U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 17

1.

The pyruvate-tricarboxylic acid cycle node: a focal point of virulence control in the enteric pathogen Yersinia pseudotuberculosis [csrA mutant]

(Submitter supplied) Whole transcriptome assessment of the Yersinia pseudotuberculosis strain YPIII. The Y. pseudotuberculosis csrA regulon was determined in Yersinia minimal minimum developed for the study. CsrA is a key regulator coordinating virulence and metabolism.
Organism:
Yersinia pseudotuberculosis
Type:
Expression profiling by array
Platform:
GPL15095
3 Samples
Download data: TXT
Series
Accession:
GSE54545
ID:
200054545
2.

The pyruvate-tricarboxylic acid cycle node: a focal point of virulence control in the enteric pathogen Yersinia pseudotuberculosis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Yersinia pseudotuberculosis
Type:
Expression profiling by array
Platform:
GPL15095
9 Samples
Download data: TXT
Series
Accession:
GSE54547
ID:
200054547
3.

The pyruvate-tricarboxylic acid cycle node: a focal point of virulence control in the enteric pathogen Yersinia pseudotuberculosis [rovA mutant]

(Submitter supplied) Whole transcriptome assessment of the Yersinia pseudotuberculosis strain YPIII. The Y. pseudotuberculosis rovA regulon was determined in Yersinia minimal minimum developed for the study. RovA is a key regulator for Yersinia virulence.
Organism:
Yersinia pseudotuberculosis
Type:
Expression profiling by array
Platform:
GPL15095
3 Samples
Download data: TXT
Series
Accession:
GSE54546
ID:
200054546
4.

The pyruvate-tricarboxylic acid cycle node: a focal point of virulence control in the enteric pathogen Yersinia pseudotuberculosis [crp mutant]

(Submitter supplied) Whole transcriptome assessment of the Yersinia pseudotuberculosis strain YPIII. The Y. pseudotuberculosis crp regulon was determined in Yersinia minimal minimum developed for the study. Crp is a key regulator coordinating virulence and metabolism.
Organism:
Yersinia pseudotuberculosis
Type:
Expression profiling by array
Platform:
GPL15095
3 Samples
Download data: TXT
Series
Accession:
GSE54544
ID:
200054544
5.

Crp induces switching of the CsrB and CsrC RNAs in Yersinia pseudotuberculosis and links nutritional status to virulence

(Submitter supplied) Colonization of the intestinal tract and dissemination into deeper tissues by the enteric patho­gen Yersinia pseudotuberculosis demands expression of a special set of virulence factors important for the initiation and the persistence of the infection. In this study we demonstrate that many virulence-associated functions are coregulated with the carbohydrate metabolism. This link is mediated by the carbon storage regulator (Csr) system, including the regulatory RNAs CsrB and CsrC, and the cAMP receptor protein (Crp), which both control virulence gene expression in response to the nutrient composition of the medium. more...
Organism:
Yersinia pseudotuberculosis; Yersinia pseudotuberculosis YPIII
Type:
Expression profiling by array
Platform:
GPL15095
4 Samples
Download data: GPR
Series
Accession:
GSE42206
ID:
200042206
6.

Complex in vivo RNA-seq analysis reveal reprogramming of Yersinia from virulent to persistent mode during infection [RNA-seq]

(Submitter supplied) We recently found that Yersinia pseudotuberculosis can be used as a model of persistent bacterial infections. We performed in vivo RNA-seq of bacteria in small cecal tissue biopsies at early and persistent stages of infection to determine strategies associated with persistence. Comprehensive analysis of mixed RNA populations from infected tissues revealed that Y. pseudotuberculosis undergoes transcriptional reprogramming with drastic down-regulation of T3SS virulence genes during persistence when the pathogen resides within the cecum. more...
Organism:
Yersinia pseudotuberculosis YPIII
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18322
7 Samples
Download data: TXT
Series
Accession:
GSE55292
ID:
200055292
7.

