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Infection with the SARS-CoV-2 B.1.351 variant is lethal in aged BALB/c mice
Models of animals that are susceptible to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection can usefully evaluate the efficacy of vaccines and therapeutics. In this study, we demonstrate that infection with the SARS-CoV-2 B.1.351 variant (TY8-612 strain) induces bodyweight loss...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8907250/ https://www.ncbi.nlm.nih.gov/pubmed/35264719 http://dx.doi.org/10.1038/s41598-022-08104-4 |
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author | Yasui, Fumihiko Matsumoto, Yusuke Yamamoto, Naoki Sanada, Takahiro Honda, Tomoko Munakata, Tsubasa Itoh, Yasushi Kohara, Michinori |
author_facet | Yasui, Fumihiko Matsumoto, Yusuke Yamamoto, Naoki Sanada, Takahiro Honda, Tomoko Munakata, Tsubasa Itoh, Yasushi Kohara, Michinori |
author_sort | Yasui, Fumihiko |
collection | PubMed |
description | Models of animals that are susceptible to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection can usefully evaluate the efficacy of vaccines and therapeutics. In this study, we demonstrate that infection with the SARS-CoV-2 B.1.351 variant (TY8-612 strain) induces bodyweight loss and inflammatory cytokine/chemokine production in wild-type laboratory mice (BALB/c and C57BL/6 J mice). Furthermore, compared to their counterparts, BALB/c mice had a higher viral load in their lungs and worse symptoms. Importantly, infecting aged BALB/c mice (older than 6 months) with the TY8-612 strain elicited a massive and sustained production of multiple pro-inflammatory cytokines/chemokines and led to universal mortality. These results indicated that the SARS-CoV-2 B.1.351 variant-infected mice exhibited symptoms ranging from mild to fatal depending on their strain and age. Our data provide insights into the pathogenesis of SARS-CoV-2 and may be useful in developing prophylactics and therapeutics. |
format | Online Article Text |
id | pubmed-8907250 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89072502022-03-11 Infection with the SARS-CoV-2 B.1.351 variant is lethal in aged BALB/c mice Yasui, Fumihiko Matsumoto, Yusuke Yamamoto, Naoki Sanada, Takahiro Honda, Tomoko Munakata, Tsubasa Itoh, Yasushi Kohara, Michinori Sci Rep Article Models of animals that are susceptible to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection can usefully evaluate the efficacy of vaccines and therapeutics. In this study, we demonstrate that infection with the SARS-CoV-2 B.1.351 variant (TY8-612 strain) induces bodyweight loss and inflammatory cytokine/chemokine production in wild-type laboratory mice (BALB/c and C57BL/6 J mice). Furthermore, compared to their counterparts, BALB/c mice had a higher viral load in their lungs and worse symptoms. Importantly, infecting aged BALB/c mice (older than 6 months) with the TY8-612 strain elicited a massive and sustained production of multiple pro-inflammatory cytokines/chemokines and led to universal mortality. These results indicated that the SARS-CoV-2 B.1.351 variant-infected mice exhibited symptoms ranging from mild to fatal depending on their strain and age. Our data provide insights into the pathogenesis of SARS-CoV-2 and may be useful in developing prophylactics and therapeutics. Nature Publishing Group UK 2022-03-09 /pmc/articles/PMC8907250/ /pubmed/35264719 http://dx.doi.org/10.1038/s41598-022-08104-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yasui, Fumihiko Matsumoto, Yusuke Yamamoto, Naoki Sanada, Takahiro Honda, Tomoko Munakata, Tsubasa Itoh, Yasushi Kohara, Michinori Infection with the SARS-CoV-2 B.1.351 variant is lethal in aged BALB/c mice |
title | Infection with the SARS-CoV-2 B.1.351 variant is lethal in aged BALB/c mice |
title_full | Infection with the SARS-CoV-2 B.1.351 variant is lethal in aged BALB/c mice |
title_fullStr | Infection with the SARS-CoV-2 B.1.351 variant is lethal in aged BALB/c mice |
title_full_unstemmed | Infection with the SARS-CoV-2 B.1.351 variant is lethal in aged BALB/c mice |
title_short | Infection with the SARS-CoV-2 B.1.351 variant is lethal in aged BALB/c mice |
title_sort | infection with the sars-cov-2 b.1.351 variant is lethal in aged balb/c mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8907250/ https://www.ncbi.nlm.nih.gov/pubmed/35264719 http://dx.doi.org/10.1038/s41598-022-08104-4 |
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