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Inactivated and Immunogenic SARS-CoV-2 for Safe Use in Immunoassays and as an Immunization Control for Non-Clinical Trials
Successful SARS-CoV-2 inactivation allows its safe use in Biosafety Level 2 facilities, and the use of the whole viral particle helps in the development of analytical methods and a more reliable immune response, contributing to the development and improvement of in vitro and in vivo assays. In order...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10386713/ https://www.ncbi.nlm.nih.gov/pubmed/37515173 http://dx.doi.org/10.3390/v15071486 |
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author | Gomes, Mariana Pierre de Barros Linhares, José Henrique Rezende dos Santos, Tiago Pereira Pereira, Renata Carvalho Santos, Renata Tourinho da Silva, Stephanie Almeida Souza, Marta Cristina de Oliveira da Silva, Juliana Fernandes Amorim Trindade, Gisela Freitas Gomes, Viviane Silva Barreto-Vieira, Débora Ferreira Carvalho, Milena Mouta Verdan França Ano Bom, Ana Paula Dinis Gardinali, Noemi Rovaris Müller, Rodrigo Alves, Nathalia dos Santos Moura, Luma da Cruz Neves, Patrícia Cristina da Costa Esteves, Gabriela Santos Schwarcz, Waleska Dias Missailidis, Sotiris Mendes, Ygara da Silva de Lima, Sheila Maria Barbosa |
author_facet | Gomes, Mariana Pierre de Barros Linhares, José Henrique Rezende dos Santos, Tiago Pereira Pereira, Renata Carvalho Santos, Renata Tourinho da Silva, Stephanie Almeida Souza, Marta Cristina de Oliveira da Silva, Juliana Fernandes Amorim Trindade, Gisela Freitas Gomes, Viviane Silva Barreto-Vieira, Débora Ferreira Carvalho, Milena Mouta Verdan França Ano Bom, Ana Paula Dinis Gardinali, Noemi Rovaris Müller, Rodrigo Alves, Nathalia dos Santos Moura, Luma da Cruz Neves, Patrícia Cristina da Costa Esteves, Gabriela Santos Schwarcz, Waleska Dias Missailidis, Sotiris Mendes, Ygara da Silva de Lima, Sheila Maria Barbosa |
author_sort | Gomes, Mariana Pierre de Barros |
collection | PubMed |
description | Successful SARS-CoV-2 inactivation allows its safe use in Biosafety Level 2 facilities, and the use of the whole viral particle helps in the development of analytical methods and a more reliable immune response, contributing to the development and improvement of in vitro and in vivo assays. In order to obtain a functional product, we evaluated several inactivation protocols and observed that 0.03% beta-propiolactone for 24 h was the best condition tested, as it promoted SARS-CoV-2 inactivation above 99.99% and no cytopathic effect was visualized after five serial passages. Moreover, RT-qPCR and transmission electron microscopy revealed that RNA quantification and viral structure integrity were preserved. The antigenicity of inactivated SARS-CoV-2 was confirmed by ELISA using different Spike-neutralizing monoclonal antibodies. K18-hACE2 mice immunized with inactivated SARS-CoV-2, formulated in AddaS0(3)(TM), presented high neutralizing antibody titers, no significant weight loss, and longer survival than controls from a lethal challenge, despite RNA detection in the oropharyngeal swab, lung, and brain. This work emphasizes the importance of using different techniques to confirm viral inactivation and avoid potentially disastrous contamination. We believe that an efficiently inactivated product can be used in several applications, including the development and improvement of molecular diagnostic kits, as an antigen for antibody production as well as a control for non-clinical trials. |
format | Online Article Text |
