Summary of Study ST002063

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001306. The data can be accessed directly via it's Project DOI: 10.21228/M8WT4R This work is supported by NIH grant, U2C- DK119886.

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Study IDST002063
Study TitleIntravenous lipopolysaccharide infusion and the bovine metabolome
Study TypeMS plasma lipidomics and metabolomics
Study SummaryThe effects of lipopolysaccharides (i.e., endotoxin; LPS) on metabolism are poorly defined in lactating dairy cattle experiencing hyperlipidemia. Our objective was to explore the effects of acute intravenous LPS administration on metabolism in late-lactation Holstein cows experiencing hyperlipidemia. Ten non-pregnant lactating Holstein cows (273 ± 35 d in milk) were administered a single bolus of saline (3 mL of saline; n = 5) or LPS (0.375 μg of LPS/kg of body weight; n = 5). Simultaneously, cows were intravenously infused a triglyceride emulsion and fasted for 16 h to induce hyperlipidemia in an attempt to model the periparturient period. Blood was sampled at routine intervals. Changes in circulating total fatty acid concentrations and inflammatory parameters were measured. Plasma samples were analyzed using untargeted lipidomics and metabolomics. Endotoxin increased circulating serum amyloid A, LPS-binding protein, and cortisol concentrations. Endotoxin administration decreased plasma lysophosphatidylcholine (LPC) concentrations and increased select plasma ceramide concentrations. These outcomes suggest modulation of the immune response and insulin action. Lipopolysaccharide decreased the ratio of phosphatidylcholine to phosphatidylethanomanine, which potentially indicate a decrease in the hepatic activation of phosphatidylethanolamine N-methyltransferase and triglyceride export. Endotoxin administration also increased plasma concentrations of pyruvic and lactic acids, and decreased plasma citric acid concentrations, which implicate the upregulation of glycolysis and downregulation of the citric acid cycle (i.e., the Warburg effect), potentially in leukocytes. Acute intravenous LPS administration decreased circulating LPC concentrations, modified ceramide and glycerophospholipid concentrations, and influenced intermediary metabolism in dairy cows experiencing hyperlipidemia.
Institute
Cornell University
DepartmentAnimal Science
LaboratoryMcFadden lab
Last NameJavaid
First NameAwais
Address400 Warren Rd, Ithaca, New York, 14850, USA
Emailaj366@cornell.edu
Phone6072287246
Submit Date2022-01-09
Raw Data AvailableYes
Raw Data File Type(s)mzXML
Analysis Type DetailLC-MS
Release Date2022-06-30
Release Version1
Awais Javaid Awais Javaid
https://dx.doi.org/10.21228/M8WT4R
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Project:

Project ID:PR001306
Project DOI:doi: 10.21228/M8WT4R
Project Title:Intravenous lipopolysaccharide infusion and the bovine metabolome
Project Type:MS lipidomics and metabolomics
Project Summary:The effects of lipopolysaccharides (i.e., endotoxin; LPS) on metabolism are poorly defined in lactating dairy cattle experiencing hyperlipidemia. Our objective was to explore the effects of acute intravenous LPS administration on metabolism in late-lactation Holstein cows experiencing hyperlipidemia. Ten non-pregnant lactating Holstein cows (273 ± 35 d in milk) were administered a single bolus of saline (3 mL of saline; n = 5) or LPS (0.375 μg of LPS/kg of body weight; n = 5). Simultaneously, cows were intravenously infused a triglyceride emulsion and fasted for 16 h to induce hyperlipidemia in an attempt to model the periparturient period. Blood was sampled at routine intervals. Changes in circulating total fatty acid concentrations and inflammatory parameters were measured. Plasma samples were analyzed using untargeted lipidomics and metabolomics. Endotoxin increased circulating serum amyloid A, LPS-binding protein, and cortisol concentrations. Endotoxin administration decreased plasma lysophosphatidylcholine (LPC) concentrations and increased select plasma ceramide concentrations. These outcomes suggest modulation of the immune response and insulin action. Lipopolysaccharide decreased the ratio of phosphatidylcholine to phosphatidylethanomanine, which potentially indicate a decrease in the hepatic activation of phosphatidylethanolamine N-methyltransferase and triglyceride export. Endotoxin administration also increased plasma concentrations of pyruvic and lactic acids, and decreased plasma citric acid concentrations, which implicate the upregulation of glycolysis and downregulation of the citric acid cycle (i.e., the Warburg effect), potentially in leukocytes. Acute intravenous LPS administration decreased circulating LPC concentrations, modified ceramide and glycerophospholipid concentrations, and influenced intermediary metabolism in dairy cows experiencing hyperlipidemia.
Institute:Animal Science
Department:Animal Science
Laboratory:McFadden lab
Last Name:Javaid
First Name:Awais
Address:400 Warren Rd, Ithaca, New York, 14850, USA
Email:aj366@cornell.edu
Phone:6072287246
Funding Source:Agriculture and Food Research Initiative grant no. 2018-67015-27548

