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Items: 1 to 20 of 198

1.

Transposon Insertion Sequencing to study the genetic interactions between V. cholerae WT cells and two mutant strains in absence or presence of subinhibitory doses of tobramycin

(Submitter supplied) This study was conducted to study which genes or functions become important or expendable in two V. cholerae mutants compared to the WT. This was assessed directly by conjugating a Mariner Transposon with WT or mutant cells and obtaining a bank of hundreds of thousands of mutants which we consider as the T=0. We then subjected these banks to 16 generations in rich media with or without 50% MIC of tobramycin (which we call T=16gen). more...
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
Type:
Other
Platform:
GPL32053
27 Samples
Download data: XLSX
Series
Accession:
GSE198341
ID:
200198341
2.

Gene expression profile of Vibrio cholerae N16961 grown in various conditions of culture

(Submitter supplied) To investigate the effect of conditions of culture on gene expression in Vibrio cholerae N16961 We then performed gene expression profiling analysis using data obtained from RNA-seq of 4 conditions of culture in biological duplicate
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30088
8 Samples
Download data: XLSX
Series
Accession:
GSE214813
ID:
200214813
3.

V. cholerae transcriptome or deleted for the tgt gene in MH, supplemented or not with tobramycin or ciprofloxacin

(Submitter supplied) We study gene expression levels of V. cholerae N16961 WT and tgt mutant strains in MH medium in the presence or not of sublethal concentration on tobramycin or ciprofloxacin
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30088
18 Samples
Download data: XLSX
Series
Accession:
GSE214520
ID:
200214520
4.

V. cholerae transcriptome in MH, supplemented or not with glucose 0.4% or maltose 0.4%

(Submitter supplied) We study gene expression levels of V. cholerae N16961 WT and crp mutant strains/V. cholerae N16961 hapR+ corrected strain, ravAviA mutant and ravAviA overexpressing strains in exponential phase in MH, MH+maltose 0.4% and MH+glucose 0.4%
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30088
45 Samples
Download data: TXT
Series
Accession:
GSE196651
ID:
200196651
5.

A mannose-sensing AraC-type transcriptional activator regulates intestinal colonization of Vibrio cholerae

(Submitter supplied) In this study, we show that ManR (VC1825) activates the transcription of the mannose operon in M9 medium supplemented with fructose or mannose, and when manR is impaired Vibrio cholerae cells fail to colonize the intestine and host survival is significantly prolonged in a fruit fly Drosophila melanogaster infection model. To identify other target genes of ManR, transcriptome analysis was performed in wild-type V. more...
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
Type:
Expression profiling by high throughput sequencing
Platform:
GPL31160
8 Samples
Download data: XLSX
Series
Accession:
GSE192900
ID:
200192900
6.

V. cholerae transcriptome without treatment and with indole or sub-MIC tobramycin

(Submitter supplied) We study gene expression levels of V. cholerae N16961 hapR+ corrected strain in exponential phase without and with indole or tobramycin.
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30088
9 Samples
Download data: TXT
Series
Accession:
GSE182561
ID:
200182561
7.

Transcriptional response to overexpressing Vibrio Seventh Pandemic -II island encoded genes

(Submitter supplied) Purpose: to characterize the regulatory targets of an AraC-like transcriptional regulator (VC0513) encoded on the Vibrio Seventh Pandemic Island -II (VSP-II) in V. cholerae O1 El Tor N16961 Methods: RNA was isolated from a wild-type N16961 carrying an IPTG-inducible copy of vc0513, vc0515, or an empty vector control Results: vc0513 induction significantly increased expression of other VSP-II encoded genes relative to the empty vector control Conclusions: our study represents the first analysis of a transcriptional regulator encoded on the VSP-II island
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30088
9 Samples
Download data: TXT, XLSX
Series
Accession:
GSE174028
ID:
200174028
8.

Zur-dependent zinc starvation response in Vibrio cholerae N16961

(Submitter supplied) Zur is a transcription factor that represses zinc starvation response genes under zinc-rich conditions. Our goal was to identify candidate Zur-regulated genes by looking for transcripts significantly upregulated in the absence of Zur.
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30088
6 Samples
Download data: CSV, TXT
Series
Accession:
GSE173966
ID:
200173966
9.

RNA-Seq for identification of differntially expressed genes by VxrB(D78E) overexpression

(Submitter supplied) Bactericidal antibiotics are powerful drugs because they not only inhibit essential bacterial functions, but convert them into toxic processes. Many bacteria are remarkably tolerant against antibiotics, due to inducible damage repair responses. How these responses promote whole population tolerance in important human pathogens is poorly understood. The two-component system VxrAB of the diarrheal pathogen Vibrio cholerae, a model system for tolerance against cell wall damaging (e.g., beta-lactam) antibiotics, is required for high-level beta-lactam tolerance. more...
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26987
6 Samples
Download data: GFF, XLSX
Series
Accession:
GSE135010
ID:
200135010
10.

