U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 20

1.

RNA sequencing provides exquisite insight into the manipulation of the alveolar macrophage by tubercle bacilli

(Submitter supplied) Mycobacterium bovis, the agent of bovine tuberculosis, causes an estimated $3 billion annual losses to global agriculture due, in part, to the limitations of current diagnostics. Development of next-generation diagnostics requires a greater understanding of the interaction between the pathogen and the bovine host. Therefore, to explore the early response of the alveolar macrophage to infection, we report the first application of RNA-sequencing to define, in exquisite detail, the transcriptomes of M. more...
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15749
78 Samples
Download data: TXT, XLSX
Series
Accession:
GSE62506
ID:
200062506
2.

The bovine alveolar macrophage (bAM) DNA methylome is resilient to infection with Mycobacterium bovis

(Submitter supplied) Whole genome bisulfite sequencing (WGBS) was used to assess the effect of M. bovis infection on the bAM DNA methylome (5-methylcytosine). The methylomes of bAM infected with M. bovis (n = 8) were compared to those of non-infected control bAM (n = 8) at 24 hours post-infection (hpi). No differences in DNA methylation (CpG or non-CpG) were observed between control and infected bAM. Analysis of DNA methylation at proximal promoter regions uncovered >250 genes harbouring intermediately methylated (IM) promoters (average methylation = 33–66%). more...
Organism:
Bos taurus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL19172
16 Samples
Download data: TXT
Series
Accession:
GSE110412
ID:
200110412
3.

Whole-transcriptome, high-throughput RNA sequence analysis of the bovine macrophage response to Mycobacterium bovis infection in vitro

(Submitter supplied) Background: Mycobacterium bovis, the causative agent of bovine tuberculosis, is an intracellular pathogen that can persist inside host macrophages during infection via a diverse range of mechanisms that subvert the host immune response. In the current study, we have analysed and compared the transcriptomes of M. bovis-infected monocyte-derived macrophages (MDM) purified from six Holstein-Friesian females with the transcriptomes of non-infected control MDM from the same animals over a 24 h period using strand-specific RNA sequencing (RNA-seq). more...
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15750
14 Samples
Download data: TXT, XLSX
Series
Accession:
GSE45439
ID:
200045439
4.

MicroRNA analysis of the bovine alveolar macrophage response to Mycobacterium bovis infection suggests pathogen survival is enhanced by miRNA regulation of endocytosis and lysosome trafficking

(Submitter supplied) Purpose: The goal of this RNA-seq study was to profile changes in miRNA expression in bovine alveolar macrophages isolated from Holstein-Friesian and challenged with M. bovis over a 48 hour time course. Background: Mycobacterium bovis, the causative agent of bovine tuberculosis, is a major infectious disease problem for global agriculture, resulting in losses of billions of Euros annually. The bacterium spreads via an airborne route and is taken up by alveolar macrophages in the lung. more...
Organism:
Bos taurus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL15749
88 Samples
Download data: TXT
Series
Accession:
GSE58883
ID:
200058883
5.

Initial host response to mycobacterial infection is orchestrated through H3K4 methylation-mediated RNA polymerase II binding at key immune function genes.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Bos taurus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL23295 GPL19172
30 Samples
Download data: BW, TXT
Series
Accession:
GSE116734
ID:
200116734
6.

Initial  host  response to mycobacterial infection is orchestrated through H3K4 methylation-mediated RNA polymerase II binding at key immune function genes [miRNA-seq]

(Submitter supplied) Massive reprogramming of the host alveolar macrophage transcriptome occurs during the initial stages of tuberculosis. In bovine tuberculosis, Mcobacterium bovis can persist and replicate within alveolar macrophages through varied mechanisms to subvert or exploit host immune responses ( REF). To determine how these transcriptional changes are regulated we performed ChIPseq analysis of H3K4 and H3K27 methylation, established histone tail markers associated with permissive and repressive chromatin states, respectively. more...
Organism:
Bos taurus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL19172
8 Samples
Download data: TXT
Series
Accession:
GSE116733
ID:
200116733
7.

Initial  host  response to mycobacterial infection is orchestrated through H3K4 methylation-mediated RNA polymerase II binding at key immune function genes [RNA-seq]

(Submitter supplied) Massive reprogramming of the host alveolar macrophage transcriptome occurs during the initial stages of tuberculosis. In bovine tuberculosis, Mcobacterium bovis can persist and replicate within alveolar macrophages through varied mechanisms to subvert or exploit host immune responses ( REF). To determine how these transcriptional changes are regulated we performed ChIPseq analysis of H3K4 and H3K27 methylation, established histone tail markers associated with permissive and repressive chromatin states, respectively. more...
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23295
8 Samples
Download data: TXT
Series
Accession:
GSE116732
ID:
200116732
8.

