Search results for "length polymorphism"

showing 10 items of 177 documents

Current Technologies for Pseudomonas spp. And Ralstonia solanacearum Detection and Molecular Typing

2008

Standard protocols for detection of phytopathogenic Pseudomonas spp. and Ralstonia solanacearum in plant material, soil, water or other sources, often still rely on the isolation of bacterial colonies on appropriate media, and/or on the use of serological techniques. However, over the last several years, molecular techniques, mainly based on PCR methods after extraction of nucleic acids from samples, have improved enough to allow a more rapid, reliable detection of these bacteria. When maximum accuracy is required the use of multiple techniques in an integrated approach is advised. Other promising technologies like flow cytometry, electronic nose or microarrays are emerging due to the need …

Ralstonia solanacearumbiologybusiness.industryPseudomonasfood and beveragesbiology.organism_classificationIsolation (microbiology)BiotechnologyMolecular typingPulsed-field gel electrophoresisMultilocus sequence typingAmplified fragment length polymorphismDNA microarraybusiness
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Mutation Analysis Identifies GUCY2D as the Major Gene Responsible for Autosomal Dominant Progressive Cone Degeneration

2008

PURPOSE. Heterozygous mutations in the GUCY2D gene, which encodes the membrane-bound retinal guanylyl cyclase-1 protein (RetGC-1), have been shown to cause autosomal dominant inherited cone degeneration and cone–rod degeneration (adCD, adCRD). The present study was a comprehensive screening of the GUCY2D gene in 27 adCD and adCRD unrelated families of these rare disorders. METHODS. Mutation analysis was performed by direct sequencing as well as PCR and subsequent restriction length polymorphism analysis (PCR/RFLP). Haplotype analysis was performed in selected patients by using microsatellite markers. RESULTS. GUCY2D gene mutations were identified in 11 (40%) of 27 patients, and all mutation…

Retinal degenerationMaleDNA Mutational AnalysisReceptors Cell SurfaceBiologyPolymerase Chain ReactionArticlemedicineElectroretinographyMissense mutationHumansGenetic Predisposition to DiseaseCodonGeneGeneticsHaplotypeRetinal DegenerationDNAmedicine.diseasePrognosisRod Cell Outer SegmentMajor geneMolecular biologyPedigreeHaplotypesGuanylate CyclaseMutationMutation testingDisease ProgressionGUCY2DFemaleRestriction fragment length polymorphism
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Bradyrhizobium sp. nodulating the Mediterranean shrub Spanish broom (Spartium junceum L.)

2002

Aims: The molecular diversity of 25 strains of rhizobia, isolated in Sicily from root nodules of the Mediterranean shrubby legume Spanish broom (Spartium junceum L.), is presented in relation to the known rhizobial reference strains. Methods and Results: Our approach to the study of the S. junceum rhizobial diversity combined the information given by the 16S and the intergenic spacer (IGS) 16S–23S rDNA polymorphic region by obtaining them in a single polymerase chain reaction (PCR) step. The PCR fragment size of the S. junceum isolates was 2400–2500 bp and that of the reference strains varied from 2400 in Bradyrhizobium strains to 2800 in Sinorhizobium strains. Inter- and intrageneric lengt…

Root noduleMolecular Sequence DataSpartiummedicine.disease_causePlant RootsPolymerase Chain ReactionApplied Microbiology and BiotechnologyBradyrhizobiumRhizobium leguminosarumRhizobiaRNA Ribosomal 16SBotanymedicineBradyrhizobiumRibosomal DNAPhylogenyGeneticsbiologyfood and beveragesFabaceaeSequence Analysis DNAGeneral Medicinebiochemical phenomena metabolism and nutritionbiology.organism_classificationSinorhizobiumDNA IntergenicRestriction fragment length polymorphismPolymorphism Restriction Fragment LengthBiotechnology
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Vigna mungo, V. radiata and V. unguiculata plants sampled in different agronomical-ecological-climatic regions of India are nodulated by Bradyrhizobi…

2009

International audience; Vigna mungo, Vigna radiata and Vigna unguiculata are important legume crops cultivated in India, but little is known about the genetic resources in native rhizobia that nodulate these species. To identify these bacteria, a core collection of 76 slow-growing isolates was built from root nodules of V. mungo, V. radiata and V. unguiculata plants grown at different sites within three agro-ecological-climatic regions of India. The genetic diversity of the bacterial collection was assessed by restriction fragment length polymorphism (RFLP) analysis of PCR-amplified DNA fragments of the 16S–23S rDNA intergenic spacer (IGS) region, and the symbiotic genes nifH and nodC. One …

