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Links from GEO DataSets

Items: 20

1.

RNA sequencing of nasal lavage samples from mock- and Streptococcus pneumoniae-infected infant and adult mice

(Submitter supplied) Acute respiratory infections (ARI), which generally begin with colonization of the mucosal surfaces of the upper respiratory tract (URT), are a leading cause of morbidity and mortality with the highest rate in infants. As a common colonizer of the URT, and one of the most prevalent causes of life-threatening infections in the pediatric population, Streptococcus pneumoniae (Spn) was used as a model pathogen to investigate the effect of age during URT infection. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
35 Samples
Download data: BW, CSV
Series
Accession:
GSE116604
ID:
200116604
2.

Type I and type III interferons drive redundant amplification loops to induce a transcriptional signature in influenza-infected airway epithelia

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
62 Samples
Download data: CEL
Series
Accession:
GSE43710
ID:
200043710
3.

Expression data from Influenza A infected mouse primary tracheal epithelial cell cultures (MTEC), from both wild-type and MAVS-/- mice

(Submitter supplied) We used microarrays to detail the global programme of gene expression in response to Influenza A (PR8) infection
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL, TXT
Series
Accession:
GSE43709
ID:
200043709
4.

Expression data from Influenza A infected mouse primary tracheal epithelial cell cultures (MTEC), from wild-type, IFNAR1-/-, IL28Ra-/- and IFNAR1-/- IL28Ra-/- double ko

(Submitter supplied) We used microarrays to detail the global programme of gene expression in response to Influenza A (PR8) infection
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
40 Samples
Download data: CEL, TXT
Series
Accession:
GSE43708
ID:
200043708
5.

Expression data from Influenza A infected mouse primary tracheal epithelial cell cultures (MTEC)

(Submitter supplied) We used microarrays to detail the global programme of gene expression in response to Influenza A (PR8) infection
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
10 Samples
Download data: CEL, TXT
Series
Accession:
GSE43707
ID:
200043707
6.

Transport of influenza A virus neuraminidase to host cell surface and virus replication are regulated by ARHGAP21 and Cdc42

(Submitter supplied) Influenza virus neuraminidase (NA), a type II transmembrane glycoprotein, is transported to the virus assembly site at the plasma membrane and is a major viral envelope component that plays a critical role in the release of progeny virions and in determination of host range restriction. Although signals/sequences in NA for translocation, sorting and raft association have been identified, little is known about the host factors that are involved in regulating the intracellular and cell surface transport of NA. more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Non-coding RNA profiling by genome tiling array
Platform:
GPL14715
6 Samples
Download data: CALLS, PAIR
Series
Accession:
GSE32878
ID:
200032878
7.

Characterization of the host defense against influenza virus infection and a secondary bacterial pneumonia infection

(Submitter supplied) Secondary bacterial infections (‘superinfection’) are a major reason for excessive mortality and hospitalizations during influenza virus infections. Here we present a longitudinal study of gene-expression changes in murine lungs during superinfection, with an initial influenza A virus (IAV) infection and a subsequent S. pneumonia (SP) infection. In addition to the well characterized impairment of the innate immune response, we identified superinfection-specific alterations in endothelial functions, including rapid downregulation in angiogenic activity and vascular regulators. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
51 Samples
Download data: CSV
Series
Accession:
GSE206534
ID:
200206534
8.

Influenza-induced inflammation drives pneumococcal otitis media

(Submitter supplied) Influenza A virus (IAV) predisposes individuals to secondary infections with the bacterium Streptococcus pneumoniae (the pneumococcus). Infections may manifest as pneumonia, sepsis, meningitis or otitis media (OM). It remains controversial as to whether secondary pneumococcal disease is due to the induction of an aberrant immune response or IAV induced immunosuppression. Moreover, as the majority of studies have been performed in the context of pneumococcal pneumonia, it remains unclear how far these findings can be extrapolated to other pneumococcal disease phenotypes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL15887
12 Samples
Download data: PAIR
Series
Accession:
GSE41098
ID:
200041098
9.

