Search results for "Structural Proteins"

showing 10 items of 109 documents

ISDR pattern and evolution in patients with chronic hepatitis C treated with standard or Peg-IFN plus ribavirin

2003

The aim of the study was to characterize the interferon sensitivity determining region (ISDR) mutation pattern and its changes at 4 weeks of treatment in a population of patients infected with hepatitis C virus (HCV) genotype 1b receiving standard or PEG-IFN plus ribavirin (RBV), to find possible early correlates of therapy outcome.Forty-five patients with chronic hepatitis due to HCV 1b were treated by PEG-IFN-α2b (n=23) or IFN-α2b (n=22) plus RBV 1000–1200 mg/day. They were classified 24 weeks after stopping therapy as sustained responders (SR), relapsers (REL) or non-responders (NR). Sixteen patients were SR, 12 REL and 17 NR. ISDR mutations were evaluated by direct sequencing at baselin…

Malemedicine.medical_treatmentHepacivirusHepacivirusViral Nonstructural Proteinsmedicine.disease_causePolyethylene GlycolPolyethylene GlycolsCohort Studieschemistry.chemical_compoundInterferonMedicinePharmacology (medical)education.field_of_studybiologyRecombinant ProteinMiddle AgedRecombinant ProteinsTreatment OutcomeInfectious DiseasesDrug Therapy CombinationFemaleHumanmedicine.drugGenotypeHepatitis C virusMolecular Sequence DataPopulationInterferon alpha-2Antiviral AgentsVirusFlaviviridaeRibavirinHumansAmino Acid SequenceeducationAntiviral AgentPharmacologyChemotherapyHepacivirubusiness.industryRibavirinInterferon-alphaHepatitis C Chronicbiology.organism_classificationVirologychemistryMutationCohort StudiebusinessSequence Alignment
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Generation of immune responses against hepatitis C virus by dendritic cells containing NS5 protein-coated microparticles.

2009

ABSTRACTDendritic cells (DCs) internalize and process antigens as well as activate cellular immune responses. The aim of this study was to determine the capacity of DCs that contain antigen-coated magnetic beads to induce immunity against the nonstructural hepatitis C virus (HCV) antigen 5 (NS5). Splenocytes derived from Fms-like tyrosine kinase receptor 3 (Flt3) ligand-pretreated BALB/c mice were incubated with magnetic beads coated with HCV NS5, lipopolysaccharide (LPS), and/or anti-CD40; purified; and used for immunization. Cellular immunity was measured using cytotoxic T-lymphocyte (CTL) and T-cell proliferation assays, intracellular cytokine staining, and a syngeneic tumor challenge us…

Microbiology (medical)Cytotoxicity ImmunologicCellular immunityLipopolysaccharidevirusesT-LymphocytesClinical BiochemistryImmunologychemical and pharmacologic phenomenaHepacivirusBiologyViral Nonstructural Proteinschemistry.chemical_compoundMiceImmune systemAntigenImmunitySplenocyteImmunology and AllergyCytotoxic T cellAnimalsCell ProliferationMice Inbred BALB Cvirus diseasesDendritic CellsCytotoxicity Tests ImmunologicVaccine ResearchMolecular biologyMicrospheresCTL*chemistryCytokinesFemaleClinical and vaccine immunology : CVI
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Rare AU-1-like G3P[9] human rotaviruses with a Kun-like NSP4 gene in children with diarrhea in Italy

2007

ABSTRACT Three G3P[9] rotaviruses, detected in children hospitalized with gastroenteritis in Palermo, Italy, were found to be genetically related to strains of either human or feline origin in the VP7, VP4, and VP6 genes. In contrast, in the NSP4 gene the viruses resembled G2P[4] human strains, suggesting a reassortment between AU-1-like and Kun-like strains.

Microbiology (medical)DiarrheaRotavirusSettore MED/07 - Microbiologia E Microbiologia ClinicaSettore MED/17 - Malattie InfettivevirusesReassortmentMolecular Sequence DataReoviridaeSequence HomologyViral Nonstructural Proteinsmedicine.disease_causeVirusRotavirus InfectionsRotavirus Phylogenetic analysesfluids and secretionsPhylogeneticsRotavirusVirologyGenotypemedicineHumansChildGenePhylogenyViral Structural Proteinsbiologyvirus diseasesSequence Analysis DNAbiology.organism_classificationVirologyDiarrheaItalymedicine.symptom
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The role of positive selection in hepatitis C virus

2008

Hepatitis C virus (HCV) is a major health problem worldwide, infecting an estimated 170 million people. In this study, we have employed a large data set of sequences (14,654 sequences from between 25 and 100 clone sequences per analyzed region and per patient) from 67 patients infected with HCV genotype 1 (23 subtype 1a and 44 subtype 1b). For all patients, a sample prior to combined therapy with alpha interferon plus ribavirin was available, whereas for some patients additional samples after 6 or 12 months of treatment were also available. Twenty-seven patients responded to treatment (12 subtype 1a and 15 subtype 1b) and forty patients did not respond to treatment (11 subtype 1a vs. 29 sub…

Microbiology (medical)Hepatitis C virusAlpha interferonHepacivirusViral Nonstructural ProteinsBiologymedicine.disease_causeMicrobiologyCohort Studieschemistry.chemical_compoundViral Envelope ProteinsSequence Analysis ProteinInterferonDrug Resistance ViralRibavirinGeneticsmedicineHumansAmino Acid SequenceSelection GeneticNS5AMolecular BiologyEcology Evolution Behavior and SystematicsChi-Square DistributionRibavirinInterferon-alphaHepatitis Cmedicine.diseaseComplementarity Determining RegionsHepatitis CVirologyHypervariable regionInfectious DiseaseschemistryImmunologyViral hepatitismedicine.drugInfection, Genetics and Evolution
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Molecular epidemiology of a hepatitis C virus outbreak in a hemodialysis unit.

