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Recombinant DnaK Orally Administered Protects Axenic European Sea Bass Against Vibriosis

Vibrio anguillarum causes high mortality in European sea bass (Dicentrarchus labrax) larviculture and is a hindering factor for successful sustainable aquaculture of this commercially valuable species. Priming of the innate immune system through administration of immunostimulants has become an impor...

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Autores principales: Yaacob, Eamy Nursaliza, Norouzitallab, Parisa, De Geest, Bruno G., Bajek, Aline, Dierckens, Kristof, Bossier, Peter, Vanrompay, Daisy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033693/
https://www.ncbi.nlm.nih.gov/pubmed/32117214
http://dx.doi.org/10.3389/fimmu.2019.03162
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author Yaacob, Eamy Nursaliza
Norouzitallab, Parisa
De Geest, Bruno G.
Bajek, Aline
Dierckens, Kristof
Bossier, Peter
Vanrompay, Daisy
author_facet Yaacob, Eamy Nursaliza
Norouzitallab, Parisa
De Geest, Bruno G.
Bajek, Aline
Dierckens, Kristof
Bossier, Peter
Vanrompay, Daisy
author_sort Yaacob, Eamy Nursaliza
collection PubMed
description Vibrio anguillarum causes high mortality in European sea bass (Dicentrarchus labrax) larviculture and is a hindering factor for successful sustainable aquaculture of this commercially valuable species. Priming of the innate immune system through administration of immunostimulants has become an important approach to control disease outbreaks in marine fish larviculture. This study was conducted to evaluate immunostimulation by Escherichia coli HSP70 (DnaK) in axenic European sea bass larvae in order to protect the larvae against vibriosis. DnaK stimulates the immune response in crustaceans and juvenile fish against bacterial infections. The use of axenic fish larvae allows to study immunostimulation in the absence of an interfering microbial community. At 7 days post-hatching, larvae received a single dose of alginate encapsulated recombinant DnaK. Two non-treated control groups in which animals either received empty alginate microparticles (C1) or no alginante microparticles (C2 and C3) were included in the study. Eighteen hours later, all larvae, except the ones from group C3 (non-infected control) were challenged with V. anguillarum (10(5) CFU, bath infection). Mortality was daily recorded until 120 h post infection and at 18, 24, and 36 h post infection, larvae were sampled for expression of immune related genes. Results showed that V. anguillarum induced an immune response in axenic sea bass larvae but that the innate immune response was incapable to protect the larvae against deadly septicaemic disease. In addition, we showed that administration of alginate encapsulated DnaK to axenic European sea bass larvae at DAH7 resulted in a significant, DnaK dose dependent, upreglation of immune sensor, regulatory and effector genes. Significant upregulation of cxcr4, cas1 and especially of hep and dic was correlated with significant higher survival rates in V. anguillarum infected larvae. In the future recombinant DnaK might perhaps be used as a novel immunostimulant in sea bass larviculture.
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spelling pubmed-70336932020-02-28 Recombinant DnaK Orally Administered Protects Axenic European Sea Bass Against Vibriosis Yaacob, Eamy Nursaliza Norouzitallab, Parisa De Geest, Bruno G. Bajek, Aline Dierckens, Kristof Bossier, Peter Vanrompay, Daisy Front Immunol Immunology Vibrio anguillarum causes high mortality in European sea bass (Dicentrarchus labrax) larviculture and is a hindering factor for successful sustainable aquaculture of this commercially valuable species. Priming of the innate immune system through administration of immunostimulants has become an important approach to control disease outbreaks in marine fish larviculture. This study was conducted to evaluate immunostimulation by Escherichia coli HSP70 (DnaK) in axenic European sea bass larvae in order to protect the larvae against vibriosis. DnaK stimulates the immune response in crustaceans and juvenile fish against bacterial infections. The use of axenic fish larvae allows to study immunostimulation in the absence of an interfering microbial community. At 7 days post-hatching, larvae received a single dose of alginate encapsulated recombinant DnaK. Two non-treated control groups in which animals either received empty alginate microparticles (C1) or no alginante microparticles (C2 and C3) were included in the study. Eighteen hours later, all larvae, except the ones from group C3 (non-infected control) were challenged with V. anguillarum (10(5) CFU, bath infection). Mortality was daily recorded until 120 h post infection and at 18, 24, and 36 h post infection, larvae were sampled for expression of immune related genes. Results showed that V. anguillarum induced an immune response in axenic sea bass larvae but that the innate immune response was incapable to protect the larvae against deadly septicaemic disease. In addition, we showed that administration of alginate encapsulated DnaK to axenic European sea bass larvae at DAH7 resulted in a significant, DnaK dose dependent, upreglation of immune sensor, regulatory and effector genes. Significant upregulation of cxcr4, cas1 and especially of hep and dic was correlated with significant higher survival rates in V. anguillarum infected larvae. In the future recombinant DnaK might perhaps be used as a novel immunostimulant in sea bass larviculture. Frontiers Media S.A. 2020-02-14 /pmc/articles/PMC7033693/ /pubmed/32117214 http://dx.doi.org/10.3389/fimmu.2019.03162 Text en Copyright © 2020 Yaacob, Norouzitallab, De Geest, Bajek, Dierckens, Bossier and Vanrompay. http://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 Immunology
Yaacob, Eamy Nursaliza
Norouzitallab, Parisa
De Geest, Bruno G.
Bajek, Aline
Dierckens, Kristof
Bossier, Peter
Vanrompay, Daisy
Recombinant DnaK Orally Administered Protects Axenic European Sea Bass Against Vibriosis
title Recombinant DnaK Orally Administered Protects Axenic European Sea Bass Against Vibriosis
title_full Recombinant DnaK Orally Administered Protects Axenic European Sea Bass Against Vibriosis
title_fullStr Recombinant DnaK Orally Administered Protects Axenic European Sea Bass Against Vibriosis
title_full_unstemmed Recombinant DnaK Orally Administered Protects Axenic European Sea Bass Against Vibriosis
title_short Recombinant DnaK Orally Administered Protects Axenic European Sea Bass Against Vibriosis
title_sort recombinant dnak orally administered protects axenic european sea bass against vibriosis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033693/
https://www.ncbi.nlm.nih.gov/pubmed/32117214
http://dx.doi.org/10.3389/fimmu.2019.03162
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