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Items: 1 to 20 of 420

1.

Ectopic expression of transcriptional regulatory proteins reveals two classes of late genes during chlamydial development, corresponding to the IB and EB cell type.

(Submitter supplied) The bacteria in the chlamydiales order are obligate intracellular parasites of eukaryotic cells. They are reliant on an infectious cycle consisting of at least three phenotypically distinct cell forms termed the reticulate body (RB), the intermediate body (IB) and the elementary body (EB). The EB is infectious but does not replicate. The RB replicates in the host cell but is non-infectious, while the IB is an intermediate form that transitions to the EB form. more...
Organism:
Chlamydia trachomatis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34870
8 Samples
Download data: TXT
Series
Accession:
GSE276506
ID:
200276506
2.

Euo is a developmental regulator that represses late genes and activates midcycle genes in C. trachomatis

(Submitter supplied) The pathogenic bacterium Chlamydia reproduces via an unusual intracellular developmental cycle in which it converts from a dividing form (reticulate body or RB) to an infectious form (elementary body or EB). The transcription factor Euo has been proposed as a developmental regulator in C. trachomatis because it repressed a number of late chlamydial promoters, which are transcribed during RB-to-EB conversion. more...
Organism:
Chlamydia trachomatis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL32238
18 Samples
Download data: XLSX
Series
Accession:
GSE202414
ID:
200202414
3.

Ectopic expression of transcriptional regulatory proteins reveals two classes of late genes during chlamydial development, corresponding to the IB and EB cell type.

(Submitter supplied) The bacteria in the chlamydiales order are obligate intracellular parasites of eukaryotic cells. They are reliant on an infectious cycle consisting of at least three phenotypically distinct cell forms termed the reticulate body (RB), the intermediate body (IB) and the elementary body (EB). The EB is infectious but does not replicate. The RB replicates in the host cell but is non-infectious, while the IB is an intermediate form that transitions to the EB form. more...
Organism:
Chlamydia trachomatis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28812
30 Samples
Download data: TXT
Series
Accession:
GSE262652
ID:
200262652
4.

Supermajority of Chlamydia trachomatis genes are activated during the first hour of infection

(Submitter supplied) The obligate intracellular bacterium Chlamydia has a unique developmental cycle that alternates between two contrasting cell types. With a hardy envelope and highly condensed genome, the small elementary body (EB) maintains limited metabolic activities yet can survive in an extracellular environment and is infectious. After entering host cells, EBs differentiate into larger and proliferating reticulate bodies (RBs). more...
Organism:
Chlamydia trachomatis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28812
12 Samples
Download data: TXT
Series
Accession:
GSE248988
ID:
200248988
5.

Transcriptomes of Chlamydia trachomatis L2 with Conditional GrgA deficiency

(Submitter supplied) To determine the role that GrgA plays in chlamydial physiology, we constructed a Chlamydia trachomatis mutant that we term L/cgad-peig, in which the chromosomal grgA (ctl0766 or ct504) has been disrupted by Targetron mutagenesis, and the plasmid carries an inducible grgA under the control of anhydrotetracycline (ATC). RNA-Seq analysis was performed for L2/cgad-peig grown with and without ATC.
Organism:
Chlamydia trachomatis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL32238
12 Samples
Download data: TXT
Series
Accession:
GSE234589
ID:
200234589
6.

Identification of the alternative sigma factor regulons of Chlamydia trachomatis using multiplexed CRISPR interference

(Submitter supplied) RNAseq analysis was performed for C. trachomatis serovar L2 after knocking down or overexpressing different sigma factors.
Organism:
Chlamydia trachomatis L2/434/Bu
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33362
48 Samples
Download data: XLSX
Series
Accession:
GSE230645
ID:
200230645
7.

