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Items: 1 to 20 of 1741

1.

RNA-seq analyses of pathogenic Burkholderia glumae under in vivo rice panicle condition

(Submitter supplied) RNA-seq based transcriptome analysis was employed to understand the genome-wide expression patterns of B. glumae BGR1 under infected rice panicle tissue.
Organism:
Burkholderia glumae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27527
3 Samples
Download data: TXT
Series
Accession:
GSE137969
ID:
200137969
2.

Transcriptional analysis of transposon mutants disrupted in glutathione or ergothioneine biosynthesis in Burkholderia thailandensis

(Submitter supplied) In this study we compare logarithmically grown Burkholderia thailadensis wildtype to a transposon mutant that is disrupted in gshA1, or gshA2, which are involved in glutathione biosynthesis or egtB, involved in ergothioneine biosynthesis using RNASeq to identify novel pathways where glutathione or ergothioneine may be involved.
Organism:
Burkholderia thailandensis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33677
8 Samples
Download data: CSV, XLSX
Series
Accession:
GSE240826
ID:
200240826
3.

RNA-seq based transcriptome analysis of plant pathogens under salt stress condition

(Submitter supplied) Plant pathogens require lethal virulence factors, susceptible hosts, and optimal environmental conditions for disease establishment. High soil salinity, exacerbated by climate change, significantly impacts agro-biological ecosystems. However, the overall interactions between plant pathogens and salt stress are not fully characterized or understood. This study examines the effects of salt stress on representative plant pathogens: Burkholderia gladioli, Pectobacterium carotovorum subsp. more...
Organism:
Pectobacterium carotovorum subsp. carotovorum; Ralstonia solanacearum; Burkholderia gladioli
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL29295 GPL34740 GPL34741
18 Samples
Download data: TXT
Series
Accession:
GSE272984
ID:
200272984
4.

TetR-like regulator BP1026B_II1561 controls aromatic amino acid biosynthesis and intracellular pathogenesis in Burkholderia pseudomallei [RNA-seq]

(Submitter supplied) We identified BP1026b_II1561 to be an important transcriptional regulator controling late stages of intracellular infection. RNA-seq analysis was performed to further investigate the regulatory network of II1561 regulation. ChIP-seq was also performed under the same conditions.
Organism:
Burkholderia pseudomallei
Type:
Expression profiling by high throughput sequencing
Platform:
GPL32930
2 Samples
Download data: XLSX
Series
Accession:
GSE273460
ID:
200273460
5.

TetR-like regulator BP1026B_II1561 controls aromatic amino acid biosynthesis and intracellular pathogenesis in Burkholderia pseudomallei [ChIP-seq]

(Submitter supplied) We identified BP1026b_II1561 to be an important transcriptional regulator controling late stages of intracellular infection. RNA-seq analysis was performed to further investigate the regulatory network of II1561 regulation. ChIP-seq was also performed under the same conditions.
Organism:
Burkholderia pseudomallei
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL32930
2 Samples
Download data: XLSX
Series
Accession:
GSE273459
ID:
200273459
6.

Transcriptome profiling of Burkholderia pseudomallei wildtype strain1026b and BP1026b_II1046::T4 insertion mutant

(Submitter supplied) We identified BP1026b_II1046 (SapR) to be an important transcriptional regulator controling surface attachment factor 1 (sap1). RNA-seq analysis was performed to further investigate the regulatory network of SapR regulation.
Organism:
Burkholderia pseudomallei
Type:
Expression profiling by high throughput sequencing
Platform:
GPL32930
6 Samples
Download data: XLSX
Series
Accession:
GSE220579
ID:
200220579
7.

Genome wide identification of BysR binding sites in Burkholderia sp. JP2-270

(Submitter supplied) To verify genes that are directly regulated by BysR, we used DNA affinity purification sequencing analysis (DAP-seq) for genome-wide recognition of BysR binding sites in vitro. The HALO-fusion BysR protein was successfully expressed and purified. After affinity purification and sequencing, at least 22 million double-end reads per sample were generated and with > 99 % of reads uniquely mapped to the JP2-270 genome. more...
Organism:
Burkholderia sp. JP2-270
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL31243
3 Samples
Download data: FA, TXT, WIG
Series
Accession:
GSE193916
ID:
200193916
8.

RNA-seq analysis of wild type and ΔbysR in Burkholderia sp. JP2-270

(Submitter supplied) Purpose: In order to identify the differentially expressed genes between wild type and ΔbysR, we performed RNA-seq analysis.Methods:All the isolates were cultured in CM medium for 24 h at 28℃. Three repetitions were performed for each treatment. The samples were sequenced on an Illumina Hiseq 2000 platform.Clean reads were obtained by removing reads containing adapter, reads containing ploy-N and low quality reads from raw data. more...
Organism:
Burkholderia sp. JP2-270
Type:
Expression profiling by high throughput sequencing
Platform:
GPL31232
6 Samples
Download data: TXT
Series
Accession:
GSE193778
ID:
200193778
9.