id | pubmed-10386713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103867132023-07-30 Inactivated and Immunogenic SARS-CoV-2 for Safe Use in Immunoassays and as an Immunization Control for Non-Clinical Trials Gomes, Mariana Pierre de Barros Linhares, José Henrique Rezende dos Santos, Tiago Pereira Pereira, Renata Carvalho Santos, Renata Tourinho da Silva, Stephanie Almeida Souza, Marta Cristina de Oliveira da Silva, Juliana Fernandes Amorim Trindade, Gisela Freitas Gomes, Viviane Silva Barreto-Vieira, Débora Ferreira Carvalho, Milena Mouta Verdan França Ano Bom, Ana Paula Dinis Gardinali, Noemi Rovaris Müller, Rodrigo Alves, Nathalia dos Santos Moura, Luma da Cruz Neves, Patrícia Cristina da Costa Esteves, Gabriela Santos Schwarcz, Waleska Dias Missailidis, Sotiris Mendes, Ygara da Silva de Lima, Sheila Maria Barbosa Viruses Article Successful SARS-CoV-2 inactivation allows its safe use in Biosafety Level 2 facilities, and the use of the whole viral particle helps in the development of analytical methods and a more reliable immune response, contributing to the development and improvement of in vitro and in vivo assays. In order to obtain a functional product, we evaluated several inactivation protocols and observed that 0.03% beta-propiolactone for 24 h was the best condition tested, as it promoted SARS-CoV-2 inactivation above 99.99% and no cytopathic effect was visualized after five serial passages. Moreover, RT-qPCR and transmission electron microscopy revealed that RNA quantification and viral structure integrity were preserved. The antigenicity of inactivated SARS-CoV-2 was confirmed by ELISA using different Spike-neutralizing monoclonal antibodies. K18-hACE2 mice immunized with inactivated SARS-CoV-2, formulated in AddaS0(3)(TM), presented high neutralizing antibody titers, no significant weight loss, and longer survival than controls from a lethal challenge, despite RNA detection in the oropharyngeal swab, lung, and brain. This work emphasizes the importance of using different techniques to confirm viral inactivation and avoid potentially disastrous contamination. We believe that an efficiently inactivated product can be used in several applications, including the development and improvement of molecular diagnostic kits, as an antigen for antibody production as well as a control for non-clinical trials. MDPI 2023-06-30 /pmc/articles/PMC10386713/ /pubmed/37515173 http://dx.doi.org/10.3390/v15071486 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gomes, Mariana Pierre de Barros Linhares, José Henrique Rezende dos Santos, Tiago Pereira Pereira, Renata Carvalho Santos, Renata Tourinho da Silva, Stephanie Almeida Souza, Marta Cristina de Oliveira da Silva, Juliana Fernandes Amorim Trindade, Gisela Freitas Gomes, Viviane Silva Barreto-Vieira, Débora Ferreira Carvalho, Milena Mouta Verdan França Ano Bom, Ana Paula Dinis Gardinali, Noemi Rovaris Müller, Rodrigo Alves, Nathalia dos Santos Moura, Luma da Cruz Neves, Patrícia Cristina da Costa Esteves, Gabriela Santos Schwarcz, Waleska Dias Missailidis, Sotiris Mendes, Ygara da Silva de Lima, Sheila Maria Barbosa Inactivated and Immunogenic SARS-CoV-2 for Safe Use in Immunoassays and as an Immunization Control for Non-Clinical Trials |
title | Inactivated and Immunogenic SARS-CoV-2 for Safe Use in Immunoassays and as an Immunization Control for Non-Clinical Trials |
title_full | Inactivated and Immunogenic SARS-CoV-2 for Safe Use in Immunoassays and as an Immunization Control for Non-Clinical Trials |
title_fullStr | Inactivated and Immunogenic SARS-CoV-2 for Safe Use in Immunoassays and as an Immunization Control for Non-Clinical Trials |
title_full_unstemmed | Inactivated and Immunogenic SARS-CoV-2 for Safe Use in Immunoassays and as an Immunization Control for Non-Clinical Trials |
title_short | Inactivated and Immunogenic SARS-CoV-2 for Safe Use in Immunoassays and as an Immunization Control for Non-Clinical Trials |
title_sort | inactivated and immunogenic sars-cov-2 for safe use in immunoassays and as an immunization control for non-clinical trials |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10386713/ https://www.ncbi.nlm.nih.gov/pubmed/37515173 http://dx.doi.org/10.3390/v15071486 |
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