Root noduleVigna spp.RadiataDIVERSITYApplied Microbiology and BiotechnologyPlant Root NodulationPolymerase Chain ReactionVignaSymbiotic genesCluster AnalysisBradyrhizobiumPhylogeny0303 health sciencesDiversitybiologyEcologyfood and beveragesFabaceae[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyRestriction fragment length polymorphismOxidoreductasesRoot Nodules PlantPolymorphism Restriction Fragment LengthDNA BacterialBradyrhizobium yuanmingensePHYLOGENYVIGNA SPP.Molecular Sequence DataIndiaN-AcetylglucosaminyltransferasesMicrobiologyBradyrhizobiumRhizobia03 medical and health sciencesVIGNA RADIATABacterial ProteinsBotanyDNA Ribosomal SpacerSYMBIOTIC GENESEcology Evolution Behavior and Systematics030304 developmental biologyRELATION HOTE-PARASITEGenetic diversity030306 microbiologyBRADYRHIZOBIUMSequence Analysis DNA15. Life on landVIGNA MUNGObiology.organism_classificationMULTI-LOCUS SEQUENCE ANALYSISMulti-locus sequence analysis
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Effects of the introduction of a biocontrol strain of Trichoderma atroviride on non target soil micro-organisms

2009

International audience; The main objective of this study was to assess the impact of the application of an antagonistic strain of Trichoderma atroviride on the native microbial soil communities. The structures of the fungal and bacterial communities were assessed by T-RFLP (terminal restriction fragment length polymorphism) method, based on T-RFLP analysis of 18S and 16S rRNA genes, respectively. Results showed that the introduction of the strain I-1237 into two soils slightly modified the microbial diversity, only for a short period of time. Nine months post-inoculation resilience took place, resulting in similar structures of the fungal and bacterial communities in the inoculated and cont…

SOIL MICROBIAL COMMUNITIES T-RFLP0303 health sciencesbiologyStrain (chemistry)030306 microbiologyMicroorganism[SDV]Life Sciences [q-bio]Soil ScienceFungi imperfecti16S ribosomal RNAbiology.organism_classificationMicrobiologyBIOCONTROL03 medical and health sciencesTerminal restriction fragment length polymorphismPOPULATION DYNAMICSMicrobial population biologyInsect ScienceTrichodermaBotany[SDE]Environmental SciencesRestriction fragment length polymorphism030304 developmental biology
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Serotypes, Antibiotic Resistance, and Class 1 Integrons in Salmonella Isolates from Pediatric Cases of Enteritis in Tehran, Iran

2011

The present study was conducted to investigate serotype distribution, antimicrobial resistance patterns, carriage of class 1 integron, and clonality of Salmonella strains isolated from patients aged 0-12 years in Tehran, Iran, during 2007-2008. A total of 139 Salmonella isolates were studied. Salmonella serotypes Enteritidis, Infantis, and Typhimurium included 84.9% of isolates, Enteritidis accounting for 41.7%. The most prevalent resistances were to doxycycline (64.7%), nalidixic acid (61.2%), tetracycline (51.8%), and streptomycin (42.8%). Fifty-three (38.1%) isolates contained class 1 integron. Eight different gene cassettes were identified, aadA1 being the most frequently encountered. P…

Salmonella typhimuriumSerotypeSettore MED/07 - Microbiologia E Microbiologia ClinicaSalmonellaNalidixic acidTetracyclineDrug resistanceIranSettore MED/42 - Igiene Generale E ApplicataIntegronmedicine.disease_causeApplied Microbiology and BiotechnologyMicrobiologyIntegronsMicrobiologyAntibiotic resistanceBacterial ProteinsDisk Diffusion Antimicrobial TestsSalmonellaDrug Resistance BacterialmedicineHumansSalmonella antibiotic resistance class 1 integrons IranAmplified Fragment Length Polymorphism AnalysisSerotypingChildbiologyInfantHospitals PediatricEnteritisAnti-Bacterial AgentsClone CellsElectrophoresis Gel Pulsed-FieldSalmonella enteritidisStreptomycinChild PreschoolSalmonella Infectionsbiology.proteinAnimal Science and ZoologyFood Sciencemedicine.drugFoodborne Pathogens and Disease
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Diagnosis of flavobacteriosis by direct amplification of rRNA genes