Euo is a developmental regulator that represses late genes and activates midcycle genes in C. trachomatis

(Submitter supplied) The pathogenic bacterium Chlamydia reproduces via an unusual intracellular developmental cycle in which it converts from a dividing form (reticulate body or RB) to an infectious form (elementary body or EB). The transcription factor Euo has been proposed as a developmental regulator in C. trachomatis because it repressed a number of late chlamydial promoters, which are transcribed during RB-to-EB conversion. more...
Organism:
Chlamydia trachomatis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL32238
16 Samples
Download data: XLSX
Series
Accession:
GSE202416
ID:
200202416
8.

Euo is a developmental regulator that represses late genes and activates midcycle genes in C. trachomatis

(Submitter supplied) The pathogenic bacterium Chlamydia reproduces via an unusual intracellular developmental cycle in which it converts from a dividing form (reticulate body or RB) to an infectious form (elementary body or EB). The transcription factor Euo has been proposed as a developmental regulator in C. trachomatis because it repressed a number of late chlamydial promoters, which are transcribed during RB-to-EB conversion. more...
Organism:
Chlamydia trachomatis
Type:
Other
Platform:
GPL32238
8 Samples
Download data: XLSX
Series
Accession:
GSE202415
ID:
200202415
9.

Dual RNA-seq of chlamydial and host cell transcriptomes during nutritional stress

(Submitter supplied) We utilized host-pathogen dual RNA-sequencing to elucidate the transcriptomes of both Chlamydia trachomatis and the infected HeLa cell during nutritional conditions that induce persistence.
Organism:
Chlamydia trachomatis L2/434/Bu; Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL30321 GPL30320
18 Samples
Download data: CSV
Series
Accession:
GSE179003
ID:
200179003
10.

Heat shock-induced transcriptomic response in Chlamydia trachomatis

(Submitter supplied) Heat shock-induced transcriptomic response in Chlamydia trachomatis
Organism:
Chlamydia trachomatis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28812
6 Samples
Download data: FA, GTF, TXT
Series
Accession:
GSE173366
ID:
200173366
11.

A GrgA-Euo-HrcA transcriptional regulatory network controls the growth and development of the obligate intracellular bacterium Chlamydia

(Submitter supplied) Effects of overexpression of Chlamydia trachomatis transcription factors GrgA, Euo and HrcA on the chlamydial transcriptome were determined.
Organism:
Chlamydia trachomatis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28812
36 Samples
Download data: TXT
Series
Accession:
GSE153747
ID:
200153747
12.

RNA Seq analysis of Chlamydia trachomatis D serovar in axenic culture

(Submitter supplied) Chlamydia trachomatis D serovar was grown in axenic culture with G6P or G6P with glutamine. The data reveal the early transcriptonal regulation in the bacteria.
Organism:
Chlamydia trachomatis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28305
9 Samples
Download data: TXT
Series
Accession:
GSE147539
ID:
200147539
13.

A primary Chlamydia trachomatis genital infection of Rhesus macaques identifies new immunodominant B-cell antigens

(Submitter supplied) To identify immunodominant antigens that elicit a humoral immune response following a primary genital infection, rhesus monkeys were inoculated cervically with Chlamydia trachomatis serovar D. Serum samples were collected and probed with a protein microarray expressing 864/894 (96.4%) of the open reading frames of the C. trachomatis serovar D genome. The antibody response was analyzed in 72 serum samples from 12 inoculated monkeys. more...
Organism:
Chlamydia trachomatis; Macaca mulatta
Type:
Protein profiling by protein array
Platform:
GPL28497
72 Samples
Download data: TXT
Series
Accession:
GSE151183
ID:
200151183
14.

DksA controls the response of the Lyme disease spirochete Borrelia burgdorferi to starvation

(Submitter supplied) The pathogenic spirochete Borrelia burgdorferi senses and responds to diverse environmental challenges, including changes in nutrient availability, throughout its natural infectious cycle in Ixodes spp. ticks and mammalian hosts. This study examined the role of the putative DnaK suppressor protein (DksA) in the transcriptional response of B. burgdorferi to starvation. Wild-type and dksA-deficient B. more...
Organism:
Yersinia pestis; Borreliella burgdorferi; Chlamydia trachomatis; Staphylococcus aureus; Coxiella burnetii; Streptococcus pyogenes
Type:
Expression profiling by array
Platform:
GPL2129
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE119023
ID:
200119023
15.

