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Links from GEO DataSets

Items: 16

1.

Mycobacterium tuberculosis Requires Phosphate-Responsive Gene Regulation to Resist Host Immunity

(Submitter supplied) Mycobacterium tuberculosis persists in the lungs of mammalian hosts despite inducing an immune response dominated by the macrophage-activating cytokine interferon-gamma (IFN-gamma). We identified the M. tuberculosis phosphate uptake system component PstA1 as a factor required to resist IFN-gamma dependent immunity. A ∆pstA1 mutant was fully virulent in IFN-gamma-/- mice but was attenuated in mice lacking the IFN-gamma-inducible nitric oxide synthase (NOS2). more...
Organism:
Mycobacterium tuberculosis CDC1551; Mycobacterium tuberculosis H37Rv; Mycobacterium tuberculosis str. Erdman = ATCC 35801
Type:
Expression profiling by array
Platform:
GPL15398
11 Samples
Download data: GPR
Series
Accession:
GSE36998
ID:
200036998
2.

Mycobacterium tuberculosis Phosphate Uptake System Component PstA2 is Not Required for Gene Regulation or Virulence

(Submitter supplied) The Mycobacterium tuberculosis genome encodes two complete high-affinity Pst phosphate-specific transporters. We previously demonstrated that a membrane-spanning component of one Pst system, PstA1, was essential both for M. tuberculosis virulence and for regulation of gene expression in response to external phosphate availability. To determine if the alternative Pst system is similarly required for virulence or gene regulation, we constructed a deletion of pstA2. more...
Organism:
Mycobacterium tuberculosis str. Erdman = ATCC 35801; Mycobacterium tuberculosis CDC1551; Mycobacterium tuberculosis H37Rv
Type:
Expression profiling by array
Platform:
GPL15398
6 Samples
Download data: GPR
Series
Accession:
GSE83812
ID:
200083812
3.

Mycobacterium tuberculosis Lsr2 is a global transcriptional regulator required for adaptation to changing oxygen levels and virulence

(Submitter supplied) To survive a dynamic host environment, Mycobacterium tuberculosis must endure a series of challenges from reactive oxygen and nitrogen stress, to drastic shifts in oxygen availability. The mycobacterial Lsr2 protein has been implicated in reactive oxygen defense via direct protection of DNA. To examine the role of Lsr2 in pathogenesis and physiology of M. tuberculosis, we generated a strain deleted for lsr2. more...
Organism:
Mycobacterium tuberculosis; Mycobacterium tuberculosis CDC1551; Mycobacterium tuberculosis H37Rv
Type:
Expression profiling by array
Platform:
GPL15398
16 Samples
Download data: GPR
Series
Accession:
GSE57948
ID:
200057948
4.

Phosphate depletion: A novel trigger for Mycobacterium tuberculosis persistence

(Submitter supplied) These data represent the global gene expression profile of Mycobacterium tuberculosis after 24 hrs and 72 hrs of inorganic phosphate starvation. Differentially regulated genes appear to include those encoding proteins involved in adaptation to phosphate starvation, namely those involved in phosphate regulation and phosphate assimilation, as well as those involved in the stringent response.
Organism:
Mycobacterium tuberculosis H37Rv; Mycobacterium tuberculosis CDC1551
Type:
Expression profiling by array
Platform:
GPL8189
6 Samples
Download data: TXT
Series
Accession:
GSE14840
ID:
200014840
5.

The carbonic anhydrase inhibitor ethoxzolamide inhibits the Mycobacterium tuberculosis PhoPR regulon and Esx-1 secretion and attenuates virulence

(Submitter supplied) The purpose of this study was to examine how ethoxzolamide modulates gene M. tuberculosis gene expression at acidic pH. We observed that ethoxzolamide downregulates genes of the PhoPR regulon.
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17879
8 Samples
Download data: TXT
Series
Accession:
GSE63917
ID:
200063917
6.

Transcriptional profiling of Mycobacterium tuberculosis Rv3852 (hns) knockout mutant

(Submitter supplied) A handful of nucleoid-associated proteins (NAPs) regulate the vast majority of genes in a bacterial cell. H-NS, the Histone-like Nucleoid-Structuring protein, is one of these NAPs and protects Escherichia coli from foreign gene expression. Though lacking any sequence similarity with E. coli H-NS, Rv3852 was annotated as the H-NS ortholog in Mycobacterium tuberculosis, as it resembles human histone H1. more...
Organism:
Mycobacterium tuberculosis H37Rv
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17280
4 Samples
Download data: TXT
Series
Accession:
GSE95181
ID:
200095181
7.

Transcriptomic analysis of Mtb H37Rv and MtbΔwhiB3 at pH 4.5

(Submitter supplied) Since WhiB3 expression was shown to be maximally upregulated at pH 4.5 and MtbΔwhiB3 was shown to be defective in survival in Ph 4.5, we did microarray at pH 4.5 so as to study comprehensive role of WhiB3 in regulating gene expression at acidic Ph
Organism:
Mycobacterium tuberculosis H37Rv
Type:
Expression profiling by array
Platform:
GPL16972
7 Samples
Download data: TXT
Series
Accession:
GSE61579
ID:
200061579
8.