Subject:

Subject ID:SU002145
Subject Type:Mammal
Subject Species:Bos taurus
Taxonomy ID:9913
Genotype Strain:Holstein dairy cows
Age Or Age Range:4- 5 years
Weight Or Weight Range:733-797
Gender:Female
Animal Housing:Tie stall
Animal Feed:TMR Ad lib
Animal Water:Ad libitum
Animal Inclusion Criteria:lactation stage, Days in milk

Factors:

Subject type: Mammal; Subject species: Bos taurus (Factor headings shown in green)

mb_sample_id local_sample_id Time
SA194101233-10336_CON-IL_12.raw12 | Treatment:CON | Category:Lipidomics
SA194102234-9855_CON-IL_12.raw12 | Treatment:CON | Category:Lipidomics
SA194103231-9852_CON-IL_12.raw12 | Treatment:CON | Category:Lipidomics
SA194104230-9609_CON-IL_12.raw12 | Treatment:CON | Category:Lipidomics
SA194105232-9610_CON-IL_12.raw12 | Treatment:CON | Category:Lipidomics
SA194106238-9785_LPS-IL_12.raw12 | Treatment:LPS | Category:Lipidomics
SA194107237-10008_LPS-IL_12.raw12 | Treatment:LPS | Category:Lipidomics
SA194108235-10218_LPS-IL_12.raw12 | Treatment:LPS | Category:Lipidomics
SA194109239-10103_LPS-IL_12.raw12 | Treatment:LPS | Category:Lipidomics
SA194110236-8473_LPS-IL_12.raw12 | Treatment:LPS | Category:Lipidomics
SA194111241-9852_CON-IL_16.raw16 | Treatment:CON | Category:Lipidomics
SA194112240-9609_CON-IL_16.raw16 | Treatment:CON | Category:Lipidomics
SA194113244-9855_CON-IL_16.raw16 | Treatment:CON | Category:Lipidomics
SA194114242-9610_CON-IL_16.raw16 | Treatment:CON | Category:Lipidomics
SA194115243-10336_CON-IL_16.raw16 | Treatment:CON | Category:Lipidomics
SA1941169609CON-IL-16_NEG.raw16 | Treatment:CON | Category:Metabolomics
SA1941179852CON-IL-16_NEG.raw16 | Treatment:CON | Category:Metabolomics
SA1941189855CON-IL-16_NEG.raw16 | Treatment:CON | Category:Metabolomics
SA19411910336CON-IL-16_NEG.raw16 | Treatment:CON | Category:Metabolomics
SA1941209610CON-IL-16_NEG.raw16 | Treatment:CON | Category:Metabolomics
SA194121249-10103_LPS-IL_16.raw16 | Treatment:LPS | Category:Lipidomics
SA194122245-10218_LPS-IL_16.raw16 | Treatment:LPS | Category:Lipidomics
SA194123246-8473_LPS-IL_16.raw16 | Treatment:LPS | Category:Lipidomics
SA194124248-9785_LPS-IL_16.raw16 | Treatment:LPS | Category:Lipidomics
SA194125247-10008_LPS-IL_16.raw16 | Treatment:LPS | Category:Lipidomics
SA19412610218LPS-IL-16_NEG.raw16 | Treatment:LPS | Category:Metabolomics
SA19412710103LPS-IL-16_NEG.raw16 | Treatment:LPS | Category:Metabolomics
SA1941288473LPS-IL-16_NEG.raw16 | Treatment:LPS | Category:Metabolomics
SA1941299785LPS-IL-16_NEG.raw16 | Treatment:LPS | Category:Metabolomics
SA19413010008LPS-IL-16_NEG.raw16 | Treatment:LPS | Category:Metabolomics
SA194131251-9852_CON-IL_24.raw24 | Treatment:CON | Category:Lipidomics
SA194132254-9855_CON-IL_24.raw24 | Treatment:CON | Category:Lipidomics
SA194133250-9609_CON-IL_24.raw24 | Treatment:CON | Category:Lipidomics
SA194134253-10336_CON-IL_24.raw24 | Treatment:CON | Category:Lipidomics
SA194135252-9610_CON-IL_24.raw24 | Treatment:CON | Category:Lipidomics
SA194136257-10008_LPS-IL_24.raw24 | Treatment:LPS | Category:Lipidomics
SA194137259-10103_LPS-IL_24.raw24 | Treatment:LPS | Category:Lipidomics
SA194138255-10218_LPS-IL_24.raw24 | Treatment:LPS | Category:Lipidomics
SA194139258-9785_LPS-IL_24.raw24 | Treatment:LPS | Category:Lipidomics
SA194140256-8473_LPS-IL_24.raw24 | Treatment:LPS | Category:Lipidomics
SA194141264-9855_CON-IL_48.raw48 | Treatment:CON | Category:Lipidomics
SA194142260-9609_CON-IL_48.raw48 | Treatment:CON | Category:Lipidomics
SA194143262-9610_CON-IL_48.raw48 | Treatment:CON | Category:Lipidomics
SA194144261-9852_CON-IL_48.raw48 | Treatment:CON | Category:Lipidomics
SA194145263-10336_CON-IL_48.raw48 | Treatment:CON | Category:Lipidomics
SA194146265-10218_LPS-IL_48.raw48 | Treatment:LPS | Category:Lipidomics
