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Boosted expression of the SARS-CoV nucleocapsid protein in tobacco and its immunogenicity in mice
Vaccines produced in plant systems are safe and economical; however, the extensive application of plant-based vaccines is mainly hindered by low expression levels of heterologous proteins in plant systems. Here, we demonstrated that the post-transcriptional gene silencing suppressor p19 protein from...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115566/ https://www.ncbi.nlm.nih.gov/pubmed/19523911 http://dx.doi.org/10.1016/j.vaccine.2009.05.073 |
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author | Zheng, Nuoyan Xia, Ran Yang, Cuiping Yin, Bojiao Li, Yin Duan, Chengguo Liang, Liming Guo, Huishan Xie, Qi |
author_facet | Zheng, Nuoyan Xia, Ran Yang, Cuiping Yin, Bojiao Li, Yin Duan, Chengguo Liang, Liming Guo, Huishan Xie, Qi |
author_sort | Zheng, Nuoyan |
collection | PubMed |
description | Vaccines produced in plant systems are safe and economical; however, the extensive application of plant-based vaccines is mainly hindered by low expression levels of heterologous proteins in plant systems. Here, we demonstrated that the post-transcriptional gene silencing suppressor p19 protein from tomato bushy stunt virus substantially enhanced the transient expression of recombinant SARS-CoV nucleocapsid (rN) protein in Nicotiana benthamiana. The rN protein in the agrobacteria-infiltrated plant leaf accumulated up to a concentration of 79 μg per g fresh leaf weight at 3 days post infiltration. BALB/c mice were intraperitoneally vaccinated with pre-treated plant extract emulsified in Freund's adjuvant. The rN protein-specific IgG in the mouse sera attained a titer about 1:1,800 following three doses of immunization, which suggested effective B-cell maturation and differentiation in mice. Antibodies of the subclasses IgG1 and IgG2a were abundantly present in the mouse sera. During vaccination of rN protein, the expression of IFN-γ and IL-10 was evidently up-regulated in splenocytes at different time points, while the expression of IL-2 and IL-4 was not. Up to now, this is the first study that plant-expressed recombinant SARS-CoV N protein can induce strong humoral and cellular responses in mice. |
format | Online Article Text |
id | pubmed-7115566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71155662020-04-02 Boosted expression of the SARS-CoV nucleocapsid protein in tobacco and its immunogenicity in mice Zheng, Nuoyan Xia, Ran Yang, Cuiping Yin, Bojiao Li, Yin Duan, Chengguo Liang, Liming Guo, Huishan Xie, Qi Vaccine Article Vaccines produced in plant systems are safe and economical; however, the extensive application of plant-based vaccines is mainly hindered by low expression levels of heterologous proteins in plant systems. Here, we demonstrated that the post-transcriptional gene silencing suppressor p19 protein from tomato bushy stunt virus substantially enhanced the transient expression of recombinant SARS-CoV nucleocapsid (rN) protein in Nicotiana benthamiana. The rN protein in the agrobacteria-infiltrated plant leaf accumulated up to a concentration of 79 μg per g fresh leaf weight at 3 days post infiltration. BALB/c mice were intraperitoneally vaccinated with pre-treated plant extract emulsified in Freund's adjuvant. The rN protein-specific IgG in the mouse sera attained a titer about 1:1,800 following three doses of immunization, which suggested effective B-cell maturation and differentiation in mice. Antibodies of the subclasses IgG1 and IgG2a were abundantly present in the mouse sera. During vaccination of rN protein, the expression of IFN-γ and IL-10 was evidently up-regulated in splenocytes at different time points, while the expression of IL-2 and IL-4 was not. Up to now, this is the first study that plant-expressed recombinant SARS-CoV N protein can induce strong humoral and cellular responses in mice. Elsevier Ltd. 2009-08-06 2009-06-11 /pmc/articles/PMC7115566/ /pubmed/19523911 http://dx.doi.org/10.1016/j.vaccine.2009.05.073 Text en Copyright © 2009 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Zheng, Nuoyan Xia, Ran Yang, Cuiping Yin, Bojiao Li, Yin Duan, Chengguo Liang, Liming Guo, Huishan Xie, Qi Boosted expression of the SARS-CoV nucleocapsid protein in tobacco and its immunogenicity in mice |
title | Boosted expression of the SARS-CoV nucleocapsid protein in tobacco and its immunogenicity in mice |
title_full | Boosted expression of the SARS-CoV nucleocapsid protein in tobacco and its immunogenicity in mice |
title_fullStr | Boosted expression of the SARS-CoV nucleocapsid protein in tobacco and its immunogenicity in mice |
title_full_unstemmed | Boosted expression of the SARS-CoV nucleocapsid protein in tobacco and its immunogenicity in mice |
title_short | Boosted expression of the SARS-CoV nucleocapsid protein in tobacco and its immunogenicity in mice |
title_sort | boosted expression of the sars-cov nucleocapsid protein in tobacco and its immunogenicity in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115566/ https://www.ncbi.nlm.nih.gov/pubmed/19523911 http://dx.doi.org/10.1016/j.vaccine.2009.05.073 |
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