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Salmonid microarrays identify intestinal genes that reliably monitor P deficiency in rainbow trout aquaculture

Nutrient-responsive genes can identify important metabolic pathways and evaluate optimal dietary levels. Using a 16K Salmo salar microarray, we identified in rainbow trout (Oncorhynchus mykiss) 21 potential phosphorus (P)-responsive genes, mainly involved in immune response, proteolysis or transport...

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Published in:Animal genetics 2007-08, Vol.38 (4), p.319-331
Main Authors: Kirchner, S, McDaniel, N.K, Sugiura, S.H, Soteropoulos, P, Tian, B, Fletcher, J.W, Ferraris, R.P
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container_start_page 319
container_title Animal genetics
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creator Kirchner, S
McDaniel, N.K
Sugiura, S.H
Soteropoulos, P
Tian, B
Fletcher, J.W
Ferraris, R.P
description Nutrient-responsive genes can identify important metabolic pathways and evaluate optimal dietary levels. Using a 16K Salmo salar microarray, we identified in rainbow trout (Oncorhynchus mykiss) 21 potential phosphorus (P)-responsive genes, mainly involved in immune response, proteolysis or transport, whose expression levels changed in the intestine after 5 days of feeding a low-P (LP) diet. Diet-induced changes in the expression levels of several genes in each fish were tightly correlated with changes in serum P, and the changes persisted for an additional 15 days after dietary P deficiency. We then evaluated these and previously identified P-responsive genes under simulated farm conditions, and monitored the intestinal gene expression from 6 h to 7 days after the trout were switched from a sufficient-P (SP) diet to a LP diet (SP[rightward arrow]LP), and from a LP diet to a SP diet (LP[rightward arrow]SP). After 7 days, mean serum P decreased 0.14 m M/day for SP[rightward arrow]LP and increased 0.10 m m/day for LP[rightward arrow]SP. The mRNA abundance of the metalloendopeptidase meprin 1α (MEP1α), the Na⁺-dependent phosphate co-transporter (NaPi2b,SLC34A2), the sulfotransferase SULT2β1 and carbonic anhydrase XIII genes all increased after SP[rightward arrow]LP and decreased after LP[rightward arrow]SP, suggesting that adaptive expression is reversible and correlated with dietary P. The duration of change in gene expression in response to SP[rightward arrow]LP was generally shorter than that of LP[rightward arrow]SP, suggesting potentially different mechanisms of adaptation to deficiency as opposed to excess. Diet-induced changes in mRNA abundance of other genes were either transient or modest. We identified, by heterologous microarray hybridization, new genes sensitive to perturbations in dietary P, and then showed that these genes can reliably monitor P deficiency under field conditions. Simultaneous changes in the expression of these P biomarkers could predict either P deficiency (to prevent economic losses to the farmers) or P excess (to prevent inadvertent pollution of nearby waters).
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Using a 16K Salmo salar microarray, we identified in rainbow trout (Oncorhynchus mykiss) 21 potential phosphorus (P)-responsive genes, mainly involved in immune response, proteolysis or transport, whose expression levels changed in the intestine after 5 days of feeding a low-P (LP) diet. Diet-induced changes in the expression levels of several genes in each fish were tightly correlated with changes in serum P, and the changes persisted for an additional 15 days after dietary P deficiency. We then evaluated these and previously identified P-responsive genes under simulated farm conditions, and monitored the intestinal gene expression from 6 h to 7 days after the trout were switched from a sufficient-P (SP) diet to a LP diet (SP[rightward arrow]LP), and from a LP diet to a SP diet (LP[rightward arrow]SP). After 7 days, mean serum P decreased 0.14 m M/day for SP[rightward arrow]LP and increased 0.10 m m/day for LP[rightward arrow]SP. The mRNA abundance of the metalloendopeptidase meprin 1α (MEP1α), the Na⁺-dependent phosphate co-transporter (NaPi2b,SLC34A2), the sulfotransferase SULT2β1 and carbonic anhydrase XIII genes all increased after SP[rightward arrow]LP and decreased after LP[rightward arrow]SP, suggesting that adaptive expression is reversible and correlated with dietary P. The duration of change in gene expression in response to SP[rightward arrow]LP was generally shorter than that of LP[rightward arrow]SP, suggesting potentially different mechanisms of adaptation to deficiency as opposed to excess. Diet-induced changes in mRNA abundance of other genes were either transient or modest. We identified, by heterologous microarray hybridization, new genes sensitive to perturbations in dietary P, and then showed that these genes can reliably monitor P deficiency under field conditions. 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The mRNA abundance of the metalloendopeptidase meprin 1α (MEP1α), the Na⁺-dependent phosphate co-transporter (NaPi2b,SLC34A2), the sulfotransferase SULT2β1 and carbonic anhydrase XIII genes all increased after SP[rightward arrow]LP and decreased after LP[rightward arrow]SP, suggesting that adaptive expression is reversible and correlated with dietary P. The duration of change in gene expression in response to SP[rightward arrow]LP was generally shorter than that of LP[rightward arrow]SP, suggesting potentially different mechanisms of adaptation to deficiency as opposed to excess. Diet-induced changes in mRNA abundance of other genes were either transient or modest. We identified, by heterologous microarray hybridization, new genes sensitive to perturbations in dietary P, and then showed that these genes can reliably monitor P deficiency under field conditions. 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source Wiley-Blackwell Read & Publish Collection
subjects Animal Feed
Animals
Aquaculture
dietary deficiency
Fish Proteins - genetics
Fish Proteins - physiology
Gene Expression Profiling
Gene Expression Regulation
Genetic Markers
immune response
intestine
Intestine, Small - metabolism
Oligonucleotide Array Sequence Analysis
Oncorhynchus mykiss
Oncorhynchus mykiss - genetics
Oncorhynchus mykiss - metabolism
Phosphorus - blood
phosphorus-responsive genes
RNA, Messenger - metabolism
Salmo salar
trout
title Salmonid microarrays identify intestinal genes that reliably monitor P deficiency in rainbow trout aquaculture
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