman, Paul Knight, Julian C. Knight, Michael Liu, Xu Lumley, Sheila F. Matthews, Philippa C. McNaughton, Anna L. Mentzer, Alexander J. Mongkolsapaya, Juthathip Oakley, Sarah Oliveira, Marta S. Peto, Timothy Ploeg, Rutger J. Ratcliff, Jeremy Robbins, Melanie J. Roberts, David J. Rudkin, Justine Russell, Rebecca A. Screaton, Gavin Semple, Malcolm G. Skelly, Donal Simmonds, Peter Stoesser, Nicole Turtle, Lance Wareing, Susan Zambon, Maria Wellcome Open Res Research Article Background: Laboratory diagnosis of SARS-CoV-2 infection (the cause of COVID-19) uses PCR to detect viral RNA (vRNA) in respiratory samples. SARS-CoV-2 RNA has also been detected in other sample types, but there is limited understanding of the clinical or laboratory significance of its detection in blood. Methods: We undertook a systematic literature review to assimilate the evidence for the frequency of vRNA in blood, and to identify associated clinical characteristics. We performed RT-PCR in serum samples from a UK clinical cohort of acute and convalescent COVID-19 cases (n=212), together with convalescent plasma samples collected by NHS Blood and Transplant (NHSBT) (n=462 additional samples). To determine whether PCR-positive blood samples could pose an infection risk, we attempted virus isolation from a subset of RNA-positive samples. Results: We identified 28 relevant studies, reporting SARS-CoV-2 RNA in 0-76% of blood samples; pooled estimate 10% (95%CI 5-18%). Among serum samples from our clinical cohort, 27/212 (12.7%) had SARS-CoV-2 RNA detected by RT-PCR. RNA detection occurred in samples up to day 20 post symptom onset, and was associated with more severe disease (multivariable odds ratio 7.5). Across all samples collected ≥28 days post symptom onset, 0/494 (0%, 95%CI 0-0.7%) had vRNA detected. Among our PCR-positive samples, cycle threshold (ct) values were high (range 33.5-44.8), suggesting low vRNA copy numbers. PCR-positive sera inoculated into cell culture did not produce any cytopathic effect or yield an increase in detectable SARS-CoV-2 RNA. There was a relationship between RT-PCR negativity and the presence of total SARS-CoV-2 antibody (p=0.02). Conclusions: vRNA was detectable at low viral loads in a minority of serum samples collected in acute infection, but was not associated with infectious SARS-CoV-2 (within the limitations of the assays used). This work helps to inform biosafety precautions for handling blood products from patients with current or previous COVID-19. F1000 Research Limited 2020-10-12 /pmc/articles/PMC7689603/ /pubmed/33283055 http://dx.doi.org/10.12688/wellcomeopenres.16002.2 Text en Copyright: © 2020 Andersson MI et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Andersson, Monique I. Arancibia-Carcamo, Carolina V. Auckland, Kathryn Baillie, J. Kenneth Barnes, Eleanor Beneke, Tom Bibi, Sagida Brooks, Tim Carroll, Miles Crook, Derrick Dingle, Kate Dold, Christina Downs, Louise O. Dunn, Laura Eyre, David W. Gilbert Jaramillo, Javier Harvala, Heli Hoosdally, Sarah Ijaz, Samreen James, Tim James, William Jeffery, Katie Justice, Anita Klenerman, Paul Knight, Julian C. Knight, Michael Liu, Xu Lumley, Sheila F. Matthews, Philippa C. McNaughton, Anna L. Mentzer, Alexander J. Mongkolsapaya, Juthathip Oakley, Sarah Oliveira, Marta S. Peto, Timothy Ploeg, Rutger J. Ratcliff, Jeremy Robbins, Melanie J. Roberts, David J. Rudkin, Justine Russell, Rebecca A. Screaton, Gavin Semple, Malcolm G. Skelly, Donal Simmonds, Peter Stoesser, Nicole Turtle, Lance Wareing, Susan Zambon, Maria SARS-CoV-2 RNA detected in blood products from patients with COVID-19 is not associated with infectious virus |
title | SARS-CoV-2 RNA detected in blood products from patients with COVID-19 is not associated with infectious virus |
title_full | SARS-CoV-2 RNA detected in blood products from patients with COVID-19 is not associated with infectious virus |
title_fullStr | SARS-CoV-2 RNA detected in blood products from patients with COVID-19 is not associated with infectious virus |
title_full_unstemmed | SARS-CoV-2 RNA detected in blood products from patients with COVID-19 is not associated with infectious virus |
title_short | SARS-CoV-2 RNA detected in blood products from patients with COVID-19 is not associated with infectious virus |
title_sort | sars-cov-2 rna detected in blood products from patients with covid-19 is not associated with infectious virus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689603/ https://www.ncbi.nlm.nih.gov/pubmed/33283055 http://dx.doi.org/10.12688/wellcomeopenres.16002.2 |
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