Similar studies for GEO DataSets (Select 200086341) - GEO DataSets

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Items: 3

Select item 2000863411.

LLQR E. coli ATCC 25922 vs wild-type E. coli ATCC 25922

(Submitter supplied) Global response to ciprofloxacin in low level quinolone resistant Escherichia coli: a shorter path to survival. Background: Bactericidal activity of quinolones in bacteria has been related to a combination of DNA fragmentation, ROS production and programmed dead cell systems. Subjacent molecular systems responsible for reduction of bactericidal effect in low-level quinolone resistance (LLQR) phenotypes remain to be clarified. more...

Organism:: Escherichia coli O157:H7 str. Sakai; Escherichia coli O157:H7 str. EDL933; Escherichia coli CFT073; Escherichia coli str. K-12 substr. MG1655; Escherichia coli ATCC 25922

Type:: Expression profiling by array

Platform:: GPL13360
8 Samples

Download data: TXT, XLSX

Series

Accession:: GSE86341

ID:: 200086341

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 2001810302.

Genome-wide screening and characterization of Actinobacillus pleuropneumoniae and its ciprofloxacin-resistant mutants

(Submitter supplied) Understanding constraints which shape antibiotic resistance is key for predicting and controlling drug resistance. Here, we performed high-throughput laboratory evolution of Actinobacillus pleuropneumoniae and its ciprofloxacin resistance-inducing derivatives.This study aims to explore the mechanism of acquired ciprofloxacin resistance in Actinobacillus pleuropneumoniae.

Organism:: Actinobacillus pleuropneumoniae

Type:: Expression profiling by high throughput sequencing

Platform:: GPL30447
6 Samples

Download data: FASTA, GFF3, TXT

Series

Accession:: GSE181030

ID:: 200181030

PubMed Full text in PMC Similar studies SRA Run Selector

Select item 2000895073.

Identification of ciprofloxacin helper drug targets by RNA-seq

(Submitter supplied) The aim of this study was to identify genes that can be targeted by helper drugs to counteract resistance towards ciprofloxacin (CIP). In order to reveal the impact of ciprofloxacin on the transcriptome, differential gene-expression analysis by RNA-seq was performed on the multidrug resistant E. coli strain ST131, treated with a clinically relevant concentration of ciprofloxacin (2 µg/mL).