Cargando…

Expression and Evaluation of a Novel PPRV Nanoparticle Antigen Based on Ferritin Self-Assembling Technology

Peste des Petits Ruminants (PPR) is a highly pathogenic disease that is classified as a World Organization for Animal Health (OIE)-listed disease. PPRV mainly infects small ruminants such as goats and sheep. In view of the global and high pathogenicity of PPRV, in this study, we proposed a novel nan...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Dan, Song, Haozhi, Li, Jialei, Liu, Xingjian, Gao, Xintao, Wu, Tong, Zhang, Zhifang, Li, Yinü
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500948/
https://www.ncbi.nlm.nih.gov/pubmed/36145650
http://dx.doi.org/10.3390/pharmaceutics14091902
_version_ 1784795349072740352
author Li, Dan
Song, Haozhi
Li, Jialei
Liu, Xingjian
Gao, Xintao
Wu, Tong
Zhang, Zhifang
Li, Yinü
author_facet Li, Dan
Song, Haozhi
Li, Jialei
Liu, Xingjian
Gao, Xintao
Wu, Tong
Zhang, Zhifang
Li, Yinü
author_sort Li, Dan
collection PubMed
description Peste des Petits Ruminants (PPR) is a highly pathogenic disease that is classified as a World Organization for Animal Health (OIE)-listed disease. PPRV mainly infects small ruminants such as goats and sheep. In view of the global and high pathogenicity of PPRV, in this study, we proposed a novel nanoparticle vaccine strategy based on ferritin (Fe) self-assembly technology. Using Helicobacter pylori (H. pylori) ferritin as an antigen delivery vector, a PPRV hemagglutinin (H) protein was fused with ferritin and then expressed and purified in both Escherichia coli (E. coli) and silkworm baculovirus expression systems. Subsequently, the nanoparticle antigens’ expression level, immunogenicity and protective immune response were evaluated. Our results showed that the PPRV hemagglutinin–ferritin (H-Fe) protein was self-assembled in silkworms, while it was difficult to observe the correctly folded nanoparticle in E. coli. Meanwhile, the expression level of the H-Fe protein was higher than that of the H protein alone. Furthermore, the immunogenicity and protective immune response of H-Fe nanoparticle antigens expressed by silkworms were improved compared with the H antigen alone. Particularly, the protective immune response of H-Fe antigens expressed in E. coli did not change, as opposed to the H antigen, which was probably due to the incomplete nanoparticle structure in E. coli. This study indicated that the use of ferritin nanoparticles as antigen delivery carriers could increase the expression of antigen proteins and improve the immunogenicity and immune effect of antigens.
format Online
Article
Text
id pubmed-9500948
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-95009482022-09-24 Expression and Evaluation of a Novel PPRV Nanoparticle Antigen Based on Ferritin Self-Assembling Technology Li, Dan Song, Haozhi Li, Jialei Liu, Xingjian Gao, Xintao Wu, Tong Zhang, Zhifang Li, Yinü Pharmaceutics Article Peste des Petits Ruminants (PPR) is a highly pathogenic disease that is classified as a World Organization for Animal Health (OIE)-listed disease. PPRV mainly infects small ruminants such as goats and sheep. In view of the global and high pathogenicity of PPRV, in this study, we proposed a novel nanoparticle vaccine strategy based on ferritin (Fe) self-assembly technology. Using Helicobacter pylori (H. pylori) ferritin as an antigen delivery vector, a PPRV hemagglutinin (H) protein was fused with ferritin and then expressed and purified in both Escherichia coli (E. coli) and silkworm baculovirus expression systems. Subsequently, the nanoparticle antigens’ expression level, immunogenicity and protective immune response were evaluated. Our results showed that the PPRV hemagglutinin–ferritin (H-Fe) protein was self-assembled in silkworms, while it was difficult to observe the correctly folded nanoparticle in E. coli. Meanwhile, the expression level of the H-Fe protein was higher than that of the H protein alone. Furthermore, the immunogenicity and protective immune response of H-Fe nanoparticle antigens expressed by silkworms were improved compared with the H antigen alone. Particularly, the protective immune response of H-Fe antigens expressed in E. coli did not change, as opposed to the H antigen, which was probably due to the incomplete nanoparticle structure in E. coli. This study indicated that the use of ferritin nanoparticles as antigen delivery carriers could increase the expression of antigen proteins and improve the immunogenicity and immune effect of antigens. MDPI 2022-09-08 /pmc/articles/PMC9500948/ /pubmed/36145650 http://dx.doi.org/10.3390/pharmaceutics14091902 Text en © 2022 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
Li, Dan
Song, Haozhi
Li, Jialei
Liu, Xingjian
Gao, Xintao
Wu, Tong
Zhang, Zhifang
Li, Yinü
Expression and Evaluation of a Novel PPRV Nanoparticle Antigen Based on Ferritin Self-Assembling Technology
title Expression and Evaluation of a Novel PPRV Nanoparticle Antigen Based on Ferritin Self-Assembling Technology
title_full Expression and Evaluation of a Novel PPRV Nanoparticle Antigen Based on Ferritin Self-Assembling Technology
title_fullStr Expression and Evaluation of a Novel PPRV Nanoparticle Antigen Based on Ferritin Self-Assembling Technology
title_full_unstemmed Expression and Evaluation of a Novel PPRV Nanoparticle Antigen Based on Ferritin Self-Assembling Technology
title_short Expression and Evaluation of a Novel PPRV Nanoparticle Antigen Based on Ferritin Self-Assembling Technology
title_sort expression and evaluation of a novel pprv nanoparticle antigen based on ferritin self-assembling technology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500948/
https://www.ncbi.nlm.nih.gov/pubmed/36145650
http://dx.doi.org/10.3390/pharmaceutics14091902
work_keys_str_mv AT lidan expressionandevaluationofanovelpprvnanoparticleantigenbasedonferritinselfassemblingtechnology
AT songhaozhi expressionandevaluationofanovelpprvnanoparticleantigenbasedonferritinselfassemblingtechnology
AT lijialei expressionandevaluationofanovelpprvnanoparticleantigenbasedonferritinselfassemblingtechnology
AT liuxingjian expressionandevaluationofanovelpprvnanoparticleantigenbasedonferritinselfassemblingtechnology
AT gaoxintao expressionandevaluationofanovelpprvnanoparticleantigenbasedonferritinselfassemblingtechnology
AT wutong expressionandevaluationofanovelpprvnanoparticleantigenbasedonferritinselfassemblingtechnology
AT zhangzhifang expressionandevaluationofanovelpprvnanoparticleantigenbasedonferritinselfassemblingtechnology
AT liyinu expressionandevaluationofanovelpprvnanoparticleantigenbasedonferritinselfassemblingtechnology