Initial  host  response to mycobacterial infection is orchestrated through H3K4 methylation-mediated RNA polymerase II binding at key immune function genes [ChIP-seq]

(Submitter supplied) Massive reprogramming of the host alveolar macrophage transcriptome occurs during the initial stages of tuberculosis. In bovine tuberculosis, Mcobacterium bovis can persist and replicate within alveolar macrophages through varied mechanisms to subvert or exploit host immune responses ( REF). To determine how these transcriptional changes are regulated we performed ChIPseq analysis of H3K4 and H3K27 methylation, established histone tail markers associated with permissive and repressive chromatin states, respectively. more...
Organism:
Bos taurus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL23295
14 Samples
Download data: BW
Series
Accession:
GSE116731
ID:
200116731
9.

Comparison of antigen stimulation response in Mycobacterium bovis-infected vs. control cattle using BOTL-5 microarray

(Submitter supplied) Bovine tuberculosis (BTB) caused by Mycobacterium bovis continues to cause substantial losses to global agriculture and has significant repercussions for human health. The advent of high throughput genomics has facilitated large scale gene expression analyses that present a novel opportunity for revealing the molecular mechanisms underlying chronic mycobacterial infection. Using this approach, we have previously shown that innate immune genes in peripheral blood mononuclear cells (PBMC) from BTB-infected animals are repressed in vivo in the absence of exogenous stimulation. more...
Organism:
Bos taurus
Type:
Expression profiling by array
Platform:
GPL5751
36 Samples
Download data: GPR
Series
Accession:
GSE12835
ID:
200012835
10.

Global gene expression of bovine monocyte-derived macrophages in response to in vitro challenge with Mycobacterium bovis

(Submitter supplied) Background: Mycobacterium bovis, the causative agent of bovine tuberculosis, is a major cause of mortality in global cattle populations. Macrophages are among the first cells types to encounter M. bovis following exposure and the response elicited by these cells is pivotal in determining the outcome of infection. Here, a functional genomics approach was undertaken to investigate global gene expression profiles in bovine monocyte-derived macrophages (MDM) purified from seven age-matched non-related females, in response to in vitro challenge with M. more...
Organism:
Bos taurus
Type:
Expression profiling by array
Platform:
GPL2112
49 Samples
Download data: CEL
Series
Accession:
GSE33309
ID:
200033309
11.

Genome-wide transcriptional profiling of peripheral blood leukocytes from cattle infected with Mycobacterium bovis

(Submitter supplied) Background: Mycobacterium bovis is the causative agent of bovine tuberculosis (BTB), a pathological infection with significant economic impact. Recent studies have highlighted the role of functional genomics to better understand the molecular mechanisms governing the host immune response to M. bovis infection. Furthermore, these studies may enable the identification of novel transcriptional markers of BTB that can augment current diagnostic tests and surveillance programmes. more...
Organism:
Bos taurus
Type:
Expression profiling by array
Platform:
GPL2112
16 Samples
Download data: CEL
Series
Accession:
GSE33359
ID:
200033359
12.

RNA-seq transcriptional profiling of peripheral blood leukocytes from cattle infected with Mycobacterium bovis

(Submitter supplied) In the present study, we have analyzed the peripheral blood leukocyte (PBL) transcriptome of eight natural M. bovis-infected and eight age- and sex-matched non-infected control Holstein-Friesian animals using RNA-seq. In addition, we compared gene expression profiles generated using RNA-seq with those previously generated using the high-density Affymetrix® GeneChip® Bovine Genome Array platform from the same PBL-extracted RNA
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15750
16 Samples
Download data: TXT, XLSX
Series
Accession:
GSE60265
ID:
200060265
13.

Comparison of Mycobacterium bovis-infected cattle versus control non-infected cattle using the BOTL-5 microarray

(Submitter supplied) Background: Bovine tuberculosis is an enduring disease of cattle that has significant repercussions for human health. The advent of high-throughput functional genomics technologies has facilitated large-scale analyses of the immune response to this disease that will ultimately lead to novel diagnostics and therapeutic targets. Analysis of mRNA abundance in peripheral blood mononuclear cells (PBMC) from six Mycobacterium bovis infected cattle and six non-infected controls was performed. more...
Organism:
Bos taurus
Type:
Expression profiling by array
Platform:
GPL5751
12 Samples
Download data: GPR
Series
Accession:
GSE8857
ID:
200008857
14.