2002

A broad-range bacterial PCR method with universal 16S rDNA targeting primers and bacterial cultivation was used to identify the putative pathogen in flavobacterial outbreaks. Restriction fragment length polymorphism (PCR-RFLP) analysis and sequencing of the partial 16S rDNA PCR products of 10 skin samples and 10 representative isolates derived from the same fish specimens revealed differences between direct molecular and cultivation-based analysis. Flavobacterium columnare-like sequences dominated in the direct molecular analysis in most cases, whereas most of the isolates belonged to a phylogenetically heterogeneous group of flavobacteria clustering with F. hibernum. F. columnare was isola…

Sequence HomologyAquatic ScienceDNA RibosomalFlavobacteriumMicrobiologySpecies SpecificityPhylogeneticsPseudomonasRNA Ribosomal 16SAnimalsPhylogenyEcology Evolution Behavior and SystematicsGeneticsBase SequencebiologyPseudomonasGene AmplificationRibosomal RNA16S ribosomal RNAbiology.organism_classificationFlavobacteriaceaeRestriction fragment length polymorphismGram-Negative Bacterial InfectionsSequence AlignmentPolymorphism Restriction Fragment LengthBacteriaFlavobacteriumDiseases of Aquatic Organisms
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ABO genotyping by PCR-RFLP and cloning and sequencing

2005

A refined PCR-RFLP based method was established to genotype ABO blood groups. The main objective of this study was to make the techniques also suitable for working with degraded DNA. Specific primer design was carried out to choose fragments shorter than 200 bp as necessary in forensic and archaeological applications. Four fragments of exon 6 and 7 of the ABO gene were amplified and digested by in total 7 restriction endonucleases. Particular attention was paid to the base changes at nucleotide positions 261(delG), 297, 526, 703, 721, 771, 796 and 1060(delC) in order to distinguish the six common alleles A101, A201, B, O01, O02 and O03. Furthermore, this method also enables determination of…

Sequence analysisBiologyPolymerase Chain ReactionABO Blood-Group Systemlaw.inventionlawABO blood group systemGenotypeHumansCloning MolecularGenotypingAllelesHistory AncientEcology Evolution Behavior and SystematicsPolymerase chain reactionGeneticsReproducibility of ResultsSequence Analysis DNAGeneral MedicineForensic MedicineRestriction enzymePhenotypeAncient DNAArchaeologyBlood StainsPostmortem ChangesAnthropologyDNA Transposable ElementsAnimal Science and ZoologyChromosome DeletionRestriction fragment length polymorphismToothPolymorphism Restriction Fragment LengthAnthropologischer Anzeiger
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A Polyphasic Approach to Study the Intraspecif ic Diversity Amongst Vibrio vulnificus Isolates

1997

Summary A polyphasic taxonomic approach using phenotypic and molecular genetic techniques, was carried out on the species Vibrio vulnificus in order to study its intraspecific diversity. Seven techniques, including phenotypic (API 20E, BIOLOG, total protein profiles, serotyping, ELISA), and genotypic methods (ribotyping and AFLP), were employed on 80 V. vulnificus strains of biotypes 1 and 2, including 9 reference cultures. The isolates came from different geographic origins (USA, Spain, Belgium, Sweden, Norway, Japan, Thailand) and types of samples (clinical, health/diseased fish, seafood, water). Diversity indexes calculated for strains of both biotypes revealed a higher phenotypic and ge…

SerotypeGeneticsGenetic diversitybiologyVibrio vulnificusbiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologyMicrobiologyRibotypingDNA profilingGenotypeAmplified fragment length polymorphismTypingEcology Evolution Behavior and SystematicsSystematic and Applied Microbiology
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Genetic population structure of Epinephelus marginatus (Pisces, Serranidae) revealed by two molecular markers

2006

In this paper, data are presented regarding the population structure of dusky grouper (Epinephelus marginatus) which was sampled in the Mediterranean Sea and Atlantic Ocean using two different molecular markers, ND2 RFLP and cytochrome b (cyt b) sequence analysis. The main objective of the study is to analyse the genetic variability of E. marginatus in the Mediterranean Sea to define how the biological characteristics of the species, such as the dispersal capability of pelagic larvae and the benthonic-sedentary life style, can affect the genetic population structure or maintaining the gene flow or determining genetic differences. Furthermore, we considered an Atlantic sample to establish th…

SerranidaebiologyEcologyCytochrome bZoologyEpinephelus marginatusbiology.organism_classificationGene flowMediterranean seaDusky grouper cyt b ND2 RFLP genetic population structureBiological dispersalAnimal Science and ZoologyGenetic variabilityRestriction fragment length polymorphism
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