Search results for "DNA Gyrase"

showing 10 items of 15 documents

Molecular characterisation of quinolone-resistant Shigella strains isolated in Tehran, Iran.

2016

Over the past few years, the number of Shigella strains resistant to nalidixic acid has increased and has made the selection of effective antimicrobial therapy more difficult. The purpose of this study was to investigate the molecular mechanism of quinolone resistance in Shigella strains. Shigella strains isolated from 1100 diarrhoeal patients in Tehran, Iran, were assessed for their susceptibility to nalidixic acid prior to PCR-RFLP and sequence analysis of their quinolone resistance genes. Among 73 Shigella strains isolated, 23 (31.5%) were resistant to nalidixic acid. The most common Shigella spp. was Shigella sonnei (54; 74.0%). Of the 23 quinolone-resistant isolates, 4 (17.4%) (includi…

0301 basic medicineMicrobiology (medical)Nalidixic acidmedicine.drug_class030106 microbiologyImmunologyShigella sonneiMicrobial Sensitivity TestsIranQuinolonesmedicine.disease_causeMicrobiologyDNA gyraseMicrobiology03 medical and health sciencesShigella flexneriDrug Resistance BacterialmedicineImmunology and AllergyHumansShigella sonneiShigellaShigella boydiiDysentery Bacillarybiologybiology.organism_classificationAntimicrobialQuinoloneVirologyAnti-Bacterial AgentsDNA GyraseGenes BacterialShigellamedicine.drugJournal of global antimicrobial resistance
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ChemInform Abstract: Pyrrolidino Enaminones Structurally Related to Gyrase Inhibitors: Synthesis, Cyclization and Pharmacological Activity.

2010

ChemistryStereochemistryBiological activityGeneral MedicineDNA gyraseCombinatorial chemistryPyrrole derivativesChemInform
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Identification of Gip as a novel phage‐encoded gyrase inhibitor protein of Corynebacterium glutamicum

2021

By targeting key regulatory hubs of their host, bacteriophages represent a powerful source for the identification of novel antimicrobial proteins. Here, a screening of small cytoplasmic proteins encoded by the CGP3 prophage of Corynebacterium glutamicum resulted in the identification of the gyrase-inhibiting protein Cg1978, termed Gip. Pull-down assays and surface plasmon resonance revealed a direct interaction of Gip with the gyrase subunit A (GyrA). The inhibitory activity of Gip was shown to be specific to the DNA gyrase of its bacterial host C. glutamicum. Overproduction of Gip in C. glutamicum resulted in a severe growth defect as well as an induction of the SOS response. Furthermore, …

DNA Replicationendocrine systemProtein subunitProphagesBiologyMicrobiologyDNA gyraseCorynebacterium glutamicum03 medical and health scienceschemistry.chemical_compoundViral Proteinsddc:570Topoisomerase II InhibitorsSOS responseMolecular BiologyProphage030304 developmental biology0303 health sciences030306 microbiologyDNA replicationAnti-Bacterial AgentsHigh-Throughput Screening AssaysCorynebacterium glutamicumchemistryBiochemistrybacteriaTopoisomerase-II InhibitorDNAhormones hormone substitutes and hormone antagonistsMolecular Microbiology
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Mechanisms of quinolone resistance in Aeromonas species isolated from humans, water and eels.

2009

Mechanisms of resistance were determined in 33 quinolone-resistant isolates of the species Aeromonas hydrophila, Aeromonas caviae, Aeromonas media, Aeromonas salmonicida, Aeromonas popoffii and Aeromonas veronii, recovered from humans, freshwater and eels. The quinolone resistance-determining regions (QRDRs) of gyrA and parC genes were sequenced in these resistant strains, as well as in 8 quinolone-sensitive Aeromonas used as controls. All quinolone-resistant Aeromonas carried point mutations in the gyrA QRDR at codon 83, respectively giving rise to substitutions Ser(83)-->Ile (32 strains) or Ser(83)-->Val (1 strain). Almost half of these isolates (48%) carried additional point mutations in…