Transcriptomic and phenotypic analysis reveals new functions for the Tat pathway in Yersinia pseudotuberculosis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Yersinia pseudotuberculosis; Yersinia pseudotuberculosis IP 32953
Type:
Expression profiling by array
Platform:
GPL15095
16 Samples
Download data: TAB, TXT
Series
Accession:
GSE80532
ID:
200080532
8.

Transcriptomic and phenotypic analysis reveals new functions for the Tat pathway in Yersinia pseudotuberculosis [dtatC-vs-ip_37C-stat]

(Submitter supplied) The Twin-arginine translocation (Tat) system promotes secretion of folded proteins that in bacteria are identified via an N-terminal signal peptide. Tat systems are associated with virulence in many bacterial pathogens and our previous studies revealed that Tat deficient Yersinia pseudotuberculosis was severely attenuated for virulence. However, in silico predictions did not reveal any obvious virulence factors among the potential Tat substrates encoded by Y. more...
Organism:
Yersinia pseudotuberculosis; Yersinia pseudotuberculosis IP 32953
Type:
Expression profiling by array
Platform:
GPL15095
4 Samples
Download data: TAB, TXT
Series
Accession:
GSE80531
ID:
200080531
9.

Transcriptomic and phenotypic analysis reveals new functions for the Tat pathway in Yersinia pseudotuberculosis [dtatC-vs-ip_37C-log]

(Submitter supplied) The Twin-arginine translocation (Tat) system promotes secretion of folded proteins that in bacteria are identified via an N-terminal signal peptide. Tat systems are associated with virulence in many bacterial pathogens and our previous studies revealed that Tat deficient Yersinia pseudotuberculosis was severely attenuated for virulence. However, in silico predictions did not reveal any obvious virulence factors among the potential Tat substrates encoded by Y. more...
Organism:
Yersinia pseudotuberculosis; Yersinia pseudotuberculosis IP 32953
Type:
Expression profiling by array
Platform:
GPL15095
4 Samples
Download data: TAB, TXT
Series
Accession:
GSE80530
ID:
200080530
10.

Transcriptomic and phenotypic analysis reveals new functions for the Tat pathway in Yersinia pseudotuberculosis [dtatC-vs-ip_26C-stat]

(Submitter supplied) The Twin-arginine translocation (Tat) system promotes secretion of folded proteins that in bacteria are identified via an N-terminal signal peptide. Tat systems are associated with virulence in many bacterial pathogens and our previous studies revealed that Tat deficient Yersinia pseudotuberculosis was severely attenuated for virulence. However, in silico predictions did not reveal any obvious virulence factors among the potential Tat substrates encoded by Y. more...
Organism:
Yersinia pseudotuberculosis IP 32953; Yersinia pseudotuberculosis
Type:
Expression profiling by array
Platform:
GPL15095
4 Samples
Download data: TAB, TXT
Series
Accession:
GSE80529
ID:
200080529
11.

Transcriptomic and phenotypic analysis reveals new functions for the Tat pathway in Yersinia pseudotuberculosis [dtatC-vs-ip_26C-log]

(Submitter supplied) The Twin-arginine translocation (Tat) system promotes secretion of folded proteins that in bacteria are identified via an N-terminal signal peptide. Tat systems are associated with virulence in many bacterial pathogens and our previous studies revealed that Tat deficient Yersinia pseudotuberculosis was severely attenuated for virulence. However, in silico predictions did not reveal any obvious virulence factors among the potential Tat substrates encoded by Y. more...
Organism:
Yersinia pseudotuberculosis; Yersinia pseudotuberculosis IP 32953
Type:
Expression profiling by array
Platform:
GPL15095
4 Samples
Download data: TAB, TXT
Series
Accession:
GSE80528
ID:
200080528
12.

