Return to study ST002556 main page

MB Sample ID: SA257072

Local Sample ID:9908_Calving_Met
Subject ID:SU002657
Subject Type:Mammal
Subject Species:Bos taurus
Taxonomy ID:9913
Weight Or Weight Range:700 kg
Gender:Female
Animal Housing:Free-stalls
Animal Feed:TMR

Select appropriate tab below to view additional metadata details:


Subject:

Subject ID:SU002657
Subject Type:Mammal
Subject Species:Bos taurus
Taxonomy ID:9913
Weight Or Weight Range:700 kg
Gender:Female
Animal Housing:Free-stalls
Animal Feed:TMR

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
9908_Calving_MetSA257072FL032794MetGroup
9908_Calving_MetSA257072FL032794CalvingTime
9908_Calving_MetSA257072FL032794MultParity

Collection:

Collection ID:CO002650
Collection Summary:All cows had blood collected in the prepartum period (-14 DRP), calving (first 24h after calving), and at diagnosis (day of metritis diagnosis). Blood was sampled from the jugular vein using a 20-gauge x 2.54-cm needle and 10-mL evacuated tube containing lithium heparin (Vacutainer, Becton, Dickinson and Company, Franklin Lakes, NJ, USA). After collection, the blood tubes were placed on ice and transported to the laboratory within 2 hours. Once in the laboratory, the blood tubes were centrifuged at 4000 g, 4 °C, for 10 min, and the plasma was stored at -80 oC for further characterization of the plasma metabolome. The frozen plasma was submitted to the University of California’s West Coast Metabolomics Center in Davis, CA for metabolome analysis. Samples were analyzed by blinded technicians using untargeted gas chromatography with time-of-flight mass spectrometry (GC-TOF-MS) in a single batch.
Sample Type:Blood (plasma)

Treatment:

Treatment ID:TR002669
Treatment Summary:This was a case-control study, hence, there were not treatments applied. Cows were self assigned to the groups. Cows that developed metritis were paired with healthy cows by days in milk.

Sample Preparation:

Sampleprep ID:SP002663
Sampleprep Summary:After collection, the blood tubes were placed on ice and transported to the laboratory within 2 hours. Once in the laboratory, the blood tubes were centrifuged at 4000 g, 4 °C, for 10 min, and the plasma was stored at -80 oC for further characterization of the plasma metabolome. The frozen plasma was submitted to the University of California’s West Coast Metabolomics Center in Davis, CA for metabolome analysis

Combined analysis:

Analysis ID AN004211
Analysis type MS
Chromatography type GC
Chromatography system Leco Pegasus IV GC
Column Restek Rtx-5Sil MS (30m x 0.25mm, 0.25um)
MS Type EI
MS instrument type GC-TOF
MS instrument name Leco Pegasus IV TOF
Ion Mode POSITIVE
Units peak heights

Chromatography:

Chromatography ID:CH003122
Chromatography Summary:Data are acquired using the following chromatographic parameters, with more details to be found in Fiehn O. et al. Plant J. 53 (2008) 691–704. Column: Restek corporation Rtx-5Sil MS (30 m length x 0.25 mm internal diameter with 0.25 μm film made of 95% dimethyl/5%diphenylpolysiloxane) Mobile phase: Helium Column temperature: 50-330°C Flow- rate: 1 mL min-1 Injection volume: 0.5 μL Injection: 25 splitless time into a multi-baffled glass liner Injection temperature: 50°C ramped to 250°C by 12°C s-1 Oven temperature program: 50°C for 1 min, then ramped at 20°C min-1 to 330°C, held constant for 5 min. The analytical GC column is protected by a 10 m long empty guard column which is cut by 20 cm intervals whenever the reference mixture QC samples indicate problems caused by column contaminations. We have validated that at this sequence of column cuts, no detrimental effects are detected with respect to peak shapes, absolute or relative metabolite retention times or reproducibility of quantifications. This chromatography method yields excellent retention and separation of primary metabolite classes (amino acids, hydroxyl acids, carbohydrates, sugar acids, sterols, aromatics, nucleosides, amines and miscellaneous compounds) with narrow peak widths of 2–3 s and very good within-series retention time reproducibility of better than 0.2 s absolute deviation of retention times. We use automatic liner exchanges after each set of 10 injections which we could show to reduce sample carryover for highly lipophilic compounds such as free fatty acids. Mass spectrometry parameters are used as follows: a Leco Pegasus IV mass spectrometer is used with unit mass resolution at 17 spectra s-1 from 80-500 Da at - 70 eV ionization energy and 1800 V detector voltage with a 230°C transfer line and a 250°C ion source.
Instrument Name:Leco Pegasus IV GC
Column Name:Restek Rtx-5Sil MS (30m x 0.25mm, 0.25um)
Column Temperature:50-330
Flow Gradient:.
Flow Rate:1 mL min-1
Solvent A:.
Solvent B:.
Chromatography Type:GC

MS:

MS ID:MS003958
Analysis ID:AN004211
Instrument Name:Leco Pegasus IV TOF
Instrument Type:GC-TOF
MS Type:EI
MS Comments:See data acquisition, processing, and reporting in "Methods.pdf" file
Ion Mode:POSITIVE
Analysis Protocol File:Methods_SC.pdf
  logo