Search results for "nuclei"

showing 10 items of 1273 documents

Genome characterisation of two Ljungan virus isolates from wild bank voles (Myodes glareolus) in Sweden

2015

Ljungan virus (LV) (family Picornaviridae, genus Parechovirus) is a suspected zoonotic pathogen with associations to human disease in Sweden. LV is a single-stranded RNA virus with a positive sense genome. There are five published Ljungan virus strains, three isolated from Sweden and two from America, and are classified into four genotypes. A further two strains described here were isolated from wild bank voles (Myodes glareolus) caught in Vastmanlands county, Sweden in 1994. These strains were sequenced using next generation pyrosequencing technology on the GS454flx platform. Genetic and phylogenetic analysis of the obtained genomes confirms isolates LV340 and LV342 as two new putative mem…

Microbiology (medical)Genes ViralGenotypeGS454ParechovirusGenome ViralMicrobiologyGenomeEvolution MolecularPhylogeneticsUntranslated Regionspositive selectionGenotypeevolutionMyodes glareolusGeneticsAnimalsSelection GeneticMolecular BiologyEcology Evolution Behavior and SystematicsPhylogenyGeneticsSwedenPicornaviridae InfectionsbiologyPhylogenetic treeArvicolinaeta1183RNA virusLjungan virusbiology.organism_classificationVirologyInfectious DiseasesLjungan virusArvicolinaeVP3ParechovirusNucleic Acid ConformationRNA Viralta1181Infection, Genetics and Evolution
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Detection of hepatitis B virus DNA by polymerase chain reaction in serum and liver of children with chronic hepatitis B negative for hepatitis B viru…

1992

Hepatitis B virus (HBV) DNA was detected by polymerase chain reaction in the serum of 87 and liver tissue of 40 children with chronic hepatitis B, negative for HBV DNA by dot blot and Southern blot hybridization, respectively. In sera HBV DNA could be detected in 73 hepatitis B surface antigen carriers; 14 were hepatitis B e antigen (HBeAg), 56 were anti-HBe-seropositive and 3 had neither HBeAg nor positive anti-HBe. In 14 anti-HBe-positive patients no HBV DNA could be found. Viral sequences in liver tissue were present in 33 specimens; 20 were HBeAg and 13 were anti-HBe-seropositive. All of the 7 negative children had anti-HBe. Our results confirm polymerase chain reaction to be a more sen…

Microbiology (medical)Hepatitis B virusAdolescentHepatitis B virus DNA polymeraseMolecular Sequence Datamedicine.disease_causePolymerase Chain ReactionHepatitis B virus PRE betaViruslaw.inventionlawMedicineHumansChildPolymerase chain reactionSouthern blotHepatitis B virusbiologyBase Sequencebusiness.industryvirus diseasesInfantNucleic Acid Hybridizationbiology.organism_classificationHepatitis BVirologydigestive system diseasesInfectious DiseasesHBeAgHepadnaviridaeLiverChild PreschoolPediatrics Perinatology and Child HealthChronic DiseaseDNA ViralbusinessThe Pediatric infectious disease journal
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Rickettsia conorii Indian Tick Typhus Strain and R. slovaca in Humans, Sicily

2012

Letter to the Editor.-- et al.

Microbiology (medical)LetterSettore MED/17 - Malattie Infettivevector-borne infectionslcsh:MedicineBacteremiaBiologyTickBoutonneuse FeverMicrobiologylcsh:Infectious and parasitic diseasesBacterial proteinBacterial ProteinsSequence Homology Nucleic AcidmedicineHumanslcsh:RC109-216Letters to the EditorSicilyCiencias VeterinariasStrain (biology)RICKETTSIOSIS SICILY TICKlcsh:RMediterranean spotted feverMediterranean spotted fever (Boutonneuse fever)zoonosisIndian tick typhus strainmedicine.diseasebiology.organism_classificationVirologyrickettsiatickRickettsia slovacaBoutonneuse feverRickettsia conoriiInfectious DiseasesCIENCIAS AGRÍCOLASRickettsia slovacaepidemiology//purl.org/becyt/ford/4.3 [https]Rickettsia conorii//purl.org/becyt/ford/4 [https]TyphusMultilocus Sequence TypingEmerging Infectious Diseases
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Characterization and multicentric validation of a common standard for Toxoplasma gondii detection using nucleic acid amplification assays.

