Ratio of dietary rumen degradable protein to rumen undegradable protein affects nitrogen partitioning but does not affect the bovine milk proteome produced by mid-lactation Holstein dairy cows

Little is known about the bovine milk proteome or whether it can be affected by diet. The objective of this study was to determine if the dietary rumen degradable protein (RDP):rumen undegradable protein (RUP) ratio could alter the bovine milk proteome. Six Holstein cows (parity: 2.5 ± 0.8) in mid l...

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Veröffentlicht in:Journal of dairy science 2017-09, Vol.100 (9), p.7246-7261
Hauptverfasser: Tacoma, R., Fields, J., Ebenstein, D.B., Lam, Y.-W., Greenwood, S.L.
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container_end_page 7261
container_issue 9
container_start_page 7246
container_title Journal of dairy science
container_volume 100
creator Tacoma, R.
Fields, J.
Ebenstein, D.B.
Lam, Y.-W.
Greenwood, S.L.
description Little is known about the bovine milk proteome or whether it can be affected by diet. The objective of this study was to determine if the dietary rumen degradable protein (RDP):rumen undegradable protein (RUP) ratio could alter the bovine milk proteome. Six Holstein cows (parity: 2.5 ± 0.8) in mid lactation were blocked by days in milk (80 ± 43 d in milk) and milk yield (57.5 ± 6.0 kg) and randomly assigned to treatment groups. The experiment was conducted as a double-crossover design consisting of three 21-d periods. Within each period, treatment groups received diets with either (1) a high RDP:RUP ratio (RDP treatment: 62.4:37.6% of crude protein) or (2) a low RDP:RUP ratio (RUP treatment: 51.3:48.7% of crude protein). Both diets were isonitrogenous and isoenergetic (crude protein: 18.5%, net energy for lactation: 1.8 Mcal/kg of dry matter). To confirm N and energy status of cows, dry matter intake was determined daily, rumen fluid samples were collected for volatile fatty acid analysis, blood samples were collected for plasma glucose, β-hydroxybutyrate, urea nitrogen, and fatty acid analysis, and total 24-h urine and fecal samples were collected for N analysis. Milk samples were collected to determine the general milk composition and the protein profile. Milk samples collected for high-abundance protein analysis were subjected to HPLC analysis to determine the content of α-casein, β-casein, and κ-casein, as well as α-lactalbumin and β-lactoglobulin. Samples collected for low-abundance protein analysis were fractionated, enriched using ProteoMiner treatment, and separated using sodium dodecyl sulfate-PAGE. After excision and digestion, the peptides were analyzed using liquid chromatography (LC) tandem mass spectrometry (MS/MS). The LC-MS/MS data were analyzed using PROC GLIMMIX of SAS (version 9.4, SAS Institute Inc., Cary, NC) and adjusted using the MULTTEST procedure. All other parameters were analyzed using PROC MIXED of SAS. No treatment differences were observed in dry matter intake, milk yield, general milk composition, plasma parameters, or rumen volatile fatty acid concentrations, indicating no shift in total energy or protein available. Milk urea N and plasma urea N concentrations were higher in the RDP group, indicating some shift in N partitioning due to diet. A total of 595 milk proteins were identified, with 83% of these proteins known to be involved in cellular processes. Although none of the low-abundance proteins identified by LC-MS/MS we
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The objective of this study was to determine if the dietary rumen degradable protein (RDP):rumen undegradable protein (RUP) ratio could alter the bovine milk proteome. Six Holstein cows (parity: 2.5 ± 0.8) in mid lactation were blocked by days in milk (80 ± 43 d in milk) and milk yield (57.5 ± 6.0 kg) and randomly assigned to treatment groups. The experiment was conducted as a double-crossover design consisting of three 21-d periods. Within each period, treatment groups received diets with either (1) a high RDP:RUP ratio (RDP treatment: 62.4:37.6% of crude protein) or (2) a low RDP:RUP ratio (RUP treatment: 51.3:48.7% of crude protein). Both diets were isonitrogenous and isoenergetic (crude protein: 18.5%, net energy for lactation: 1.8 Mcal/kg of dry matter). To confirm N and energy status of cows, dry matter intake was determined daily, rumen fluid samples were collected for volatile