Cargando…

Evaluation of Immunogenicity, Protective Immunity on Aquaculture Pathogenic Vibrio and Fermentation of Vibrio alginolyticus Flagellin FlaC Protein

BACKGROUND: Vibrio are the main pathogenic bacteria in aquaculture. The flagellin protein C (FlaC) of Vibrio alginolyticus has good immunogenicity and the prospect of potential application in a vaccine. OBJECTIVES: We aimed to evaluate the immunogenicity, protective immunity, and prokaryotic express...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Chen, Kang, Chao, Rong, Na, Wu, Nana, Chen, Chunlin, Wu, Sanqiao, Zhang, Xiaoying, Liu, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Institute of Genetic Engineering and Biotechnology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080974/
https://www.ncbi.nlm.nih.gov/pubmed/32195288
http://dx.doi.org/10.29252/ijb.2628
_version_ 1783508089158238208
author Chen, Chen
Kang, Chao
Rong, Na
Wu, Nana
Chen, Chunlin
Wu, Sanqiao
Zhang, Xiaoying
Liu, Xiang
author_facet Chen, Chen
Kang, Chao
Rong, Na
Wu, Nana
Chen, Chunlin
Wu, Sanqiao
Zhang, Xiaoying
Liu, Xiang
author_sort Chen, Chen
collection PubMed
description BACKGROUND: Vibrio are the main pathogenic bacteria in aquaculture. The flagellin protein C (FlaC) of Vibrio alginolyticus has good immunogenicity and the prospect of potential application in a vaccine. OBJECTIVES: We aimed to evaluate the immunogenicity, protective immunity, and prokaryotic expression fermentation of V. alginolyticus FlaC protein for the vaccine in aquaculture. MATERIAL AND METHODS: A molecular cloning method was used to construct the expression strain of FlaC protein, and the protein was purified with Ni-affinity chromatography. Polyclonal antiserum was prepared via mice immunized with the FlaC protein. The Western blot and enzyme-linked immunosorbent assay (ELISA) were used to check the specificity and titre of the antiserum. ELISA and pull-down assay detected the interaction between FlaC protein antiserum and Vibrio. The immune protection function of FlaC protein was detected with mice actively immunized with FlaC protein and challenged by V. alginolyticus and V. parahaemolyticus. The optimal expression conditions for FlaC protein were detected using an L(9)(3(4)) orthogonal design model. RESULTS: The expression strain of FlaC protein was obtained successfully, and purified FlaC protein was prepared using a mice polyclonal antibody. The FlaC protein antiserum held a high specificity, and the titre was 13200. The antiserum directly interacted with V. alginolyticus and V. parahaemolyticus, and the FlaC protein demonstrated a significant immune protection function (50%) against V. alginolyticus infection and some immune protection function (41.66%) against V. parahaemolyticus. The optimal expression conditions for FlaC protein included a strain OD(600) value of 0.8, final isopropyl-β-d-thiogalactoside (IPTG) concentration of 0.1 mmol/L, an inducing time of 8 hours, and an inducing temperature of 28°C. CONCLUSIONS: This study showed that the FlaC protein possesses a significant immunogenicity and immune protection effect and obtained the optimal fermentation conditions. It is expected to be a potential vaccine against V. alginolyticus and V. parahaemolyticus.
