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Items: 1 to 20 of 40

1.

Inactivation of Pseudomonas putida KT2440 pyruvate dehydrogenase relieves catabolite repression and improves the usefulness of this strain as a tool in biotechnology

(Submitter supplied) Pyruvate dehydrogenase (PDH) catalyses the irreversible decarboxylation of pyruvate to acetyl-CoA, which feeds the tricarboxylic acids cycle. We analysed how the lack of PDH affects Pseudomonas putida metabolism. Inactivating PDH generated a strain that can no longer use compounds whose assimilation converges into pyruvate, including sugars and several amino acids. Compounds generating acetyl-CoA supported growth. more...
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18287
6 Samples
Download data: TXT
Series
Accession:
GSE263208
ID:
200263208
2.

RNA-Seq analysis for the study "tRNA epitranscriptome determines pathogenicity of the opportunistic pathogen Pseudomonas aeruginosa"

(Submitter supplied) The success of bacterial pathogens depends on the coordinated expression of virulence determinants. Regulatory circuits that drive pathogenesis are complex, multilayered, and incompletely understood. Here, we reveal that alterations in tRNA modifications define pathogenic phenotypes in the opportunistic pathogen Pseudomonas aeruginosa. We demonstrate that the enzymatic activity of GidA leads to the introduction of a carboxymethylaminomethyl modification in selected tRNAs. more...
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18287
6 Samples
Download data: XLSX
Series
Accession:
GSE149304
ID:
200149304
3.

tRNA epitranscriptome determines pathogenicity of the opportunistic pathogen Pseudomonas aeruginosa

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Pseudomonas aeruginosa UCBPP-PA14; Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL18287 GPL27892
18 Samples
Download data: BED
Series
Accession:
GSE149306
ID:
200149306
4.

Effect of long-term exposure of platinum nanopariticles on gene expression of Pseudomonas aeruginosa PAO1

(Submitter supplied) Previous synthesized Pt NPs were selected to evaluate the influences on bacterial resistance, and a typical pathogenic microbe P. aeruginosa was chosen as model bacteria. After 60-day PtNPs exposure, we found under 12.5 μg/mL of platinum nanoparticles (PtNPs) exposure for ~7200 generations, the IC50 of evolved Pseudomonas aeruginosa PAO1 to imipenem (IPM) and ciprofloxacin (CIP) reduced 77.0% and 87.8%, respectively. more...
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18287
9 Samples
Download data: CSV
Series
Accession:
GSE218408
ID:
200218408
5.

The dual GGDEF/EAL domain enzyme PA0285 is a Pseudomonas species housekeeping phosphodiesterase regulating early attachment and biofilm architecture

(Submitter supplied) Bacterial lifestyles are dictated by the conditions encountered during colonization of a specific ecological niche or host. A wide range of environmental stimuli triggers sensory modules, that modify activity of proteins, or/and initiate a transfer of information in complex regulatory networks, which modulate gene expression, and therefore adaptation. The transition between planktonic and biofilm growth is dependent on the homeostasis of the intracellular second messenger c-di-GMP. more...
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18287
12 Samples
Download data: TXT
Series
Accession:
GSE223663
ID:
200223663
6.

RNA Seq of passages of a small colony variant P. aeruginosa clinical isolate

(Submitter supplied) Purpose : The goal of this study was to use RNA Seq to explore the correlation of gene expression of a collection of clinical P. aeruginosa isolates to various phenotypes, such as colony morphology, c-di-GMP production and biofilm formation Methods : mRNA profiles were generated for Pseudomonas aerugionsa clinical samples by deep sequencing.Ribosomal RNA was removed by using the RiboZero Bacteria kit (Illumina). more...
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL26913 GPL18287
22 Samples
Download data: XLSX
Series
Accession:
GSE147921
ID:
200147921
7.