fatty acid analysis, blood samples were collected for plasma glucose, β-hydroxybutyrate, urea nitrogen, and fatty acid analysis, and total 24-h urine and fecal samples were collected for N analysis. Milk samples were collected to determine the general milk composition and the protein profile. Milk samples collected for high-abundance protein analysis were subjected to HPLC analysis to determine the content of α-casein, β-casein, and κ-casein, as well as α-lactalbumin and β-lactoglobulin. Samples collected for low-abundance protein analysis were fractionated, enriched using ProteoMiner treatment, and separated using sodium dodecyl sulfate-PAGE. After excision and digestion, the peptides were analyzed using liquid chromatography (LC) tandem mass spectrometry (MS/MS). The LC-MS/MS data were analyzed using PROC GLIMMIX of SAS (version 9.4, SAS Institute Inc., Cary, NC) and adjusted using the MULTTEST procedure. All other parameters were analyzed using PROC MIXED of SAS. No treatment differences were observed in dry matter intake, milk yield, general milk composition, plasma parameters, or rumen volatile fatty acid concentrations, indicating no shift in total energy or protein available. Milk urea N and plasma urea N concentrations were higher in the RDP group, indicating some shift in N partitioning due to diet. A total of 595 milk proteins were identified, with 83% of these proteins known to be involved in cellular processes. Although none of the low-abundance proteins identified by LC-MS/MS were affected by diet, feeding a diet high in RUP decreased β-casein, κ-casein, and total milk casein concentration. Further investigations of the interactions between diet and the milk protein profile are needed to manipulate the milk proteome using diet.</description><identifier>ISSN: 0022-0302</identifier><identifier>EISSN: 1525-3198</identifier><identifier>DOI: 10.3168/jds.2017-12647</identifier><identifier>PMID: 28711247</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>3-hydroxybutyric acid ; alpha-casein ; Animals ; beta-casein ; beta-lactoglobulin ; bioactive ; blood glucose ; blood sampling ; Cattle ; crude protein ; dairy cows ; Dietary Proteins - metabolism ; digestion ; dry matter intake ; energy ; excision ; fatty acid composition ; feces ; Female ; high performance liquid chromatography ; Holstein ; kappa-casein ; lactalbumin ; Lactation ; low-abundance protein ; milk ; milk protein ; Milk Proteins - metabolism ; milk yield ; nitrogen ; Nitrogen - metabolism ; peptides ; polyacrylamide gel electrophoresis ; Pregnancy ; proteome ; Proteome - metabolism ; proteomics ; Random Allocation ; Rumen - metabolism ; rumen fluids ; sodium ; sodium dodecyl sulfate ; Tandem Mass Spectrometry ; urea nitrogen ; urine ; volatile fatty acids</subject><ispartof>Journal of dairy science, 2017-09, Vol.100 (9), p.7246-7261</ispartof><rights>2017 American Dairy Science Association</rights><rights>The Authors. Published by the Federation of Animal Science Societies and Elsevier Inc. on behalf of the American Dairy Science Association®. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c472t-8e37d31b959f71cbfc827320b07d3efd9a5309ef5a086f9ce17d3b155b0869703</citedby><cites>FETCH-LOGICAL-c472t-8e37d31b959f71cbfc827320b07d3efd9a5309ef5a086f9ce17d3b155b0869703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022030217306665$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28711247$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tacoma, R.</creatorcontrib><creatorcontrib>Fields, J.</creatorcontrib><creatorcontrib>Ebenstein, D.B.</creatorcontrib><creatorcontrib>Lam, Y.-W.</creatorcontrib><creatorcontrib>Greenwood, S.L.</creatorcontrib><title>Ratio of dietary rumen degradable protein to rumen undegradable protein affects nitrogen partitioning but does not affect the bovine milk proteome produced by mid-lactation Holstein dairy cows</title><title>Journal of dairy science</title><addtitle>J Dairy Sci</addtitle><description>Little is known about the bovine milk proteome or whether it can be affected by diet. The objective of this study was to determine if the dietary rumen degradable protein (RDP):rumen undegradable protein (RUP) ratio could alter the bovine milk proteome. Six Holstein cows (parity: 2.5 ± 0.8) in mid lactation were blocked by days in milk (80 ± 43 d in milk) and milk yield (57.5 ± 6.0 kg) and randomly assigned to treatment groups. The experiment was conducted