SA194147266-8473_LPS-IL_48.raw48 | Treatment:LPS | Category:Lipidomics
SA194148267-10008_LPS-IL_48.raw48 | Treatment:LPS | Category:Lipidomics
SA194149269-10103_LPS-IL_48.raw48 | Treatment:LPS | Category:Lipidomics
SA194150268-9785_LPS-IL_48.raw48 | Treatment:LPS | Category:Lipidomics
SA194151211-9852_CON-IL_4.raw4 | Treatment:CON | Category:Lipidomics
SA194152210-9609_CON-IL_4.raw4 | Treatment:CON | Category:Lipidomics
SA194153214-9855_CON-IL_4.raw4 | Treatment:CON | Category:Lipidomics
SA194154213-10336_CON-IL_4.raw4 | Treatment:CON | Category:Lipidomics
SA194155212-9610_CON-IL_4.raw4 | Treatment:CON | Category:Lipidomics
SA194156216-8473_LPS-IL_4.raw4 | Treatment:LPS | Category:Lipidomics
SA194157218-9785_LPS-IL_4.raw4 | Treatment:LPS | Category:Lipidomics
SA194158217-10008_LPS-IL_4.raw4 | Treatment:LPS | Category:Lipidomics
SA194159215-10218_LPS-IL_4.raw4 | Treatment:LPS | Category:Lipidomics
SA194160219-10103_LPS-IL_4.raw4 | Treatment:LPS | Category:Lipidomics
SA194161222-9610_CON-IL_8.raw8 | Treatment:CON | Category:Lipidomics
SA194162220-9609_CON-IL_8.raw8 | Treatment:CON | Category:Lipidomics
SA194163224-9855_CON-IL_8.raw8 | Treatment:CON | Category:Lipidomics
SA194164223-10336_CON-IL_8.raw8 | Treatment:CON | Category:Lipidomics
SA194165221-9852_CON-IL_8.raw8 | Treatment:CON | Category:Lipidomics
SA1941669855CON-IL-8_NEG.raw8 | Treatment:CON | Category:Metabolomics
SA19416710336CON-IL-8_NEG.raw8 | Treatment:CON | Category:Metabolomics
SA1941689852CON-IL-8_NEG.raw8 | Treatment:CON | Category:Metabolomics
SA1941699609CON-IL-8_NEG.raw8 | Treatment:CON | Category:Metabolomics
SA1941709610CON-IL-8_NEG.raw8 | Treatment:CON | Category:Metabolomics
SA194171227-10008_LPS-IL_8.raw8 | Treatment:LPS | Category:Lipidomics
SA194172229-10103_LPS-IL_8.raw8 | Treatment:LPS | Category:Lipidomics
SA194173228-9785_LPS-IL_8.raw8 | Treatment:LPS | Category:Lipidomics
SA194174226-8473_LPS-IL_8.raw8 | Treatment:LPS | Category:Lipidomics
SA194175225-10218_LPS-IL_8.raw8 | Treatment:LPS | Category:Lipidomics
SA1941768473LPS-IL-8_NEG.raw8 | Treatment:LPS | Category:Metabolomics
SA1941779785LPS-IL-8_NEG.raw8 | Treatment:LPS | Category:Metabolomics
SA19417810103LPS-IL-8_NEG.raw8 | Treatment:LPS | Category:Metabolomics
SA19417910008LPS-IL-8_NEG.raw8 | Treatment:LPS | Category:Metabolomics
SA19418010218LPS-IL-8_NEG.raw8 | Treatment:LPS | Category:Metabolomics
SA194098QC_3_NEG.raw. | Treatment:. | Category:Metabolomics
SA194099QC_1_NEG.raw. | Treatment:. | Category:Metabolomics
SA194100QC_2_NEG.raw. | Treatment:. | Category:Metabolomics
SA194078202-9610_CON-IL_0.raw- | Treatment:CON | Category:Lipidomics
SA194079204-9855_CON-IL_0.raw- | Treatment:CON | Category:Lipidomics
SA194080200-9609_CON-IL_0.raw- | Treatment:CON | Category:Lipidomics
SA194081201-9852_CON-IL_0.raw- | Treatment:CON | Category:Lipidomics
SA194082203-10336_CON-IL_0.raw- | Treatment:CON | Category:Lipidomics
SA19408310336CON-IL-0_NEG.raw- | Treatment:CON | Category:Metabolomics
SA1940849610CON-IL-0_NEG.raw- | Treatment:CON | Category:Metabolomics
SA1940859852CON-IL-0_NEG.raw- | Treatment:CON | Category:Metabolomics
SA1940869855CON-IL-0_NEG.raw- | Treatment:CON | Category:Metabolomics
SA1940879609CON-IL-0_NEG.raw- | Treatment:CON | Category:Metabolomics
SA194088206-8473_LPS-IL_0.raw- | Treatment:LPS | Category:Lipidomics
SA194089209-10103_LPS-IL_0.raw- | Treatment:LPS | Category:Lipidomics
SA194090208-9785_LPS-IL_0.raw- | Treatment:LPS | Category:Lipidomics
SA194091205-10218_LPS-IL_0.raw- | Treatment:LPS | Category:Lipidomics
SA194092207-10008_LPS-IL_0.raw- | Treatment:LPS | Category:Lipidomics
SA19409310008LPS-IL-0_NEG.raw- | Treatment:LPS | Category:Metabolomics
SA1940948473LPS-IL-0_NEG.raw- | Treatment:LPS | Category:Metabolomics
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Collection:

