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Inactivation of SARS-CoV-2 and COVID-19 Patient Samples for Contemporary Immunology and Metabolomics Studies

Due to the severity of COVID-19 disease, the U.S. Centers for Disease Control and Prevention and World Health Organization recommend that manipulation of active viral cultures of SARS-CoV-2 and respiratory secretions from COVID-19 patients be performed in biosafety level (BSL)3 laboratories. Therefo...

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Autores principales: Eddins, Devon J., Bassit, Leda C., Chandler, Joshua D., Haddad, Natalie S., Musall, Kathryn L., Yang, Junkai, Kosters, Astrid, Dobosh, Brian S., Hernández, Mindy R., Ramonell, Richard P., Tirouvanziam, Rabindra M., Lee, F. Eun-Hyung, Zandi, Keivan, Schinazi, Raymond F., Ghosn, Eliver E. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164212/
https://www.ncbi.nlm.nih.gov/pubmed/35173021
http://dx.doi.org/10.4049/immunohorizons.2200005
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author Eddins, Devon J.
Bassit, Leda C.
Chandler, Joshua D.
Haddad, Natalie S.
Musall, Kathryn L.
Yang, Junkai
Kosters, Astrid
Dobosh, Brian S.
Hernández, Mindy R.
Ramonell, Richard P.
Tirouvanziam, Rabindra M.
Lee, F. Eun-Hyung
Zandi, Keivan
Schinazi, Raymond F.
Ghosn, Eliver E. B.
author_facet Eddins, Devon J.
Bassit, Leda C.
Chandler, Joshua D.
Haddad, Natalie S.
Musall, Kathryn L.
Yang, Junkai
Kosters, Astrid
Dobosh, Brian S.
Hernández, Mindy R.
Ramonell, Richard P.
Tirouvanziam, Rabindra M.
Lee, F. Eun-Hyung
Zandi, Keivan
Schinazi, Raymond F.
Ghosn, Eliver E. B.
author_sort Eddins, Devon J.
collection PubMed
description Due to the severity of COVID-19 disease, the U.S. Centers for Disease Control and Prevention and World Health Organization recommend that manipulation of active viral cultures of SARS-CoV-2 and respiratory secretions from COVID-19 patients be performed in biosafety level (BSL)3 laboratories. Therefore, it is imperative to develop viral inactivation procedures that permit samples to be transferred to lower containment levels (BSL2), while maintaining the fidelity of complex downstream assays to expedite the development of medical countermeasures. In this study, we demonstrate optimal conditions for complete viral inactivation following fixation of infected cells with commonly used reagents for flow cytometry, UVC inactivation in sera and respiratory secretions for protein and Ab detection, heat inactivation following cDNA amplification for droplet-based single-cell mRNA sequencing, and extraction with an organic solvent for metabolomic studies. Thus, we provide a suite of viral inactivation protocols for downstream contemporary assays that facilitate sample transfer to BSL2, providing a conceptual framework for rapid initiation of high-fidelity research as the COVID-19 pandemic continues.
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spelling pubmed-91642122022-06-04 Inactivation of SARS-CoV-2 and COVID-19 Patient Samples for Contemporary Immunology and Metabolomics Studies Eddins, Devon J. Bassit, Leda C. Chandler, Joshua D. Haddad, Natalie S. Musall, Kathryn L. Yang, Junkai Kosters, Astrid Dobosh, Brian S. Hernández, Mindy R. Ramonell, Richard P. Tirouvanziam, Rabindra M. Lee, F. Eun-Hyung Zandi, Keivan Schinazi, Raymond F. Ghosn, Eliver E. B. Immunohorizons Article Due to the severity of COVID-19 disease, the U.S. Centers for Disease Control and Prevention and World Health Organization recommend that manipulation of active viral cultures of SARS-CoV-2 and respiratory secretions from COVID-19 patients be performed in biosafety level (BSL)3 laboratories. Therefore, it is imperative to develop viral inactivation procedures that permit samples to be transferred to lower containment levels (BSL2), while maintaining the fidelity of complex downstream assays to expedite the development of medical countermeasures. In this study, we demonstrate optimal conditions for complete viral inactivation following fixation of infected cells with commonly used reagents for flow cytometry, UVC inactivation in sera and respiratory secretions for protein and Ab detection, heat inactivation following cDNA amplification for droplet-based single-cell mRNA sequencing, and extraction with an organic solvent for metabolomic studies. Thus, we provide a suite of viral inactivation protocols for downstream contemporary assays that facilitate sample transfer to BSL2, providing a conceptual framework for rapid initiation of high-fidelity research as the COVID-19 pandemic continues. 2022-02-16 /pmc/articles/PMC9164212/ /pubmed/35173021 http://dx.doi.org/10.4049/immunohorizons.2200005 Text en https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the CC BY 4.0 Unported license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Eddins, Devon J.
Bassit, Leda C.
Chandler, Joshua D.
Haddad, Natalie S.
Musall, Kathryn L.
Yang, Junkai
Kosters, Astrid
Dobosh, Brian S.
Hernández, Mindy R.
Ramonell, Richard P.
Tirouvanziam, Rabindra M.
Lee, F. Eun-Hyung
Zandi, Keivan
Schinazi, Raymond F.
Ghosn, Eliver E. B.
Inactivation of SARS-CoV-2 and COVID-19 Patient Samples for Contemporary Immunology and Metabolomics Studies
title Inactivation of SARS-CoV-2 and COVID-19 Patient Samples for Contemporary Immunology and Metabolomics Studies
title_full Inactivation of SARS-CoV-2 and COVID-19 Patient Samples for Contemporary Immunology and Metabolomics Studies
title_fullStr Inactivation of SARS-CoV-2 and COVID-19 Patient Samples for Contemporary Immunology and Metabolomics Studies
title_full_unstemmed Inactivation of SARS-CoV-2 and COVID-19 Patient Samples for Contemporary Immunology and Metabolomics Studies
title_short Inactivation of SARS-CoV-2 and COVID-19 Patient Samples for Contemporary Immunology and Metabolomics Studies
title_sort inactivation of sars-cov-2 and covid-19 patient samples for contemporary immunology and metabolomics studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164212/
https://www.ncbi.nlm.nih.gov/pubmed/35173021
http://dx.doi.org/10.4049/immunohorizons.2200005
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