Cargando…

Association between adaptive immunity and neutrophil dynamics in zebrafish (Danio rerio) infected by a parasitic ciliate

The protective immune response in zebrafish (Danio rerio) against the parasitic ciliate Ichthyophthirius multifiliis, targeting host skin, fins and gills, comprises an accelerated and manifold elevated immunoglobulin gene expression as well as a significantly elevated number of neutrophils at infect...

Descripción completa

Detalles Bibliográficos
Autores principales: Jørgensen, Louise von Gersdorff, Korbut, Rozalia, Jeberg, Sandra, Kania, Per Walter, Buchmann, Kurt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133357/
https://www.ncbi.nlm.nih.gov/pubmed/30204772
http://dx.doi.org/10.1371/journal.pone.0203297
_version_ 1783354493159604224
author Jørgensen, Louise von Gersdorff
Korbut, Rozalia
Jeberg, Sandra
Kania, Per Walter
Buchmann, Kurt
author_facet Jørgensen, Louise von Gersdorff
Korbut, Rozalia
Jeberg, Sandra
Kania, Per Walter
Buchmann, Kurt
author_sort Jørgensen, Louise von Gersdorff
collection PubMed
description The protective immune response in zebrafish (Danio rerio) against the parasitic ciliate Ichthyophthirius multifiliis, targeting host skin, fins and gills, comprises an accelerated and manifold elevated immunoglobulin gene expression as well as a significantly elevated number of neutrophils at infected sites. Experimental fish were subjected to a primary I. multifiliis infection followed by a series of secondary exposures before they were challenged by a high dosage of infective theronts. Immunized fish responded immediately with a protective response suggesting existence of immunological memory whereas fish exposed to the parasite for the first time obtained a marked infection. The primary response to infection was dominated by expression of genes encoding acute phase reactants and inflammatory cytokines as well as recruitment of neutrophils at infected locations. Immunized fish showed a significantly upregulated immunoglobulin gene expression following challenge, which indicates existence of a secondary response effected by antibodies. Both responses induced a significantly elevated expression of the Th2 signature cytokine Il13. The increased presence of neutrophils in immunized fish suggests that innate cell mediated immunity supplements or influence the protective response against the parasite.
format Online
Article
Text
id pubmed-6133357
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-61333572018-09-27 Association between adaptive immunity and neutrophil dynamics in zebrafish (Danio rerio) infected by a parasitic ciliate Jørgensen, Louise von Gersdorff Korbut, Rozalia Jeberg, Sandra Kania, Per Walter Buchmann, Kurt PLoS One Research Article The protective immune response in zebrafish (Danio rerio) against the parasitic ciliate Ichthyophthirius multifiliis, targeting host skin, fins and gills, comprises an accelerated and manifold elevated immunoglobulin gene expression as well as a significantly elevated number of neutrophils at infected sites. Experimental fish were subjected to a primary I. multifiliis infection followed by a series of secondary exposures before they were challenged by a high dosage of infective theronts. Immunized fish responded immediately with a protective response suggesting existence of immunological memory whereas fish exposed to the parasite for the first time obtained a marked infection. The primary response to infection was dominated by expression of genes encoding acute phase reactants and inflammatory cytokines as well as recruitment of neutrophils at infected locations. Immunized fish showed a significantly upregulated immunoglobulin gene expression following challenge, which indicates existence of a secondary response effected by antibodies. Both responses induced a significantly elevated expression of the Th2 signature cytokine Il13. The increased presence of neutrophils in immunized fish suggests that innate cell mediated immunity supplements or influence the protective response against the parasite. Public Library of Science 2018-09-11 /pmc/articles/PMC6133357/ /pubmed/30204772 http://dx.doi.org/10.1371/journal.pone.0203297 Text en © 2018 Jørgensen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Jørgensen, Louise von Gersdorff
Korbut, Rozalia
Jeberg, Sandra
Kania, Per Walter
Buchmann, Kurt
Association between adaptive immunity and neutrophil dynamics in zebrafish (Danio rerio) infected by a parasitic ciliate
title Association between adaptive immunity and neutrophil dynamics in zebrafish (Danio rerio) infected by a parasitic ciliate
title_full Association between adaptive immunity and neutrophil dynamics in zebrafish (Danio rerio) infected by a parasitic ciliate
title_fullStr Association between adaptive immunity and neutrophil dynamics in zebrafish (Danio rerio) infected by a parasitic ciliate
title_full_unstemmed Association between adaptive immunity and neutrophil dynamics in zebrafish (Danio rerio) infected by a parasitic ciliate
title_short Association between adaptive immunity and neutrophil dynamics in zebrafish (Danio rerio) infected by a parasitic ciliate
title_sort association between adaptive immunity and neutrophil dynamics in zebrafish (danio rerio) infected by a parasitic ciliate
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133357/
https://www.ncbi.nlm.nih.gov/pubmed/30204772
http://dx.doi.org/10.1371/journal.pone.0203297
work_keys_str_mv AT jørgensenlouisevongersdorff associationbetweenadaptiveimmunityandneutrophildynamicsinzebrafishdaniorerioinfectedbyaparasiticciliate
AT korbutrozalia associationbetweenadaptiveimmunityandneutrophildynamicsinzebrafishdaniorerioinfectedbyaparasiticciliate
AT jebergsandra associationbetweenadaptiveimmunityandneutrophildynamicsinzebrafishdaniorerioinfectedbyaparasiticciliate
AT kaniaperwalter associationbetweenadaptiveimmunityandneutrophildynamicsinzebrafishdaniorerioinfectedbyaparasiticciliate
AT buchmannkurt associationbetweenadaptiveimmunityandneutrophildynamicsinzebrafishdaniorerioinfectedbyaparasiticciliate