2014

ABSTRACT The molecular diagnosis of toxoplasmosis essentially relies upon laboratory-developed methods and suffers from lack of standardization, hence the large diversity of performances between laboratories. Moreover, quantifications of parasitic loads differ among centers, a fact which prevents the possible prediction of the severity of this disease as a function of parasitic loads. The objectives of this multicentric study performed in eight proficient laboratories of the Molecular Biology Pole of the French National Reference Center for Toxoplasmosis (NRC-T) were (i) to assess the suitability of a lyophilized preparation of Toxoplasma gondii as a common standard for use in this PCR-base…

Microbiology (medical)MESH: Reference Standards*MESH: Molecular Diagnostic Techniques/methods*MESH: Parasite Load/standards[SDV]Life Sciences [q-bio]Toxoplasma gondiidiagnosticParasitic loadsParasite LoadMESH: Nucleic Acid Amplification Techniques/standards*MESH: Toxoplasma/isolation & purification*medicineMolecular diagnostic techniquesHumansNational levelReference standardsMESH: Parasite Load/methodsstandardizationMESH: HumansbiologyMESH: Nucleic Acid Amplification Techniques/methods*Toxoplasma gondiiNucleic acid amplification techniqueMESH: Toxoplasmosis/diagnosis*MESH: Molecular Diagnostic Techniques/standards*Reference Standardsbiology.organism_classificationmedicine.diseaseVirologyToxoplasmosisquantification3. Good healthMESH: FranceMolecular Diagnostic TechniquesImmunologyNucleic acidMESH: Toxoplasma/geneticsParasitologyFranceNucleic Acid Amplification TechniquesToxoplasmaToxoplasmosisJournal of clinical microbiology
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Freezing and storage at -20 °C provides adequate preservation of Toxoplasma gondii DNA for retrospective molecular analysis.

2014

Equipe EA MERS; International audience; Nucleic acid-based testing has become crucial for toxoplasmosis diagnosis. For retrospective (forensic or scientific) studies, optimal methods must be employed for DNA long-term storage. We compared Toxoplasma gondii detection before and after DNA storage using real-time PCR. No significant differences were found depending on duration or storage conditions at -20 °C or -80 °C.

Microbiology (medical)Time Factors[SDV]Life Sciences [q-bio]educationBiologyReal-Time Polymerase Chain ReactionSpecimen HandlingToxoplasma gondii DNAchemistry.chemical_compoundparasitic diseasesFreezingmedicineRetrospective Studiestoxoplasma gondiiDNA storageToxoplasma gondiiamniotic fluidGeneral MedicineDNA Protozoanmedicine.diseasebiology.organism_classificationVirologyToxoplasmosisDna storageMolecular analysisInfectious DiseasesReal-time polymerase chain reaction[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologychemistryMolecular Diagnostic Techniquescongenital toxoplasmosisNucleic acidMESH: DNA Protozoan/isolation&purification; Freezing; Molecular Diagnostic Technics/methods; Specimen Handling/methods; Toxoplasmosis/diagnosisreal-Time PCRToxoplasmaDNAToxoplasmosisDiagnostic microbiology and infectious disease
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Evaluation of the Amplex eazyplex Loop-Mediated Isothermal Amplification Assay for Rapid Diagnosis of Pneumocystis jirovecii Pneumonia

2020

ABSTRACT Quantitative PCR (qPCR) assays are the gold standard for diagnosis of Pneumocystis jirovecii pneumonia (PCP). However, they are laborious and require skilled personnel. Therefore, execution outside regular working hours of the molecular biology laboratory is limited. The eazyplex P. jirovecii assay (PJA) uses loop-mediated isothermal amplification for detection of P. jirovecii. It is performed directly with respiratory specimens, without the need for special skills, and delivers a result within 3 to 25 min. The goal of our study was to compare the performance of the eazyplex PJA with that of established P. jirovecii qPCR assays. All archived bronchoalveolar lavage fluid (BALF) samp…

Microbiology (medical)Working hoursmedicine.diagnostic_testbusiness.industryPneumonia PneumocystisPneumocystis jirovecii PneumoniaLoop-mediated isothermal amplificationTime to resultMycologyGold standard (test)Pneumocystis cariniiSensitivity and SpecificityMicrobiologyReal-time polymerase chain reactionBronchoalveolar lavageMolecular Diagnostic TechniquesPneumocystis cariniiparasitic diseasesHumansMedicineProspective StudiesbusinessBronchoalveolar Lavage FluidNucleic Acid Amplification TechniquesRetrospective StudiesJournal of Clinical Microbiology
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Sequence polymorphism of mitochondrial DNA control region in Japanese.

