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Sample GSM4173977 Query DataSets for GSM4173977
Status Public on Nov 19, 2019
Title Control S. sonnei culture 1
Sample type SRA
Source name S. sonnei culture
Organism Shigella sonnei
Characteristics strain: 53G transformed with pFPV25.1
incubation temperature: 28.5C
collection point: OD reached 0.6
Growth protocol Bacteria were firsts grown at 37C O/N from glycerol stocks on tryptic soy agar plates containing 0.01% Congo red and 100 ug/ml Carbenicillin. One single smooth colony accumulating Congo red was selected and cultured O/N in tryptic soy broth containing 100 ug/ml Carbenicillin at 37C with agitation. O/N culture was then diluted 50x in tryptic soy broth containing 25 ug/ml Carbenicillin and grown at 37C with agitation until culture reached an OD of 0.55-0.65 at 600 nm. Bacteria for control cultures were then diluted 50x and incubated at 28.5C in a total of 5 ml until they reached an OD of 0.55-0.65. The remaining of the original culture was instead spun down and further processed for injections. (see S. sonnei infected larvae sample)
Extracted molecule total RNA
Extraction protocol Samples were snap frozen at -80°C, then 100 μl of RNA protect bacteria reagent (Qiagen) was added, followed by mechanical trituration with a pestle blender. Samples were supplemented with 100 μl of 30 mM Tris-HCl/1 mM EDTA solution at pH = 8, 33 μl of 50 mg/ml lysozyme (Thermo Scientific), 33 μl of proteinase K >600 U/ml (Thermo Scientific) and shaken for 20 min RT. Lysis was completed by adding 700 μl of RTL buffer (Qiagen), 3 μl of 1 M dithiothreitol (Sigma-Aldrich) and mechanical disruption. Undigested debris were spun down 3 min 10000 rpm and the supernatant was supplemented with 500 μl of 100% ethanol prior loading onto RNeasy mini columns (Qiagen). From this step onwards, the manufacturer’s guidelines were followed for RNA purification. RNA quality and integrity were assessed by using NanoDrop and Non-denaturing agarose gel electrophoresis. For further quality check, RNA sequencing, library construction and reads count, samples were outsourced to Vertis Biotechnologie AG (Freising, Germany). Bacterial and host mRNA were enriched prior library preparation by using Ribo-Zero Gold rRNA Removal Kit (Epidemiology, Illumina, San Diego, California).
The rRNA depleted RNA samples were first fragmented using ultrasound (4 pulses of 30 s each at 4°C). Then, an oligonucleotide adapter was ligated to the 3' end of the RNA molecules. First-strand cDNA synthesis was performed using M-MLV reverse transcriptase and the 3’ adapter as primer. The first-strand cDNA was purified and the 5' Illumina TruSeq sequencing adapter was ligated to the 3' end of the antisense cDNA. The resulting cDNA was PCR-amplified to about 10-20 ng/μl using a high fidelity DNA polymerase . The cDNA was purified using the Agencourt AMPure XP kit (Beckman Coulter Genomics). For Illumina NextSeq sequencing, the samples were pooled in approximately equimolar amounts. The cDNA pool was size fractionated in the size range of 200 – 550 bp using a preparative agarose gel. The primers used for PCR amplification were designed for TruSeq sequencing according to the instructions of Illumina. The cDNA pools were sequenced on an Illumina NextSeq 500 system using 75 bp read length.
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NextSeq 500
Description zebrafish_processed_data.tsv
Data processing Base-calling was perform online during the sequencing procedure with the Real-Time Analysis (RTA) software version 2.4.11 and System Suite Version
Conversion of the bcl2 file to de-multiplexed gzipped fastq files was performed using the bcl2fastq script v. provided by Illumina.
Quality and adapter trimming of fastq files was performed with trimmomatic-0.36.jar SE using parameters: -phred33;ILLUMINACLIP:adapter:2:30:10;SLIDINGWINDOW:4:15;LEADING:3;TRAILING:3;MINLEN:30
Mapping of the reads to the genomes was performed with bowtie2 using parameter --local
Read counting was performed with featureCounts version 1.5.0-p1
Genome_build: GRCz11 (Danio rerio), ASM28371v1 (S. sonnei 53G)
Supplementary_files_format_and_content: tab-separated values (TSV) files include geneID, gene name, gene description, log2foldchange (Deseq2), pvalue (Deseq2), padj (Deseq2), chromosome name, position (start, end and strand), length, reads and RPKM per each sample
Submission date Nov 18, 2019
Last update date Nov 20, 2019
Contact name Vincenzo Torraca
Phone +447519097861
Organization name LSHTM
Street address Keppel street
City London
State/province London
ZIP/Postal code WC1E 7HT
Country United Kingdom
Platform ID GPL27764
Series (1)
GSE140544 Dual RNA-seq of zebrafish larvae infected with Shigella sonnei
BioSample SAMN13319877
SRA SRX7175303

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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