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Targeting the conserved coronavirus octamer motif GGAAGAGC is a strategy for the development of coronavirus vaccine
BACKGROUND: Coronaviruses are pathogens of humans and animals that cause widespread and costly diseases. The development of effective strategies to combat the threat of coronaviruses is therefore a top priority. The conserved coronavirus octamer motif 5’GGAAGAGC3’ exists in the 3’ untranslated regio...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652495/ https://www.ncbi.nlm.nih.gov/pubmed/37968733 http://dx.doi.org/10.1186/s12985-023-02231-8 |
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author | Lin, Ching-Hung Hsieh, Feng-Cheng Chang, Yu-Chia Yang, Cheng-Yao Hsu, Hsuan-Wei Yang, Chun-Chun Tam, Hon-Man-Herman Wu, Hung-Yi |
author_facet | Lin, Ching-Hung Hsieh, Feng-Cheng Chang, Yu-Chia Yang, Cheng-Yao Hsu, Hsuan-Wei Yang, Chun-Chun Tam, Hon-Man-Herman Wu, Hung-Yi |
author_sort | Lin, Ching-Hung |
collection | PubMed |
description | BACKGROUND: Coronaviruses are pathogens of humans and animals that cause widespread and costly diseases. The development of effective strategies to combat the threat of coronaviruses is therefore a top priority. The conserved coronavirus octamer motif 5’GGAAGAGC3’ exists in the 3’ untranslated region of all identified coronaviruses. In the current study, we aimed to examine whether targeting the coronavirus octamer motif GGAAGAGC is a promising approach to develop coronavirus vaccine. METHODS: Plaque assays were used to determine the titers of mouse hepatitis virus (MHV)-A59 octamer mutant (MHVoctm) and wild-type (wt) MHV-A59 (MHVwt). Western blotting was used for the determination of translation efficiency of MHVoctm and MHVwt. Plaque assays and RT-qPCR were employed to examine whether MHVoctm was more sensitive to interferon treatment than MHVwt. Weight loss, clinical signs, survival rate, viral RNA detection and histopathological examination were used to evaluate whether MHVoctm was a vaccine candidate against MHVwt infection in BALB/c mice. RESULTS: In this study, we showed that (i) the MHVoctm with mutation of coronavirus octamer was able to grow to high titers but attenuated in mice, (ii) with the reduced multiplicity of infection (MOI), the difference in gene expression between MHVoctm and MHVwt became more evident in cultured cells, (iii) MHVoctm was more sensitive to interferon treatment than MHVwt and (iv) mice inoculated with MHVoctm were protected from MHVwt infection. CONCLUSIONS: Based on the results obtained from cultured cells, it was suggested that the synergistic effects of octamer mutation, multiplicity of infection and immune response may be a mechanism explaining the distinct phenotypes of octamer-mutated coronavirus in cell culture and mice. In addition, targeting the conserved coronavirus octamer motif is a strategy for development of coronavirus vaccine. Since the conserved octamer exists in all coronaviruses, this strategy of targeting the conserved octamer motif can also be applied to other human and animal coronaviruses for the development of coronavirus vaccines, especially the emergence of novel coronaviruses such as SARS-CoV-2, saving time and cost for vaccine development and disease control. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12985-023-02231-8. |
format | Online Article Text |
id | pubmed-10652495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106524952023-11-15 Targeting the conserved coronavirus octamer motif GGAAGAGC is a strategy for the development of coronavirus vaccine Lin, Ching-Hung Hsieh, Feng-Cheng Chang, Yu-Chia Yang, Cheng-Yao Hsu, Hsuan-Wei Yang, Chun-Chun Tam, Hon-Man-Herman Wu, Hung-Yi Virol J Research BACKGROUND: Coronaviruses are pathogens of humans and animals that cause widespread and costly diseases. The development of effective strategies to combat the threat of coronaviruses is therefore a top priority. The conserved coronavirus octamer motif 5’GGAAGAGC3’ exists in the 3’ untranslated region of all identified coronaviruses. In the current study, we aimed to examine whether targeting the coronavirus octamer motif GGAAGAGC is a promising approach to develop coronavirus vaccine. METHODS: Plaque assays were used to determine the titers of mouse hepatitis virus (MHV)-A59 octamer mutant (MHVoctm) and wild-type (wt) MHV-A59 (MHVwt). Western blotting was used for the determination of translation efficiency of MHVoctm and MHVwt. Plaque assays and RT-qPCR were employed to examine whether MHVoctm was more sensitive to interferon treatment than MHVwt. Weight loss, clinical signs, survival rate, viral RNA detection and histopathological examination were used to evaluate whether MHVoctm was a vaccine candidate against MHVwt infection in BALB/c mice. RESULTS: In this study, we showed that (i) the MHVoctm with mutation of coronavirus octamer was able to grow to high titers but attenuated in mice, (ii) with the reduced multiplicity of infection (MOI), the difference in gene expression between MHVoctm and MHVwt became more evident in cultured cells, (iii) MHVoctm was more sensitive to interferon treatment than MHVwt and (iv) mice inoculated with MHVoctm were protected from MHVwt infection. CONCLUSIONS: Based on the results obtained from cultured cells, it was suggested that the synergistic effects of octamer mutation, multiplicity of infection and immune response may be a mechanism explaining the distinct phenotypes of octamer-mutated coronavirus in cell culture and mice. In addition, targeting the conserved coronavirus octamer motif is a strategy for development of coronavirus vaccine. Since the conserved octamer exists in all coronaviruses, this strategy of targeting the conserved octamer motif can also be applied to other human and animal coronaviruses for the development of coronavirus vaccines, especially the emergence of novel coronaviruses such as SARS-CoV-2, saving time and cost for vaccine development and disease control. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12985-023-02231-8. BioMed Central 2023-11-15 /pmc/articles/PMC10652495/ /pubmed/37968733 http://dx.doi.org/10.1186/s12985-023-02231-8 Text en © The Author(s) 2023 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Lin, Ching-Hung Hsieh, Feng-Cheng Chang, Yu-Chia Yang, Cheng-Yao Hsu, Hsuan-Wei Yang, Chun-Chun Tam, Hon-Man-Herman Wu, Hung-Yi Targeting the conserved coronavirus octamer motif GGAAGAGC is a strategy for the development of coronavirus vaccine |
title | Targeting the conserved coronavirus octamer motif GGAAGAGC is a strategy for the development of coronavirus vaccine |
title_full | Targeting the conserved coronavirus octamer motif GGAAGAGC is a strategy for the development of coronavirus vaccine |
title_fullStr | Targeting the conserved coronavirus octamer motif GGAAGAGC is a strategy for the development of coronavirus vaccine |
title_full_unstemmed | Targeting the conserved coronavirus octamer motif GGAAGAGC is a strategy for the development of coronavirus vaccine |
title_short | Targeting the conserved coronavirus octamer motif GGAAGAGC is a strategy for the development of coronavirus vaccine |
title_sort | targeting the conserved coronavirus octamer motif ggaagagc is a strategy for the development of coronavirus vaccine |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652495/ https://www.ncbi.nlm.nih.gov/pubmed/37968733 http://dx.doi.org/10.1186/s12985-023-02231-8 |
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