Transcriptional response of C.trachomatis to early-cycle and mid-cycle iron-starvation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Chlamydia trachomatis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24258
28 Samples
Download data
Series
Accession:
GSE106763
ID:
200106763
16.

Transcriptional response of C.trachomatis to mid-cycle iron-starvation

(Submitter supplied) Mid-cycle C. trachomatis differentially regulates a subset of genes in response to iron-starvation
Organism:
Chlamydia trachomatis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24258
20 Samples
Download data: XLSX
Series
Accession:
GSE106762
ID:
200106762
17.

Transcriptional response of C.trachomatis to early-cycle iron-starvation

(Submitter supplied) Early-cycle C. trachomatis differentially regulates a subset of genes in response to iron-starvation
Organism:
Chlamydia trachomatis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24258
8 Samples
Download data: XLSX
Series
Accession:
GSE106761
ID:
200106761
18.

Genome-wide analysis of the regulatory function mediated by the small regulatory psm-mec RNA of methicillin-resistant Staphylococcus aureus

(Submitter supplied) Several methicillin resistance (SCCmec) clusters characteristic of hospital-associated methicillin-resistant Staphylococcus aureus (MRSA) strains harbor the psm-mec locus. In addition to encoding the cytolysin, phenol-soluble modulin (PSM) mec, this locus has been attributed gene regulatory functions. Here we employed genome-wide transcriptional profiling to define the regulatory function of the psm-mec locus. more...
Organism:
Staphylococcus aureus; Coxiella burnetii; Borreliella burgdorferi; Chlamydia trachomatis; Yersinia pestis; Streptococcus pyogenes
Type:
Expression profiling by array
Platform:
GPL2129
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE51366
ID:
200051366
19.

Role of the PhoP-PhoQ Gene Regulatory System in Adaptation of Yersinia pestis to Environmental Stress in the Flea Digestive Tract

(Submitter supplied) The Yersinia pestis PhoPQ gene regulatory system is induced during infection of the flea digestive tract and is required to produce adherent biofilm in the foregut, which greatly enhances bacterial transmission during a flea bite. To understand the in vivo context of PhoPQ induction and to determine PhoP-regulated targets in the flea, we undertook whole genome comparative transcriptional profiling of Y. more...
Organism:
Yersinia pestis; Coxiella burnetii; Chlamydia trachomatis; Streptococcus pyogenes; Borreliella burgdorferi; Staphylococcus aureus
Type:
Expression profiling by array
Platform:
GPL2129
40 Samples
Download data: CEL, CHP
Series
Accession:
GSE61558
ID:
200061558
20.

Toxin mediates sepsis caused by methicillin-resistant Staphylococcus epidermidis

(Submitter supplied) Bacterial sepsis is a major killer in hospitalized patients. Coagulase-negative staphylococci (CNS) with the leading species Staphylococcus epidermidis are the most frequent causes of nosocomial sepsis, with most infectious isolates being methicillin resistant. However, which bacterial factors underlie the pathogenesis of CNS sepsis is unknown. While it has been commonly believed that invariant structures on the surface of CNS trigger sepsis by causing an over-reaction of the immune system, we show here that sepsis caused my methicillin-resistant S. more...
Organism:
Staphylococcus epidermidis ATCC 12228; Chlamydia trachomatis D/UW-3/CX; Coxiella burnetii; Rickettsia rickettsii; Chlamydia muridarum; Staphylococcus epidermidis RP62A; Staphylococcus epidermidis; Staphylococcus aureus subsp. aureus MW2; Granulibacter bethesdensis; Chlamydia pneumoniae AR39; Borreliella burgdorferi B31; Coxiella burnetii RSA 493; Chlamydia caviae GPIC; Staphylococcus haemolyticus JCSC1435
Type:
Expression profiling by array
Platform:
GPL4692
15 Samples
Download data: CEL, CHP
Series
Accession:
GSE85265
ID:
200085265
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