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Defending against pathogens – immunological priming and its molecular basis in a sea anemone, cnidarian

Cnidarians, in general, are long-lived organisms and hence may repeatedly encounter common pathogens during their lifespans. It remains unknown whether these early diverging animals possess some type of immunological reaction that strengthens the defense response upon repeated infections, such as th...

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Autores principales: Brown, Tanya, Rodriguez-Lanetty, Mauricio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667181/
https://www.ncbi.nlm.nih.gov/pubmed/26628080
http://dx.doi.org/10.1038/srep17425
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author Brown, Tanya
Rodriguez-Lanetty, Mauricio
author_facet Brown, Tanya
Rodriguez-Lanetty, Mauricio
author_sort Brown, Tanya
collection PubMed
description Cnidarians, in general, are long-lived organisms and hence may repeatedly encounter common pathogens during their lifespans. It remains unknown whether these early diverging animals possess some type of immunological reaction that strengthens the defense response upon repeated infections, such as that described in more evolutionary derived organisms. Here we show results that sea anemones that had previously encountered a pathogen under sub-lethal conditions had a higher survivorship during a subsequently lethal challenge than naïve anemones that encountered the pathogen for the first time. Anemones subjected to the lethal challenge two and four weeks after the sub-lethal exposure presented seven- and five-fold increases in survival, respectively, compared to the naïve anemones. However, anemones challenged six weeks after the sub-lethal exposure showed no increase in survivorship. We argue that this short-lasting priming of the defense response could be ecologically relevant if pathogen encounters are restricted to short seasons characterized by high stress. Furthermore, we discovered significant changes in proteomic profiles between naïve sea anemones and those primed after pathogen exposure suggesting a clear molecular signature associated with immunological priming in cnidarians. Our findings reveal that immunological priming may have evolved much earlier in the tree of life than previously thought.
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spelling pubmed-46671812015-12-03 Defending against pathogens – immunological priming and its molecular basis in a sea anemone, cnidarian Brown, Tanya Rodriguez-Lanetty, Mauricio Sci Rep Article Cnidarians, in general, are long-lived organisms and hence may repeatedly encounter common pathogens during their lifespans. It remains unknown whether these early diverging animals possess some type of immunological reaction that strengthens the defense response upon repeated infections, such as that described in more evolutionary derived organisms. Here we show results that sea anemones that had previously encountered a pathogen under sub-lethal conditions had a higher survivorship during a subsequently lethal challenge than naïve anemones that encountered the pathogen for the first time. Anemones subjected to the lethal challenge two and four weeks after the sub-lethal exposure presented seven- and five-fold increases in survival, respectively, compared to the naïve anemones. However, anemones challenged six weeks after the sub-lethal exposure showed no increase in survivorship. We argue that this short-lasting priming of the defense response could be ecologically relevant if pathogen encounters are restricted to short seasons characterized by high stress. Furthermore, we discovered significant changes in proteomic profiles between naïve sea anemones and those primed after pathogen exposure suggesting a clear molecular signature associated with immunological priming in cnidarians. Our findings reveal that immunological priming may have evolved much earlier in the tree of life than previously thought. Nature Publishing Group 2015-12-02 /pmc/articles/PMC4667181/ /pubmed/26628080 http://dx.doi.org/10.1038/srep17425 Text en Copyright © 2015, Macmillan Publishers Limited 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
Brown, Tanya
Rodriguez-Lanetty, Mauricio
Defending against pathogens – immunological priming and its molecular basis in a sea anemone, cnidarian
title Defending against pathogens – immunological priming and its molecular basis in a sea anemone, cnidarian
title_full Defending against pathogens – immunological priming and its molecular basis in a sea anemone, cnidarian
title_fullStr Defending against pathogens – immunological priming and its molecular basis in a sea anemone, cnidarian
title_full_unstemmed Defending against pathogens – immunological priming and its molecular basis in a sea anemone, cnidarian
title_short Defending against pathogens – immunological priming and its molecular basis in a sea anemone, cnidarian
title_sort defending against pathogens – immunological priming and its molecular basis in a sea anemone, cnidarian
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667181/
https://www.ncbi.nlm.nih.gov/pubmed/26628080
http://dx.doi.org/10.1038/srep17425
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