Genome-wide screening of VxrB binding sites in Vibrio cholerae

(Submitter supplied) Bactericidal antibiotics are powerful drugs because they not only inhibit essential bacterial functions, but convert them into toxic processes. Many bacteria are remarkably tolerant against antibiotics, due to inducible damage repair responses. How these responses promote whole population tolerance in important human pathogens is poorly understood. The two-component system VxrAB of the diarrheal pathogen Vibrio cholerae, a model system for tolerance against cell wall damaging (e.g., beta-lactam) antibiotics, is required for high-level beta-lactam tolerance. more...
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26987
8 Samples
Download data: GFF, XLSX
Series
Accession:
GSE135009
ID:
200135009
11.

MerR and ChrR mediate blue light induced photo-oxidative stress response at the transcriptional level in Vibrio cholerae

(Submitter supplied) Blue light (BL) is a major environmental factor that affects the physiology, behavior, and infectivity of bacteria as it contributes to the generation of reactive oxygen species (ROS) while increasing photo-oxidative stress in cells. However, precise photo-oxidative response mechanism in non-phototrophic bacteria is yet to be elucidated. In this study, we investigated the effect of BL in Vibrio cholerae by using genetics and transcriptome profiling. more...
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21692
14 Samples
Download data: XLSX
Series
Accession:
GSE79911
ID:
200079911
12.

Genome-wide ParB2-DNA and RctB-DNA interaction analyses in Vibrio cholerae

(Submitter supplied) Replication and segregation are the two main processes that maintain chromosomes in growing cells. In bacteria, replication and transcription have been proposed to provide motive force in chromosome segregation. Recently, ParB2, a segregation protein, encoded by V. cholerae chromosome II (chrII) was also found to influence chrII replication. V. cholerae chrII replication is primarily controlled by its specific initiator protein, RctB. more...
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961; Vibrio cholerae
Type:
Genome binding/occupancy profiling by array
Platform:
GPL20909
8 Samples
Download data: TXT
Series
Accession:
GSE72978
ID:
200072978
13.

Vibrio cholerae N16961 cpxA*

(Submitter supplied) Transcriptional profiling comparing a V. cholerae cpxA* mutant relative to WT at an OD600 of 1.
Organism:
Vibrio cholerae; Vibrio cholerae O1 biovar El Tor str. N16961
Type:
Expression profiling by array
Platform:
GPL3651
6 Samples
Download data: GPR
Series
Accession:
GSE55037
ID:
200055037
14.

Vibrio cholerae N16961 overexpression of CpxR

(Submitter supplied) Transcriptionnal profiling comparing a V. Choleare ∆cpxR mutant harboring either (pBAD33-cpxR) or empty (pBAD33) grown for 1h under inducing conditions.
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
Type:
Expression profiling by array
Platform:
GPL3651
4 Samples
Download data: TXT
Series
Accession:
GSE54081
ID:
200054081
15.

Expression analysis of Vibrio cholerae O395N1 delta-nqrA-F mutant

(Submitter supplied) Investigation of whole genome gene expression level changes in a Vibrio cholerae O395N1 delta-nqrA-F mutant, compared to the wild-type strain.
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961; Vibrio cholerae
Type:
Expression profiling by array
Platform:
GPL18506
3 Samples
Download data: PAIR
Series
Accession:
GSE56387
ID:
200056387
16.

Effect of cFP on gene expression in Vibiro cholerae

(Submitter supplied) Vibrio cholerae is a Gram negative, motile, facultative anaerobic bacterium, and the causative agent of cholera, a severe diarrhoeal disease, which untreated can rapidly lead to dehydration, hypotensive shock, and death. Cholera is a significant human disease that is estimated to affect 3-5 million people each year. The mechanism by which V. cholerae regulates virulence gene expression in vivo is unknown, but a number of studies have suggested that low molecular weight signally molecules may be important in modulating gene expression. more...
Organism:
Vibrio cholerae O1 biovar El Tor str. N16961; Vibrio cholerae
Type:
Expression profiling by array
Platform:
GPL15619
4 Samples
Download data: MEV
Series
Accession:
GSE38272
ID:
200038272
17.

Transcriptional analysis of a Vibrio choleare rpoH mutant vs wild-type after a heat-shock

(Submitter supplied) Vibrio cholerae, the cause of cholera, can grow in a variety of environments outside of human hosts. During infection, the pathogen must adapt to significant environmental alterations, including the elevated temperature of the human gastrointestinal tract. σ32, an alternative sigma factor encoded by rpoH, activates transcription of genes involved in the heat-shock response in several bacterial species. more...
Organism:
Vibrio cholerae; Vibrio cholerae O1 biovar El Tor str. N16961
Type:
Expression profiling by array
Platform:
GPL3651
6 Samples
Download data: TXT
Series
Accession:
GSE6097
ID:
200006097
18.

Illumina NovaSeq 6000 (Vibrio cholerae O1 biovar El Tor str. N16961)

Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
1 Series
27 Samples
Download data
Platform
Accession:
GPL32053
ID:
100032053
19.

Illumina NextSeq 500 (Vibrio cholerae O1 biovar El Tor str. N16961)

Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
1 Series
8 Samples
Download data
Platform
Accession:
GPL31160
ID:
100031160
20.

Illumina HiSeq 2000 (Vibrio cholerae O1 biovar El Tor str. N16961)

Organism:
Vibrio cholerae O1 biovar El Tor str. N16961
6 Series
95 Samples
Download data
Platform
Accession:
GPL30088
ID:
100030088
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