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Items: 1 to 20 of 1858

1.

Response of Vibrio cholerae to exogenous peptidoglycan

(Submitter supplied) Using transcriptomics, we studied the transcriptional response of Vibrio cholerae to 10 min of exogenously supplied peptidoglycan at 300 µg/mL.
Organism:
Vibrio cholerae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30059
6 Samples
Download data: XLSX
Series
Accession:
GSE216690
ID:
200216690
2.

MatP local enrichment delays segregation independently of tetramer formation and septal anchoring in Vibrio cholerae [HiSC2]

(Submitter supplied) Vibrio cholerae harbours a primary chromosome derived from the monochromosomal ancestor of the Vibrionales (ChrI) and a secondary chromosome derived from a megaplasmid (ChrII). Both carry a single origin of replication with replication terminating in a diametrically opposite zone, TerI and TerII, respectively. The choreography of TerI and TerII segregation determines when and where cell division occurs. more...
Organism:
Vibrio cholerae
Type:
Other
Platforms:
GPL34020 GPL25005
23 Samples
Download data: FA, TXT
Series
Accession:
GSE273190
ID:
200273190
3.

MatP local enrichment delays segregation independently of tetramer formation and septal anchoring in Vibrio cholerae

(Submitter supplied) Vibrio cholerae harbours a primary chromosome derived from the monochromosomal ancestor of the Vibrionales (ChrI) and a secondary chromosome derived from a megaplasmid (ChrII). Both carry a single origin of replication with replication terminating in a diametrically opposite zone, TerI and TerII, respectively. The choreography of TerI and TerII segregation determines when and where cell division occurs. more...
Organism:
Vibrio cholerae
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL31913
14 Samples
Download data: FA, TXT
Series
Accession:
GSE273189
ID:
200273189
4.

MatP local enrichment delays segregation independently of tetramer formation and septal anchoring in Vibrio cholerae [3C]

(Submitter supplied) Vibrio cholerae harbours a primary chromosome derived from the monochromosomal ancestor of the Vibrionales (ChrI) and a secondary chromosome derived from a megaplasmid (ChrII). Both carry a single origin of replication with replication terminating in a diametrically opposite zone, TerI and TerII, respectively. The choreography of TerI and TerII segregation determines when and where cell division occurs. more...
Organism:
Vibrio cholerae
Type:
Other
Platform:
GPL19265
2 Samples
Download data: FA, MATRIX
Series
Accession:
GSE273188
ID:
200273188
5.

RILseq of proQ-3XFLAG in V. cholerae

(Submitter supplied) Gene regulation at the post-transcriptional level is prevalent in all domains of life. In bacteria, ProQ-like proteins have emerged as important RNA chaperones facilitating RNA stability and RNA duplex formation. In the major human pathogen V. cholerae, post-transcriptional gene regulation is key for virulence, biofilm formation, and antibiotic resistance, yet the role of ProQ has not been studied. Here, we show that ProQ interacts with hundreds of transcripts in V. cholerae, including the highly abundant FlaX small RNA (sRNA). Global analyses of RNA duplex formation using RIL-Seq (RNA interaction by ligation and sequencing) revealed a vast network of ProQ-assisted interactions and identified a role for FlaX in motility regulation. Specifically, FlaX base-pairs with multiple sites on the flaB flagellin mRNA, preventing 30S ribosome binding and translation initiation. V. cholerae cells lacking flaX display impaired motility gene expression, altered flagella composition, and reduced swimming in liquid environments. Our results provide a global view on ProQ-mediated RNA duplex formation and pinpoint the mechanistic and phenotypic consequences associated with ProQ-associated sRNAs in V. cholerae.
Organism:
Vibrio cholerae
Type:
Other
Platform:
GPL33935
4 Samples
Download data: XLSX
Series
Accession:
GSE275761
ID:
200275761
6.

RIPseq of proQ-3XFLAG in V. cholerae

(Submitter supplied) Gene regulation at the post-transcriptional level is prevalent in all domains of life. In bacteria, ProQ-like proteins have emerged as important RNA chaperones facilitating RNA stability and RNA duplex formation. In the major human pathogen V. cholerae, post-transcriptional gene regulation is key for virulence, biofilm formation, and antibiotic resistance, yet the role of ProQ has not been studied. Here, we show that ProQ interacts with hundreds of transcripts in V. cholerae, including the highly abundant FlaX small RNA (sRNA). Global analyses of RNA duplex formation using RIL-Seq (RNA interaction by ligation and sequencing) revealed a vast network of ProQ-assisted interactions and identified a role for FlaX in motility regulation. Specifically, FlaX base-pairs with multiple sites on the flaB flagellin mRNA, preventing 30S ribosome binding and translation initiation. V. cholerae cells lacking flaX display impaired motility gene expression, altered flagella composition, and reduced swimming in liquid environments. Our results provide a global view on ProQ-mediated RNA duplex formation and pinpoint the mechanistic and phenotypic consequences associated with ProQ-associated sRNAs in V. cholerae.
Organism:
Vibrio cholerae C6706
Type:
Other
Platform:
GPL34845
12 Samples
Download data: XLSX
Series
Accession:
GSE275750
ID:
200275750
7.

