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Links from GEO DataSets

Items: 20

1.

Transcriptional Profile of Mycobacterium tuberculosis Replicating in Human Type II Alveolar Epithelial A549 cell line

(Submitter supplied) Infection with Mycobacterium tuberculosis (M. tb) is initiated when an aerosol droplet carrying a few bacilli is inhaled into an alveolus. Alveolar epithelial cells (AEC) (type II and type I) are among the first cells encountered by the infecting bacteria and greatly outnumber macrophages in the alveolus. M. tb replicates dramatically (>20,000 fold) in a “non-migrating” compartment in the lung prior to the development of the cell-mediated immune response in aerosol-infected mice (Wolf AJ, 2008). more...
Organism:
Mycobacterium tuberculosis; Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4057
6 Samples
Download data: GPR
Series
Accession:
GSE58466
ID:
200058466
2.

Transcriptional profiling of Mycobacterium tuberculosis H37Rv in whole blood from HIV- and HIV+ individuals

(Submitter supplied) Mycobacterium tuberculosis (M. tb), the cause of tuberculosis (TB), utilizes the blood circulation to spread systemically and establish infection, and the risk of developing active TB (pulmonary and extrapulmonary) is significantly increased in individuals infected with human immunodeficiency virus (HIV). In this work, we have used DNA microarray analysis to investigate the transcriptome of M. tb replicating in human whole blood from both HIV-negative and HIV-positive donors compared to M. more...
Organism:
Mycobacterium tuberculosis H37Rv; Mycobacterium tuberculosis
Type:
Expression profiling by array
Platform:
GPL4057
24 Samples
Download data: GPR
Series
Accession:
GSE49760
ID:
200049760
3.

Trancriptional Profile of Mycobacterium tuberculosis Replicating at in Artificial Intraocular Fluid

(Submitter supplied) Intraocular tuberculosis (IOTB) is a significant cause of visual morbidity in TB-endemic countries. However, pathogenesis of Mycobacterium tuberculosis (M. tb) in the ocular compartment is poorly defined. IOTB is paucibacillary in a vast majority of patients although M. tb has been detected in both the retinal pigment epithelial (RPE) cells (Rao et al. 2006) and in the intraocular fluid (IOF) (Aggarwal et al., 2016; Bajgai et al., 2017) in some cases. more...
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by array
Platform:
GPL4057
6 Samples
Download data: GPR
Series
Accession:
GSE216603
ID:
200216603
4.

Mycobacterium tuberculosis and macrophage response

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by array
Platform:
GPL4057
33 Samples
Download data: GPR
Series
Accession:
GSE7963
ID:
200007963
5.

The global transcriptional profile of Mycobacterium tuberculosis during human macrophages infection

(Submitter supplied) During lung infection Mycobacterium tuberculosis (Mtb) resides in macrophages and subverts the bactericidal mechanisms of these professional phagocytes. In this work we have analyzed by DNA microarray technique the global transcription profile of Mtb infecting primary human macrophages in order to identify putative bacterial pathogenic factors that can be relevant for the intracellular survival of Mtb. more...
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by array
Platform:
GPL4057
11 Samples
Download data: GPR
Series
Accession:
GSE6209
ID:
200006209
6.

Genome-Wide Expression Profiling Identifies Type 1 Interferon Response Pathways in Active Tuberculosis

(Submitter supplied) Whole-genome expression profiling on a cohort of TB patients. Tuberculosis patients above 15 years of age were recruited from an outpatient tuberculosis clinic in central Jakarta (Indonesia). Randomly selected control subjects with the same sex and age (+/-10%) were recruited from neighboring households, with first degree relatives excluded.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6883
71 Samples
Download data: TXT
Series
Accession:
GSE56153
ID:
200056153
7.

The Mycobacterium tuberculosis ECF sigma Factor sE: role in global gene expression and survival in macrophages

(Submitter supplied) In previously published work, we identified three Mycobacterium tuberculosis sigma (s) factor genes responding to heat shock (sigB, sigE and sigH ). Two of them (sigB and sigE ) also responded to SDS exposure. As these responses to stress suggested that the s factors encoded by these genes could be involved in pathogenicity, we are studying their role in physiology and virulence. In this work, we characterize a sigE mutant of M. more...
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by array
Platform:
GPL2787
15 Samples
Download data: TXT
Series
Accession:
GSE8664
ID:
200008664
8.

AmpliSeq Transcriptome Analysis of Human Alveolar and Monocyte-Derived Macrophages Over Time in Response to Mycobacterium tuberculosis infection

(Submitter supplied) Human alveolar macrophages (HAM) are primary bacterial niche and immune response cells during Mycobacterium tuberculosis (M.tb) infection, and human blood monocyte-derived macrophages (MDM) are a model for investigating M.tb-macrophage interactions. Here, we use a targeted RNA-Seq method to measure transcriptome-wide changes in RNA expression patterns of freshly obtained HAM (used within 6 h) and 6 day cultured MDM upon M.tb infection over time (2, 24 and 72 h), in both uninfected and infected cells from three donors each. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL17303
36 Samples
Download data: TXT
Series
Accession:
GSE114371
ID:
200114371
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.

The influence of reduced oxygen availability on gene expression in Laboratory (H37Rv) and clinical strains (S7 and S10) of Mycobacterium tuberculosis

(Submitter supplied) Mycobacterium tuberculosis has the ability to persist within the host in a clinically latent stage. One important condition believed to contribute to latency is reduced access to oxygen but the response of M. tuberculosis to hypoxia is partially characterized. Virtually all dormant models against tuberculosis the vaccine tested in animals used laboratory strains H37Rv or Erdman strains. But major outbreaks of TB occur with the strains that have widely different genotypes and phenotypes compare to H37Rv. more...
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by array
Platform:
GPL18388
9 Samples
Download data: TXT
Series
Accession:
GSE55863
ID:
200055863
11.

