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A bioconjugate vaccine against Brucella abortus produced by engineered Escherichia coli

Brucellosis, mainly caused by Brucella, is a widespread zoonotic disease worldwide, with no available effective vaccine for human use. Recently, bioconjugate vaccines against Brucella have been prepared in Yersinia enterocolitica O:9 (YeO9), whose O-antigen structure is similar to that of Brucella a...

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Autores principales: Li, Shulei, Huang, Jing, Wang, Kangfeng, Liu, Yan, Guo, Yan, Li, Xiang, Wu, Jun, Sun, Peng, Wang, Yufei, Zhu, Li, Wang, Hengliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995886/
https://www.ncbi.nlm.nih.gov/pubmed/36911199
http://dx.doi.org/10.3389/fbioe.2023.1121074
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author Li, Shulei
Huang, Jing
Wang, Kangfeng
Liu, Yan
Guo, Yan
Li, Xiang
Wu, Jun
Sun, Peng
Wang, Yufei
Zhu, Li
Wang, Hengliang
author_facet Li, Shulei
Huang, Jing
Wang, Kangfeng
Liu, Yan
Guo, Yan
Li, Xiang
Wu, Jun
Sun, Peng
Wang, Yufei
Zhu, Li
Wang, Hengliang
author_sort Li, Shulei
collection PubMed
description Brucellosis, mainly caused by Brucella, is a widespread zoonotic disease worldwide, with no available effective vaccine for human use. Recently, bioconjugate vaccines against Brucella have been prepared in Yersinia enterocolitica O:9 (YeO9), whose O-antigen structure is similar to that of Brucella abortus. However, the pathogenicity of YeO9 still hinders the large-scale production of these bioconjugate vaccines. Here, an attractive system for the preparation of bioconjugate vaccines against Brucella was established in engineered E. coli. Briefly, the OPS gene cluster of YeO9 was modularized into five individual fragments and reassembled using synthetic biological methods through standardized interfaces, then introduced into E. coli. After confirming the synthesis of targeted antigenic polysaccharides, the exogenous protein glycosylation system (PglL system) was used to prepare the bioconjugate vaccines. A series of experiments were conducted to demonstrate that the bioconjugate vaccine could effectively evoke humoral immune responses and induce the production of specific antibodies against B. abortus A19 lipopolysaccharide. Furthermore, the bioconjugate vaccines provide protective roles in both lethal and non-lethal challenge of B. abortus A19 strain. Using the engineered E. coli as a safer chassis to prepare bioconjugate vaccines against B. abortus paves the way for future industrial applications.
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spelling pubmed-99958862023-03-10 A bioconjugate vaccine against Brucella abortus produced by engineered Escherichia coli Li, Shulei Huang, Jing Wang, Kangfeng Liu, Yan Guo, Yan Li, Xiang Wu, Jun Sun, Peng Wang, Yufei Zhu, Li Wang, Hengliang Front Bioeng Biotechnol Bioengineering and Biotechnology Brucellosis, mainly caused by Brucella, is a widespread zoonotic disease worldwide, with no available effective vaccine for human use. Recently, bioconjugate vaccines against Brucella have been prepared in Yersinia enterocolitica O:9 (YeO9), whose O-antigen structure is similar to that of Brucella abortus. However, the pathogenicity of YeO9 still hinders the large-scale production of these bioconjugate vaccines. Here, an attractive system for the preparation of bioconjugate vaccines against Brucella was established in engineered E. coli. Briefly, the OPS gene cluster of YeO9 was modularized into five individual fragments and reassembled using synthetic biological methods through standardized interfaces, then introduced into E. coli. After confirming the synthesis of targeted antigenic polysaccharides, the exogenous protein glycosylation system (PglL system) was used to prepare the bioconjugate vaccines. A series of experiments were conducted to demonstrate that the bioconjugate vaccine could effectively evoke humoral immune responses and induce the production of specific antibodies against B. abortus A19 lipopolysaccharide. Furthermore, the bioconjugate vaccines provide protective roles in both lethal and non-lethal challenge of B. abortus A19 strain. Using the engineered E. coli as a safer chassis to prepare bioconjugate vaccines against B. abortus paves the way for future industrial applications. Frontiers Media S.A. 2023-02-23 /pmc/articles/PMC9995886/ /pubmed/36911199 http://dx.doi.org/10.3389/fbioe.2023.1121074 Text en Copyright © 2023 Li, Huang, Wang, Liu, Guo, Li, Wu, Sun, Wang, Zhu and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Li, Shulei
Huang, Jing
Wang, Kangfeng
Liu, Yan
Guo, Yan
Li, Xiang
Wu, Jun
Sun, Peng
Wang, Yufei
Zhu, Li
Wang, Hengliang
A bioconjugate vaccine against Brucella abortus produced by engineered Escherichia coli
title A bioconjugate vaccine against Brucella abortus produced by engineered Escherichia coli
title_full A bioconjugate vaccine against Brucella abortus produced by engineered Escherichia coli
title_fullStr A bioconjugate vaccine against Brucella abortus produced by engineered Escherichia coli
title_full_unstemmed A bioconjugate vaccine against Brucella abortus produced by engineered Escherichia coli
title_short A bioconjugate vaccine against Brucella abortus produced by engineered Escherichia coli
title_sort bioconjugate vaccine against brucella abortus produced by engineered escherichia coli
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995886/
https://www.ncbi.nlm.nih.gov/pubmed/36911199
http://dx.doi.org/10.3389/fbioe.2023.1121074
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