Effects of available phosphorus source and concentration on performance and expression of sodium phosphate type IIb cotransporter, vitamin D-1 alpha-hydroxylase, and vitamin D-24-hydroxylase mRNA in broiler chicks
dc.contributor.author | Omara, Islam I. | en |
dc.contributor.author | Mou, C. T. | en |
dc.contributor.author | Persia, Michael E. | en |
dc.contributor.author | Wong, Eric A. | en |
dc.contributor.department | Animal and Poultry Sciences | en |
dc.date.accessioned | 2021-09-27T14:42:19Z | en |
dc.date.available | 2021-09-27T14:42:19Z | en |
dc.date.issued | 2020-04-01 | en |
dc.date.updated | 2021-09-27T14:42:15Z | en |
dc.description.abstract | This experiment was conducted to examine the effect of 2 phosphorus (P) sources on broiler performance to day 14. The P bioavailability was estimated using bird performance and tibia ash measurements, whereas P digestibility, intestinal P transporter, kidney vitamin D-1α-hydroxylase, and vitamin D-24-hydroxylase mRNA abundances were also determined. Slope regression analysis was used to determine the bioavailability of dicalcium phosphate (Dical P) and nanocalcium phosphate (Nano P) with dietary available P (AvP) set to 0.20% P (control) using AvP from the major ingredients and Dical P. The experimental treatments were achieved by supplementation with either Dical P or Nano P to generate 0.24, 0.28, 0.32, and 0.36% AvP. A total of 648-day-old unsexed broiler chicks were divided into 72 birds per treatment (8 replicate cages of 9 birds). Slope regression analysis showed positive linear relationships between BW, feed intake (FI), tibia ash weight (TAW), and tibia ash percentage (TAP) with dietary Dical P and Nano P levels. Comparisons between regression slopes for Dical P and Nano P fed birds were not significantly different for BW, feed intake, tibia ash weight, and tibia ash percentage, indicating similar P bioavailability from Dical P and Nano P. There were interactions between P source and AvP for feed efficiency (FE) and apparent ileal P digestibility (AIPD). Dicalcium phosphate had greater FE than Nano P at 0.28% AvP and greater AIPD than Nano P at 0.24% AvP. The addition of AvP from Dical P and Nano P resulted in reduced sodium phosphate cotransporter mRNA abundance in the duodenum in a dose–dependent response. In the kidney, vitamin D-1α-hydroxylase mRNA abundance was greater at 0.36% Nano P compared with control, but there was no difference with Dical P. There was no difference in vitamin D-24-hydroxylase mRNA abundance between control and supplementation with Nano P or Dical P. In conclusion, Nano P and Dical P had the same bioavailability but had different effects on gene expression. | en |
dc.description.version | Published version | en |
dc.format.extent | Pages 1822-1831 | en |
dc.format.extent | 10 page(s) | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.doi | https://doi.org/10.1016/j.psj.2019.12.035 | en |
dc.identifier.eissn | 1525-3171 | en |
dc.identifier.issn | 0032-5791 | en |
dc.identifier.issue | 4 | en |
dc.identifier.orcid | Wong, Eric [0000-0002-1891-5466] | en |
dc.identifier.other | S0032-5791(20)30008-0 (PII) | en |
dc.identifier.pmid | 32241462 | en |
dc.identifier.uri | http://hdl.handle.net/10919/105081 | en |
dc.identifier.volume | 99 | en |
dc.language.iso | en | en |
dc.publisher | Elsevier | en |
dc.relation.uri | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000525955500003&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=930d57c9ac61a043676db62af60056c1 | en |
dc.rights | Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International | en |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | en |
dc.subject | Life Sciences & Biomedicine | en |
dc.subject | Agriculture, Dairy & Animal Science | en |
dc.subject | Agriculture | en |
dc.subject | dicalcium phosphate | en |
dc.subject | nanophosphate | en |
dc.subject | phosphate transporter | en |
dc.subject | vitamin D hydroxylase | en |
dc.subject | DIETARY NONPHYTATE PHOSPHORUS | en |
dc.subject | P-I DIET | en |
dc.subject | GROWTH-PERFORMANCE | en |
dc.subject | MINERAL PHOSPHORUS | en |
dc.subject | SMALL-INTESTINE | en |
dc.subject | D-RECEPTOR | en |
dc.subject | PHYTASE | en |
dc.subject | DIGESTIBILITY | en |
dc.subject | TRANSPORTER | en |
dc.subject | SUPPLEMENTS | en |
dc.subject | Dairy & Animal Science | en |
dc.subject | 0605 Microbiology | en |
dc.subject | 0702 Animal Production | en |
dc.subject | 0908 Food Sciences | en |
dc.subject.mesh | Duodenum | en |
dc.subject.mesh | Kidney | en |
dc.subject.mesh | Animals | en |
dc.subject.mesh | Chickens | en |
dc.subject.mesh | Calcium Phosphates | en |
dc.subject.mesh | Phosphorus, Dietary | en |
dc.subject.mesh | Steroid Hydroxylases | en |
dc.subject.mesh | Avian Proteins | en |
dc.subject.mesh | RNA, Messenger | en |
dc.subject.mesh | Diet | en |
dc.subject.mesh | Random Allocation | en |
dc.subject.mesh | Biological Availability | en |
dc.subject.mesh | Dose-Response Relationship, Drug | en |
dc.subject.mesh | Animal Feed | en |
dc.subject.mesh | Dietary Supplements | en |
dc.subject.mesh | Sodium-Phosphate Cotransporter Proteins, Type IIb | en |
dc.subject.mesh | Nanoparticles | en |
dc.subject.mesh | Vitamin D3 24-Hydroxylase | en |
dc.title | Effects of available phosphorus source and concentration on performance and expression of sodium phosphate type IIb cotransporter, vitamin D-1 alpha-hydroxylase, and vitamin D-24-hydroxylase mRNA in broiler chicks | en |
dc.title.serial | Poultry Science | en |
dc.type | Article - Refereed | en |
dc.type.dcmitype | Text | en |
dc.type.other | Article | en |
dc.type.other | Journal | en |
dcterms.dateAccepted | 2019-12-10 | en |
pubs.organisational-group | /Virginia Tech | en |
pubs.organisational-group | /Virginia Tech/Agriculture & Life Sciences | en |
pubs.organisational-group | /Virginia Tech/Agriculture & Life Sciences/Animal and Poultry Sciences | en |
pubs.organisational-group | /Virginia Tech/All T&R Faculty | en |
pubs.organisational-group | /Virginia Tech/Agriculture & Life Sciences/CALS T&R Faculty | en |
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