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Items: 1 to 20 of 216

1.

Transcriptional changes associated with chemical induction of adenylyl cyclase activity in Mtb

(Submitter supplied) Goal: Assess transcriptional changes in Mtb associated with activation of adenylyl cyclase activity in the bacterium, by treatment with the Rv1625c agonist V-59 or activation of the TetOn-cAMP construct. Specifically, address changes in transcription of cholestrrol utilization genes, during growth of Mtb in cholesterol media. Method: WT, Rv1625c knockout, and Rv1625c Complement strains of Mtb were grown in cholesterol-based media and treated with V-59 or vehicle control (DMSO). more...
Organism:
Mycobacterium tuberculosis CDC1551
Type:
Expression profiling by high throughput sequencing
Platform:
GPL31090
16 Samples
Download data: TXT
Series
Accession:
GSE190875
ID:
200190875
2.

AC2P20 selectively kills M. tuberculosis at acidic pH by depleting free thiols

(Submitter supplied) In this study, AC2P20 was prioritized for continued study to test the hypothesis that it was targeting Mtb pathways associated with pH-driven adaptation. RNAseq transcriptional profiling studies showed AC2P20 modulates expression of genes associated with redox-homeostasis. Gene enrichment analysis revealed that the AC2P20 transcriptional profile had significant overlap with a previously characterized pH-selective inhibitor, AC2P36. more...
Organism:
Mycobacterium tuberculosis CDC1551
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20114
4 Samples
Download data: XLSX
Series
Accession:
GSE151884
ID:
200151884
3.

Mycobacterium tuberculosis Sensor Kinase DosS Modulates the Autophagosome in a DosR-independent Manner

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mycobacterium tuberculosis; Homo sapiens; Mycobacterium tuberculosis H37Rv; Mycobacterium tuberculosis CDC1551; Macaca mulatta
Type:
Expression profiling by array
Platforms:
GPL10183 GPL18320
14 Samples
Download data: TXT
Series
Accession:
GSE118869
ID:
200118869
4.

Mycobacterium tuberculosis Sensor Kinase DosS Modulates the Autophagosome in a DosR-independent Manner [II]

(Submitter supplied) Transcriptional profiling of bacterial RNA samples from infected Rhesus Bone Marrow Derived Macrophages (RhBMDMs) compared to RNA isolated from respective in vitro grwon cultures viz M. tuberculosis H37Rv or Isogeneic mutant MtbdosS
Organism:
Mycobacterium tuberculosis; Mycobacterium tuberculosis H37Rv; Mycobacterium tuberculosis CDC1551
Type:
Expression profiling by array
Platform:
GPL18320
6 Samples
Download data: TXT
Series
Accession:
GSE118867
ID:
200118867
5.

Targeting Mycobacterium tuberculosis Sensitivity to Thiol Stress at Acidic pH Kills the Bacterium and Potentiates Antibiotics

(Submitter supplied) The purpose of this study was to characterize the mechanism of action of the small molecule AC2P36
Organism:
Mycobacterium tuberculosis CDC1551
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20114
8 Samples
Download data: XLSX
Series
Accession:
GSE89106
ID:
200089106
6.

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 CDC1551; Mycobacterium tuberculosis H37Rv; Mycobacterium tuberculosis str. Erdman = ATCC 35801
Type:
Expression profiling by array
Platform:
GPL15398
6 Samples
Download data: GPR
Series
Accession:
GSE83812
ID:
200083812
7.

A Lysosomal In Vitro Exposure (LivE) Model to Identify Pathways Critical for Mycobacterium tuberculosis Intracellular Persistence

(Submitter supplied) Increasing experimental evidence supports that Mycobacterium tuberculosis (Mtb) has evolved strategies to survive within the lysosomes from activated macrophages, which may represent a reservoir for persistent mycobacteria. To further our knowledge in Mtb response to the lysosomal environment, we profiled the global transcriptional activity of Mtb in a lysosomal in vitro exposure (LivE) model. At inhibitory conditions of lysosomal SF (iLivE), which did not kill but arrested mycobacterial replication thereby mimicking persistence, Mtb expresses a unique transcriptome, where genes involved in general stress response, metabolic reprogramming, cell wall remodeling, respiration, oxidative stress and dormancy response were found to be significantly modulated. more...
Organism:
Mycobacterium tuberculosis CDC1551
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20114
15 Samples
Download data: TXT
Series
Accession:
GSE68337
ID:
200068337
8.

Elucidating the effects of the macrophage environment on the efficacy of anti-mycobacterial drugs

(Submitter supplied) We examined the transcriptional responses of intracellular M. tuberculosis exposed to different front-line drugs during macrophage infection. Our data reveal that Mtb experiences amplification of multiple host-derived pressures following drug exposure. The stresses from the host environment have a dominant impact on Mtb gene expression to the extent that the transcriptional profiles cluster according to environment, ie. more...
Organism:
Mycobacterium tuberculosis; Mycobacterium tuberculosis CDC1551
Type:
Expression profiling by array
Platform:
GPL19382
40 Samples
Download data: TXT
Series
Accession:
GSE62942
ID:
200062942
9.

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
10.

Accumulation of inorganic polyphosphate mediates metabolic downshift and antibiotic tolerance in Mycobacterium tuberculosis

(Submitter supplied) The stringent response, involving the regulatory molecules inorganic polyphosphate (poly P) and (p)ppGpp, is believed to mediate Mycobacterium tuberculosis persistence. In this study, we identified a novel exopolyphosphatase responsible for poly P hydrolysis. Using two different poly P-accumulating M. tuberculosis recombinant strains, we found that increased poly P content drives the organisms into early growth arrest, and contributes to tolerance to the cell wall-active agent isoniazid, increased resistance to stress conditions, and improved survival in macrophages. more...
Organism:
Mycobacterium tuberculosis CDC1551
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18715
9 Samples
Download data: TXT
Series
Accession:
GSE57868
ID:
200057868
11.

