2019
DOI: 10.1016/j.aquaculture.2019.734396
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Yeast as a protein source during smoltification of Atlantic salmon (Salmo salar L.), enhances performance and modulates health

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Cited by 39 publications
(34 citation statements)
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“…(70,71). It has been reported that feeding Atlantic salmon with a Candida utilis-supplemented diet increases the expression of aquaporin-8ab (aqp8ab) and modulates the expression other immune-related genes, indicating that inclusion of yeast in fish diets may enhance their performance and health status (72). The differential expression of aquaporins aqp8a and aqp9b in our study point to their possible role in modulating the immune response upon yeast exposure.…”
Section: Discussionsupporting
confidence: 55%
“…(70,71). It has been reported that feeding Atlantic salmon with a Candida utilis-supplemented diet increases the expression of aquaporin-8ab (aqp8ab) and modulates the expression other immune-related genes, indicating that inclusion of yeast in fish diets may enhance their performance and health status (72). The differential expression of aquaporins aqp8a and aqp9b in our study point to their possible role in modulating the immune response upon yeast exposure.…”
Section: Discussionsupporting
confidence: 55%
“…Furthermore, feed intake was higher in one- to three-week-old broiler chickens fed with diets supplemented with 17% CP from bacterial meal than in those fed with control diets ( Schøyen et al., 2007a ). In the latter studies, yeast may have enhanced the palatability of the diets by stimulating umami taste receptors in taste buds ( Liu et al., 2018 ), in a similar way as in fish diets ( Kasumyan and Døving, 2003 , Sahlmann et al., 2019 ). However, this was not observed in our study, and to our knowledge, no studies relating feed intake to the palatability of yeast in broiler chicken diets are available; thus, further investigation is encouraged.…”
Section: Discussionmentioning
confidence: 99%
“…Next, 50 μL of the primary antibody was added to each well and plates were incubated for 90 min at 37 °C. The primary antibodies used were as follows: monoclonal anti-IgD, monoclonal anti-IgM, polyclonal anti-IFNγ or polyclonal anti-IL-1β at 1:200 dilution as reported by Sahlmann, Djordjevic ( 36 ) and kindly donated by Dr. Luis Mercado. Next, 50 μL of a secondary antibody diluted to 1:7000 (goat anti-mouse IgG-HRP or mouse anti-rabbit IgG-HRP) was added and incubated for 60 min at 37°C.…”
Section: Methodsmentioning
confidence: 99%