Genome-wide Assessment of Antimicrobial Tolerance in Yersinia pseudotuberculosis Under Ciprofloxacin Stress

(Submitter supplied) Yersinia pseudotuberculosis is a Gram-negative bacterium capable of causing gastrointestinal infection and is closely related to the highly virulent plague bacillus Yersinia pestis. Infection by both species are currently treatable with antibiotics such as ciprofloxacin, a quinolone-class drug of major clinical importance in the treatment of many other infections. Our current understanding of the mechanism of action of ciprofloxacin is that it inhibits DNA replication by targeting DNA gyrase, and that resistance is primarily due to mutation at this target site, along with generic efflux and detoxification strategies. more...
Organism:
Yersinia pseudotuberculosis IP 32953
Type:
Other
Platform:
GPL27002
3 Samples
Download data: TXT
Series
Accession:
GSE135236
ID:
200135236
13.

Transciptional profile of Escherichia coli O157:H7 TUV93-0 inhibitor mutants in MEM-HEPES

(Submitter supplied) Tpx, FolX and WrbA were identified as a targets for type 3 secretion inhibititors in pull-down assays.The transcriptional profile of Escherichia coli O157:H7 and isogenic mutants grown in MEM-HEPES were determined.
Organism:
Escherichia coli O157:H7; Escherichia coli
Type:
Expression profiling by array
Platform:
GPL3051
4 Samples
Download data: GPR, TXT
Series
Accession:
GSE23001
ID:
200023001
14.

Loss of CNFy toxin-induced inflammation drives Yersinia pseudotuberculosis into persistency

(Submitter supplied) Gastrointestinal infections caused by enteric yersiniae can become persistent and complicated by relapsing enteritis and severe autoimmune disorders. To establish a persistent infection, the bacteria have to cope with hostile surroundings when they transmigrate through the intestinal epithelium and colonize underlying gut-associated lymphatic tissues. How the bacteria gain a foothold in the face of host immune responses is poorly understood. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
18 Samples
Download data: TAB, XLS
Series
Accession:
GSE98802
ID:
200098802
15.

Hemochromatosis drives acute lethal intestinal responses to hyper-yersiniabactin-producing Yersinia pseudotuberculosis

(Submitter supplied) Hemachromatosis (iron-overload) increases host susceptibility to siderophilic bacterial infections that cause serious complications, but the underlying mechanisms remain elusive. The present study demonstrates that oral infection with hyper-yersiniabactin (Ybt) producing Yersinia pseudotuberculosis Δfur mutant (termed Δfur) results in severe systemic infection and acute mortality to hemochromatotic mice due to rapid disruption of the intestinal barrier. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
9 Samples
Download data: TXT
Series
Accession:
GSE180888
ID:
200180888
16.

Inflammatory monocytes promote granuloma control of Yersinia infection

(Submitter supplied) Granulomas are organized immune cell aggregates formed in response to chronic infection or antigen persistence. The bacterial pathogen Yersinia pseudotuberculosis (Yp) blocks innate inflammatory signalling and immune defence, inducing neutrophil-rich pyogranulomas (PGs) within lymphoid tissues. Here we uncover that Yp also triggers PG formation within the murine intestinal mucosa. Mice lacking circulating monocytes fail to form defined PGs, have defects in neutrophil activation and succumb to Yp infection. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
9 Samples
Download data: XLSX
Series
Accession:
GSE194334
ID:
200194334
17.

Enteric pathogens induce tissue tolerance and prevent neuronal loss from subsequent infections

(Submitter supplied) The enteric nervous system (ENS) controls several intestinal functions including motility and nutrient handling, which can be disrupted by infection-induced neuropathies or neuronal cell death. We investigated possible tolerance mechanisms preventing neuronal loss and disruption in gut motility after pathogen exposure. We found that following enteric infections, muscularis macrophages (MMs) acquire a tissue-protective phenotype that prevents neuronal loss and dysmotility during subsequent challenge with unrelated pathogens. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
12 Samples
Download data: XLSX
Series
Accession:
GSE182294
ID:
200182294
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=3|qty=7|blobid=MCID_66a36e9f57bd0c1190abe02e|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Support Center