Cargando…
Effects of predation stress and food ration on perch gut microbiota
BACKGROUND: Gut microbiota provide functions of importance to influence hosts’ food digestion, metabolism, and protection against pathogens. Factors that affect the composition and functions of gut microbial communities are well studied in humans and other animals; however, we have limited knowledge...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801810/ https://www.ncbi.nlm.nih.gov/pubmed/29409543 http://dx.doi.org/10.1186/s40168-018-0400-0 |
_version_ | 1783298412882427904 |
---|---|
author | Zha, Yinghua Eiler, Alexander Johansson, Frank Svanbäck, Richard |
author_facet | Zha, Yinghua Eiler, Alexander Johansson, Frank Svanbäck, Richard |
author_sort | Zha, Yinghua |
collection | PubMed |
description | BACKGROUND: Gut microbiota provide functions of importance to influence hosts’ food digestion, metabolism, and protection against pathogens. Factors that affect the composition and functions of gut microbial communities are well studied in humans and other animals; however, we have limited knowledge of how natural food web factors such as stress from predators and food resource rations could affect hosts’ gut microbiota and how it interacts with host sex. In this study, we designed a two-factorial experiment exposing perch (Perca fluviatilis) to a predator (pike, Esox lucius), and different food ratios, to examine the compositional and functional changes of perch gut microbiota based on 16S rRNA amplicon sequencing. We also investigated if those changes are host sex dependent. RESULTS: We showed that overall gut microbiota composition among individual perch significantly responded to food ration and predator presence. We found that species richness decreased with predator presence, and we identified 23 taxa from a diverse set of phyla that were over-represented when a predator was present. For example, Fusobacteria increased both at the lowest food ration and at predation stress conditions, suggesting that Fusobacteria are favored by stressful situations for the host. In concordance, both food ration and predation stress seemed to influence the metabolic repertoire of the gut microbiota, such as biosynthesis of other secondary metabolites, metabolism of cofactors, and vitamins. In addition, the identified interaction between food ration and sex emphasizes sex-specific responses to diet quantity in gut microbiota. CONCLUSIONS: Collectively, our findings emphasize an alternative state in gut microbiota with responses to changes in natural food webs depending on host sex. The obtained knowledge from this study provided us with an important perspective on gut microbiota in a food web context. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-018-0400-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5801810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58018102018-02-14 Effects of predation stress and food ration on perch gut microbiota Zha, Yinghua Eiler, Alexander Johansson, Frank Svanbäck, Richard Microbiome Research BACKGROUND: Gut microbiota provide functions of importance to influence hosts’ food digestion, metabolism, and protection against pathogens. Factors that affect the composition and functions of gut microbial communities are well studied in humans and other animals; however, we have limited knowledge of how natural food web factors such as stress from predators and food resource rations could affect hosts’ gut microbiota and how it interacts with host sex. In this study, we designed a two-factorial experiment exposing perch (Perca fluviatilis) to a predator (pike, Esox lucius), and different food ratios, to examine the compositional and functional changes of perch gut microbiota based on 16S rRNA amplicon sequencing. We also investigated if those changes are host sex dependent. RESULTS: We showed that overall gut microbiota composition among individual perch significantly responded to food ration and predator presence. We found that species richness decreased with predator presence, and we identified 23 taxa from a diverse set of phyla that were over-represented when a predator was present. For example, Fusobacteria increased both at the lowest food ration and at predation stress conditions, suggesting that Fusobacteria are favored by stressful situations for the host. In concordance, both food ration and predation stress seemed to influence the metabolic repertoire of the gut microbiota, such as biosynthesis of other secondary metabolites, metabolism of cofactors, and vitamins. In addition, the identified interaction between food ration and sex emphasizes sex-specific responses to diet quantity in gut microbiota. CONCLUSIONS: Collectively, our findings emphasize an alternative state in gut microbiota with responses to changes in natural food webs depending on host sex. The obtained knowledge from this study provided us with an important perspective on gut microbiota in a food web context. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-018-0400-0) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-06 /pmc/articles/PMC5801810/ /pubmed/29409543 http://dx.doi.org/10.1186/s40168-018-0400-0 Text en © The Author(s). 2018 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 Zha, Yinghua Eiler, Alexander Johansson, Frank Svanbäck, Richard Effects of predation stress and food ration on perch gut microbiota |
title | Effects of predation stress and food ration on perch gut microbiota |
title_full | Effects of predation stress and food ration on perch gut microbiota |
title_fullStr | Effects of predation stress and food ration on perch gut microbiota |
title_full_unstemmed | Effects of predation stress and food ration on perch gut microbiota |
title_short | Effects of predation stress and food ration on perch gut microbiota |
title_sort | effects of predation stress and food ration on perch gut microbiota |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801810/ https://www.ncbi.nlm.nih.gov/pubmed/29409543 http://dx.doi.org/10.1186/s40168-018-0400-0 |
work_keys_str_mv | AT zhayinghua effectsofpredationstressandfoodrationonperchgutmicrobiota AT eileralexander effectsofpredationstressandfoodrationonperchgutmicrobiota AT johanssonfrank effectsofpredationstressandfoodrationonperchgutmicrobiota AT svanbackrichard effectsofpredationstressandfoodrationonperchgutmicrobiota |