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Tripartite species interaction: eukaryotic hosts suffer more from phage susceptible than from phage resistant bacteria
BACKGROUND: Evolutionary shifts in bacterial virulence are often associated with a third biological player, for instance temperate phages, that can act as hyperparasites. By integrating as prophages into the bacterial genome they can contribute accessory genes, which can enhance the fitness of their...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5387238/ https://www.ncbi.nlm.nih.gov/pubmed/28399796 http://dx.doi.org/10.1186/s12862-017-0930-2 |
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author | Wendling, Carolin C. Piecyk, Agnes Refardt, Dominik Chibani, Cynthia Hertel, Robert Liesegang, Heiko Bunk, Boyke Overmann, Jörg Roth, Olivia |
author_facet | Wendling, Carolin C. Piecyk, Agnes Refardt, Dominik Chibani, Cynthia Hertel, Robert Liesegang, Heiko Bunk, Boyke Overmann, Jörg Roth, Olivia |
author_sort | Wendling, Carolin C. |
collection | PubMed |
description | BACKGROUND: Evolutionary shifts in bacterial virulence are often associated with a third biological player, for instance temperate phages, that can act as hyperparasites. By integrating as prophages into the bacterial genome they can contribute accessory genes, which can enhance the fitness of their prokaryotic carrier (lysogenic conversion). Hyperparasitic influence in tripartite biotic interactions has so far been largely neglected in empirical host-parasite studies due to their inherent complexity. Here we experimentally address whether bacterial resistance to phages and bacterial harm to eukaryotic hosts is linked using a natural tri-partite system with bacteria of the genus Vibrio, temperate vibriophages and the pipefish Syngnathus typhle. We induced prophages from all bacterial isolates and constructed a three-fold replicated, fully reciprocal 75 × 75 phage-bacteria infection matrix. RESULTS: According to their resistance to phages, bacteria could be grouped into three distinct categories: highly susceptible (HS-bacteria), intermediate susceptible (IS-bacteria), and resistant (R-bacteria). We experimentally challenged pipefish with three selected bacterial isolates from each of the three categories and determined the amount of viable Vibrio counts from infected pipefish and the expression of pipefish immune genes. While the amount of viable Vibrio counts did not differ between bacterial groups, we observed a significant difference in relative gene expression between pipefish infected with phage susceptible and phage resistant bacteria. CONCLUSION: These findings suggest that bacteria with a phage-susceptible phenotype are more harmful against a eukaryotic host, and support the importance of hyperparasitism and the need for an integrative view across more than two levels when studying host-parasite evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-017-0930-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5387238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53872382017-04-11 Tripartite species interaction: eukaryotic hosts suffer more from phage susceptible than from phage resistant bacteria Wendling, Carolin C. Piecyk, Agnes Refardt, Dominik Chibani, Cynthia Hertel, Robert Liesegang, Heiko Bunk, Boyke Overmann, Jörg Roth, Olivia BMC Evol Biol Research Article BACKGROUND: Evolutionary shifts in bacterial virulence are often associated with a third biological player, for instance temperate phages, that can act as hyperparasites. By integrating as prophages into the bacterial genome they can contribute accessory genes, which can enhance the fitness of their prokaryotic carrier (lysogenic conversion). Hyperparasitic influence in tripartite biotic interactions has so far been largely neglected in empirical host-parasite studies due to their inherent complexity. Here we experimentally address whether bacterial resistance to phages and bacterial harm to eukaryotic hosts is linked using a natural tri-partite system with bacteria of the genus Vibrio, temperate vibriophages and the pipefish Syngnathus typhle. We induced prophages from all bacterial isolates and constructed a three-fold replicated, fully reciprocal 75 × 75 phage-bacteria infection matrix. RESULTS: According to their resistance to phages, bacteria could be grouped into three distinct categories: highly susceptible (HS-bacteria), intermediate susceptible (IS-bacteria), and resistant (R-bacteria). We experimentally challenged pipefish with three selected bacterial isolates from each of the three categories and determined the amount of viable Vibrio counts from infected pipefish and the expression of pipefish immune genes. While the amount of viable Vibrio counts did not differ between bacterial groups, we observed a significant difference in relative gene expression between pipefish infected with phage susceptible and phage resistant bacteria. CONCLUSION: These findings suggest that bacteria with a phage-susceptible phenotype are more harmful against a eukaryotic host, and support the importance of hyperparasitism and the need for an integrative view across more than two levels when studying host-parasite evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-017-0930-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-04-11 /pmc/articles/PMC5387238/ /pubmed/28399796 http://dx.doi.org/10.1186/s12862-017-0930-2 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Wendling, Carolin C. Piecyk, Agnes Refardt, Dominik Chibani, Cynthia Hertel, Robert Liesegang, Heiko Bunk, Boyke Overmann, Jörg Roth, Olivia Tripartite species interaction: eukaryotic hosts suffer more from phage susceptible than from phage resistant bacteria |
title | Tripartite species interaction: eukaryotic hosts suffer more from phage susceptible than from phage resistant bacteria |
title_full | Tripartite species interaction: eukaryotic hosts suffer more from phage susceptible than from phage resistant bacteria |
title_fullStr | Tripartite species interaction: eukaryotic hosts suffer more from phage susceptible than from phage resistant bacteria |
title_full_unstemmed | Tripartite species interaction: eukaryotic hosts suffer more from phage susceptible than from phage resistant bacteria |
title_short | Tripartite species interaction: eukaryotic hosts suffer more from phage susceptible than from phage resistant bacteria |
title_sort | tripartite species interaction: eukaryotic hosts suffer more from phage susceptible than from phage resistant bacteria |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5387238/ https://www.ncbi.nlm.nih.gov/pubmed/28399796 http://dx.doi.org/10.1186/s12862-017-0930-2 |
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