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Links from GEO DataSets

Items: 7

1.

Comparative transcriptome analysis of Brucella canis MucR mutant strain and its parent strain RM6/66

(Submitter supplied) Purpose:To uncover the related mechanisms underlie virulence attenuation of Brucella canis MucR mutant strain. Methods:Three Brucella canis RM6/66 strains and three Brucella canis ΔmucR strains were grown in TSB at 37℃ until the log phase was reached, total RNA was isolated using the TRIzol according to the manufacturer’s instructions.The sequencing library of each RNA sample was prepared by using NEB Next Ultra Directional RNA Library Prep Kit for Illumina as recommended by the manufacturer. more...
Organism:
Brucella canis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28970
6 Samples
Download data: TXT
Series
Accession:
GSE155748
ID:
200155748
2.

Expression Data from Brucella abortus strain 2308 and isogenic mucR mutant cells

(Submitter supplied) MucR is one of the few transcriptional regulatory proteins that has been linked to Brucella pathogenesis. We used custom-made Affymetrix B. abortus strain 2308 derived GeneChips to copare the gene expression properties of wild type and isogenic mucR mutant cells.
Organism:
Brucella abortus
Type:
Expression profiling by array
Platform:
GPL15577
4 Samples
Download data: CEL, CHP
Series
Accession:
GSE40532
ID:
200040532
3.

Brucella MucR acts as an H-NS-like protein to silence virulence genes and structure the nucleoid 

(Submitter supplied) Histone-like nucleoid structuring (H-NS) and H-NS-like proteins serve as global gene silencers and work with antagonistic transcriptional activators (counter- silencers) to properly coordinate the expression of virulence genes in pathogenic bacteria. In Brucella, MucR has been proposed as a novel H-NS-like gene silencer, but direct experimental evidence is lacking. Here, we show that MucR serves as an H-NS-like silencer of the Brucella abortus genes encoding the polar autotransporter adhesins BtaE and BmaC, the c-di-GMP-specific phosphodiesterase BpdB, and the quorum-sensing regulator BabR. more...
Organism:
Brucella abortus 2308
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other
Platform:
GPL33491
12 Samples
Download data: CSV, TXT
Series
Accession:
GSE234935
ID:
200234935
4.

Comparative transcriptome analysis of artificially induced rough-type Brucella strain RM57 and its parent strain

(Submitter supplied) Purpose: To uncover the related mechanisms underlie virulence attenuation of RM57 vaccine candidate. Methods: Three Brucella melitensis M1981 strains and three Brucella melitensis RM57 strains were grown in TSB at 37℃ until the log phase was reached, total RNA was isolated using the TRIzol according to the manufacturer’s instructions.The sequencing library of each RNA sample was prepared by using NEB Next Ultra Directional RNA Library Prep Kit for Illumina as recommended by the manufacturer.The HiSeq 4000 platform was used to perform the transcriptome sequencing. more...
Organism:
Brucella melitensis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26681
6 Samples
Download data: TXT
Series
Accession:
GSE131394
ID:
200131394
5.

Transcripyome analysis of Brucella melitensis 16M and otpR mutant using Solexa/Illumina platform

(Submitter supplied) We sequenced the mRNA of Brucella melitensis 16M and otpR mutant under acid stress to identify genes that were regulated by regulator OtpR.
Organism:
Brucella melitensis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17325
2 Samples
Download data: TXT, XLS
Series
Accession:
GSE48165
ID:
200048165
6.

ChIP-seq analyses of 10 quorum sensing regulators in Pseudomonas aeruginosa

(Submitter supplied) The Pseudomonas aeruginosa quorum-sensing (QS) systems contribute to bacterial homeostasis and pathogenicity. Although many regulators have been characterized to control the production of virulence factors and QS signaling molecules, its detailed regulatory mechanisms still remain elusive. Here, we performed chromatin immunoprecipitation followed by high-throughput DNA sequencing (ChIP-seq) on 10 key QS regulators. more...
Organism:
Pseudomonas aeruginosa
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18644
20 Samples
Download data: TXT
Series
Accession:
GSE65356
ID:
200065356
7.

RNA-seq analysis of stimulated canine macrophage by Brucella canis

(Submitter supplied) A lot of attempts have been made to understand the immunopathological mechanisms of Brucella canis infection because of the importance of the disease in both public and clinical aspects. However, previous mechanisms are not still revealed. Therefore, in vitro models, which mimic to in vivo infection route using a canine epithelial cell, D17 cell, and a canine macrophage, DH82 cell, was used to solve the clues by analysis of transcriptomes in the cells. more...
Organism:
Canis lupus familiaris
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25760
14 Samples
Download data: FPKM_TRACKING
Series
Accession:
GSE134331
ID:
200134331
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