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Items: 1 to 20 of 142

1.

Comparative Ribo-Seq of Staphylococcus aureus harboring A2058-unmodified ribosomes and m6A2058-modified ribosomes

(Submitter supplied) A total of 10 cDNA libraries were constructed, representing 3 and 2 independent biological replicates of S. aureus strain KES34 (unmodified ribosomes) and KES30 (m6A2058-modified ribosomes), respectively. Translational efficiency (RPF/mRNA ratios), total mRNA abundance and ribosome density of each ORFs were calculated.
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL17452
10 Samples
Download data: TXT
Series
Accession:
GSE168265
ID:
200168265
2.

G-quadruplex DNA as a target for pathogenic bacteria: efficacy of an extended naphthalene diimide ligand and mode of action

(Submitter supplied) Guanidine DNA quadruplex (G4-DNA) structures convey a distinctive layer of epigenetic information that is critical for the regulation of key biological activities and processes as genome transcription regulation, replication and repair. Despite several works that have been published recently, the information regarding their role and possible use as therapeutic drug targets in bacteria is still scarce. more...
Organism:
Escherichia coli; Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL17452 GPL14548
8 Samples
Download data: RPKM
Series
Accession:
GSE178890
ID:
200178890
3.

High resolution definition of the Staphylococcus aureus WalKR regulon

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL18481 GPL17452
19 Samples
Download data
Series
Accession:
GSE212321
ID:
200212321
4.

High resolution definition of the Staphylococcus aureus WalKR regulon [RNA-seq]

(Submitter supplied) Here, we use a panel of defined walKR mutants and functional genomics including ChIP-seq to confirm a high-resolution consensus WalR DNA-binding motif and characterise a 61-gene direct regulon
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17452
6 Samples
Download data: CSV
Series
Accession:
GSE212319
ID:
200212319
5.

Integration of Metabolomics and Transcriptomics Reveals Changes in MRSA Exposed to Terpinen-4-ol

(Submitter supplied) Staphylococcus aureus (S. aureus) is a gram-positive bacterium that causes a wide range of diseases. Terpinen-4-ol is a monoterpene component contained in most plant essential oils with good antibacterial activity. In this study, terpinen-4-ol effectively inhibited 13 strains of S. aureus, and effectively inhibited the biofilm of MRSA. Metabolomics and transcriptomics were used to elucidate changes in MRSA cells exposed to terpinen-4-ol. more...
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17452
6 Samples
Download data: TXT
Series
Accession:
GSE157638
ID:
200157638
6.

Microbiome characterization using transfer RNA sequencing

(Submitter supplied) Here we report a direct tRNA sequencing protocol and software to simultaneously examine the composition and biological activity of naturally occurring microbial communities. Our analysis of mouse gut microbiome with tRNA-seq and 16S ribosomal RNA gene amplicons revealed comparable microbial community structures, and additional physiological insights into the microbiome through tRNA abundance and modifications.
Organism:
Bacillus subtilis; mouse gut metagenome; Barnesiella viscericola; Escherichia coli; Staphylococcus aureus
Type:
Non-coding RNA profiling by high throughput sequencing
6 related Platforms
28 Samples
Download data: TXT, XLSX
Series
Accession:
GSE100263
ID:
200100263
7.

Lysogenization of Staphylococcus aureus RN450 by phages phi11 and phi80alpha leads to the activation of the SigB regulon

(Submitter supplied) Staphylococcus aureus is a major opportunistic pathogen and notable efforts are currently under way to develop new methods to combat staphylococcal infections. It is becoming increasingly clear that understanding the ecology of pathogenic bacteria is important to design improved disinfection and therapeutic strategies. Like many microbes, S. aureus commonly forms biofilms on various biotic and abiotic surfaces. more...
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17452
6 Samples
Download data: TXT
Series
Accession:
GSE111012
ID:
200111012
8.