1998

Sequence polymorphisms of the mitochondrial DNA (mtDNA) control region, hypervariable regions I and II, from 100 unrelated Japanese were determined by PCR amplification and direct sequencing. Sequences of 404 nucleotides for hypervariable region I and 379 nucleotides for region II were obtained. Variable sites (85 and 45) were revealed in region I and region II, respectively, as compared to the reference sequence, and a total of 96 different genetic patterns from both regions I and II were determined. A point mutation heteroplasmy was observed at the ratio of approximately 50:50 from one individual at the sequence position 151 showing a nucleotide transition from C to T. The probability of …

Mitochondrial DNAGenotypeSequence analysisPopulationMolecular Sequence DataBiologyDNA MitochondrialPolymerase Chain ReactionPathology and Forensic MedicineJapanHumansPoint MutationeducationDNA PrimersmtDNA control regionGeneticseducation.field_of_studyPolymorphism GeneticBase SequenceNucleic acid sequenceSequence Analysis DNALocus Control RegionHeteroplasmyHypervariable regionGenetics PopulationGenetic markerLawForensic science international
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Mitochondrial genome of Suberites domuncula: palindromes and inverted repeats are abundant in non-coding regions.

2007

The 26,300-nucleotide sequence of the mitochondrial DNA (mtDNA) molecule of the demosponge Suberites domuncula (Olivi, 1792), the largest in size yet found in Porifera, has been determined. We describe the second hadromerid sponge mitochondrial genome that contains the same set of 41 genes as the hadromerid sponge Tethya actinia, including trnMe(cau), trnI2(cau), trnR2(ucu), and atp9, all of which are transcribed in the same direction. Furthermore, rRNA genes for the small and large ribosomal subunit are very long, rns is indeed the longest among Metazoa (1833 bp). Intergenic regions (IGR) comprise about 25% of S. domuncula mtDNA and include numerous direct and inverted repeats, as well as …

Mitochondrial DNAInverted repeatMolecular Sequence DataSuberites ficusDNA MitochondrialIntergenic regionRNA TransferSpecies SpecificityLarge ribosomal subunitSequence Homology Nucleic AcidGeneticsAnimalsGenePhylogenyRepetitive Sequences Nucleic AcidGeneticsPorifera ; Hadromerida ; mtDNA ; mitochondrial evolution ; polymorphismsBase CompositionbiologyBase SequenceGenetic VariationGeneral MedicineRibosomal RNAbiology.organism_classificationSuberites domunculaGenome MitochondrialDNA IntergenicSuberitesGene
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Mitochondrial interference by anti-HIV drugs: mechanisms beyond Pol-γ inhibition.

2011

The combined pharmacological approach to the treatment of HIV infection, known as highly active antiretroviral therapy (HAART), has dramatically reduced AIDS-related morbidity and mortality. However, its use has been associated with serious adverse reactions, of which those resulting from mitochondrial dysfunction are particularly widespread. Nucleos(t)ide-reverse transcriptase inhibitors (NRTIs) have long been considered the main source of HAART-related mitochondrial toxicity due to their ability to inhibit Pol-γ, the DNA polymerase responsible for the synthesis of mitochondrial DNA. Nevertheless, accumulating evidence points to a more complex relationship between these organelles and NRTI…

Mitochondrial DNAMitochondrial DiseasesNucleic Acid Synthesis InhibitorDNA polymeraseAnti-HIV Agentsmedicine.medical_treatmentDNA-Directed DNA PolymeraseMitochondrionPharmacologyToxicologyAntiretroviral Therapy Highly ActivemedicineAnimalsHumansNucleic Acid Synthesis InhibitorsPharmacologyProteasebiologyvirus diseasesmedicine.diseaseReverse transcriptaseDNA Polymerase gammaMitochondriaMitochondrial toxicityToxicitybiology.proteinReverse Transcriptase InhibitorsTrends in pharmacological sciences
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Characterization of the length polymorphism in the A + T-rich region of the Drosophila obscura group species

1993

In the twelve Drosophila obscura group species studied, belonging to the affinis, obscura, and pseudoobscura subgroups, the mitochondrial DNA length ranges from 15.8 to 17.2 kb. This length polymorphism is mainly due to insertions/deletions in the variable region of the A + T-rich region. In addition, one species (D. tristis) possess a tandem duplication of a 470-bp fragment that contains the replication origin. The same duplication has occurred at least twice in the Drosophila evolutionary history due to the fact that the repetition is analogous to repetitions found in the four species of the D. melanogaster complex. By comparing the nucleotide sequence of the conserved region in D. ambigu…

Mitochondrial DNAMolecular Sequence DataRestriction MappingDNA RecombinantDNA MitochondrialConserved sequenceSpecies SpecificityMolecular evolutionDrosophilidaeSequence Homology Nucleic AcidGene duplicationGeneticsAnimalsMolecular BiologyEcology Evolution Behavior and SystematicsGeneticsPolymorphism GeneticbiologyBase SequenceAdenineNucleic acid sequencebiology.organism_classificationNucleic Acid ConformationDrosophilaTandem exon duplicationDrosophila obscuraSequence AlignmentPlasmidsThymidine
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