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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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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. |
format | Online Article Text |
id | pubmed-4667181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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