Transcriptomics analysis during the transient ceftazidime tolerance of Burkholderia pseudomallei

(Submitter supplied) B. pseudomallei strain K96243 is sensitive to the drug ceftazidime (CAZ), but has been shown to exhibit transient CAZ tolerance when in a biofilm form. To investigate an observed shift in gene expression profile during ceftazidime (CAZ) tolerance and to better understand the mechanistic aspects of this transient tolerance, RNA-sequencing was performed on B. pseudomallei K96243 from the following three growth states: planktonic-free, biofilm, and planktonic shedding cells. more...
Organism:
Burkholderia pseudomallei K96243
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29815
9 Samples
Download data: FPKM_TRACKING, GTF, XLSX
Series
Accession:
GSE168275
ID:
200168275
10.

An investigation of Burkholderia cepacia complex methylomes via SMRT sequencing and mutant analysis

(Submitter supplied) While nucleotide sequences determine an organism’s proteins, methylation of the nucleotides themselves can confer additional properties. In bacteria, differences in methylation can be used to identify incoming DNA, for example from bacteriophages. Restriction enzymes detect the methylation status at specific sequence motifs, and cleave improperly methylated, foreign DNA. Furthermore, methylation of key genetic regions can influence gene expression and hence phenotype. more...
Organism:
Burkholderia cenocepacia H111
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23128
4 Samples
Download data: TXT
Series
Accession:
GSE147038
ID:
200147038
11.

RegAB Two-Component System Homolog of Burkholderia pseudomallei is the Master Regulator of Redox Control and involved in Virulence.

(Submitter supplied) Burkholderia pseudomallei, the etiological agent of melioidosis in humans and animals, often occupies environmental niches and infection sites characterized by limited concentrations of oxygen. Versatile genomic features enable this pathogen to maintain its physiology and virulence under hypoxia, but the crucial regulatory networks employed to switch from oxygen dependent respiration to alternative terminal electron acceptors (TEA) like nitrate, remains poorly understood. more...
Organism:
Burkholderia pseudomallei K96243; Burkholderia pseudomallei
Type:
Expression profiling by genome tiling array
Platform:
GPL16432
44 Samples
Download data: PAIR, TXT
Series
Accession:
GSE159521
ID:
200159521
12.

Overexpression of a histone-like nucleoid structuring protein in Burkholderia multivorans affects several traits dependent on the cell envelope

(Submitter supplied) Burkholderia cepacia complex bacteria comprise opportunistic pathogens causing chronic respiratory infections in cystic fibrosis (CF) patients. These microorganisms produce exopolysaccharides which are considered virulence determinants. Here, we report the isolation of an evolved nonmucoid variant (17616nmv) after the ancestor, Burkholderia multivorans ATCC 17616, was subjected to prolonged stationary phase. more...
Organism:
Burkholderia multivorans; Burkholderia cenocepacia J2315; Burkholderia multivorans ATCC 17616
Type:
Expression profiling by array
Platform:
GPL13356
6 Samples
Download data: CEL
Series
Accession:
GSE162693
ID:
200162693
13.

Dissecting the co-transcriptome landscape of plants and microbiota

(Submitter supplied) Interactions between plants and each neighboring microbial species are fundamental building blocks that collectively determine the structure and function of the plant microbiota, but the molecular basis of such interactions is poorly characterized. Here, we monocolonized Arabidopsis leaves with nine plant-associated bacteria from all major phyla of the plant microbiota and profiled co-transcriptomes of plants and bacteria. more...
Organism:
Plantibacter sp. Leaf1; Rhizobium sp. Leaf155; Acinetobacter sp. Leaf130; Arthrobacter sp. Soil763; Flavobacterium sp. Root935; Arabidopsis thaliana; Pedobacter sp. Leaf176; Burkholderia sp. Leaf177; Chryseobacterium sp. Leaf404; Exiguobacterium sp. Leaf187
Type:
Expression profiling by high throughput sequencing
10 related Platforms
125 Samples
Download data: FNA, TXT
Series
Accession:
GSE150422
ID:
200150422
14.

