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Sample GSM4973292 Query DataSets for GSM4973292
Status Public on Dec 22, 2020
Title USA500 NRS385 Planktonic 10 hour
Sample type SRA
 
Source name bacterial cells
Organism Staphylococcus aureus
Characteristics strain: NRS385
genotype: Wildtype
growth medium: TSB
growth conditions: Static planktonic, 10 h, 37°C
Treatment protocol Samples were stored at -80°C prior to RNA extraction.
Growth protocol Overnight S. aureus cultures were used to inoculate fresh tryptic soy broth at an optical density (OD600) of 0.5 in 96-well microtiter plates, in biological triplicate. Test cultures were grown for 5 h, 10 h and 24 h at 37°C in a static incubator prior to collection. To collect planktonic samples, 75 μL of supernatant was removed from the top of each well, and those for like strains were pooled. Samples were immediately combined with 5 mL of ice-cold PBS, and pelleted by refrigerated centrifugation for subsequent RNA isolation. For biofilm samples, the remaining supernatant was removed and biofilm containing wells were washed three times with 200 μL of ice-cold PBS. Ice-cold PBS was added a final time, pipetted vigorously to disrupt biofilm cells, and like strains were pooled. Samples were then immediately combined with an additional 5 mL of ice-cold PBS and pelleted by refrigerated centrifugation for subsequent RNA isolation.
Extracted molecule total RNA
Extraction protocol Total bacterial RNA was isolated utilizing an RNeasy Kit (Qiagen) and contaminating DNA was removed by treatment with TURBO DNA-free kit (Ambion). Samples with a RIN of >9.7 measured by Agilent 2100 Bioanalyzer system and corresponding RNA 6000 Nano kit (Agilent) were used in this study. Ribosomal RNA was removed using a Ribo-Zero Kit for Gram-positive Bacteria (Illumina) and MICROBExpress Bacterial mRNA enrichment kit (Agilent).
Library construction was performed using the TruSeq Stranded mRNA Kit from Illumina omitting mRNA enrichment steps.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NextSeq 500
 
Data processing Raw data files (.fastq) were exported from the Illumina BaseSpace Server
Raw data files (.fastq) were imported into Qiagen CLC Genomics Workbench (version 20) as paired-end reads for analysis and adapter indices trimmed.
Reads corresponding to ribosomal RNA were filtered out and removed
Gene expression values were calculated using the Expression Browser tool
Differential expression between biofilm and planktonic samples were generated for each strain and timepoint individually using the Differential Expression in Two Groups tool
Fold change comparisons were exported in excel format
Genome_build: The accession number for the Genbank genome files used as reference are: USA100 (NC_002745), USA200 (NC_002952), USA300 (NC_007793), USA400 (NC_003923), and USA500 (NC_007793).
Supplementary_files_format_and_content: Differential expression in biofilm populations relative to their planktonic counterpart are presented as fold-change values in excel format.
 
Submission date Dec 14, 2020
Last update date Dec 22, 2020
Contact name Lindsey N Shaw
Organization name University of South Florida
Department CMMB
Street address 4202 E Fowler Avenue
City Tampa
State/province FL
ZIP/Postal code 33620
Country USA
 
Platform ID GPL24034
Series (1)
GSE163153 Temporal transcriptomic analysis of five Staphylococcus aureus strains' biofilms and planktonic counterparts
Relations
BioSample SAMN17077268
SRA SRX9682666

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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