DNA Topoisomerase IVDNA BacterialAeromonas caviaemedicine.drug_classDNA Mutational AnalysisMutation MissenseDrug resistanceMicrobial Sensitivity TestsQuinolonesMicrobiologyMicrobiologyBacterial ProteinsDrug Resistance BacterialmedicineAnimalsHumansPoint MutationMolecular BiologyEelsbiologyGeneral MedicineSequence Analysis DNAbiochemical phenomena metabolism and nutritionQuinolonebiology.organism_classificationAnti-Bacterial AgentsAeromonas hydrophilaAeromonas salmonicidaAeromonasAmino Acid SubstitutionDNA GyraseAeromonas mediaAeromonasGram-Negative Bacterial InfectionsWater MicrobiologyAeromonas veroniiResearch in microbiology
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Spontaneous Quinolone Resistance in the Zoonotic Serovar of Vibrio vulnificus

2009

ABSTRACT This work demonstrates that Vibrio vulnificus biotype 2, serovar E, an eel pathogen able to infect humans, can become resistant to quinolone by specific mutations in gyrA (substitution of isoleucine for serine at position 83) and to some fluoroquinolones by additional mutations in parC (substitution of lysine for serine at position 85). Thus, to avoid the selection of resistant strains that are potentially pathogenic for humans, antibiotics other than quinolones must be used to treat vibriosis on farms.

DNA Topoisomerase IVDNA BacterialSerotypeBiologiamedicine.drug_classMolecular Sequence DataAntibioticsMutation MissenseMicrobiologiaPublic Health MicrobiologyVibrio vulnificusQuinolonesApplied Microbiology and BiotechnologyDNA gyraseMicrobiologyBacterial ProteinsVibrionaceaeDrug Resistance BacterialmedicineAnimalsVibrio vulnificusPathogenEelsEcologybiologySequence Analysis DNAbiology.organism_classificationQuinoloneVirologyAnti-Bacterial AgentsDNA GyrasebacteriaBacteriaFood ScienceBiotechnologyApplied and Environmental Microbiology
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An MLSA approach for the taxonomic update of the Splendidus clade, a lineage containing several fish and shellfish pathogenic Vibrio spp.

2016

A multilocus sequence analysis was undertaken in order to redefine the Splendidus clade of the genus Vibrio, a large group of species containing several pathogenic members that affect fish and shellfish, and are difficult to identify through both phenotypic and genotypic approaches. The study included analysis of partial sequences of recA, gyrB, mreB, rpoD and pyrH genes, as well as the 16S rRNA gene. Seventeen type strain species were included that were complemented with other reference strains and a collection of isolates tentatively identified as members of this clade, as well as a set of other Vibrio species. The clade was well defined and stable in all analyses, and was confirmed to co…

DNA Bacterial0301 basic medicineVibrio cyclitrophicusSequence analysisLineage (evolution)030106 microbiologyZoologySigma FactorApplied Microbiology and BiotechnologyMicrobiologyMicrobiologyFish Diseases03 medical and health sciencesTransferasesRNA Ribosomal 16SAnimalsCladePhylogenyEcology Evolution Behavior and SystematicsShellfishShellfishVibrioBase SequencebiologyStrain (biology)FishesSubcladeDNA-Directed RNA PolymerasesSequence Analysis DNAbiology.organism_classification16S ribosomal RNAOstreidaeBacterial Typing TechniquesRec A RecombinasesDNA GyraseSeasonsMultilocus Sequence TypingSystematic and Applied Microbiology
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Multilocus sequence analysis of the central clade of the genus Vibrio by using the 16S rRNA, recA, pyrH, rpoD, gyrB, rctB and toxR genes.

2009

The central clade of the genus Vibrio, also called the Vibrio core group, comprises six species that are tightly related (DNA–DNA reassociation values are very close to 70 % for most species pairs). Identification of novel strains to the species level within this group is troublesome and results are quite often dependent on the methodology employed. Therefore, this group represents an excellent framework to test the robustness of multilocus sequence analysis (MLSA) not only for inferring phylogeny but also as an identification tool without the need for DNA–DNA hybridization assays. The genes selected, 16S rRNA, recA, pyrH, rpoD, gyrB, rctB and toxR, were amplified by direct PCR from 44 Vibr…

