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Links from GEO DataSets

Items: 17

1.

Pharmacologic disruption of agr quorum sensing in Staphylococcus aureus promotes host defense against skin and soft tissue infections

(Submitter supplied) Drug discovery for novel anti-infectives is essential to meet the global health threat of antibiotic resistant bacterial infections, including those caused by Staphylococcus aureus1,2. Because ~90% of S. aureus infections involve skin and soft tissues (SSTIs)3,4, we hypothesized that developing anti-virulence therapeutics5,6 for SSTIs could minimize pressure on resistance development while sparing conventional antibiotics for control of systemic infections. more...
Organism:
Staphylococcus aureus; Staphylococcus aureus subsp. aureus USA300
Type:
Expression profiling by array
Platform:
GPL8069
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE52978
ID:
200052978
2.

The quorum-sensing agr system protects Staphylococcus aureus from oxidative stress

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27158
18 Samples
Download data
Series
Accession:
GSE207045
ID:
200207045
3.

The quorum-sensing agr system protects Staphylococcus aureus from oxidative stress (overnight growth)

(Submitter supplied) The agr quorum-sensing system clearly links Staphylococcus aureus metabolism to virulence, but little is known about how agr alters metabolism to affect cell survival during severe stress. Recently, we reported that agr activity increases survival of bacteria during treatment with lethal concentrations of H2O2, a crucial host defense against S. aureus.  Here we report that protection by agr extends to growth resumption during the exit from stationary phase. more...
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27158
12 Samples
Download data: TSV
Series
Accession:
GSE206916
ID:
200206916
4.

The quorum-sensing agr system protects Staphylococcus aureus from oxidative stress (5 hour growth)

(Submitter supplied) The agr quorum-sensing system clearly links Staphylococcus aureus metabolism to virulence, but little is known about how agr alters metabolism to affect cell survival during severe stress. Recently, we reported that agr activity increases survival of bacteria during treatment with lethal concentrations of H2O2, a crucial host defense against S. aureus.  Here we report that protection by agr extends to growth resumption during the exit from stationary phase. more...
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27158
6 Samples
Download data: TSV
Series
Accession:
GSE206889
ID:
200206889
5.

Evolution of virulence control by the staphylococcal agr quorum-sensing regulator

(Submitter supplied) The Staphylococcus aureus accessory gene regulator (agr) is a prototype quorum-sensing system in Gram-positive bacteria and a paradigmatic example of gene regulation by a small regulatory RNA, RNAIII. Using genome-wide transcriptional profiling in the community-associated methicillin-resistant (CA-MRSA) strain MW2, we demonstrate here that in contrast to the current model of target gene regulation by agr, a large subset of agr-regulated genes is controlled independently of RNAIII. more...
Organism:
Borreliella burgdorferi B31; Chlamydia trachomatis D/UW-3/CX; Staphylococcus haemolyticus JCSC1435; Chlamydia muridarum; Staphylococcus epidermidis RP62A; Staphylococcus aureus subsp. aureus MW2; Chlamydia pneumoniae AR39; Coxiella burnetii RSA 493; Granulibacter bethesdensis; Coxiella burnetii; Rickettsia rickettsii; Staphylococcus aureus; Staphylococcus epidermidis ATCC 12228; Chlamydia caviae GPIC
Type:
Expression profiling by array
Platform:
GPL4692
27 Samples
Download data: CEL, CHP
Series
Accession:
GSE10165
ID:
200010165
6.

The ubiquitous human skin commensal Staphylococcus hominis protects against opportunistic pathogens

(Submitter supplied) Staphylococcus hominis is frequently isolated from human skin and we hypothesize that it may protect the cutaneous barrier from opportunistic pathogens. We determined that S. hominis makes six unique auto inducing peptide (AIP) signals that inhibit the major virulence factor accessory gene regulator (agr) quorum sensing system of Staphylococcus aureus. We solved and confirmed the structures of three novel AIP signals in conditioned media by mass spectrometry, then validated synthetic AIP activity against all S. more...
Organism:
Staphylococcus hominis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL32101
6 Samples
Download data: TXT
Series
Accession:
GSE199818
ID:
200199818
7.

Effect of apicidin on gene expression in Staphylococcus aureus USA300 strain LAC

(Submitter supplied) The fungal metabolite apicidin acts as a quorum sensing inhibitor in Staphylococcus aureus. Here we use RNA-sequencing to examine the effect of apicidin on gene expression, comparing to untreated wild-type and an agr quorum sensing mutant.
Organism:
Staphylococcus aureus subsp. aureus USA300
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17544
9 Samples
Download data: CSV
Series
Accession:
GSE125741
ID:
200125741
8.