Collection ID:CO002138
Collection Summary:Blood was collected via coccygeal venipuncture after the morning milking during the baseline period and at -0.5, 0, 4, 8, 16, 24, and 48 h, relative to saline or LPS administration. Plasma samples were incubated on ice for 30 min before centrifugation.
Collection Protocol ID:N/A
Collection Protocol Filename:Collection_Protocol.docx
Collection Protocol Comments:N/A
Sample Type:Blood (plasma)
Collection Method:Blood collection using venipuncture needle
Collection Location:Coccygeal venipuncture
Collection Frequency:At interval of -0.5, 0, 4, 8, 16, 24, and 48 h respectively
Collection Duration:1 min
Volumeoramount Collected:10ml
Storage Conditions:-20℃
Collection Vials:10 ml blood vial
Storage Vials:Eppendorf tubes 2ml
Collection Tube Temp:4°C

Treatment:

Treatment ID:TR002157
Treatment Summary:Sterile saline (CON; n = 5) or 2) LPS (0.375 μg of LPS/kg of BW in sterile saline; Escherichia coli O55:B5; Sigma Aldrich, St. Louis, MO; n = 5)
Treatment Protocol ID:N/A
Treatment Protocol Filename:N
A

Sample Preparation:

Sampleprep ID:SP002151
Sampleprep Summary:Untargeted lipidomics samples were prepared by dissolving in dicholormethane/ methanol ( MeOH; 2:1). Untargeted metabolomics was done by centrifugation, samples were re-suspended with 60% ACN prior to analysis. FOR details please refer to publication Wang et al 2022.

Combined analysis:

Analysis ID AN003362
Analysis type MS
Chromatography type Reversed phase
Chromatography system Vanquish UHPLC system
Column Accucore C30 (150 x 2.1mm,2.6um)
MS Type ESI
MS instrument type Single quadrupole
MS instrument name Thermo Q Exactive HF hybrid Orbitrap
Ion Mode UNSPECIFIED
Units Normalized ion intensity

Chromatography:

Chromatography ID:CH002488
Chromatography Summary:Chromatographic separation was performed on a Vanquish UHPLC system with an Accucore C30, 2.6 μm column (2.1 mm id × 150mm) coupled to a Q Exactive™ Hybrid Quadrupole-Orbitrap High Resolution Mass Spectrometer (Thermo Fisher Scientific, San Jose, CA) and generated data was processed using LipidSearch™ software version 4.1 (Thermo Scientific),
Methods Filename:Genenral_method_for_Untargeted_Metabolomics_Mar2020.docx
Instrument Name:Vanquish UHPLC system
Column Name:Accucore C30 (150 x 2.1mm,2.6um)
Chromatography Type:Reversed phase

MS:

MS ID:MS003131
Analysis ID:AN003362
Instrument Name:Thermo Q Exactive HF hybrid Orbitrap
Instrument Type:Single quadrupole
MS Type:ESI
MS Comments:Please refer to publication Wang et al 2022.
Ion Mode:UNSPECIFIED
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