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Improved plaque assay for human coronaviruses 229E and OC43

In light of the COVID-19 pandemic, studies that work to understand SARS-CoV-2 are urgently needed. In turn, the less severe human coronaviruses such as HCoV-229E and OC43 are drawing newfound attention. These less severe coronaviruses can be used as a model to facilitate our understanding of the hos...

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Autores principales: Bracci, Nicole, Pan, Han-Chi, Lehman, Caitlin, Kehn-Hall, Kylene, Lin, Shih-Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7759117/
https://www.ncbi.nlm.nih.gov/pubmed/33391888
http://dx.doi.org/10.7717/peerj.10639
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author Bracci, Nicole
Pan, Han-Chi
Lehman, Caitlin
Kehn-Hall, Kylene
Lin, Shih-Chao
author_facet Bracci, Nicole
Pan, Han-Chi
Lehman, Caitlin
Kehn-Hall, Kylene
Lin, Shih-Chao
author_sort Bracci, Nicole
collection PubMed
description In light of the COVID-19 pandemic, studies that work to understand SARS-CoV-2 are urgently needed. In turn, the less severe human coronaviruses such as HCoV-229E and OC43 are drawing newfound attention. These less severe coronaviruses can be used as a model to facilitate our understanding of the host immune response to coronavirus infection. SARS-CoV-2 must be handled under biosafety level 3 (BSL-3) conditions. Therefore, HCoV-229E and OC43, which can be handled at BSL-2 provide an alternative to SARS-CoV-2 for preclinical screening and designing of antivirals. However, to date, there is no published effective and efficient method to titrate HCoVs other than expensive indirect immunostaining. Here we present an improved approach using an agarose-based conventional plaque assay to titrate HCoV 229E and OC43 with mink lung epithelial cells, Mv1Lu. Our results indicate that titration of HCoV 229E and OC43 with Mv1Lu is consistent and reproducible. The titers produced are also comparable to those produced using human rhabdomyosarcoma (RD) cells. More importantly, Mv1Lu cells display a higher tolerance for cell-cell contact stress, decreased temperature sensitivity, and a faster growth rate. We believe that our improved low-cost plaque assay can serve as an easy tool for researchers conducting HCoV research.
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spelling pubmed-77591172020-12-31 Improved plaque assay for human coronaviruses 229E and OC43 Bracci, Nicole Pan, Han-Chi Lehman, Caitlin Kehn-Hall, Kylene Lin, Shih-Chao PeerJ Biotechnology In light of the COVID-19 pandemic, studies that work to understand SARS-CoV-2 are urgently needed. In turn, the less severe human coronaviruses such as HCoV-229E and OC43 are drawing newfound attention. These less severe coronaviruses can be used as a model to facilitate our understanding of the host immune response to coronavirus infection. SARS-CoV-2 must be handled under biosafety level 3 (BSL-3) conditions. Therefore, HCoV-229E and OC43, which can be handled at BSL-2 provide an alternative to SARS-CoV-2 for preclinical screening and designing of antivirals. However, to date, there is no published effective and efficient method to titrate HCoVs other than expensive indirect immunostaining. Here we present an improved approach using an agarose-based conventional plaque assay to titrate HCoV 229E and OC43 with mink lung epithelial cells, Mv1Lu. Our results indicate that titration of HCoV 229E and OC43 with Mv1Lu is consistent and reproducible. The titers produced are also comparable to those produced using human rhabdomyosarcoma (RD) cells. More importantly, Mv1Lu cells display a higher tolerance for cell-cell contact stress, decreased temperature sensitivity, and a faster growth rate. We believe that our improved low-cost plaque assay can serve as an easy tool for researchers conducting HCoV research. PeerJ Inc. 2020-12-21 /pmc/articles/PMC7759117/ /pubmed/33391888 http://dx.doi.org/10.7717/peerj.10639 Text en © 2020 Bracci et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Biotechnology
Bracci, Nicole
Pan, Han-Chi
Lehman, Caitlin
Kehn-Hall, Kylene
Lin, Shih-Chao
Improved plaque assay for human coronaviruses 229E and OC43
title Improved plaque assay for human coronaviruses 229E and OC43
title_full Improved plaque assay for human coronaviruses 229E and OC43
title_fullStr Improved plaque assay for human coronaviruses 229E and OC43
title_full_unstemmed Improved plaque assay for human coronaviruses 229E and OC43
title_short Improved plaque assay for human coronaviruses 229E and OC43
title_sort improved plaque assay for human coronaviruses 229e and oc43
topic Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7759117/
https://www.ncbi.nlm.nih.gov/pubmed/33391888
http://dx.doi.org/10.7717/peerj.10639
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