format Online
Article
Text
id pubmed-7080974
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher National Institute of Genetic Engineering and Biotechnology
record_format MEDLINE/PubMed
spelling pubmed-70809742020-03-19 Evaluation of Immunogenicity, Protective Immunity on Aquaculture Pathogenic Vibrio and Fermentation of Vibrio alginolyticus Flagellin FlaC Protein Chen, Chen Kang, Chao Rong, Na Wu, Nana Chen, Chunlin Wu, Sanqiao Zhang, Xiaoying Liu, Xiang Iran J Biotechnol Research Article BACKGROUND: Vibrio are the main pathogenic bacteria in aquaculture. The flagellin protein C (FlaC) of Vibrio alginolyticus has good immunogenicity and the prospect of potential application in a vaccine. OBJECTIVES: We aimed to evaluate the immunogenicity, protective immunity, and prokaryotic expression fermentation of V. alginolyticus FlaC protein for the vaccine in aquaculture. MATERIAL AND METHODS: A molecular cloning method was used to construct the expression strain of FlaC protein, and the protein was purified with Ni-affinity chromatography. Polyclonal antiserum was prepared via mice immunized with the FlaC protein. The Western blot and enzyme-linked immunosorbent assay (ELISA) were used to check the specificity and titre of the antiserum. ELISA and pull-down assay detected the interaction between FlaC protein antiserum and Vibrio. The immune protection function of FlaC protein was detected with mice actively immunized with FlaC protein and challenged by V. alginolyticus and V. parahaemolyticus. The optimal expression conditions for FlaC protein were detected using an L(9)(3(4)) orthogonal design model. RESULTS: The expression strain of FlaC protein was obtained successfully, and purified FlaC protein was prepared using a mice polyclonal antibody. The FlaC protein antiserum held a high specificity, and the titre was 13200. The antiserum directly interacted with V. alginolyticus and V. parahaemolyticus, and the FlaC protein demonstrated a significant immune protection function (50%) against V. alginolyticus infection and some immune protection function (41.66%) against V. parahaemolyticus. The optimal expression conditions for FlaC protein included a strain OD(600) value of 0.8, final isopropyl-β-d-thiogalactoside (IPTG) concentration of 0.1 mmol/L, an inducing time of 8 hours, and an inducing temperature of 28°C. CONCLUSIONS: This study showed that the FlaC protein possesses a significant immunogenicity and immune protection effect and obtained the optimal fermentation conditions. It is expected to be a potential vaccine against V. alginolyticus and V. parahaemolyticus. National Institute of Genetic Engineering and Biotechnology 2019-09-01 /pmc/articles/PMC7080974/ /pubmed/32195288 http://dx.doi.org/10.29252/ijb.2628 Text en Copyright: © 2019 The Author(s); Published by National Institute of Genetic Engineering and Biotechnology. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article, distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits others to copy and redistribute material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Research Article
Chen, Chen
Kang, Chao
Rong, Na
Wu, Nana
Chen, Chunlin
Wu, Sanqiao
Zhang, Xiaoying
Liu, Xiang
Evaluation of Immunogenicity, Protective Immunity on Aquaculture Pathogenic Vibrio and Fermentation of Vibrio alginolyticus Flagellin FlaC Protein
title Evaluation of Immunogenicity, Protective Immunity on Aquaculture Pathogenic Vibrio and Fermentation of Vibrio alginolyticus Flagellin FlaC Protein
title_full Evaluation of Immunogenicity, Protective Immunity on Aquaculture Pathogenic Vibrio and Fermentation of Vibrio alginolyticus Flagellin FlaC Protein
title_fullStr Evaluation of Immunogenicity, Protective Immunity on Aquaculture Pathogenic Vibrio and Fermentation of Vibrio alginolyticus Flagellin FlaC Protein
title_full_unstemmed Evaluation of Immunogenicity, Protective Immunity on Aquaculture Pathogenic Vibrio and Fermentation of Vibrio alginolyticus Flagellin FlaC Protein
title_short Evaluation of Immunogenicity, Protective Immunity on Aquaculture Pathogenic Vibrio and Fermentation of Vibrio alginolyticus Flagellin FlaC Protein
title_sort evaluation of immunogenicity, protective immunity on aquaculture pathogenic vibrio and fermentation of vibrio alginolyticus flagellin flac protein
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080974/
https://www.ncbi.nlm.nih.gov/pubmed/32195288
http://dx.doi.org/10.29252/ijb.2628
work_keys_str_mv AT chenchen evaluationofimmunogenicityprotectiveimmunityonaquaculturepathogenicvibrioandfermentationofvibrioalginolyticusflagellinflacprotein
AT kangchao evaluationofimmunogenicityprotectiveimmunityonaquaculturepathogenicvibrioandfermentationofvibrioalginolyticusflagellinflacprotein
AT rongna evaluationofimmunogenicityprotectiveimmunityonaquaculturepathogenicvibrioandfermentationofvibrioalginolyticusflagellinflacprotein
AT wunana evaluationofimmunogenicityprotectiveimmunityonaquaculturepathogenicvibrioandfermentationofvibrioalginolyticusflagellinflacprotein
AT chenchunlin evaluationofimmunogenicityprotectiveimmunityonaquaculturepathogenicvibrioandfermentationofvibrioalginolyticusflagellinflacprotein
AT wusanqiao evaluationofimmunogenicityprotectiveimmunityonaquaculturepathogenicvibrioandfermentationofvibrioalginolyticusflagellinflacprotein
AT zhangxiaoying evaluationofimmunogenicityprotectiveimmunityonaquaculturepathogenicvibrioandfermentationofvibrioalginolyticusflagellinflacprotein
AT liuxiang evaluationofimmunogenicityprotectiveimmunityonaquaculturepathogenicvibrioandfermentationofvibrioalginolyticusflagellinflacprotein