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Sample GSM375565 Query DataSets for GSM375565
Status Public on Jun 01, 2009
Title udder_healthy_24h_rep3_3
Sample type RNA
 
Source name mammary gland tissue, healthy, external control
Organism Bos taurus
Characteristics tissue: udder
infection: uninfected
time: 24h
Treatment protocol E. coli 1303 was isolated from clinical cases; Inoculum Dose: Bovine mastitis isolate E. coli 1303 belongs to the major E. coli phylogenetic group A (E. coli collection of reference strains, ECOR-A). According to a multiplex PCR-based screening for virulence-associated genes of pathogenic E. coli, this strain does not represent an extraintestinal or intestinal pathogenic E. coli isolate. Only the genes coding for type 1 fimbriae, F17 fimbriae, antigen 43, the ferric citrate siderophore system and the EAST1 toxin could be detected. Bacteria were kept cryo-conserved (Mikrobank-system CryobankTM, Mast Diagnostika, Reinfeld, Germany) for subsequent infections. Bacteria were plated on Columbia sheep blood agar and incubated (37°C) for 24h. A few colonies were transferred to a tube of brain-heart infusion broth (Oxoid, Wesel, Germany) and incubated for 6h (37°C); then a 100_l sample was transferred to a tube of trypticase soy broth (9.9ml, Oxoid, Wesel, Germany). Serial dilutions were made after 18h to prepare the desired inoculum dose of 500CFU/2ml 0.9% sterile, pyrogen free saline. The inoculum dose was plated for control and ranged from 421-613CFU/2ml. Inoculum was administered intracisternally in one quarter through the teat canal. Cows were slaughtered after 6h. Samples from untreated quarters from healthy animals served as controls.
Growth protocol 10 healthy, primiparous, midlactating German Holstein Frisian cows; no history of clinical mastitis; quarter milk samples less than 50,000 somatic cells/ml and free of mastitis pathogens; oestrus synchronized with Cloprostenol (Prostaglandin-F2alpha-analogue, Selectavet,Weyarn), before trial cows were entirely milked out with 20 I.U. Oxytocin i.v. (Veyx-Pharma, Schwarzenborn).
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from bovine mammary gland tissue with the Trizol method according to the manufacturers protocol
Label biotin
Label protocol total RNA was transcribed and labeled with Affymetrix Kits (One-Cycle cDNA Synthesis and IVT Labeling Kit) according to the manufacturers protocol
 
Hybridization protocol fragmented cRNA was hybridized to Affymetrix GeneChip Bovine Genome Arrays and washed and stained with Affymetrix Wash&Stain Kit on an Affymetrix Fluidics Station 450
Scan protocol Affymetrix GeneChip Scanner 3000
Description udder tissue, healthy untreated animal
Data processing RMA Normalization
 
Submission date Feb 26, 2009
Last update date Jun 30, 2009
Contact name Stefan Krebs
E-mail(s) krebs-st@lmb.uni-muenchen.de
Phone 0049-89-2180 76715
Organization name Ludwig-Maximilian University
Department Gene Center
Lab Lafuga Genomics
Street address Feodor-Lynen-Str. 25
City Munich
ZIP/Postal code 81377
Country Germany
 
Platform ID GPL2112
Series (2)
GSE15019 Transcriptome analysis of bovine mammary gland tissue treated with E. coli for 6 hours
GSE15025 E. coli infection induces distinct local and systemic transcriptome responses in the mammary gland

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
AFFX-BioB-3_at 6.8740
AFFX-BioB-5_at 7.1218
AFFX-BioB-M_at 7.4147
AFFX-BioC-3_at 7.1809
AFFX-BioC-5_at 6.7260
AFFX-BioDn-3_at 10.8486
AFFX-BioDn-5_at 9.6275
AFFX-Bt_Cyph_3_at 10.4350
AFFX-Bt_Cyph_5_at 9.0271
AFFX-Bt_Cyph_M_at 9.5079
AFFX-Bt_eIF-4E_3_at 8.4842
AFFX-Bt_eIF-4E_5_at 4.5669
AFFX-Bt_eIF-4E_M_at 6.3042
AFFX-Bt_GST_3_at 7.3541
AFFX-Bt_GST_5_at 7.3567
AFFX-Bt_GST_M_at 6.9223
AFFX-Bt_Lacphor_5_s_at 14.1204
AFFX-Bt_Lacphor_M_s_at 14.0658
AFFX-Bt-A00196-1_s_at 3.5714
AFFX-Bt-AB076373-1_at 3.4856

Total number of rows: 24128

Table truncated, full table size 561 Kbytes.




Supplementary file Size Download File type/resource
GSM375565.CEL.gz 1.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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