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Symbiont-derived sphingolipids modulate mucosal homeostasis and B cells in teleost fish
Symbiotic bacteria and mucosal immunoglobulins have co-evolved for millions of years in vertebrate animals. Symbiotic bacteria products are known to modulate different aspects of the host immune system. We recently reported that Flectobacillus major is a predominant species that lives in the gill an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155239/ https://www.ncbi.nlm.nih.gov/pubmed/27966609 http://dx.doi.org/10.1038/srep39054 |
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author | Sepahi, Ali Cordero, Héctor Goldfine, Howard Esteban, Maria Ángeles Salinas, Irene |
author_facet | Sepahi, Ali Cordero, Héctor Goldfine, Howard Esteban, Maria Ángeles Salinas, Irene |
author_sort | Sepahi, Ali |
collection | PubMed |
description | Symbiotic bacteria and mucosal immunoglobulins have co-evolved for millions of years in vertebrate animals. Symbiotic bacteria products are known to modulate different aspects of the host immune system. We recently reported that Flectobacillus major is a predominant species that lives in the gill and skin mucosal surfaces of rainbow trout (Oncorhynchus mykiss). F. major is known to produce sphingolipids of a unique molecular structure. Here we propose a role for F. major and its sphingolipids in the regulation of B cell populations in rainbow trout, as well as an essential role for sphingolipids in trout mucosal homeostasis. We found that F. major-specific IgT titers are confined to the gill and skin mucus, whereas F. major-specific IgM titers are only detected in serum. Live F. major cells are able to stimulate sustained IgT expression and secretion in gills. F. major sphingolipids modulate the growth of trout total skin and gill symbiotic bacteria. In vivo systemic administration of F. major sphingolipids changes the proportion of IgT(+) to IgM(+) B cells in trout HK. These results demonstrate the key role of the symbiont F. major and its sphingolipids in mucosal homeostasis via the modulation of mucosal and systemic Igs and B cells. |
format | Online Article Text |
id | pubmed-5155239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51552392016-12-28 Symbiont-derived sphingolipids modulate mucosal homeostasis and B cells in teleost fish Sepahi, Ali Cordero, Héctor Goldfine, Howard Esteban, Maria Ángeles Salinas, Irene Sci Rep Article Symbiotic bacteria and mucosal immunoglobulins have co-evolved for millions of years in vertebrate animals. Symbiotic bacteria products are known to modulate different aspects of the host immune system. We recently reported that Flectobacillus major is a predominant species that lives in the gill and skin mucosal surfaces of rainbow trout (Oncorhynchus mykiss). F. major is known to produce sphingolipids of a unique molecular structure. Here we propose a role for F. major and its sphingolipids in the regulation of B cell populations in rainbow trout, as well as an essential role for sphingolipids in trout mucosal homeostasis. We found that F. major-specific IgT titers are confined to the gill and skin mucus, whereas F. major-specific IgM titers are only detected in serum. Live F. major cells are able to stimulate sustained IgT expression and secretion in gills. F. major sphingolipids modulate the growth of trout total skin and gill symbiotic bacteria. In vivo systemic administration of F. major sphingolipids changes the proportion of IgT(+) to IgM(+) B cells in trout HK. These results demonstrate the key role of the symbiont F. major and its sphingolipids in mucosal homeostasis via the modulation of mucosal and systemic Igs and B cells. Nature Publishing Group 2016-12-14 /pmc/articles/PMC5155239/ /pubmed/27966609 http://dx.doi.org/10.1038/srep39054 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Sepahi, Ali Cordero, Héctor Goldfine, Howard Esteban, Maria Ángeles Salinas, Irene Symbiont-derived sphingolipids modulate mucosal homeostasis and B cells in teleost fish |
title | Symbiont-derived sphingolipids modulate mucosal homeostasis and B cells in teleost fish |
title_full | Symbiont-derived sphingolipids modulate mucosal homeostasis and B cells in teleost fish |
title_fullStr | Symbiont-derived sphingolipids modulate mucosal homeostasis and B cells in teleost fish |
title_full_unstemmed | Symbiont-derived sphingolipids modulate mucosal homeostasis and B cells in teleost fish |
title_short | Symbiont-derived sphingolipids modulate mucosal homeostasis and B cells in teleost fish |
title_sort | symbiont-derived sphingolipids modulate mucosal homeostasis and b cells in teleost fish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155239/ https://www.ncbi.nlm.nih.gov/pubmed/27966609 http://dx.doi.org/10.1038/srep39054 |
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