Cargando…

Functional Genomic Analysis of the Impact of Camelina (Camelina sativa) Meal on Atlantic Salmon (Salmo salar) Distal Intestine Gene Expression and Physiology

The inclusion of plant meals in diets of farmed Atlantic salmon can elicit inflammatory responses in the distal intestine (DI). For the present work, fish were fed a standard fish meal (FM) diet or a diet with partial replacement of FM with solvent-extracted camelina meal (CM) (8, 16, or 24 % CM inc...

Descripción completa

Detalles Bibliográficos
Autores principales: Brown, Tyler D., Hori, Tiago S., Xue, Xi, Ye, Chang Lin, Anderson, Derek M., Rise, Matthew L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911373/
https://www.ncbi.nlm.nih.gov/pubmed/27255337
http://dx.doi.org/10.1007/s10126-016-9704-x
_version_ 1782438115274653696
author Brown, Tyler D.
Hori, Tiago S.
Xue, Xi
Ye, Chang Lin
Anderson, Derek M.
Rise, Matthew L.
author_facet Brown, Tyler D.
Hori, Tiago S.
Xue, Xi
Ye, Chang Lin
Anderson, Derek M.
Rise, Matthew L.
author_sort Brown, Tyler D.
collection PubMed
description The inclusion of plant meals in diets of farmed Atlantic salmon can elicit inflammatory responses in the distal intestine (DI). For the present work, fish were fed a standard fish meal (FM) diet or a diet with partial replacement of FM with solvent-extracted camelina meal (CM) (8, 16, or 24 % CM inclusion) during a 16-week feeding trial. A significant decrease in growth performance was seen in fish fed all CM inclusion diets (Hixson et al. in Aquacult Nutr 22:615–630, 2016). A 4x44K oligonucleotide microarray experiment was carried out and significance analysis of microarrays (SAM) and rank products (RP) methods were used to identify differentially expressed genes between the DIs of fish fed the 24 % CM diet and those fed the FM diet. Twelve features representing six known transcripts and two unknowns were identified as CM responsive by both SAM and RP. The six known transcripts (including thioredoxin and ependymin), in addition to tgfb, mmp13, and GILT, were studied using qPCR with RNA templates from all four experimental diet groups. All six microarray-identified genes were confirmed to be CM responsive, as was tgfb and mmp13. Histopathological analyses identified signs of inflammation in the DI of salmon fed CM-containing diets, including lamina propria and sub-epithelial mucosa thickening, infiltration of eosinophilic granule cells, increased goblet cells and decreased enterocyte vacuolization. All of these were significantly altered in 24 % CM compared to all other diets, with the latter two also altered in 16 % CM compared with 8 % CM and control diet groups. Significant correlation was seen between histological parameters as well as between five of the qPCR analyzed genes and histological parameters. These molecular biomarkers of inflammation arising from long-term dietary CM exposure will be useful in the development of CM-containing diets that do not have deleterious effects on salmon growth or physiology. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10126-016-9704-x) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4911373
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-49113732016-07-05 Functional Genomic Analysis of the Impact of Camelina (Camelina sativa) Meal on Atlantic Salmon (Salmo salar) Distal Intestine Gene Expression and Physiology Brown, Tyler D. Hori, Tiago S. Xue, Xi Ye, Chang Lin Anderson, Derek M. Rise, Matthew L. Mar Biotechnol (NY) Original Article The inclusion of plant meals in diets of farmed Atlantic salmon can elicit inflammatory responses in the distal intestine (DI). For the present work, fish were fed a standard fish meal (FM) diet or a diet with partial replacement of FM with solvent-extracted camelina meal (CM) (8, 16, or 24 % CM inclusion) during a 16-week feeding trial. A significant decrease in growth performance was seen in fish fed all CM inclusion diets (Hixson et al. in Aquacult Nutr 22:615–630, 2016). A 4x44K oligonucleotide microarray experiment was carried out and significance analysis of microarrays (SAM) and rank products (RP) methods were used to identify differentially expressed genes between the DIs of fish fed the 24 % CM diet and those fed the FM diet. Twelve features representing six known transcripts and two unknowns were identified as CM responsive by both SAM and RP. The six known transcripts (including thioredoxin and ependymin), in addition to tgfb, mmp13, and GILT, were studied using qPCR with RNA templates from all four experimental diet groups. All six microarray-identified genes were confirmed to be CM responsive, as was tgfb and mmp13. Histopathological analyses identified signs of inflammation in the DI of salmon fed CM-containing diets, including lamina propria and sub-epithelial mucosa thickening, infiltration of eosinophilic granule cells, increased goblet cells and decreased enterocyte vacuolization. All of these were significantly altered in 24 % CM compared to all other diets, with the latter two also altered in 16 % CM compared with 8 % CM and control diet groups. Significant correlation was seen between histological parameters as well as between five of the qPCR analyzed genes and histological parameters. These molecular biomarkers of inflammation arising from long-term dietary CM exposure will be useful in the development of CM-containing diets that do not have deleterious effects on salmon growth or physiology. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10126-016-9704-x) contains supplementary material, which is available to authorized users. Springer US 2016-06-02 2016 /pmc/articles/PMC4911373/ /pubmed/27255337 http://dx.doi.org/10.1007/s10126-016-9704-x Text en © The Author(s) 2016 Open Access This 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.
spellingShingle Original Article
Brown, Tyler D.
Hori, Tiago S.
Xue, Xi
Ye, Chang Lin
Anderson, Derek M.
Rise, Matthew L.
Functional Genomic Analysis of the Impact of Camelina (Camelina sativa) Meal on Atlantic Salmon (Salmo salar) Distal Intestine Gene Expression and Physiology
title Functional Genomic Analysis of the Impact of Camelina (Camelina sativa) Meal on Atlantic Salmon (Salmo salar) Distal Intestine Gene Expression and Physiology
title_full Functional Genomic Analysis of the Impact of Camelina (Camelina sativa) Meal on Atlantic Salmon (Salmo salar) Distal Intestine Gene Expression and Physiology
title_fullStr Functional Genomic Analysis of the Impact of Camelina (Camelina sativa) Meal on Atlantic Salmon (Salmo salar) Distal Intestine Gene Expression and Physiology
title_full_unstemmed Functional Genomic Analysis of the Impact of Camelina (Camelina sativa) Meal on Atlantic Salmon (Salmo salar) Distal Intestine Gene Expression and Physiology
title_short Functional Genomic Analysis of the Impact of Camelina (Camelina sativa) Meal on Atlantic Salmon (Salmo salar) Distal Intestine Gene Expression and Physiology
title_sort functional genomic analysis of the impact of camelina (camelina sativa) meal on atlantic salmon (salmo salar) distal intestine gene expression and physiology
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911373/
https://www.ncbi.nlm.nih.gov/pubmed/27255337
http://dx.doi.org/10.1007/s10126-016-9704-x
work_keys_str_mv AT browntylerd functionalgenomicanalysisoftheimpactofcamelinacamelinasativamealonatlanticsalmonsalmosalardistalintestinegeneexpressionandphysiology
AT horitiagos functionalgenomicanalysisoftheimpactofcamelinacamelinasativamealonatlanticsalmonsalmosalardistalintestinegeneexpressionandphysiology
AT xuexi functionalgenomicanalysisoftheimpactofcamelinacamelinasativamealonatlanticsalmonsalmosalardistalintestinegeneexpressionandphysiology
AT yechanglin functionalgenomicanalysisoftheimpactofcamelinacamelinasativamealonatlanticsalmonsalmosalardistalintestinegeneexpressionandphysiology
AT andersonderekm functionalgenomicanalysisoftheimpactofcamelinacamelinasativamealonatlanticsalmonsalmosalardistalintestinegeneexpressionandphysiology
AT risematthewl functionalgenomicanalysisoftheimpactofcamelinacamelinasativamealonatlanticsalmonsalmosalardistalintestinegeneexpressionandphysiology