Negative feedback of cyclic di-GMP levels optimizes switching between sessile and motile lifestyles in Vibrio cholerae [RNA-seq]

(Submitter supplied) The signaling molecule cyclic di-GMP (cdG) controls the switch between bacterial motility and biofilm production, and fluctuations in cellular levels of cdG have been implicated in Vibrio cholerae pathogenesis. Intracellular concentrations of cdG are controlled by the interplay of diguanylate cyclase (DGC) enzymes, which synthesize cdG to promote biofilms, and phosphodiesterase (PDE) enzymes, which hydrolyse cdG to drive motility. more...
Organism:
Vibrio cholerae C6706
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34804
45 Samples
Download data: BEDGRAPH, TSV
Series
Accession:
GSE274216
ID:
200274216
8.

Negative feedback of cyclic di-GMP levels optimizes switching between sessile and motile lifestyles in Vibrio cholerae [ChIP-seq]

(Submitter supplied) The signaling molecule cyclic di-GMP (cdG) controls the switch between bacterial motility and biofilm production, and fluctuations in cellular levels of cdG have been implicated in Vibrio cholerae pathogenesis. Intracellular concentrations of cdG are controlled by the interplay of diguanylate cyclase (DGC) enzymes, which synthesize cdG to promote biofilms, and phosphodiesterase (PDE) enzymes, which hydrolyse cdG to drive motility. more...
Organism:
Vibrio cholerae C6706
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL34804
91 Samples
Download data: BEDGRAPH, BW
Series
Accession:
GSE274215
ID:
200274215
9.

RNAseq of WT + pctrl, ∆flaX + pctrl and ∆flaX + pPflaAX in V. cholerae

(Submitter supplied) Gene regulation at the post-transcriptional level is prevalent in all domains of life. In bacteria, ProQ-like proteins have emerged as important RNA chaperones facilitating RNA stability and RNA duplex formation. In the major human pathogen V. cholerae, post-transcriptional gene regulation is key for virulence, biofilm formation, and antibiotic resistance, yet the role of ProQ has not been studied. Here, we show that ProQ interacts with hundreds of transcripts in V. cholerae, including the highly abundant FlaX small RNA (sRNA). Global analyses of RNA duplex formation using RIL-Seq (RNA interaction by ligation and sequencing) revealed a vast network of ProQ-assisted interactions and identified a role for FlaX in motility regulation. Specifically, FlaX base-pairs with multiple sites on the flaB flagellin mRNA, preventing 30S ribosome binding and translation initiation. V. cholerae cells lacking flaX display impaired motility gene expression, altered flagella composition, and reduced swimming in liquid environments. Our results provide a global view on ProQ-mediated RNA duplex formation and pinpoint the mechanistic and phenotypic consequences associated with ProQ-associated sRNAs in V. cholerae.
Organism:
Vibrio cholerae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33935
18 Samples
Download data: XLSX
Series
Accession:
GSE275822
ID:
200275822
10.

TsrA regulates gene expression of horizontally acquired elements in Vibrio cholerae via both H-NS dependent and independent mechanisms

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Vibrio cholerae
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL34020 GPL31913 GPL28681
76 Samples
Download data: BEDGRAPH, H5, TSV
Series
Accession:
GSE250408
ID:
200250408
11.

TsrA regulates gene expression of horizontally acquired elements in Vibrio cholerae via both H-NS dependent and independent mechanisms [RNA-Seq]

(Submitter supplied) Vibrio cholerae, the causative agent of the diarrheal disease cholera, poses an ongoing health threat due to its wide repertoire of horizontally acquired elements (HAEs) and virulence factors. New clinical isolates of the bacterium with improved fitness abilities, often associated with HAEs, frequently emerge. The appropriate control and expression of such genetic elements is critical for the bacteria to thrive in different environments. more...
Organism:
Vibrio cholerae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34020
19 Samples
Download data: H5, R, TSV
Series
Accession:
GSE250406
ID:
200250406
12.

TsrA regulates gene expression of horizontally acquired elements in Vibrio cholerae via both H-NS dependent and independent mechanisms [IPOD-HR]

(Submitter supplied) Vibrio cholerae, the causative agent of the diarrheal disease cholera, poses an ongoing health threat due to its wide repertoire of horizontally acquired elements (HAEs) and virulence factors. New clinical isolates of the bacterium with improved fitness abilities, often associated with HAEs, frequently emerge. The appropriate control and expression of such genetic elements is critical for the bacteria to thrive in different environments. more...
Organism:
Vibrio cholerae
Type:
Other
Platforms:
GPL28681 GPL31913 GPL34020
57 Samples
Download data: BEDGRAPH, NARROWPEAK
Series
Accession:
GSE250405
ID:
200250405
13.