Inflammation induced by influenza virus impairs innate control of human pneumococcal carriage

(Submitter supplied) Secondary bacterial pneumonia following influenza infection is a significant cause of mortality worldwide. Upper respiratory tract pneumococcal carriage is important as both determinants of disease and population transmission. The immunological mechanisms that contain pneumococcal carriage are well-studied in mice but remain unclear in humans. Loss of this control of carriage following influenza infection is associated with secondary bacterial pneumonia during seasonal and pandemic outbreaks. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
96 Samples
Download data: CSV
10.

Predictive signature of murine and human host response to typical and atypical pneumonia

(Submitter supplied) Using gene expression data we developed a predictive signture to discriminate between typical bacterial, atyipcal bacterial, and viral pnuemonia in murine samples and validated it against open source human datasets.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL8321
126 Samples
Download data: CEL
Series
Accession:
GSE214051
ID:
200214051
11.

Systemic approaches reveal anti-adipogenic signals at the onset of obesity–related inflammation in white adipose tissue [ChIP-seq]

(Submitter supplied) HFD feeding induces a rapid adipocyte progenitors (APs) proliferation in visceral adipose tissue (vWAT), followed by a block of differentiation. In contrast, subcutaneous adipose tissue (scWAT), in obesity, undergoes trans-differentiation of beige adipocytes to white and, consequently, a hyperplastic growth at later stages. We performed ChIP-seq to profile RNA pol II recruitment and the global epigenetic changes of H3K4me1 and H3K27Ac induced by HFD feeding.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
96 Samples
Download data: BW
Series
Accession:
GSE132726
ID:
200132726
12.

Systemic approaches reveal anti-adipogenic signals at the onset of obesity–related inflammation in white adipose tissue [RNA-seq]

(Submitter supplied) HFD feeding induces a rapid adipocyte progenitors (APs) proliferation in visceral adipose tissue (vWAT), followed by a block of differentiation. In contrast, subcutaneous adipose tissue (scWAT), in obesity, undergoes trans-differentiation of beige adipocytes to white and, consequently, a hyperplastic growth at later stages. We performed RNA-seq to investigate the global transcriptomic changes induced by HFD feeding
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
72 Samples
Download data: TXT
Series
Accession:
GSE132706
ID:
200132706
13.

Characterization of antibiotic resistance and host-microbiome interactions in the human upper respiratory tract during influenza infection

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
human metagenome
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL26213 GPL26212
69 Samples
Download data
Series
Accession:
GSE126902
ID:
200126902
14.

Characterization of antibiotic resistance and host-microbiome interactions in the human upper respiratory tract during influenza infection [RNA-Seq]

(Submitter supplied) Antibiotic resistance genes expressed in the upper respiratory tract of patients infected with influenza viruses were associated with the microbial community and microbial activities. Interactions between the host systemic responses to influenza infection and ARG expression highlight the importance of antibiotic resistance in viral-bacterial co-infection.
Organism:
human metagenome
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26213
35 Samples
Download data: TXT
Series
Accession:
GSE126901
ID:
200126901
15.

Characterization of antibiotic resistance and host-microbiome interactions in the human upper respiratory tract during influenza infection [16s rRNA gene V4 region]

(Submitter supplied) Antibiotic resistance genes expressed in the upper respiratory tract of patients infected with influenza viruses were associated with the microbial community and microbial activities. Interactions between the host systemic responses to influenza infection and ARG expression highlight the importance of antibiotic resistance in viral-bacterial co-infection.
Organism:
human metagenome
Type:
Other
Platform:
GPL26212
34 Samples
Download data: HDF5
Series
Accession:
GSE126900
ID:
200126900
16.

Characterization of antibiotic resistance and host-microbiome interactions in the human upper respiratory tract during influenza infection [human host RNA-seq]

(Submitter supplied) Antibiotic resistance genes expressed in the upper respiratory tract of patients infected with influenza viruses were associated with the microbial community and microbial activities. Interactions between the host systemic responses to influenza infection and ARG expression highlight the importance of antibiotic resistance in viral-bacterial co-infection.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
56 Samples
Download data: TSV
17.

