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Digestive tract morphology and enzyme activities of juvenile diploid and triploid Atlantic salmon (Salmo salar) fed fishmeal-based diets with or without fish protein hydrolysates

Triploid, sterile Atlantic salmon (Salmo salar) could make a contribution to the development of the farming industry, but uncertainties about the performance and welfare of triploids have limited their adoption by farmers. In this study, we compared the ontogeny of digestive tract morphology and enz...

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Autores principales: Martínez-Llorens, Silvia, Peruzzi, Stefano, Falk-Petersen, Inger-Britt, Godoy-Olmos, Sergio, Ulleberg, Lars Olav, Tomás-Vidal, Ana, Puvanendran, Velmurugu, Odei, Derrick Kwame, Hagen, Ørjan, Fernandes, Jorge M. O., Jobling, Malcolm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801030/
https://www.ncbi.nlm.nih.gov/pubmed/33429419
http://dx.doi.org/10.1371/journal.pone.0245216
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author Martínez-Llorens, Silvia
Peruzzi, Stefano
Falk-Petersen, Inger-Britt
Godoy-Olmos, Sergio
Ulleberg, Lars Olav
Tomás-Vidal, Ana
Puvanendran, Velmurugu
Odei, Derrick Kwame
Hagen, Ørjan
Fernandes, Jorge M. O.
Jobling, Malcolm
author_facet Martínez-Llorens, Silvia
Peruzzi, Stefano
Falk-Petersen, Inger-Britt
Godoy-Olmos, Sergio
Ulleberg, Lars Olav
Tomás-Vidal, Ana
Puvanendran, Velmurugu
Odei, Derrick Kwame
Hagen, Ørjan
Fernandes, Jorge M. O.
Jobling, Malcolm
author_sort Martínez-Llorens, Silvia
collection PubMed
description Triploid, sterile Atlantic salmon (Salmo salar) could make a contribution to the development of the farming industry, but uncertainties about the performance and welfare of triploids have limited their adoption by farmers. In this study, we compared the ontogeny of digestive tract morphology and enzyme activities (pepsin, trypsin, chymotrypsin, alkaline phosphatase and aminopeptidase) of diploid and triploid Atlantic salmon. Fish were fed diets based on fishmeal (STD) or a mix of fishmeal and hydrolysed fish proteins (HFM) whilst being reared at low temperature from start-feeding to completion of the parr-smolt transformation. Fish weights for each ploidy and feed combination were used to calculate thermal growth coefficients (TGCs) that spanned this developmental period, and the data were used to examine possible relationships between enzyme activities and growth. At the end of the experiment, faeces were collected and analyzed to determine the apparent digestibility coefficients (ADCs) of the dietary amino acids (AAs). Digestive tract histo-morphology did not differ substantially between ploidies and generally reflected organ maturation and functionality. There were no consistent differences in proteolytic enzyme activities resulting from the inclusion of HFM in the diet, nor was there improved digestibility and AA bioavailability of the HFM feed in either diploid or triploid fish. The triploid salmon had lower ADCs than diploids for most essential and non-essential AAs in both diets (STD and HFM), but without there being any indication of lower intestinal protease activity in triploid fish. When trypsin-to-chymotrypsin activity and trypsin and alkaline phosphatase (ALP) ratios (T:C and T:ALP, respectively) were considered in combination with growth data (TGC) low T:C and T:ALP values coincided with times of reduced fish growth, and vice versa, suggesting that T:C and T:ALP may be used to predict recent growth history and possible growth potential.