Differentially Expressed Genes of Pseudomonas aeruginosa Isolates from Eyes with Keratitis and Healthy Conjunctival Sacs

(Submitter supplied) P. aeruginosa isolates from keratitis and healthy conjunctival sacs were obtained. The transcriptome profile of P. aeruginosa was characterized by a high throughput RNA-seq strategy using the Illumina HiSeq 2500 platform. The DEGs were analyzed with DESeq and validated through quantitative real-time polymerase chain reaction (PCR) and with experimental mice.
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18287
7 Samples
Download data: FNA, TXT
Series
Accession:
GSE209539
ID:
200209539
8.

Enterococcus faecalis antagonizes Pseudomonas aeruginosa growth in mixed-species interactions

(Submitter supplied) Enterococcus faecalis is often co-isolated with Pseudomonas aeruginosa in mixed-species biofilm-associated infections of wounds and the urinary tract. As a defence strategy, the host innately restricts iron availability at infection sites. Despite their co-prevalence, the polymicrobial interactions of these two pathogens in low iron conditions, such as those found in the host, remains unexplored. Here we show that E. more...
Organism:
Enterococcus faecalis; Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL23172 GPL31024 GPL18287
30 Samples
Download data: TXT
Series
Accession:
GSE190090
ID:
200190090
9.

Phenotypic and integrated analysis of a comprehensive Pseudomonas aeruginosa PAO1 library of mutants lacking cyclic-di-GMP-related genes

(Submitter supplied) Pseudomonas aeruginosa is a Gram-negative bacterium able to survive and adapt in a multitude of niches as well as thriving within many different hosts. This versatility lies within a large genome of ca 6Mbp and a tight control in the expression of thousands of genes. Among the regulatory mechanisms widely spread in bacteria, cyclic-di-GMP signaling is one which influences all levels of control. It is made by diguanylate cyclases and broken by phosphodiesterases while the intracellular level of this molecule drives phenotypic responses. more...
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18287
6 Samples
Download data: TXT
Series
Accession:
GSE203348
ID:
200203348
10.

Antibacterial mechanism of the Asp - Asp - Asp - Tyr peptide

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Pseudomonas aeruginosa; Escherichia coli
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL18133 GPL18287
20 Samples
Download data
Series
Accession:
GSE192347
ID:
200192347
11.

Antibacterial mechanism of the Asp - Asp - Asp - Tyr peptide [P. aeruginosa]

(Submitter supplied) Previously, we found that ASP-ASP-ASP-TYR (DDDY) from Dendrobium aphyllum has a minimum inhibitory concentration of 36.15 mg/mL against Pseudomonas aeruginosa. Here, we explored the antibacterial mechanism of DDDY and its potential preservation applications. Metabolomic and transcriptomic analyses revealed that DDDY mainly affects genes involved in P. aeruginosa membrane transport and amino acid metabolism pathways. more...
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18287
10 Samples
Download data: TXT
Series
Accession:
GSE192340
ID:
200192340
12.

Dual effect: High NADH levels contribute to efflux-mediated antibiotic resistance but drive ROS lethality

(Submitter supplied) In light of the antibiotic crisis, emerging strategies to sensitize bacteria to available antibiotics should be explored. Several studies on the mechanisms of killing suggest that bactericidal antibiotic activity is enforced through the generation of reactive oxygen species (ROS lethality hypothesis). Here, we artificially manipulated the redox homeostasis of the model opportunistic pathogen Pseudomonas aeruginosa using specific enzymes that catalyze either the formation or oxidation of NADH. more...
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18287
8 Samples
Download data: CSV
Series
Accession:
GSE188801
ID:
200188801
13.

Using small RNA-Seq to identify differential small RNA content of bacterial outer membrane vesicles (OMVs) secreted by Pseudomonas aeruginosa in response to tobramycin exposure

(Submitter supplied) Characterization of the sRNA content of OMVs harvested from Pseudomonas aeruginosa strain PA14 LB cultue with and without tobramycin (1ug/mL)
Organism:
Pseudomonas aeruginosa
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL18287
6 Samples
Download data: XLS
Series
Accession:
GSE183895
ID:
200183895
14.

