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Caenorhabditis elegans employs innate and learned aversion in response to bacterial toxic metabolites tambjamine and violacein
Bacteriovorus eukaryotes such as nematodes are one of the major natural predators of bacteria. In their defense bacteria have evolved a number of strategies to avoid predation, including the production of deterrent or toxic metabolites, however little is known regarding the response of predators tow...
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/PMC4935850/ https://www.ncbi.nlm.nih.gov/pubmed/27384057 http://dx.doi.org/10.1038/srep29284 |
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author | Ballestriero, Francesco Nappi, Jadranka Zampi, Giuseppina Bazzicalupo, Paolo Di Schiavi, Elia Egan, Suhelen |
author_facet | Ballestriero, Francesco Nappi, Jadranka Zampi, Giuseppina Bazzicalupo, Paolo Di Schiavi, Elia Egan, Suhelen |
author_sort | Ballestriero, Francesco |
collection | PubMed |
description | Bacteriovorus eukaryotes such as nematodes are one of the major natural predators of bacteria. In their defense bacteria have evolved a number of strategies to avoid predation, including the production of deterrent or toxic metabolites, however little is known regarding the response of predators towards such bacterial defenses. Here we use the nematode C. elegans as a model to study a predators’ behavioral response towards two toxic bacterial metabolites, tambjamine YP1 and violacein. We found that C. elegans displays an innate avoidance behavior towards tambjamine YP1, however requires previous exposure to violacein before learning to avoid this metabolite. The learned avoidance of violacein is specific, reversible, is mediated via the nematode olfactory apparatus (aversive olfactory learning) and is reduced in the absence of the neurotransmitter serotonin. These multiple strategies to evade bacterial toxic metabolites represent a valuable behavioral adaptation allowing bacteriovorus predators to distinguish between good and bad food sources, thus contributing to the understanding of microbial predator-prey interactions. |
format | Online Article Text |
id | pubmed-4935850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49358502016-07-08 Caenorhabditis elegans employs innate and learned aversion in response to bacterial toxic metabolites tambjamine and violacein Ballestriero, Francesco Nappi, Jadranka Zampi, Giuseppina Bazzicalupo, Paolo Di Schiavi, Elia Egan, Suhelen Sci Rep Article Bacteriovorus eukaryotes such as nematodes are one of the major natural predators of bacteria. In their defense bacteria have evolved a number of strategies to avoid predation, including the production of deterrent or toxic metabolites, however little is known regarding the response of predators towards such bacterial defenses. Here we use the nematode C. elegans as a model to study a predators’ behavioral response towards two toxic bacterial metabolites, tambjamine YP1 and violacein. We found that C. elegans displays an innate avoidance behavior towards tambjamine YP1, however requires previous exposure to violacein before learning to avoid this metabolite. The learned avoidance of violacein is specific, reversible, is mediated via the nematode olfactory apparatus (aversive olfactory learning) and is reduced in the absence of the neurotransmitter serotonin. These multiple strategies to evade bacterial toxic metabolites represent a valuable behavioral adaptation allowing bacteriovorus predators to distinguish between good and bad food sources, thus contributing to the understanding of microbial predator-prey interactions. Nature Publishing Group 2016-07-07 /pmc/articles/PMC4935850/ /pubmed/27384057 http://dx.doi.org/10.1038/srep29284 Text en Copyright © 2016, 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 Ballestriero, Francesco Nappi, Jadranka Zampi, Giuseppina Bazzicalupo, Paolo Di Schiavi, Elia Egan, Suhelen Caenorhabditis elegans employs innate and learned aversion in response to bacterial toxic metabolites tambjamine and violacein |
title | Caenorhabditis elegans employs innate and learned aversion in response to bacterial toxic metabolites tambjamine and violacein |
title_full | Caenorhabditis elegans employs innate and learned aversion in response to bacterial toxic metabolites tambjamine and violacein |
title_fullStr | Caenorhabditis elegans employs innate and learned aversion in response to bacterial toxic metabolites tambjamine and violacein |
title_full_unstemmed | Caenorhabditis elegans employs innate and learned aversion in response to bacterial toxic metabolites tambjamine and violacein |
title_short | Caenorhabditis elegans employs innate and learned aversion in response to bacterial toxic metabolites tambjamine and violacein |
title_sort | caenorhabditis elegans employs innate and learned aversion in response to bacterial toxic metabolites tambjamine and violacein |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4935850/ https://www.ncbi.nlm.nih.gov/pubmed/27384057 http://dx.doi.org/10.1038/srep29284 |
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