An in vivo atlas of host-pathogen transcriptomes during Streptococcus pneumoniae colonization and disease

(Submitter supplied) D’Mello et al. detail host-pathogen interaction gene expression profiles of Streptococcus pneumoniae (Spn) and its infected host at disease relevant anatomical sites using mice as experimental models. The authors identify the core and organ-specific transcriptomes of Spn, show that bacterial and host gene expression profiles are highly distinct during asymptomatic colonization versus disease-causing infection, and demonstrate that Spn and host genes with high levels of expression contribute to pathogenesis or host defense, respectively.
Organism:
Mus musculus; Streptococcus pneumoniae
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL28625 GPL21103 GPL22283
44 Samples
Download data: TXT
Series
Accession:
GSE150788
ID:
200150788
18.

Epithelial cells maintain memory of prior infection with Streptococcus pneumoniae through di-methylation of histone H3

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL16791 GPL17692
27 Samples
Download data: BW, CEL, NARROWPEAK
Series
Accession:
GSE230142
ID:
200230142
19.

Epithelial cells maintain memory of prior infection with Streptococcus pneumoniae through di-methylation of histone H3 [ChIPseq]

(Submitter supplied) Epithelial cells are the first point of contact for bacteria entering the respiratory tract. Streptococcus pneumoniae is an obligatory human pathobiont of the nasal mucosa, carried asymptomatically but also the cause of severe pneumoniae. The role of the epithelium in maintaining homeostatic interactions or mounting an inflammatory response to invasive S. pneumoniae is currently poorly understood. However, studies have shown that chromatin modifications, at the histone level, induced by bacterial pathogens interfere with the host transcriptional program and promote infection. In this study, we demonstrate that S. pneumoniae actively induces di-methylation of histone H3 on lysine 4 (H3K4me2), which persists for at least 9 days upon clearance of bacteria with antibiotics. We show that infection establishes a unique epigenetic program affecting the transcriptional response of epithelial cells, rendering them more permissive upon secondary infection. Our results establish H3K4me2 as a unique modification induced by infection, distinct from H3K4me3, which localizes to enhancer regions genome-wide. Therefore, this study reveals evidence that bacterial infection leaves a memory in epithelial cells after bacterial clearance, in an epigenomic mark, thereby altering cellular responses for subsequent infections.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
15 Samples
Download data: BW, NARROWPEAK
Series
Accession:
GSE230141
ID:
200230141
20.

Epithelial cells maintain memory of prior infection with Streptococcus pneumoniae through di-methylation of histone H3 [Affymetrix]

(Submitter supplied) Epithelial cells are the first point of contact for bacteria entering the respiratory tract. Streptococcus pneumoniae is an obligatory human pathobiont of the nasal mucosa, carried asymptomatically but also the cause of severe pneumoniae. The role of the epithelium in maintaining homeostatic interactions or mounting an inflammatory response to invasive S. pneumoniae is currently poorly understood. However, studies have shown that chromatin modifications, at the histone level, induced by bacterial pathogens interfere with the host transcriptional program and promote infection. In this study, we demonstrate that S. pneumoniae actively induces di-methylation of histone H3 on lysine 4 (H3K4me2), which persists for at least 9 days upon clearance of bacteria with antibiotics. We show that infection establishes a unique epigenetic program affecting the transcriptional response of epithelial cells, rendering them more permissive upon secondary infection. Our results establish H3K4me2 as a unique modification induced by infection, distinct from H3K4me3, which localizes to enhancer regions genome-wide. Therefore, this study reveals evidence that bacterial infection leaves a memory in epithelial cells after bacterial clearance, in an epigenomic mark, thereby altering cellular responses for subsequent infections. Transcriptome analysis aimed at testing whether cells respond differently in the primary (1°) and secondary (2°) infection. Differential gene expression and gene set enrichment analysis performed.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17692
12 Samples
Download data: CEL
Series
Accession:
GSE230138
ID:
200230138
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