Maturation of polycistronic mRNA by RNase Y and its associated Y-complex in Gram-positive bacteria

(Submitter supplied) Endonucleolytic cleavage within polycistronic mRNAs can lead to differential stability and discordant abundance among co-transcribed genes. RNase Y, the major endonuclease for mRNA decay in Bacillus subtilis, was originally identified for its cleavage activity towards the cggR-gapA operon, an event that differentiates the expression of a glycolytic enzyme from its transcriptional regulator. A three-protein Y-complex (YlbF, YmcA, and YaaT) was recently identified that is also required for this cleavage in vivo, raising the possibility that it is an accessory factor acting to regulate RNase Y. more...
Organism:
Bacillus subtilis; Staphylococcus aureus
Type:
Other
Platforms:
GPL17452 GPL18561
16 Samples
Download data: WIG
Series
Accession:
GSE108295
ID:
200108295
9.

Changes in relative transcript amounts caused by hydrogen sulfide treatment, calprotectin treatment, and deletion of CstR in Staphylococcus Aureus

(Submitter supplied) The Staphylococcus aureus strain Newman uses the dithiol-containing repressor CstR to sense sulfide stress via reactive sulfur species (RSS), allowing transcription of a mitochondrial-like sulfide oxidation system, the core of which is genetically linked to methicillin resistance determinants in MRSA strains. The cytoplasm maintains an excess of reduced relative to oxidized low molecular weight (LMW) thiols that are protective against oxidative stress and transition metal (Zn, Cd and Cu) toxicity, buffering these ions to low “free” concentrations via formation of coordination complexes. more...
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL19006 GPL17452
18 Samples
Download data: TXT
Series
Accession:
GSE99432
ID:
200099432
10.

Downregulation of autolysin-encoding genes by phage-derived lytic proteins inhibits biofilm formation in Staphylococcus aureus

(Submitter supplied) Phage-derived lytic proteins are a promising alternative to conventional antimicrobials. One of their most interesting properties is that they do not readily select for resistant strains, which is likely due to the fact that their targets are essential for the viability of the bacterial cell. Moreover, genetic engineering allows the design of new "tailor-made" proteins that may exhibit improved antibacterial properties. more...
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17452
6 Samples
Download data: TXT
Series
Accession:
GSE94512
ID:
200094512
11.

Response to low-level phage predation in Staphylococcus aureus biofilms

(Submitter supplied) An important lesson from the war on pathogenic bacteria has been the need to understand the physiological responses and evolution of natural microbial communities. Bacterial populations in the environment are generally forming biofilms subject to some level of phage predation. These multicellular communities are notoriously resistant to antimicrobials and, consequently, very difficult to eradicate. This has sparked the search for new therapeutic alternatives, including phage therapy. This study demonstrates that S. aureus biofilms formed in the presence of a non-lethal dose of phage phiIPLA-RODI exhibit a unique physiological state that could potentially benefit both the host and the predator. Thus, biofilms formed under phage pressure are thicker and have a greater DNA content. Also, the virus-infected biofilm displayed major transcriptional differences compared to an untreated control. Significantly, RNA-seq data revealed activation of the stringent response, which could slow down the advance of the bacteriophage within the biofilm. The end result would be an equilibrium that would help bacterial cells to withstand environmental challenges, while maintaining a reservoir of sensitive bacterial cells available to the phage upon reactivation of the dormant carrier population.
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17452
6 Samples
Download data: TXT
Series
Accession:
GSE87706
ID:
200087706
12.

TSS-EMOTE, a refined protocol for a more complete and less biased global mapping of transcription start sites in bacterial pathogens.

(Submitter supplied) Background Bacteria rely on efficient gene regulatory mechanisms to switch between genetic programs when they are facing new environments. Although this regulation can occur at many different levels, one of the key steps is the initiation of transcription. Identification of the first nucleotide transcribed by the RNA polymerase is therefore essential to understand the underlying regulatory processes, since this provides insight on promoter strength and binding sites for transcriptional regulators, and additionally reveals the exact 5' untranslated region of the transcripts, which often contains elements that regulate translation. more...
Organism:
Acinetobacter baumannii; Staphylococcus aureus; Staphylococcus epidermidis; Klebsiella aerogenes
Type:
Expression profiling by high throughput sequencing; Other
4 related Platforms
30 Samples
Download data: TSV
Series
Accession:
GSE85110
ID:
200085110
13.

