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Evaluation of glutathione-binding protein A of Haemophilus parasuis as a vaccine candidate in a mouse model

The virulent strains of Haemophilus parasuis are the causative agents of Glässer’s disease, which can cause systemic infection and result in polyserositis, meningitis and arthritis. The development of novel, effective vaccines would be beneficial to preventing H. parasuis infections. Here, we report...

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Autores principales: ZHANG, Yanhe, LI, Gang, XIE, Fang, LIU, Siguo, WANG, Chunlai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289258/
https://www.ncbi.nlm.nih.gov/pubmed/27840377
http://dx.doi.org/10.1292/jvms.16-0327
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author ZHANG, Yanhe
LI, Gang
XIE, Fang
LIU, Siguo
WANG, Chunlai
author_facet ZHANG, Yanhe
LI, Gang
XIE, Fang
LIU, Siguo
WANG, Chunlai
author_sort ZHANG, Yanhe
collection PubMed
description The virulent strains of Haemophilus parasuis are the causative agents of Glässer’s disease, which can cause systemic infection and result in polyserositis, meningitis and arthritis. The development of novel, effective vaccines would be beneficial to preventing H. parasuis infections. Here, we report a novel immunogenic protein, glutathione-binding protein A (GbpA), which can elicit a significant humoral antibody response and confer significant protection against challenge with a lethal dose of a highly virulent H. parasuis strain. The H. parasuis strain can be fully eliminated in the immunized mice. The results indicate that GbpA has the potential to be used as an effective component of a new vaccine against H. parasuis.
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spelling pubmed-52892582017-02-08 Evaluation of glutathione-binding protein A of Haemophilus parasuis as a vaccine candidate in a mouse model ZHANG, Yanhe LI, Gang XIE, Fang LIU, Siguo WANG, Chunlai J Vet Med Sci Bacteriology The virulent strains of Haemophilus parasuis are the causative agents of Glässer’s disease, which can cause systemic infection and result in polyserositis, meningitis and arthritis. The development of novel, effective vaccines would be beneficial to preventing H. parasuis infections. Here, we report a novel immunogenic protein, glutathione-binding protein A (GbpA), which can elicit a significant humoral antibody response and confer significant protection against challenge with a lethal dose of a highly virulent H. parasuis strain. The H. parasuis strain can be fully eliminated in the immunized mice. The results indicate that GbpA has the potential to be used as an effective component of a new vaccine against H. parasuis. The Japanese Society of Veterinary Science 2016-11-11 2017-01 /pmc/articles/PMC5289258/ /pubmed/27840377 http://dx.doi.org/10.1292/jvms.16-0327 Text en ©2017 The Japanese Society of Veterinary Science http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Bacteriology
ZHANG, Yanhe
LI, Gang
XIE, Fang
LIU, Siguo
WANG, Chunlai
Evaluation of glutathione-binding protein A of Haemophilus parasuis as a vaccine candidate in a mouse model
title Evaluation of glutathione-binding protein A of Haemophilus parasuis as a vaccine candidate in a mouse model
title_full Evaluation of glutathione-binding protein A of Haemophilus parasuis as a vaccine candidate in a mouse model
title_fullStr Evaluation of glutathione-binding protein A of Haemophilus parasuis as a vaccine candidate in a mouse model
title_full_unstemmed Evaluation of glutathione-binding protein A of Haemophilus parasuis as a vaccine candidate in a mouse model
title_short Evaluation of glutathione-binding protein A of Haemophilus parasuis as a vaccine candidate in a mouse model
title_sort evaluation of glutathione-binding protein a of haemophilus parasuis as a vaccine candidate in a mouse model
topic Bacteriology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289258/
https://www.ncbi.nlm.nih.gov/pubmed/27840377
http://dx.doi.org/10.1292/jvms.16-0327
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