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A diet-change modulates the previously established bacterial gut community in juvenile brown trout (Salmo trutta)

The aim of the present study was to investigate the impact of dietary plant proteins on the gut microbiome of first feeding brown trout (Salmo trutta) reproduced from wild stocks and to evaluate whether the initial microbiome of brown trout fry can be permanently manipulated by the first feeding die...

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Autores principales: Michl, Stéphanie C., Beyer, Matt, Ratten, Jenni-Marie, Hasler, Mario, LaRoche, Julie, Schulz, Carsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382790/
https://www.ncbi.nlm.nih.gov/pubmed/30787388
http://dx.doi.org/10.1038/s41598-019-38800-7
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author Michl, Stéphanie C.
Beyer, Matt
Ratten, Jenni-Marie
Hasler, Mario
LaRoche, Julie
Schulz, Carsten
author_facet Michl, Stéphanie C.
Beyer, Matt
Ratten, Jenni-Marie
Hasler, Mario
LaRoche, Julie
Schulz, Carsten
author_sort Michl, Stéphanie C.
collection PubMed
description The aim of the present study was to investigate the impact of dietary plant proteins on the gut microbiome of first feeding brown trout (Salmo trutta) reproduced from wild stocks and to evaluate whether the initial microbiome of brown trout fry can be permanently manipulated by the first feeding diet. Therefore, brown trout fry was fed diets based on either 0%, 50% or 90% plant-derived proteins from first feeding onwards and via 16S rRNA gene sequencing a strong dietary influence on the bacterial gut community on phylum and order level was detected. Proteobacteria and Fusobacteria were significantly enhanced when fishmeal was integrated into the experimental diet, whereas plant-derived proteins significantly promoted Firmicutes and Bacteroidetes. In order to evaluate whether the first feeding diet had a permanent effect on the initially established microbial gut community of juvenile brown trout, a cross-over diet-change was applied 61 days post first feeding. 48 days after the diet-change, the gut microbiome of all dietary groups was significantly different from the one initially established after first feeding. Moreover, the first feeding diet had no statistically significant influence on the gut microbiome after the diet-change, demonstrating no permanent effect on the gut microbiome formation.
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spelling pubmed-63827902019-02-22 A diet-change modulates the previously established bacterial gut community in juvenile brown trout (Salmo trutta) Michl, Stéphanie C. Beyer, Matt Ratten, Jenni-Marie Hasler, Mario LaRoche, Julie Schulz, Carsten Sci Rep Article The aim of the present study was to investigate the impact of dietary plant proteins on the gut microbiome of first feeding brown trout (Salmo trutta) reproduced from wild stocks and to evaluate whether the initial microbiome of brown trout fry can be permanently manipulated by the first feeding diet. Therefore, brown trout fry was fed diets based on either 0%, 50% or 90% plant-derived proteins from first feeding onwards and via 16S rRNA gene sequencing a strong dietary influence on the bacterial gut community on phylum and order level was detected. Proteobacteria and Fusobacteria were significantly enhanced when fishmeal was integrated into the experimental diet, whereas plant-derived proteins significantly promoted Firmicutes and Bacteroidetes. In order to evaluate whether the first feeding diet had a permanent effect on the initially established microbial gut community of juvenile brown trout, a cross-over diet-change was applied 61 days post first feeding. 48 days after the diet-change, the gut microbiome of all dietary groups was significantly different from the one initially established after first feeding. Moreover, the first feeding diet had no statistically significant influence on the gut microbiome after the diet-change, demonstrating no permanent effect on the gut microbiome formation. Nature Publishing Group UK 2019-02-20 /pmc/articles/PMC6382790/ /pubmed/30787388 http://dx.doi.org/10.1038/s41598-019-38800-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Michl, Stéphanie C.
Beyer, Matt
Ratten, Jenni-Marie
Hasler, Mario
LaRoche, Julie
Schulz, Carsten
A diet-change modulates the previously established bacterial gut community in juvenile brown trout (Salmo trutta)
title A diet-change modulates the previously established bacterial gut community in juvenile brown trout (Salmo trutta)
title_full A diet-change modulates the previously established bacterial gut community in juvenile brown trout (Salmo trutta)
title_fullStr A diet-change modulates the previously established bacterial gut community in juvenile brown trout (Salmo trutta)
title_full_unstemmed A diet-change modulates the previously established bacterial gut community in juvenile brown trout (Salmo trutta)
title_short A diet-change modulates the previously established bacterial gut community in juvenile brown trout (Salmo trutta)
title_sort diet-change modulates the previously established bacterial gut community in juvenile brown trout (salmo trutta)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382790/
https://www.ncbi.nlm.nih.gov/pubmed/30787388
http://dx.doi.org/10.1038/s41598-019-38800-7
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