Differential transcriptome profiling of P. aeruginosa PAO1 with oxythiamine treatment

(Submitter supplied) We report antibacterial potency of oxythiamine, which is a known transketolase inhibitor in eukaryotes. Oxythiamine inhibited the growth of P. aeruginosa PAO1 and clinical isolates in thiamine-depleted medium only. Metabolic and trascriptomic analyses indicated that oxythiamine was converted to oxythiamine pyrophosphate that subsequently inhibited several vitamin B1-dependent enzymes. Furthermore, a system-level perturbation of thiamine metabolism sensitized P. more...
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18287
4 Samples
Download data: XLSX
Series
Accession:
GSE181354
ID:
200181354
15.

Bacterial defenses against natural antibiotics promote collateral resilience to clinical antibiotics

(Submitter supplied) To characterize the defense mechanisms P. aeruginosa has evolved in response to its most toxic phenazine, pyocyanin, we performed a genome-wide transposon sequencing (TnSeq) screen in which the mutant library was exposed to PYO under carbon starvation in order to maximize PYO toxicity, and genes for which transposon mutants were significantly enriched or depleted were identified.
Organism:
Pseudomonas aeruginosa
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18287
4 Samples
Download data: TXT
Series
Accession:
GSE148769
ID:
200148769
16.

The Fem system in Pseudomonas aeruginosa functions as an ExsA-regulated interspecies signaling pathway

(Submitter supplied) Bacterial interspecies interactions shape the function and structural dynamics of microbial communities and affect disease progression of polymicrobial infections. Here, we present data suggesting that the FemA-FemR-FemI (Fem) cell surface signaling system in P. aeruginosa serves as an interspecies signaling pathway between P. aeruginosa and Mycobacterium species. The Fem system is regulated by the type three secretion system (T3SS) regulator ExsA. more...
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18287
6 Samples
Download data: TXT
Series
Accession:
GSE164773
ID:
200164773
17.

Dkstatin-treated Pseudomonas aeruginosa trascriptome

(Submitter supplied) To better understand the effects of Dkstatin treatment, we compared transcriptome landscapes of PAO1 grown without or with either Dkstatin. A global view of the entire transcriptome uncovered the substantial differences between cells treated with Dkstatin-1 or Dkstatin-2.
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18287
6 Samples
Download data: XLSX
Series
Accession:
GSE163248
ID:
200163248
18.

Adaptation of Pseudomonas aeruginosa to cultivation in standard laboratory conditions

(Submitter supplied) We studied adaptation of the metabolically versatile bacterium Pseudomonas aeruginosa to standard laboratory conditions by propagating mismatch repair-deficient P. aeruginosa in exponential phase for 24 days in rich medium. In the selective environment of this large-bottleneck mutation accumulation experiment, the bacteria developed shorter lag phases, higher growth rates and higher maximum cell densities. more...
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18287
32 Samples
Download data: XLSX
Series
Accession:
GSE146906
ID:
200146906
19.

Transcriptional response of Pseudomonas aeruginosa PA3 to bacteriophage PaP3 infection

(Submitter supplied) Explore the genome-scale phage–host interactions across different developmental infection stages
Organism:
Pseudomonas aeruginosa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18287
18 Samples
Download data: TXT
Series
Accession:
GSE129181
ID:
200129181
20.

Transcriptional response of Pseudomonas aeruginosa PAO1r to bacteriophage phiYY infection

(Submitter supplied) Explore the genome-scale phage–host interactions across different developmental infection stages
Organism:
Pseudomonas aeruginosa; Pseudomonas phage phiYY
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL18287 GPL26342
12 Samples
Download data: TXT
Series
Accession:
GSE128811
ID:
200128811
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