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Design of a multi-epitope vaccine against brucellosis fused to IgG-fc by an immunoinformatics approach

INTRODUCTION: Brucella, a type of intracellular Gram-negative bacterium, has unique features and acts as a zoonotic pathogen. It can lead to abortion and infertility in animals. Eliminating brucellosis becomes very challenging once it spreads among both humans and animals, putting a heavy burden on...

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Autores principales: Wu, Aodi, Wang, Yueli, Ali, Adnan, Xu, Zhenyu, Zhang, Dongsheng, Zhumanov, Kairat, Sheng, Jinliang, Yi, Jihai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625910/
https://www.ncbi.nlm.nih.gov/pubmed/37937155
http://dx.doi.org/10.3389/fvets.2023.1238634
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author Wu, Aodi
Wang, Yueli
Ali, Adnan
Xu, Zhenyu
Zhang, Dongsheng
Zhumanov, Kairat
Sheng, Jinliang
Yi, Jihai
author_facet Wu, Aodi
Wang, Yueli
Ali, Adnan
Xu, Zhenyu
Zhang, Dongsheng
Zhumanov, Kairat
Sheng, Jinliang
Yi, Jihai
author_sort Wu, Aodi
collection PubMed
description INTRODUCTION: Brucella, a type of intracellular Gram-negative bacterium, has unique features and acts as a zoonotic pathogen. It can lead to abortion and infertility in animals. Eliminating brucellosis becomes very challenging once it spreads among both humans and animals, putting a heavy burden on livestock and people worldwide. Given the increasing spread of brucellosis, it is crucial to develop improved vaccines for susceptible animals to reduce the disease’s impact. METHODS: In this study, we effectively used an immunoinformatics approach with advanced computer software to carefully identify and analyze important antigenic parts of Brucella abortus. Subsequently, we skillfully designed chimeric peptides to enhance the vaccine’s strength and effectiveness. We used computer programs to find four important parts of the Brucella bacteria that our immune system recognizes. Then, we carefully looked for eight parts that are recognized by a type of white blood cell called cytotoxic T cells, six parts recognized by T helper cells, and four parts recognized by B cells. We connected these parts together using a special link, creating a strong new vaccine. To make the vaccine even better, we added some extra parts called molecular adjuvants. These included something called human β-defensins 3 (hBD-3) that we found in a database, and another part that helps the immune system called PADRE. We attached these extra parts to the beginning of the vaccine. In a new and clever way, we made the vaccine even stronger by attaching a part from a mouse’s immune system to the end of it. This created a new kind of vaccine called MEV-Fc. We used advanced computer methods to study how well the MEV-Fc vaccine interacts with certain receptors in the body (TLR-2 and TLR-4). RESULTS: In the end, Immunosimulation predictions showed that the MEV-Fc vaccine can make the immune system respond strongly, both in terms of cells and antibodies. DISCUSSION: In summary, our results provide novel insights for the development of Brucella vaccines. Although further laboratory experiments are required to assess its protective effect.
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spelling pubmed-106259102023-11-07 Design of a multi-epitope vaccine against brucellosis fused to IgG-fc by an immunoinformatics approach Wu, Aodi Wang, Yueli Ali, Adnan Xu, Zhenyu Zhang, Dongsheng Zhumanov, Kairat Sheng, Jinliang Yi, Jihai Front Vet Sci Veterinary Science INTRODUCTION: Brucella, a type of intracellular Gram-negative bacterium, has unique features and acts as a zoonotic pathogen. It can lead to abortion and infertility in animals. Eliminating brucellosis becomes very challenging once it spreads among both humans and animals, putting a heavy burden on livestock and people worldwide. Given the increasing spread of brucellosis, it is crucial to develop improved vaccines for susceptible animals to reduce the disease’s impact. METHODS: In this study, we effectively used an immunoinformatics approach with advanced computer software to carefully identify and analyze important antigenic parts of Brucella abortus. Subsequently, we skillfully designed chimeric peptides to enhance the vaccine’s strength and effectiveness. We used computer programs to find four important parts of the Brucella bacteria that our immune system recognizes. Then, we carefully looked for eight parts that are recognized by a type of white blood cell called cytotoxic T cells, six parts recognized by T helper cells, and four parts recognized by B cells. We connected these parts together using a special link, creating a strong new vaccine. To make the vaccine even better, we added some extra parts called molecular adjuvants. These included something called human β-defensins 3 (hBD-3) that we found in a database, and another part that helps the immune system called PADRE. We attached these extra parts to the beginning of the vaccine. In a new and clever way, we made the vaccine even stronger by attaching a part from a mouse’s immune system to the end of it. This created a new kind of vaccine called MEV-Fc. We used advanced computer methods to study how well the MEV-Fc vaccine interacts with certain receptors in the body (TLR-2 and TLR-4). RESULTS: In the end, Immunosimulation predictions showed that the MEV-Fc vaccine can make the immune system respond strongly, both in terms of cells and antibodies. DISCUSSION: In summary, our results provide novel insights for the development of Brucella vaccines. Although further laboratory experiments are required to assess its protective effect. Frontiers Media S.A. 2023-10-23 /pmc/articles/PMC10625910/ /pubmed/37937155 http://dx.doi.org/10.3389/fvets.2023.1238634 Text en Copyright © 2023 Wu, Wang, Ali, Xu, Zhang, Zhumanov, Sheng and Yi. 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 Veterinary Science
Wu, Aodi
Wang, Yueli
Ali, Adnan
Xu, Zhenyu
Zhang, Dongsheng
Zhumanov, Kairat
Sheng, Jinliang
Yi, Jihai
Design of a multi-epitope vaccine against brucellosis fused to IgG-fc by an immunoinformatics approach
title Design of a multi-epitope vaccine against brucellosis fused to IgG-fc by an immunoinformatics approach
title_full Design of a multi-epitope vaccine against brucellosis fused to IgG-fc by an immunoinformatics approach
title_fullStr Design of a multi-epitope vaccine against brucellosis fused to IgG-fc by an immunoinformatics approach
title_full_unstemmed Design of a multi-epitope vaccine against brucellosis fused to IgG-fc by an immunoinformatics approach
title_short Design of a multi-epitope vaccine against brucellosis fused to IgG-fc by an immunoinformatics approach
title_sort design of a multi-epitope vaccine against brucellosis fused to igg-fc by an immunoinformatics approach
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625910/
https://www.ncbi.nlm.nih.gov/pubmed/37937155
http://dx.doi.org/10.3389/fvets.2023.1238634
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