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SRX1470931: GSM1967942: 0 h ΔyrlA/B replicate 2; Homo sapiens; Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 9.3M spots, 931.2M bases, 518.4Mb downloads

Submitted by: NCBI (GEO)
Study: Dual RNA-seq – Dual RNA-seq of further sRNA mutants
show Abstracthide Abstract
Bacteria possess many small noncoding RNAs whose regulatory roles in pathogenesis are little understood due to a paucity of macroscopic phenotypes in standard virulence assays. Here, we use a novel Dual RNA-seq approach for a single-step simultaneous RNA profiling in both pathogen and host to reveal molecular phenotypes of sRNAs during infection with Salmonella Typhimurium. We identify a new PhoP/Q-activated small RNA which upon bacterial internalization acts to temporally control the expression of both, invasion-associated effectors and virulence genes required for intracellular survival. This riboregulatory activity is shown to adjust the human response to replicating Salmonella, and have a pervasive impact on host RNA expression both inside and outside protein-coding regions including infection-specific alterations of an array of long noncoding RNAs. Our study provides a paradigm for a comprehensive RNA-based analysis of intracellular bacterial pathogens without their physical purification from a host and a new discovery route for hidden functions of pathogen genes. Overall design: Dual RNA-seq of further sRNA mutants
Sample: 0 h ΔyrlA/B replicate 2
SAMN04327162 • SRS1198098 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: miRvana kit for total RNA (Ambion) The total RNA samples were first fragmented using ultrasound (4 pulses of 30 s each). Then, RNAs <20 nt were removed using the Agencourt RNAClean XP kit (Beckman Coulter Genomics). This was followed by a dephosphorylation with Antarctic Phosphatase (AP, NEB) and re-phosphorylation with T4 Polynucleotide Kinase (PNK, NEB). Oligonucleotide adapters were ligated to the 5' and 3' ends of the RNA samples. First-strand cDNA synthesis was performed using M-MLV reverse transcriptase and the 3' adapter as primer. The resulting cDNAs were amplified with PCR using a high fidelity DNA polymerase. The cDNA was purified using the Agencourt AMPure XP kit (Beckman Coulter Genomics) and was analyzed by capillary electrophoresis. For Illumina NextSeq sequencing, the samples were pooled in approximately equimolar amounts. An aliquot of the size fractionated pool was analyzed by capillary electrophoresis.
Experiment attributes:
GEO Accession: GSM1967942
Links:
Runs: 1 run, 9.3M spots, 931.2M bases, 518.4Mb
Run# of Spots# of BasesSizePublished
SRR29814819,312,967931.2M518.4Mb2015-12-11

ID:
2079805

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