as a double-crossover design consisting of three 21-d periods. Within each period, treatment groups received diets with either (1) a high RDP:RUP ratio (RDP treatment: 62.4:37.6% of crude protein) or (2) a low RDP:RUP ratio (RUP treatment: 51.3:48.7% of crude protein). Both diets were isonitrogenous and isoenergetic (crude protein: 18.5%, net energy for lactation: 1.8 Mcal/kg of dry matter). To confirm N and energy status of cows, dry matter intake was determined daily, rumen fluid samples were collected for volatile fatty acid analysis, blood samples were collected for plasma glucose, β-hydroxybutyrate, urea nitrogen, and fatty acid analysis, and total 24-h urine and fecal samples were collected for N analysis. Milk samples were collected to determine the general milk composition and the protein profile. Milk samples collected for high-abundance protein analysis were subjected to HPLC analysis to determine the content of α-casein, β-casein, and κ-casein, as well as α-lactalbumin and β-lactoglobulin. Samples collected for low-abundance protein analysis were fractionated, enriched using ProteoMiner treatment, and separated using sodium dodecyl sulfate-PAGE. After excision and digestion, the peptides were analyzed using liquid chromatography (LC) tandem mass spectrometry (MS/MS). The LC-MS/MS data were analyzed using PROC GLIMMIX of SAS (version 9.4, SAS Institute Inc., Cary, NC) and adjusted using the MULTTEST procedure. All other parameters were analyzed using PROC MIXED of SAS. No treatment differences were observed in dry matter intake, milk yield, general milk composition, plasma parameters, or rumen volatile fatty acid concentrations, indicating no shift in total energy or protein available. Milk urea N and plasma urea N concentrations were higher in the RDP group, indicating some shift in N partitioning due to diet. A total of 595 milk proteins were identified, with 83% of these proteins known to be involved in cellular processes. Although none of the low-abundance proteins identified by LC-MS/MS were affected by diet, feeding a diet high in RUP decreased β-casein, κ-casein, and total milk casein concentration. Further investigations of the interactions between diet and the milk protein profile are needed to manipulate the milk proteome using diet.</description><subject>3-hydroxybutyric acid</subject><subject>alpha-casein</subject><subject>Animals</subject><subject>beta-casein</subject><subject>beta-lactoglobulin</subject><subject>bioactive</subject><subject>blood glucose</subject><subject>blood sampling</subject><subject>Cattle</subject><subject>crude protein</subject><subject>dairy cows</subject><subject>Dietary Proteins - metabolism</subject><subject>digestion</subject><subject>dry matter intake</subject><subject>energy</subject><subject>excision</subject><subject>fatty acid composition</subject><subject>feces</subject><subject>Female</subject><subject>high performance liquid chromatography</subject><subject>Holstein</subject><subject>kappa-casein</subject><subject>lactalbumin</subject><subject>Lactation</subject><subject>low-abundance protein</subject><subject>milk</subject><subject>milk protein</subject><subject>Milk Proteins - metabolism</subject><subject>milk yield</subject><subject>nitrogen</subject><subject>Nitrogen - metabolism</subject><subject>peptides</subject><subject>polyacrylamide gel electrophoresis</subject><subject>Pregnancy</subject><subject>proteome</subject><subject>Proteome - metabolism</subject><subject>proteomics</subject><subject>Random Allocation</subject><subject>Rumen - metabolism</subject><subject>rumen fluids</subject><subject>sodium</subject><subject>sodium dodecyl sulfate</subject><subject>Tandem Mass Spectrometry</subject><subject>urea nitrogen</subject><subject>urine</subject><subject>volatile fatty acids</subject><issn>0022-0302</issn><issn>1525-3198</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkkuLFDEUhYMozji6dSlZuqk2j05VZSPIoI4wIIiuQx43PRmrkjZJtcy_86eZfjgoKK5Ccr6c3Nx7EHpOyYrTfnx168qKETp0lPXr4QE6p4KJjlM5PkTnhDDWEU7YGXpSym3bUkbEY3TGxoFSth7O0Y9PuoaEk8cuQNX5DudlhogdbLJ22kyAtzlVCBHXdNKW-BdVew-2FhxDzWnTqK3ONTTvGOIGm6Vil6DJqZ5QXG8Am7QLEfAcpq9HpzQfLN1iwWFz1xTXTdrWfZURX6WpHF5zOrRSbfpenqJHXk8Fnp3WC_Tl3dvPl1fd9cf3Hy7fXHd2PbDajcAHx6mRQvqBWuPtyAbOiCHtGLyTWnAiwQtNxt5LC7SdGyqEaXs5EH6BXh99t4uZwVmINetJbXOYW9dU0kH9qcRwozZpp3ouiGSiGbw8GeT0bYFS1RyKhWnSEdJSFCOECEL4uP4vSiUjbeh9Lxu6OqI2p1Iy-PuKKFH7hKiWELVPiDokpF148fs_7vFfkWjAeASgdXMXIKtiA8Q2j5Db2JRL4V_ePwHPidAf</recordid><startdate>20170901</startdate><enddate>20170901</enddate><creator>Tacoma, R.