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Links from GEO DataSets

Items: 7

1.

Metabolic reprogramming with the induction of toxin production of Clostridioides difficile during the stationary phase

(Submitter supplied) Systems biology approach of Clostridioides difficile to analyze the temporal changes in the intracellular and extracellular metabolme, transcriptome and proteome along the growth curve in casamino acids medium and the connection to toxin production.
Organism:
Clostridioides difficile 630
Type:
Expression profiling by array
Platform:
GPL25054
16 Samples
Download data: CSV, TXT
Series
Accession:
GSE115054
ID:
200115054
2.

Influence of L-lactate and low glucose concentrations on the metabolism and the toxin formation of Clostridioides difficile

(Submitter supplied) Metabolomic and transcriptomic analysis of changes in the exponential and stationary phase of Clostridioides difficile after cultivation in casamino acids medium (reference) and supplemented with L-lactate or glucose and the connection to toxin production.
Organism:
Clostridioides difficile 630
Type:
Expression profiling by array
Platform:
GPL25054
16 Samples
Download data: TXT, XLSX
Series
Accession:
GSE149911
ID:
200149911
3.

L-lactate supplementation influences toxin production of Clostridioides difficile via energy metabolism

(Submitter supplied) Metabolomic and transcriptomic analysis of changes in the exponential and stationary phase of Clostridioides difficile after cultivation in casamino acids medium (reference) and supplemented with L-lactate and the connection to toxin production.
Organism:
Clostridioides difficile 630
Type:
Expression profiling by array
Platform:
GPL25054
8 Samples
Download data: TXT, XLSX
Series
Accession:
GSE139354
ID:
200139354
4.

Clostridium difficile transcriptome of strain R20291 in response to cysteine by using a time-resolved RNA-seqencing

(Submitter supplied) The incidence of Clostridium difficile infection has been steadily rising over the past decade. Its increased rate is associated with the specific NAP1/BI/027 strains which are “hypervirulent” and have led to several large outbreaks since their emergence. However, the relation between their outbreaks and virulence regulation mechanisms remains unclear. It has been reported that the major virulence factor TcdA and TcdB in C. more...
Organism:
Clostridioides difficile R20291
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24374
12 Samples
Download data: XLSX
Series
Accession:
GSE107961
ID:
200107961
5.

Clostridium difficile CD630E: growth with 10 mM cysteine in PY vs growth in PY

(Submitter supplied) Comparison of Clostridium difficile transcriptome of strain CD630E grown for 10 hours in PY (supplemented with mild concentration of cysteine) versus PYC (PY supplemented with 10 mM of cysteine). Experimental procedure was designed to investigate the influence of cysteine on toxins production and the regulatory network involved.
Organism:
Clostridioides difficile
Type:
Expression profiling by array
Platform:
GPL10556
8 Samples
Download data: GPR, TXT
Series
Accession:
GSE22423
ID:
200022423
6.

Iron regulation in Clostridioides difficile

(Submitter supplied) The response to iron limitation of several bacteria is regulated by the ferric uptake regulator (Fur). The Fur-regulated transcriptional, translational and metabolic networks of the Gram-positive, pathogen Clostridioides difficile were investigated by a combined RNA sequencing, proteomic, metabolomic and electron microscopy approach. At high iron conditions (760 g/l) the C. difficile fur mutant displayed a growth deficiency compared to wild type C. difficile cells. more...
Organism:
Clostridioides difficile 630
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25590
12 Samples
Download data: TXT
Series
Accession:
GSE120189
ID:
200120189
7.

Effect of tcdR mutation in Clostridium difficile sporulation

(Submitter supplied) Clostridium difficile is an important nosocomial pathogen and the leading cause of hospital-acquired diarrhea. Antibiotic use is the primary risk factor for the development of C. difficile-associated disease because it disrupts normal protective gut flora and enables C. difficile to colonize the colon. C. difficile damages host tissue by secreting toxins and disseminates by forming spores. The toxin-encoding genes, tcdA and tcdB are part of a pathogenicity locus, which also encodes the gene tcdR that codes for the toxin genes positive regulator. more...
Organism:
Clostridioides difficile
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22304
4 Samples
Download data: XLS
Series
Accession:
GSE85395
ID:
200085395
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Supplemental Content

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