Transcriptional response of bovine macrophages after infection with two Argentinean Mycobacterium bovis isolates

(Submitter supplied) Infection of cattle with Mycobacterium bovis causes severe financial hardship in many countries, in addition to presenting a health risk for humans. As an intracellular pathogen, M. bovis, adapted to survive and thrive within the intramacrophage environment. However, little is known about expression patterns in the macrophage, particularly in the bovine host. In this study, DNA microarray analysis was used to detect genes expressed in Holstein bovine macrophages derived from peripheral blood mononuclear cells infected during four hours with two Argentinean strains of M. more...
Organism:
Bos taurus
Type:
Expression profiling by array
Platform:
GPL2112
10 Samples
Download data: CEL
Series
Accession:
GSE39819
ID:
200039819
15.

Transcriptional response of bovine moncocyte-derived macrophages to infection with strains of Mycobacterium bovis and Mycobacterium avium subspecies paratuberculosis

(Submitter supplied) Mycobacterium bovis (M. bovis) and Mycobacterium avium subspecies paratuberculosis (MAP) are important pathogens of cattle, causing bovine tuberculosis and Johne’s disease respectively. M. bovis and MAP infect residential macrophages in the lung and intestines respectively and subvert the macrophage biology to create a survival niche. To investigate this interaction we simultaneously studied the transcriptional response of bovine monocyte-derived macrophages to infection with two strains of M. more...
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11153
80 Samples
Download data: TXT
Series
Accession:
GSE104211
ID:
200104211
16.

Transcriptional profiling of disease progression in bovine tuberculosis and the identification of potential diagnostic biomarkers

(Submitter supplied) The definition of biomarkers correlating with disease progression could have impact on the rational design of novel diagnostic approaches for bovine tuberculosis in cattle. We have used the advantages of the murine model to identify promising candidates in the host transcriptome post-infection. RNA from BALB/c splenocytes and lung cells after aerogenic Mycobacterium bovis infection were with high-density microarrays to defining biomarkers of disease progression. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
25 Samples
Download data: TXT
Series
Accession:
GSE33058
ID:
200033058
17.

Transcriptome microRNA profiling of bovine mammary epithelial cells challenged with Escherichia coli or Staphylococcus aureus bacteria reveals pathogen directed microRNA expression profiles

(Submitter supplied) Purpose: The goal of this study is to explore the role of miRNAs in dairy cow response to E. coli and S. aureus, mastitis causing pathogens, is not well understood. Results: The global expression of miRNAs in bovine mammary epithelial cells (MAC-T cells) challenged with heat-inactivated Staphylococcus aureus (S. aureus) or Escherichia coli (E. coli) bacteria (treatments: 6, 12, 24 and 48 hr) and without challenge (control: 0, 6, 12, 24 and 48 hr) was profiled using next-generation-sequencing. more...
Organism:
Bos taurus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL17875
13 Samples
Download data: TXT
Series
Accession:
GSE51979
ID:
200051979
18.

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
19.

Transcription analysis of the porcine alveolar macrophage (PAM) response to co-infection of porcine reproductive and respiratory syndrome virus (PRRSV) and M. hyopneumoniae (Mhp)

(Submitter supplied) Investigation of whole genome gene expression level changes in porcine alveolar macrophage response to co-infection of PRRSV and M. hyopneumoniae The results in this study will be further described in Bin li et al., 2013. BMC genomics.
Organism:
Sus scrofa
Type:
Expression profiling by array
Platform:
GPL17577
24 Samples
Download data: PAIR
Series
Accession:
GSE49882
ID:
200049882
20.

Profiling microRNA expression in bovine alveolar macrophages using RNA-seq

(Submitter supplied) In this study, we determined the miRNA expression profile of bovine alveolar macrophages, using next-generation sequencing strategy. On an Illumina HiSeq 2000 machine, we sequenced 8 miRNA libraries, prepared from small RNA fractions of alveolar macrophages isolated from 8 different healthy animals (Bos taurus). From the data, the potential novel miRNAs were predicted, and the expression levels of the known miRNAs were determined. more...
Organism:
Bos taurus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL15749
8 Samples
Download data: TXT
Series
Accession:
GSE41138
ID:
200041138
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=3|qty=5|blobid=MCID_66d1ebfab1cb767cd2ea47c0|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Support Center