</creator><creator>Fields, J.</creator><creator>Ebenstein, D.B.</creator><creator>Lam, Y.-W.</creator><creator>Greenwood, S.L.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20170901</creationdate><title>Ratio of dietary rumen degradable protein to rumen undegradable protein affects nitrogen partitioning but does not affect the bovine milk proteome produced by mid-lactation Holstein dairy cows</title><author>Tacoma, R. ; 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The objective of this study was to determine if the dietary rumen degradable protein (RDP):rumen undegradable protein (RUP) ratio could alter the bovine milk proteome. Six Holstein cows (parity: 2.5 ± 0.8) in mid lactation were blocked by days in milk (80 ± 43 d in milk) and milk yield (57.5 ± 6.0 kg) and randomly assigned to treatment groups. The experiment was conducted as a double-crossover design consisting of three 21-d periods. Within each period, treatment groups received diets with either (1) a high RDP:RUP ratio (RDP treatment: 62.4:37.6% of crude protein) or (2) a low RDP:RUP ratio (RUP treatment: 51.3:48.7% of crude protein). Both diets were isonitrogenous and isoenergetic (crude protein: 18.5%, net energy for lactation: 1.8 Mcal/kg of dry matter). To confirm N and energy status of cows, dry matter intake was determined daily, rumen fluid samples were collected for volatile fatty acid analysis, blood samples were collected for plasma glucose, β-hydroxybutyrate, urea nitrogen, and fatty acid analysis, and total 24-h urine and fecal samples were collected for N analysis. Milk samples were collected to determine the general milk composition and the protein profile. Milk samples collected for high-abundance protein analysis were subjected to HPLC analysis to determine the content of α-casein, β-casein, and κ-casein, as well as α-lactalbumin and β-lactoglobulin. Samples collected for low-abundance protein analysis were fractionated, enriched using ProteoMiner treatment, and separated using sodium dodecyl sulfate-PAGE. After excision and digestion, the peptides were analyzed using liquid chromatography (LC) tandem mass spectrometry (MS/MS). The LC-MS/MS data were analyzed using PROC GLIMMIX of SAS (version 9.4, SAS Institute Inc., Cary, NC) and adjusted using the MULTTEST procedure. All other parameters were analyzed using PROC MIXED of SAS. No treatment differences were observed in dry matter intake, milk yield, general milk composition, plasma parameters, or rumen volatile fatty acid concentrations, indicating no shift in total energy or protein available. Milk urea N and plasma urea N concentrations were higher in the RDP group, indicating some shift in N partitioning due to diet. A total of 595 milk proteins were identified, with 83% of these proteins known to be involved in cellular processes. Although none of the low-abundance proteins identified by LC-MS/MS were affected by diet, feeding a diet high in RUP decreased β-casein, κ-casein, and total milk casein concentration. Further investigations of the interactions between diet and the milk protein profile are needed to manipulate the milk proteome using diet.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28711247</pmid><doi>10.3168/jds.2017-12647</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record>
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subjects 3-hydroxybutyric acid
alpha-casein
Animals
beta-casein
beta-lactoglobulin
bioactive
blood glucose
blood sampling
Cattle
crude protein
dairy cows
Dietary Proteins - metabolism
digestion
dry matter intake
energy
excision
fatty acid composition
feces
Female
high performance liquid chromatography
Holstein
kappa-casein
lactalbumin
Lactation
low-abundance protein
milk
milk protein
Milk Proteins - metabolism
milk yield
nitrogen
Nitrogen - metabolism
peptides
polyacrylamide gel electrophoresis
Pregnancy
proteome
Proteome - metabolism
proteomics
Random Allocation
Rumen - metabolism
rumen fluids
sodium
sodium dodecyl sulfate
Tandem Mass Spectrometry
urea nitrogen
urine
volatile fatty acids
title Ratio of dietary rumen degradable protein to rumen undegradable protein affects nitrogen partitioning but does not affect the bovine milk proteome produced by mid-lactation Holstein dairy cows
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