The Mycobacterium tuberculosis Clp Gene Regulator is Required for in vitro Reactivation from Hypoxia-induced Dormancy

(Submitter supplied) The isogenic Mtb:ΔRv2745c mutant is significantly more sensitive normoxia conditions after a period of hypoxia, relative to wild-type Mtb, implicating a role for ClgR in response to reactivation, in vivo. Both hypoxia and reaeration treatment led to dysregulation of the σH regulon in the isogenic mutant, Mtb:ΔRv2745c. Induction of clgR in Mtb did lead to Clp protease induction, indicating that clgR plays a role in differntially activating downstream genes in a condition dependent manner. more...
Organism:
Mycobacterium tuberculosis CDC1551; Mycobacterium tuberculosis H37Rv
Type:
Expression profiling by array
Platform:
GPL18320
54 Samples
Download data: GPR
Series
Accession:
GSE64065
ID:
200064065
12.

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 CDC1551; Mycobacterium tuberculosis H37Rv; Mycobacterium tuberculosis
Type:
Expression profiling by array
Platform:
GPL15398
16 Samples
Download data: GPR
Series
Accession:
GSE57948
ID:
200057948
13.

The Mycobacterium tuberculosis Rv2745c Plays an Important Role in Responding to Redox Stress

(Submitter supplied) The Rv2745c (clgR) gene encodes a Clp protease gene regulator that is induced in response to a variety of stress conditions and potentially plays a role in Mtb pathogenesis. The isogenic Mtb:ΔRv2745c mutant is significantly more sensitive to in vitro redox stress generated by diamide, relative to wild-type Mtb, implicating a role for ClgR in the management of intraphagosomal redox stress. Redox stress led to dysregulation of the σH regulon in the isogenic mutant, Mtb:ΔRv2745c. more...
Organism:
Mycobacterium tuberculosis CDC1551; Mycobacterium tuberculosis H37Rv
Type:
Expression profiling by array
Platform:
GPL18320
27 Samples
Download data: GPR
Series
Accession:
GSE55817
ID:
200055817
14.

Transcriptome analysis of M.tuberculosis using RNA-seq indicates WhiB6 repression of dormancy associated genes

(Submitter supplied) Tuberculosis is an infectious disease, with latent infection with Mycobacterium tuberculosis (M.tb) affecting 1/3 of humanity. It can remain quiescent for long time, making eradication very difficult. To do so, M.tb need to carefully orchestrate its gene expression to survive immune response and starvation but still be able to reactivate to enable transmission to new hosts. Here we used whole transcriptome deep sequencing to compare gene expression between wild type M.tb and a strain with its whiB6, a gene encoding a putative redox-sensing transcription factor, disrupted by a transposon. more...
Organism:
Mycobacterium tuberculosis CDC1551
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16065
6 Samples
Download data: TXT
Series
Accession:
GSE40941
ID:
200040941
15.

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 str. Erdman = ATCC 35801; Mycobacterium tuberculosis CDC1551; Mycobacterium tuberculosis H37Rv
Type:
Expression profiling by array
Platform:
GPL15398
11 Samples
Download data: GPR
Series
Accession:
GSE36998
ID:
200036998
16.

Mycobacterium tuberculosis CDC1551 WT/sigI mutant

(Submitter supplied) Transcription profile of WT compare to sigma factor sigI deletion mutant at OD1 and OD2.
Organism:
Mycobacterium tuberculosis; Mycobacterium tuberculosis CDC1551
Type:
Expression profiling by array
Platform:
GPL15148
2 Samples
Download data: GPR
Series
Accession:
GSE35231
ID:
200035231
17.

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
18.

The unique roles of DosT and DosS in DosR regulon induction and Mycobacterium tuberculosis dormancy

(Submitter supplied) In Mycobacterium tuberculosis, the sensor kinases DosT and DosS activate the transcriptional regulator DosR, resulting in the induction of the DosR regulon, important for anaerobic survival and perhaps latent infection. The individual and collective roles of these sensors has been postulated biochemically, but their roles have remained unclear in vivo. This work demonstrates distinct and additive roles for each sensor during anaerobic dormancy. more...
Organism:
Mycobacterium tuberculosis H37Rv; Mycobacterium tuberculosis CDC1551
Type:
Expression profiling by array
Platform:
GPL8768
36 Samples
Download data: GPR
Series
Accession:
GSE16811
ID:
200016811
19.

BCG vaccine strains lack narK2 and narX induction and exhibit altered phenotypes during dormancy

(Submitter supplied) Mycobacterium tuberculosis is the causative agent of tuberculosis, a disease that affects one-third of the world’s population. The sole extant vaccine for tuberculosis is the live attenuated Mycobacterium bovis bacille Calmette-Guerin (BCG). We examined 13 representative BCG strains from around the world to ascertain their ability to express DosR-regulated dormancy antigens. These are known to be recognized by T-cells of M. more...
Organism:
Mycobacterium tuberculosis variant bovis; Mycobacterium tuberculosis H37Rv; Mycobacterium tuberculosis variant bovis BCG; Mycobacterium tuberculosis CDC1551
Type:
Expression profiling by array
Platform:
GPL6807
30 Samples
Download data: TXT
Series
Accession:
GSE11315
ID:
200011315
20.

Illumina NextSeq 500 (Mycobacterium tuberculosis CDC1551)

Organism:
Mycobacterium tuberculosis CDC1551
1 Series
16 Samples
Download data
Platform
Accession:
GPL31090
ID:
100031090
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