RNA Atlas of Bacterial Human Pathogens Uncovers Stress Dynamics Linked to Bacterial Infections

(Submitter supplied) Pathogenic bacteria encounter a variety of stressful host environments during infection. Their responses to meet these challenges protect them from deadly damages and aid in adaption to harmful environments. Bacterial products critical for this protection are therefore interesting as suitable targets for new antimicrobials. To shed light on the complex array of molecular pathways involved in bacterial stress responses we challenged 32 diverse human pathogenic bacteria to 11 infection related stress conditions and catalogued their transcriptomes. more...
Organism:
Helicobacter pylori; Enterococcus faecalis; Campylobacter jejuni; Francisella tularensis; Acinetobacter baumannii; Neisseria gonorrhoeae; Escherichia coli; Shigella flexneri; Aggregatibacter actinomycetemcomitans; Haemophilus influenzae; Staphylococcus aureus subsp. aureus MRSA252; Staphylococcus aureus subsp. aureus MSSA476; Borreliella burgdorferi; Pseudomonas aeruginosa; Legionella pneumophila; Klebsiella pneumoniae; Yersinia pseudotuberculosis; Vibrio cholerae; Streptococcus suis; Streptococcus agalactiae; Streptococcus pneumoniae; Mycobacterium tuberculosis; Burkholderia pseudomallei; Neisseria meningitidis; Staphylococcus epidermidis; Streptococcus pyogenes; Listeria monocytogenes; Salmonella enterica; Achromobacter xylosoxidans
Type:
Expression profiling by high throughput sequencing
30 related Platforms
1122 Samples
Download data: TXT
Series
Accession:
GSE152295
ID:
200152295
15.

Burkholderia cenocepacia K56-2 transcriptomic profile during the early contacts with surface of host bronchial epithelial cells

(Submitter supplied) In this work, high-throughput RNA sequencing was used to assess transcriptomic alteration in Burkholderia cenocepacia K56-2 in the early stages of interaction with host-cell surface. Giant plasma membrane vesicles (GPMVs) from 16HBE14o- bronchial epithelial cell line were produced and used as a cell-like alternative. RNAseq was performed and the expression of the adherent (GPMV-attached) and non-adherent (planktonic control) bacteria were compared. more...
Organism:
Burkholderia cenocepacia
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28995
6 Samples
Download data: TXT
Series
Accession:
GSE155982
ID:
200155982
16.

Establishing the copper response of Burkholderia cenocepacia K56-2

(Submitter supplied) Purpose - To establish the response of B. cenocepacia K56-2 to growth in copper, and to characterise the BCAM0442/3 copper-sensing TCS. Methods - RNA-seq of the response WT and Δbcam0442/3 B. cenocepacia K56-2 to mid-log phase growth in LB with or without 1 mM CuCl2 was performed. Results - Characterisation of the overall response of B. cenocepacia K56-2 to copper, as well as establishing that BCAM0442/3 regulates the CopABCDE system in B. more...
Organism:
Burkholderia cenocepacia
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29736
12 Samples
Download data: CSV
Series
Accession:
GSE166960
ID:
200166960
17.

Genomic features and virulence characteristics of a rare Burkholderia thailandensis strain causing human infection

(Submitter supplied) Introduction. Burkholderia thailandensis is a clinically rare opportunistic pathogen in the genus Burkholderia, and the genomic features and virulence characteristics of B. thailandensis strains that cause human infection remain unclear.Gap Statement. B. thailandensis strains with different virulence induce different host innate immune responses in vitro.Aim. This work aimed to understand the sequence diversity, phylogenetic relationship, and virulence of B. more...
Organism:
Burkholderia thailandensis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23641
6 Samples
Download data: TXT
Series
Accession:
GSE147369
ID:
200147369
18.

B. pseudomallei genes differentially expressed during host cell infection

(Submitter supplied) Prokaryotic cell transcriptomics have been limited to mixed or sub-population dynamics and individuality of cells within heterogeneous populations. This significantly hampers further knowledge into spatiotemporal and stage-specific processes of prokaryotic cells within complex environments. Herein, we developed a ‘TRANSITomic’ approach to profile transcriptomes of single Burkholderia pseudomallei (Bp) cells as they transit through host cell infection at defined stages, yielding pathophysiological insights. more...
Organism:
Burkholderia mallei; Burkholderia pseudomallei
Type:
Expression profiling by array
Platform:
GPL29071
9 Samples
Download data: TXT
Series
Accession:
GSE156938
ID:
200156938
19.

Transcriptional responses of fungi (Rhizopus microsporus host [ATCC5 2813] and non-host [ATCC 11559] isolates) and bacteria (Burkholderia sp B13 ) to interaction with each other at a distance (pre-contact) and during physical contact.

(Submitter supplied) The goal of this study was to identify reciprocal commnication between fungi and bacteria during a mutualistic and antagonistin interaction at two time points.
Organism:
Rhizopus microsporus ATCC 52813; Burkholderia sp. b13
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL23355 GPL23356 GPL23357
24 Samples
Download data: TXT
Series
Accession:
GSE98095
ID:
200098095
20.

Methylome sequencing of Burkholderia pseudomallei D286, H10, PMC2000, R15 and 982

(Submitter supplied) We report the methylome sequencing and annotation of Burkholderia pseudomallei D286 based on high-throughput profiling using PacBio SMRT technology
Organism:
Burkholderia pseudomallei
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL18301
5 Samples
Download data: TXT
Series
Accession:
GSE137930
ID:
200137930
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