Inactivation of the response regulator AgrA has a pleiotropic effect on biofilm formation, pathogenesis and stress response in Staphylococcus lugdunensis

(Submitter supplied) Exploration of the the transcriptomic consequences of the complete deletion of agrA gene in Staphylococcus lugdunensis. Overall, the ΔagrA deletion significantly affected the expression of 400 genes. Among them, 149 were upregulated and 251 were downregulated.
Organism:
Staphylococcus lugdunensis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29710
8 Samples
Download data: TAB
Series
Accession:
GSE181857
ID:
200181857
9.

RNA sequencing and gene analysis of unstimulated and stimulated MRSA cultures

(Submitter supplied) Aim: the goal of this study is to compare Quorum sensing related gene expression in MRSA cultures incubated with an aza-derivative
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24034
4 Samples
Download data: XLSX
Series
Accession:
GSE161844
ID:
200161844
10.

Impact of compound VU0026921 on S. aureus transcriptional profile

(Submitter supplied) Compound VU0026921 is antimicrobial to S. aureus in a manner modulated by Mn. To elucidate information regarding the mechanism of action of VU0026921, we performed RNA sequencing of S. aureus exposed to VU0026921 in the presence or absence of excess Mn
Organism:
Staphylococcus aureus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26273
12 Samples
Download data: TXT
Series
Accession:
GSE128062
ID:
200128062
11.

Manganese detoxification by Staphylococcus aureus

(Submitter supplied) Manganese (Mn) is an essential micronutrient critical for the pathogenesis of Staphylococcus aureus, a significant cause of human morbidity and mortality. Paradoxically, excess Mn is toxic, therefore maintaining intracellular Mn homeostasis is required for survival. To identify gene candidates that contribute to manganese detoxification, we compared the transcriptional response of S. aureus cells exposed to 1 mM MnCl2 and those that were untreated.
Organism:
Staphylococcus aureus subsp. aureus str. Newman
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25976
6 Samples
Download data: TXT
Series
Accession:
GSE124285
ID:
200124285
12.

YAP promotes cell-autonomous immune responses in vitro to tackle intra-cellular Staphylococcus aureus

(Submitter supplied) Transcriptional cofactors YAP/TAZ have recently been found to support autophagy and inflammation, which are part of cell autonomous immunity and are critical in antibacterial defense. Here, we studied the role of YAP against Staphylococcus aureus using CRISPR/Cas9-mutated HEK293 cells and a primary cell-based organoid model. We found that S. aureus infection increases YAP transcriptional activity, which is required to reduce intracellular S. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL31975
12 Samples
Download data: CSV
Series
Accession:
GSE197181
ID:
200197181
13.

Dermal and hypodermal macrophages and dendritic cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL21493 GPL24247 GPL17021
42 Samples
Download data: BED, CSV, MTX, TSV, XLSX
Series
Accession:
GSE228445
ID:
200228445
14.

Transcriptomic profile of hypodermal adventitia fibroblasts from Csf1f/f and Tek-crexCsf1f/f mice

(Submitter supplied) In order to explore and compare the transcriptomic profile of hypodermal adventitia fibroblasts, fibroblasts were isolated via flow cytometry mouse hypodermis and were subjected to RNA-sequencing analysis.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21493
12 Samples
Download data: XLSX
Series
Accession:
GSE228443
ID:
200228443
15.

Single-cell transcriptomic profile of CD45+ and CD45- cells from dermis and hypodermis of C57BL/6 mice

(Submitter supplied) In order to explore and compare the transcriptomic profile of leucocytes and stromal cells present in the dermis and hypodermis of C57BL/6 mice, isolated cells from each of these skin layers were subjected to single-cell RNA-sequencing analysis.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21493
8 Samples
Download data: MTX, TSV
Series
Accession:
GSE228018
ID:
200228018
16.

Single-cell epigenomic analysis of hypodermal macrophages from Csf1r-cre x Igf1-flox mice.

(Submitter supplied) To explore the effect of cell-autonomous Igf1 expression on hypodermal macrophages, these cells were isolated from Csf1r-cre x Igf1-flox mice and subjected to single-cell ATAC-sequencing.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
4 Samples
Download data: BED, CSV, TSV
Series
Accession:
GSE227859
ID:
200227859
17.

Transcriptomic profile of dermal and hypodermal CCR2+ macrophages, CCR2- macrophages and dendritic cells from C57BL/6 mice

(Submitter supplied) In order to explore and compare the transcriptomic profile of CCR2+ macrophages, CCR2- macrophages and dendritic cells present in the dermis and hypodermis of C57BL/6 mice, isolated cells were subjected to RNA-sequencing analysis.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
18 Samples
Download data: XLSX
Series
Accession:
GSE227758
ID:
200227758
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