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Protist predation can select for bacteria with lowered susceptibility to infection by lytic phages

BACKGROUND: Consumer-resource interactions constitute one of the most common types of interspecific antagonistic interaction. In natural communities, complex species interactions are likely to affect the outcomes of reciprocal co-evolution between consumers and their resource species. Individuals fa...

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Autores principales: Örmälä-Odegrip, Anni-Maria, Ojala, Ville, Hiltunen, Teppo, Zhang, Ji, Bamford, Jaana KH, Laakso, Jouni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4425896/
https://www.ncbi.nlm.nih.gov/pubmed/25947228
http://dx.doi.org/10.1186/s12862-015-0341-1
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author Örmälä-Odegrip, Anni-Maria
Ojala, Ville
Hiltunen, Teppo
Zhang, Ji
Bamford, Jaana KH
Laakso, Jouni
author_facet Örmälä-Odegrip, Anni-Maria
Ojala, Ville
Hiltunen, Teppo
Zhang, Ji
Bamford, Jaana KH
Laakso, Jouni
author_sort Örmälä-Odegrip, Anni-Maria
collection PubMed
description BACKGROUND: Consumer-resource interactions constitute one of the most common types of interspecific antagonistic interaction. In natural communities, complex species interactions are likely to affect the outcomes of reciprocal co-evolution between consumers and their resource species. Individuals face multiple enemies simultaneously, and consequently they need to adapt to several different types of enemy pressures. In this study, we assessed how protist predation affects the susceptibility of bacterial populations to infection by viral parasites, and whether there is an associated cost of defence on the competitive ability of the bacteria. As a study system we used Serratia marcescens and its lytic bacteriophage, along with two bacteriovorous protists with distinct feeding modes: Tetrahymena thermophila (particle feeder) and Acanthamoeba castellanii (surface feeder). The results were further confirmed with another study system with Pseudomonas and Tetrahymena thermophila. RESULTS: We found that selection by protist predators lowered the susceptibility to infections by lytic phages in Serratia and Pseudomonas. In Serratia, concurrent selection by phages and protists led to lowered susceptibility to phage infections and this effect was independent from whether the bacteria shared a co-evolutionary history with the phage population or not. Bacteria that had evolved with phages were overall more susceptible to phage infection (compared to bacteria with history with multiple enemies) but they were less vulnerable to the phages they had co-evolved with than ancestral phages. Selection by bacterial enemies was costly in general and was seen as a lowered fitness in absence of phages, measured as a biomass yield. CONCLUSIONS: Our results show the significance of multiple species interactions on pairwise consumer-resource interaction, and suggest potential overlap in defending against predatory and parasitic enemies in microbial consumer-resource communities. Ultimately, our results could have larger scale effects on eco-evolutionary community dynamics.
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spelling pubmed-44258962015-05-10 Protist predation can select for bacteria with lowered susceptibility to infection by lytic phages Örmälä-Odegrip, Anni-Maria Ojala, Ville Hiltunen, Teppo Zhang, Ji Bamford, Jaana KH Laakso, Jouni BMC Evol Biol Research Article BACKGROUND: Consumer-resource interactions constitute one of the most common types of interspecific antagonistic interaction. In natural communities, complex species interactions are likely to affect the outcomes of reciprocal co-evolution between consumers and their resource species. Individuals face multiple enemies simultaneously, and consequently they need to adapt to several different types of enemy pressures. In this study, we assessed how protist predation affects the susceptibility of bacterial populations to infection by viral parasites, and whether there is an associated cost of defence on the competitive ability of the bacteria. As a study system we used Serratia marcescens and its lytic bacteriophage, along with two bacteriovorous protists with distinct feeding modes: Tetrahymena thermophila (particle feeder) and Acanthamoeba castellanii (surface feeder). The results were further confirmed with another study system with Pseudomonas and Tetrahymena thermophila. RESULTS: We found that selection by protist predators lowered the susceptibility to infections by lytic phages in Serratia and Pseudomonas. In Serratia, concurrent selection by phages and protists led to lowered susceptibility to phage infections and this effect was independent from whether the bacteria shared a co-evolutionary history with the phage population or not. Bacteria that had evolved with phages were overall more susceptible to phage infection (compared to bacteria with history with multiple enemies) but they were less vulnerable to the phages they had co-evolved with than ancestral phages. Selection by bacterial enemies was costly in general and was seen as a lowered fitness in absence of phages, measured as a biomass yield. CONCLUSIONS: Our results show the significance of multiple species interactions on pairwise consumer-resource interaction, and suggest potential overlap in defending against predatory and parasitic enemies in microbial consumer-resource communities. Ultimately, our results could have larger scale effects on eco-evolutionary community dynamics. BioMed Central 2015-05-07 /pmc/articles/PMC4425896/ /pubmed/25947228 http://dx.doi.org/10.1186/s12862-015-0341-1 Text en © Örmälä-Odegrip et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Örmälä-Odegrip, Anni-Maria
Ojala, Ville
Hiltunen, Teppo
Zhang, Ji
Bamford, Jaana KH
Laakso, Jouni
Protist predation can select for bacteria with lowered susceptibility to infection by lytic phages
title Protist predation can select for bacteria with lowered susceptibility to infection by lytic phages
title_full Protist predation can select for bacteria with lowered susceptibility to infection by lytic phages
title_fullStr Protist predation can select for bacteria with lowered susceptibility to infection by lytic phages
title_full_unstemmed Protist predation can select for bacteria with lowered susceptibility to infection by lytic phages
title_short Protist predation can select for bacteria with lowered susceptibility to infection by lytic phages
title_sort protist predation can select for bacteria with lowered susceptibility to infection by lytic phages
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4425896/
https://www.ncbi.nlm.nih.gov/pubmed/25947228
http://dx.doi.org/10.1186/s12862-015-0341-1
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