RNAseq of VP882 phage activation in V. cholerae

(Submitter supplied) Many, if not all, bacteria use quorum sensing (QS) to control gene expression and collective behaviours, and more recently QS has also been discovered in bacteriophages (phages). Phages can produce communication molecules of their own, or “listen in” on the host’s communication processes, in order to switch between lytic and lysogenic modes of infection. In this project, we studied the interaction of Vibrio cholerae, the causative agent of cholera disease, with the lysogenic vibriophage VP882. more...
Organism:
Vibrio cholerae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25005
18 Samples
Download data: XLSX
Series
Accession:
GSE247770
ID:
200247770
14.

RNAseq of VP882 and VP882 ∆vpdS phage activation in V. cholerae

(Submitter supplied) Many, if not all, bacteria use quorum sensing (QS) to control gene expression and collective behaviours, and more recently QS has also been discovered in bacteriophages (phages). Phages can produce communication molecules of their own, or “listen in” on the host’s communication processes, in order to switch between lytic and lysogenic modes of infection. In this project, we studied the interaction of Vibrio cholerae, the causative agent of cholera disease, with the lysogenic vibriophage VP882. more...
Organism:
Vibrio cholerae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33935
18 Samples
Download data: XLSX
Series
Accession:
GSE247769
ID:
200247769
15.

RIPseq of VP882 phage activation in V. cholerae

(Submitter supplied) Many, if not all, bacteria use quorum sensing (QS) to control gene expression and collective behaviours, and more recently QS has also been discovered in bacteriophages (phages). Phages can produce communication molecules of their own, or “listen in” on the host’s communication processes, in order to switch between lytic and lysogenic modes of infection. In this project, we studied the interaction of Vibrio cholerae, the causative agent of cholera disease, with the lysogenic vibriophage VP882. more...
Organism:
Vibrio cholerae
Type:
Other
Platform:
GPL33935
12 Samples
Download data: XLSX
Series
Accession:
GSE247768
ID:
200247768
16.

RILseq of VP882 phage activation in V. cholerae

(Submitter supplied) Many, if not all, bacteria use quorum sensing (QS) to control gene expression and collective behaviours, and more recently QS has also been discovered in bacteriophages (phages). Phages can produce communication molecules of their own, or “listen in” on the host’s communication processes, in order to switch between lytic and lysogenic modes of infection. In this project, we studied the interaction of Vibrio cholerae, the causative agent of cholera disease, with the lysogenic vibriophage VP882. more...
Organism:
Vibrio cholerae
Type:
Other
Platform:
GPL33935
12 Samples
Download data: XLSX
Series
Accession:
GSE247767
ID:
200247767
17.

Chromosomal integrons are genetically and functionally isolated units of genomes

(Submitter supplied) Integrons are genetic elements that enable bacterial adaptation by collecting new genes encoded in integron cassettes (ICs) to create a reservoir of adaptive functions. These cassettes typically lack their own promoters and rely on the integron platform for their expression. Integrons, well-known for spreading antibiotic resistance genes in clinically relevant Gram-negative species, include Mobile Integrons (MIs), that transport over 170 resistance genes. more...
Organism:
Vibrio cholerae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28681
12 Samples
Download data: TSV
Series
Accession:
GSE247496
ID:
200247496
18.

A TetR-family regulator of an RND efflux system that directs artemisinin resistance in Vibrio cholerae

(Submitter supplied) Artemisinin (ARS) displayed bactericidal activity against Vibrio cholerae. To assess the mechanistic details of its antibacterial action, we have isolated V. cholerae mutants with enhanced ARS resistance and identified a gene (VCA0767), whose loss-of-function resulted in the ARS resistance phenotypes. This gene (atrR) encodes a TetR family transcriptional regulator, and its deletion mutant displayed the reduction in ARS-induced ROS formation and DNA damage. more...
Organism:
Vibrio cholerae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21023
8 Samples
Download data: TXT
Series
Accession:
GSE245142
ID:
200245142
19.

Molecular mechanisms of increased survival of Vibrio cholerae flrA mutant in amoeba

(Submitter supplied) Mutation in flagellar transcriptional regulatory gene (flrA) result in increased V. cholerae growth and intracellular survival in the amoeba host Acanthamoeba castellanii. To identify molecular mechanisms behind the increased survival and growth of the flrA mutant transcriptomics assay was done.
Organism:
Vibrio cholerae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21023
5 Samples
Download data: TSV
Series
Accession:
GSE215287
ID:
200215287
20.

RNAseq analysis of Vibrio cholerae A1552 WT and ∆rvvA (∆VCA0257)

(Submitter supplied) RNA-sequencing of Vibrio cholerae A1552 wild-type and ∆VCA0257 (∆rvvA) strains grown under virulence-inducing conditions (AKI).
Organism:
Vibrio cholerae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21023
6 Samples
Download data: CSV
Series
Accession:
GSE230781
ID:
200230781
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