The mutual effect of Staphylococcus epidermidis and Staphylococcus aureus in dual species biofilms as revealed by RNA-Seq

(Submitter supplied) We examined the differential gene expression of Staphylococcus epidermidis and Staphylococcus epidermidis in dual species biofilms. Therefore, we performed RNA-Seq on single and dual species biofilms and we compared the gene expression levels in dual species biofilms to those in single species biofilms.
Organism:
Staphylococcus epidermidis; Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL21653 GPL17452 GPL21652
9 Samples
Download data: XLSX
Series
Accession:
GSE79575
ID:
200079575
14.

A master virulence regulator of S. aureus inactivated during carriage in man

(Submitter supplied) It remains unclear how the bacterial populations which colonise many healthy humans occasionally give rise to severe disease. Staphylococcus aureus represents one such population. Here we describe mutations in invasive S. aureus which arose during human colonisation and inactivated rsp, a transcription factor. RNA-Seq was used to generate mRNA profiles of genes controlled by rsp.
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17452
12 Samples
Download data: TXT
Series
Accession:
GSE67448
ID:
200067448
15.

Ribosome hibernation factor promotes Staphyloccocal survival and differentially represses translation

(Submitter supplied) We sequenced a total of 16 cDNA libararies derived from fragmented total mRNA and ribosome protected mRNAs from S. aureus hpf mutant (NE838) and its parental strain JE2 grown in tryptic soy broth (TSB) or minimal medium (MM). The data represented 2 independent biological replicates.
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL17452
16 Samples
Download data: TXT
Series
Accession:
GSE74197
ID:
200074197
16.

Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and △Rsp MRSA Transcriptomes

(Submitter supplied) Purpose: Next-generation sequencing (NGS) has revolutionized systems-based analysis of gene regulon. The goal of this study is to investigate the genes regulated by Rsp in MRSA BD02-25 Methods: mRNA profiles of wild-type (WT) and Rsp knockout (△Rsp) MRSA at mid-logarithmic growth phase (4h) were generated by deep sequencing, respectively in duplicate samples, using the Hiseq2000 (Illumina, CA) sequencer. more...
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17452
4 Samples
Download data: TXT
Series
Accession:
GSE67344
ID:
200067344
17.

In situ Staphylococcus aureus gene expression in a human prosthetic joint infection

(Submitter supplied) Little is known about regulation of gene activity of the major pathogen Staphylococcus aureus during actual human infection. Here we characterize the transcriptome using deep RNA sequencing and the metabolome using NMR of S. aureus infected joint fluid derived from an acute human prosthetic joint infection, and compare them with the genome, transcriptome and metabolome of an isolate obtained from the sample grown in vitro (LB medium). more...
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17452
4 Samples
Download data: TXT
Series
Accession:
GSE62091
ID:
200062091
18.

RNA-seq reveals differential gene expression in Staphylococcus aureus at single-nucleotide resolution

(Submitter supplied) Staphylococcus aureus is a gram-positive cocci and an important human commensal bacteria and pathogen. S. aureus infections are increasingly difficult to treat because of the emergence of highly resistant MRSA (Methicillin-resistant S. aureus) strains. Here we present a method to study differential gene expression in S. aureus using high-throughput RNA-sequencing (RNA-seq). We use RNA-seq to examine the differential gene expression in S. more...
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17452
3 Samples
Download data: WIG
Series
Accession:
GSE48896
ID:
200048896
19.

Illumina HiSeq 2000 (Staphylococcus aureus)

Organism:
Staphylococcus aureus
18 Series
123 Samples
Download data
Platform
Accession:
GPL17452
ID:
100017452
20.

YP_18_Total_KES30_rep2

Organism:
Staphylococcus aureus
Source name:
YP_18_Total_KES30_bacterial cells
Platform:
GPL17452
Series:
GSE168265
Download data: TXT
Sample
Accession:
GSM5135231
ID:
305135231
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