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spelling pubmed-78010302021-01-22 Digestive tract morphology and enzyme activities of juvenile diploid and triploid Atlantic salmon (Salmo salar) fed fishmeal-based diets with or without fish protein hydrolysates Martínez-Llorens, Silvia Peruzzi, Stefano Falk-Petersen, Inger-Britt Godoy-Olmos, Sergio Ulleberg, Lars Olav Tomás-Vidal, Ana Puvanendran, Velmurugu Odei, Derrick Kwame Hagen, Ørjan Fernandes, Jorge M. O. Jobling, Malcolm PLoS One Research Article Triploid, sterile Atlantic salmon (Salmo salar) could make a contribution to the development of the farming industry, but uncertainties about the performance and welfare of triploids have limited their adoption by farmers. In this study, we compared the ontogeny of digestive tract morphology and enzyme activities (pepsin, trypsin, chymotrypsin, alkaline phosphatase and aminopeptidase) of diploid and triploid Atlantic salmon. Fish were fed diets based on fishmeal (STD) or a mix of fishmeal and hydrolysed fish proteins (HFM) whilst being reared at low temperature from start-feeding to completion of the parr-smolt transformation. Fish weights for each ploidy and feed combination were used to calculate thermal growth coefficients (TGCs) that spanned this developmental period, and the data were used to examine possible relationships between enzyme activities and growth. At the end of the experiment, faeces were collected and analyzed to determine the apparent digestibility coefficients (ADCs) of the dietary amino acids (AAs). Digestive tract histo-morphology did not differ substantially between ploidies and generally reflected organ maturation and functionality. There were no consistent differences in proteolytic enzyme activities resulting from the inclusion of HFM in the diet, nor was there improved digestibility and AA bioavailability of the HFM feed in either diploid or triploid fish. The triploid salmon had lower ADCs than diploids for most essential and non-essential AAs in both diets (STD and HFM), but without there being any indication of lower intestinal protease activity in triploid fish. When trypsin-to-chymotrypsin activity and trypsin and alkaline phosphatase (ALP) ratios (T:C and T:ALP, respectively) were considered in combination with growth data (TGC) low T:C and T:ALP values coincided with times of reduced fish growth, and vice versa, suggesting that T:C and T:ALP may be used to predict recent growth history and possible growth potential. Public Library of Science 2021-01-11 /pmc/articles/PMC7801030/ /pubmed/33429419 http://dx.doi.org/10.1371/journal.pone.0245216 Text en © 2021 Martínez-Llorens et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are credited.
spellingShingle Research Article
Martínez-Llorens, Silvia
Peruzzi, Stefano
Falk-Petersen, Inger-Britt
Godoy-Olmos, Sergio
Ulleberg, Lars Olav
Tomás-Vidal, Ana
Puvanendran, Velmurugu
Odei, Derrick Kwame
Hagen, Ørjan
Fernandes, Jorge M. O.
Jobling, Malcolm
Digestive tract morphology and enzyme activities of juvenile diploid and triploid Atlantic salmon (Salmo salar) fed fishmeal-based diets with or without fish protein hydrolysates
title Digestive tract morphology and enzyme activities of juvenile diploid and triploid Atlantic salmon (Salmo salar) fed fishmeal-based diets with or without fish protein hydrolysates
title_full Digestive tract morphology and enzyme activities of juvenile diploid and triploid Atlantic salmon (Salmo salar) fed fishmeal-based diets with or without fish protein hydrolysates
title_fullStr Digestive tract morphology and enzyme activities of juvenile diploid and triploid Atlantic salmon (Salmo salar) fed fishmeal-based diets with or without fish protein hydrolysates
title_full_unstemmed Digestive tract morphology and enzyme activities of juvenile diploid and triploid Atlantic salmon (Salmo salar) fed fishmeal-based diets with or without fish protein hydrolysates
title_short Digestive tract morphology and enzyme activities of juvenile diploid and triploid Atlantic salmon (Salmo salar) fed fishmeal-based diets with or without fish protein hydrolysates
title_sort digestive tract morphology and enzyme activities of juvenile diploid and triploid atlantic salmon (salmo salar) fed fishmeal-based diets with or without fish protein hydrolysates
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801030/
https://www.ncbi.nlm.nih.gov/pubmed/33429419
http://dx.doi.org/10.1371/journal.pone.0245216
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