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Sample GSM4331725 Query DataSets for GSM4331725
Status Public on Feb 22, 2020
Title t13_Klox_aM
Sample type SRA
 
Source name chronic wound
Organism Staphylococcus aureus
Characteristics strain: spa type t13595
condition: S. aureus t13595 + K. oxytoca co-culture, exponential phase
origin: clinical isolate
collection date: Feb. 14, 2013
reference genome name: 1280.1985_Staphylococcus_aureus
eference genome: JAAFYO000000000.1
Treatment protocol Main cultures were started in water bath under constant shaking (80–85 rpm) at 37ºC in 120 mL pre-warmed RPMI medium. The monocultures were initiated with an OD600 of 0.05 while co-cultures were inoculated with an OD600 of 0.025 of each isolate to a total of 0.05. Samples were collected at mid-exponential phase (2-2.5 h, OD600 ±0.5) and at 90 min within the stationary growth phase (4-5 h, OD600 ±1.0). To mimic biofilm conditions, serial dilutions were performed with monocultures or mixed cultures of t111, t13595, Bt plus Ko, and these were plated onto RPMI agar and incubated at 37 ºC for 24 hr to form a homogeneous plate with coalescent individual colonies.
Growth protocol Bacterial isolates were grown in RPMI liquid medium and RPMI agar
Extracted molecule total RNA
Extraction protocol Immediately after obtaining the cell pellet, 100 µl of killing buffer was added. Mechanical cell disruption was carried out with a Teflon vessel and a disruption ball filled with liquid N2 and pre-cooled in liquid N2 . The resulting cell powder was resuspended in 4 ml of lysis solution by repeated pipetting and transfer into 1 ml aliquots. Subsequently, one volume of acid phenol solution was added to cell lysate, and mixed on a tube shaker. Centrifugation and supernatant transfer into a new tube were followed by the addition of one volume acid phenol solution. This procedure was repeated twice; first by the addition of one volume chloroform/IAA and then by the addition of Na-Acetate and isopropanol for overnight precipitation. RNA extraction was carried out by centrifugation at 4°C, where the pellet was washed twice with 80% ethanol, dry at room temperature, and dissolved in nuclease-free water. DNase Digestion and RNA clean-up (Qiagen, Hilden, Germany) were performed following manufacturer’s protocol. RNA concentration was determined by Nanodrop spectrophotometer (Thermo Fisher Scientific, Waltham, USA) and RNA quality assessment was carried out by Agilent 2100 Bioanalyzer.
cDNA libraries were constructed using the Ion Total RNA-Seq Kit v2 (Life Technologies, Carlsbad, CA) and the manufacturer’s recommended protocol.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Ion Torrent Proton
 
Description liquid culture
Processed_data_rpkm_t13595.txt
Processed_data_rpkm_t13595.txt
Data processing mapping of reads was done using: bowtie2 --local
SAM files were converted to BAM files using SAM tools
BAM files were converted to RPKM values using BED-tools
RPKM values were normalized using the TMM (Trimmed Median Mean) method in T-REx (doi: 10.1186/s12864-015-1834-4)
Genome_build: 1280.1984_Staphylococcus_aureus GenBank: JAAFYP000000000.1 42 rc DNA linear BCT 09-FEB-2020
Genome_build: 1428.155_Bacillus_thuringiensis Genbank: JAAFYT000000000.1
Genome_build: 571.31_Klebsiella_oxytoca GenBank: JAAFYN000000000.1 59 rc DNA linear BCT 09-FEB-2020
Genome_build: 1280.1985_Staphylococcus_aureus GenBank: JAAFYO000000000.1 37 rc DNA linear BCT 09-FEB-2020
Supplementary_files_format_and_content: Tab delimited text file
 
Submission date Feb 21, 2020
Last update date Feb 22, 2020
Contact name Anne de Jong
E-mail(s) anne.de.jong@rug.nl
Phone +31 50 363 2047
Organization name university of Groningen
Department Molecular Genetics
Street address Nijenborgh 7
City Groningen
ZIP/Postal code 9747 AG
Country Netherlands
 
Platform ID GPL20673
Series (1)
GSE145732 Pathogen-pathogen interactions, a way to soothe virulence?
Relations
BioSample SAMN14162268
SRA SRX7779293

Supplementary file Size Download File type/resource
GSM4331725_t13595_7am.rpkm.gz 93.1 Kb (ftp)(http) RPKM
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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