In-vivo Gene Signatures of Mycobacterium tuberculosis In C3HeB/FeJ Mice

(Submitter supplied) In-vivo Gene Signatures of Mycobacterium tuberculosis In C3HeB/FeJ Mice
Organism:
Mycobacterium tuberculosis CDC1551; Mycobacterium tuberculosis H37Rv
Type:
Expression profiling by array
Platform:
GPL18320
12 Samples
Download data: GPR
Series
Accession:
GSE70765
ID:
200070765
9.

Mycobacterium tuberculosis H37Rv (WT) versus Mut1 and Comp1

(Submitter supplied) Transcriptional profiling of H37Rv (WT), Mut1 and Comp1 bacteria under aerobic (Aer/0 day, i.e 0 D) and hypoxic conditions (Hyp/5 days standing culture, i.e 5 D). Mut1: H37Rv carrying devR gene disruption by in frame insertion of kanamycin resistance cassette and expressing DevRN-Kan fusion protein. Comp1: Mut1 complemented with low copy number plasmid carrying devR gene expressed from its native constitutive upstream promoter. more...
Organism:
Mycobacterium tuberculosis H37Rv
Type:
Expression profiling by array
Platform:
GPL13729
17 Samples
Download data: TXT
Series
Accession:
GSE30264
ID:
200030264
10.

Mycobacterium tuberculosis transcription factor, EmbR regulates expression of virulence factors that aid in ex vivo and in vivo survival

(Submitter supplied) We report RNAseq analysis of Mycobacterium tuberculosis strain that lack transcription factor EmbR and the isogenic wild type. We identify the genes whose expression is altred by the mutation and show that genes associated with virulende are downregulated in EmbR KO cells.
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27507
8 Samples
Download data: TXT
Series
Accession:
GSE154673
ID:
200154673
11.

Mycobacterium tuberculosis transcriptional responses to acidic pH and carbon source

(Submitter supplied) The purpose of this study was to examine how Mtb integrates acidic pH and available carbon sources as environmental cues to regulate its metabolism and growth rate. RNA-seq transcriptional profiling of M. tuberculosis growing at acidic or neutral pH, in pyruvate or glycerol, was examined. These studies identified carbon source-dependent and -independent pH-dependent adaptations.
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17879
8 Samples
Download data: XLS
Series
Accession:
GSE52020
ID:
200052020
12.

M. tuberculosis Rv3263 Knockout

(Submitter supplied) We determine gene expression profile for the knockout of Rv3263 (DNA Methyltransferase) and compared to wildtype M. tuberculosis.
Organism:
Mycobacterium tuberculosis H37Rv
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17967
2 Samples
Download data: TXT, WIG
Series
Accession:
GSE52551
ID:
200052551
13.

Analysis of the effects of the methyltransferase encoded by Rv3263 on gene expression in M. tuberculosis

(Submitter supplied) DNA methylation affects gene expression in many organisms. To determine to effects of DNA methylation on gene expression in M. tuberculosis, we genetically deleted a predicted DNA methyltransferase encoded by Rv3263 and subjected wildtype, mutant, and complemented strains to global expression analysis.
Organism:
Mycobacterium tuberculosis H37Rv
Type:
Expression profiling by array
Platform:
GPL17082
9 Samples
Download data: CEL
Series
Accession:
GSE46432
ID:
200046432
14.

M. tuberculosis transcriptional profile of delta pepD strain vs wild-type strain

(Submitter supplied) pepD is regulated by a 2CS, MprAB, and impacts upon the regulation of sigE, an important M.tb sigma factor. Here we examine the global impact of gene regulation in a delta pepD mutant strain.
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by array
Platform:
GPL5774
5 Samples
Download data: TXT
Series
Accession:
GSE17587
ID:
200017587
15.

Cholesterol's effect on M. tuberculosis

(Submitter supplied) 2 experiments: (1) Mtb, Tween vs Cholesterol at 3 & 24hrs (2) CDC1551 vs kstR mutant of CDC1551, with and w/o Cholesterol
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by array
Platform:
GPL4057
12 Samples
Download data: GPR
Series
Accession:
GSE13978
ID:
200013978
16.

Mycobacterium tuberculosis TraSH experiment: Growth in wild type C57BL/6J versus iNOS-/- mice

(Submitter supplied) A M. tuberculosis transposon library was used to infect WT and iNOS-/- mice. Surviving mutants were recovered from spleens, genomic DNA was extracted, and labeled probes were synthesized from transposon ends. Probes from each WT mouse were hybridized with probes from a similar iNOS-/- mouse.
Organism:
Mycobacterium tuberculosis
Type:
Other
Platform:
GPL9051
26 Samples
Download data: GPR
Series
Accession:
GSE17706
ID:
200017706
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