DNA BacterialSequence analysisMolecular Sequence DataSigma FactorBiologyMicrobiologyBacterial ProteinsPhylogeneticsVibrionaceaeTransferasesRNA Ribosomal 16SCladeGeneEcology Evolution Behavior and SystematicsPhylogenyVibrioGeneticsBase CompositionGeneral MedicineSequence Analysis DNARibosomal RNA16S ribosomal RNAbiology.organism_classificationVibrioDNA-Binding ProteinsRec A RecombinasesDNA GyraseTranscription FactorsInternational journal of systematic and evolutionary microbiology
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Antimicrobial Activity, in silico Molecular Docking, ADMET and DFT Analysis of Secondary Metabolites from Roots of Three Ethiopian Medicinal Plants

2021

Mathewos Anza,1 Milkyas Endale,1 Luz Cardona,2 Diego Cortes,3 Rajalakshmanan Eswaramoorthy,1 Jesus Zueco,4 Hortensia Rico,4 Maria Trelis,5 Belen Abarca2 1Department of Applied Chemistry, School of Applied Natural Science, Adama Science and Technology University, Adama, Ethiopia; 2Department of Organic Chemistry, Faculty of Chemistry, University of Valencia, Burjassot, Spain; 3Department of Pharmacology, Faculty of Pharmacy, University of Valencia, Burjassot, Spain; 4Department of Microbiology and Ecology, Faculty of Pharmacy, University of Valencia, Burjassot, Spain; 5Parasites and Health Research Group, Department of Pharmacy, Pharmaceutical Technology and Parasitology, Faculty of Pharmacy…

Euphorbia schimperianaStereochemistryRanunculaceaeBiochemistry Genetics and Molecular Biology (miscellaneous)BiochemistryDNA gyrasechemistry.chemical_compoundDFT analysisUvaria scheffleriLupeolOriginal ResearchClematis burgensisbiologyDihydrochalconemolecular dockingCoumarinAntimicrobialbiology.organism_classificationComputer Science ApplicationsADMETchemistryAdvances and Applications in Bioinformatics and ChemistryChemistry (miscellaneous)Docking (molecular)antimicrobialAntibacterial activityAdvances and Applications in Bioinformatics and Chemistry : AABC
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Real-time PCR detection of Pseudomonas aeruginosa in clinical and municipal wastewater and genotyping of the ciprofloxacin-resistant isolates

2006

Real-time quantification of Pseudomonas aeruginosa was performed in various wastewater systems including clinical, municipal wastewaters and inflow from a wastewater treatment plant. The highest concentrations of P. aeruginosa-specific targets were detected in clinical wastewaters. Limitations of the detection system resulting from inhibition or cross-reaction were identified. Ciprofloxacin-resistant P. aeruginosa strains were isolated after specific enrichment from clinical and municipal wastewaters. In some cases they were also cultivated from effluent of a wastewater treatment plant, and from its downstream river water. A total of 119 isolates were phenotypically characterized as ciprofl…

GeneticsEcologyPseudomonas aeruginosabiochemical phenomena metabolism and nutritionRibosomal RNABiologybacterial infections and mycosesmedicine.disease_causebiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologyDNA gyraseMicrobiologyCiprofloxacinGenotypemedicineGenotypingAntibacterial agentmedicine.drugPseudomonadaceaeFEMS Microbiology Ecology
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GyrA sequence-based typing of Legionella.

2000

Comparative sequence analysis of a 423-bp segment of the gyrA gene including a region homologous to the quinolone resistance-determining region (QRDR) of other species was evaluated as a novel typing method for Legionella strains. The study was performed with 29 reference strains representing 11 different Legionella species, with various serogroups, and with 13 clinical isolates of L. pneumophila. Pulsed-field gel electrophoresis and serotyping were employed for comparison of the clinical isolates. QRDR sequencing proved to be a highly discriminative tool for typing Legionellae, and permitted identification of species, serogroups and even different strains within serogroup 1. None of the is…

Microbiology (medical)SerotypeDNA BacterialLegionellaSequence analysisImmunologyLegionellaSensitivity and SpecificityMicrobiologyRestriction fragmentAnti-Infective AgentsGenotypePulsed-field gel electrophoresisImmunology and AllergyHumansTypingGenetics4-QuinolonesbiologyMolecular epidemiologyGeneral Medicinebiochemical phenomena metabolism and nutritionbacterial infections and mycosesbiology.organism_classificationElectrophoresis Gel Pulsed-FieldDNA Topoisomerases Type IIDNA GyraseGenes Bacterialbiology.proteinMedical microbiology and immunology
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