Alveolar macrophages from tuberculosis patients display an altered inflammatory gene expression profile

(Submitter supplied) Alveolar macrophages (AMs) are major targets of Mycobacterium tuberculosis (Mtb) infection, critical during the progression of active tuberculosis (TB). The complex immunopathology of TB generates diverse microenvironments in the lung, which shape immune responses by AMs. In the current study, we perform whole genome microarray transcriptional profiling on RNA isolated from AMs from TB patients (AMsTB) compared to AMs from control subjects (AMsCT) using bronchoalveolar lavage (BAL). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
7 Samples
Download data: TXT
Series
Accession:
GSE98750
ID:
200098750
12.

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
13.

Transcriptional profile of Mycobacterium tuberculosis in an in vitro model of intraocular tuberculosis

(Submitter supplied) We studied M. tuberculosis transcriptome by whole genome microarray for the identification of key pathogenic determinants that are involved in the pathogenesis of intraocular tuberculosis.
Organism:
Mycobacterium tuberculosis; Mycobacterium tuberculosis H37Rv
Type:
Expression profiling by array
Platform:
GPL25141
8 Samples
Download data: TXT
Series
Accession:
GSE115292
ID:
200115292
14.

Response of M. tuberculosis to 8 hour exposure to vitamin C

(Submitter supplied) Transcriptional profiling of M.tuberculosis to 10 mM vitamin C at 8 h. This was compared to gene expression profile of untreated M. tuberculosis culture.
Organism:
Mycobacterium tuberculosis H37Rv
Type:
Expression profiling by array
Platform:
GPL18055
7 Samples
Download data: TXT
Series
Accession:
GSE60376
ID:
200060376
15.

Transcriptional profile of Beijing/East-Asian Mycobacterium tuberculosis isolates

(Submitter supplied) Transcriptional profile comparison among Beijing and non-Beijing M. tuberculosis isolates.
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by array
Platform:
GPL8893
6 Samples
Download data: TXT
Series
Accession:
GSE83677
ID:
200083677
16.

Mycobacterium tuberculosis gene expression during adaptation to stationary phase and low-oxygen dormancy

(Submitter supplied) The innate mechanisms used by Mycobacterium tuberculosis to persist during periods of non-proliferation are central to understanding the physiology of the bacilli during latent disease. We have used whole genome expression profiling to expose adaptive mechanisms initiated by M. tuberculosis in two common models of M. tuberculosis non-proliferation. The first of these models was a standard growth curve in which gene expression changes were followed from exponential growth through the transition to stationary phase. more...
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by array
Platform:
GPL5714
54 Samples
Download data: TXT
Series
Accession:
GSE8786
ID:
200008786
17.

Human alveolar macrophage response to Mycobacterium tuberculosis: immune characteristics underlying large inter-individual variability.

(Submitter supplied) This is a replication study on human alveolar macrophages (HAMs) from a smaller cohort from South Africa in order to support the RNA data of a relatively larger cohort from the US (Ohio & Texas). In this replication cohort, using full RNA-seq, a substantial portion of significant differentially expressed RNAs overlap with those identified with Ampliseq from the larger cohort over time, yielding similar enriched functional terms, e.g., interferon, interleukin, and IDO1 signaling.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21290
30 Samples
Download data: XLSX
Series
Accession:
GSE223863
ID:
200223863
18.

Alveolar macrophage immunobiology and functional genomics: Unlocking human to human variation in host response to M. tuberculosis

(Submitter supplied) An innovative, high-throughput approach was proposed to identify key gene expression profiles and regulatory polymorphisms affecting innate immunity to TB by studying interactions between M.tb and human alveolar macrophages (AMs). We systematically analyzed interactions of a virulent M.tb strain with freshly isolated human AMs from 28 healthy adult donors, measuring host RNA expression and secreted candidate proteins associated with TB pathogenesis over 72h. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17303
124 Samples
Download data: TXT
19.

Mycobacterium tuberulosis H37Rv strains: Control vs. Chelerythrine

(Submitter supplied) Transcriptional profiling of Mycobacterium tuberculosis H37Rv strains comparing control DMSO treated strains with chelerythrine treated strains. Goal was to determine the effects of chelerythrine against Mycobacterium tuberculosis H37Rv strains.
Organism:
Mycobacterium tuberculosis; Mycobacterium tuberculosis H37Rv
Type:
Expression profiling by array
Platform:
GPL10895
2 Samples
Download data: PDF, TXT
Series
Accession:
GSE24035
ID:
200024035
20.

Reaeration timecourse from a defined hypoxia model

(Submitter supplied) Reaeration timecourse from a defined hypoxia model in Mycobacterium tuberculosis. The mechanism by which mycobacteria return to a replicating state upon re-exposure to favorable conditions is not well understood. In this study, we utilized reaeration from a defined hypoxia model to characterize the adaptive response of Mycobacterium tuberculosis (MTB) following a return to favorable growth conditions. more...
Organism:
Mycobacterium tuberculosis
Type:
Expression profiling by array
Platforms:
GPL10364 GPL4293 GPL5774
33 Samples
Download data: GPR
Series
Accession:
GSE21590
ID:
200021590
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