2005

ABSTRACT We analyzed a hepatitis C virus (HCV) transmission case in the hemodialysis unit of a private clinic by sequencing two genome regions of virus isolates from a number of patients attending this unit and some external controls. The analysis of 337 nucleotides (nt) in the NS5B region did not provide enough resolution to ascertain which patients were actually involved in the outbreak and the potential source. Nevertheless, this region allowed the exclusion of several patients as putative sources of the transmission case based on their genotypes and phylogenetic relationships. On the other hand, the analysis of several 472-nt-long clone sequences per sample in a more rapidly evolving re…

Microbiology (medical)MaleEpidemiologyHepatitis C virusMolecular Sequence DataHepacivirusBiologyViral Nonstructural Proteinsmedicine.disease_causeVirusDisease Outbreakschemistry.chemical_compoundFlaviviridaeViral Envelope ProteinsmedicineHumansGenetic variabilityNS5BCross InfectionMolecular EpidemiologyMolecular epidemiologyOutbreakSequence Analysis DNAbiology.organism_classificationVirologyHepatitis CHypervariable regionHemodialysis Units HospitalchemistryFemaleJournal of clinical microbiology
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Identification of group A porcine rotavirus strains bearing a novel VP4 (P) genotype in Italian swine herds.

2007

ABSTRACT The VP4 gene of a G5 Italian porcine rotavirus strain, 344/04-1, was nontypeable by PCR genotyping. The amino acid sequence of the full-length VP4 protein had low identity (≤76.6%) with the homologous sequences of representative strains of the remaining P genotypes, providing evidence for a novel P genotype.

Microbiology (medical)RotavirusGenotypeSwinevirusesMolecular Sequence DataReoviridaeViral Nonstructural Proteinsmedicine.disease_causeGroup AVirusRotavirus Infectionsfluids and secretionsRotavirusVirologyGenotypemedicineAnimalsPeptide sequenceGenotypingAntigens ViralGlycoproteinsToxins BiologicalSwine DiseasesbiologyStrain (biology)virus diseasesSequence Analysis DNAbiology.organism_classificationVirologyItalyCapsid Proteins
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Identification of a multi-reassortant G12P[9] rotavirus with novel VP1, VP2, VP3 and NSP2 genotypes in a child with acute gastroenteritis.

2015

The G12 rotavirus genotype is globally emerging to cause severe gastroenteritis in children. Common G12 rotaviruses have either a Wa-like or DS-1-like genome constellation, while some G12 strains may have unusual genome composition. In this study, we determined the full-genome sequence of a G12P[9] strain (ME848/12) detected in a child hospitalized with acute gastroenteritis in Italy in 2012. Strain ME848/12 showed a complex genetic constellation (G12-P[9]-I17-R12-C12-M11-A12-N12-T7-E6-H2), likely derived from multiple reassortment events, with the VP1, VP2, VP3 and NSP2 genes being established as novel genotypes R12, C12, M11 and N12, respectively. Gathering sequence data on human and anim…

Microbiology (medical)RotavirusGenotypingSettore MED/07 - Microbiologia E Microbiologia ClinicavirusesReassortmentHuman rotaviruGenome ViralBiologymedicine.disease_causeMicrobiologyGenomeRotavirus InfectionsReassortmentRotavirusGenotypeGeneticsmedicineHumansMolecular BiologyGenotypingGeneEcology Evolution Behavior and SystematicsPhylogenyGeneticsWhole genome sequencingViral Structural ProteinsSequence Analysis RNAStrain (biology)virus diseasesVirologyFull genome sequencingGastroenteritisInterspecies transmissionInfectious DiseasesChild PreschoolG12P[9]Reassortant VirusesInfection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases
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Molecular Analysis of the VP7, VP4, VP6, NSP4, and NSP5/6 Genes of a Buffalo Rotavirus Strain: Identification of the Rare P[3] Rhesus Rotavirus-Like …

2003

ABSTRACT We report the detection and molecular characterization of a rotavirus strain, 10733, isolated from the feces of a buffalo calf affected with diarrhea in Italy. Strain 10733 was classified as a P[3] rotavirus, as the VP8* trypsin cleavage product of the VP4 protein revealed a high amino acid identity (96.2%) with that of rhesus rotavirus strain RRV (P5B[3]), used as the recipient virus in the human-simian reassortant vaccine. Analysis of the VP7 gene product revealed that strain 10733 possessed G6 serotype specificity, a type common in ruminants, with an amino acid identity to G6 rotavirus strains ranging from 88 to 98%, to Venezuelan bovine strain BRV033, and Hungarian human strain…

Microbiology (medical)SerotypeDiarrheaRotavirusGenes ViralSwinevirusesReassortmentMolecular Sequence DataReoviridaeCattle DiseasesBiologyViral Nonstructural Proteinsmedicine.disease_causePolymerase Chain ReactionVirusBirdsFecesfluids and secretionsRotavirusVirologyGenotypemedicineAnimalsHumansAmino Acid SequenceHorsesGeneAntigens ViralAllelesPhylogenyGeneticsViral Structural ProteinsSequence Homology Amino Acidvirus diseasesbiology.organism_classificationVirologyMacaca mulattaDiarrheaCapsid ProteinsCattlemedicine.symptomSequence Alignment
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In Silico Insights into the SARS CoV-2 Main Protease Suggest NADH Endogenous Defences in the Control of the Pandemic Coronavirus Infection

2020

COVID-19 is a pandemic health emergency faced by the entire world. The clinical treatment of the severe acute respiratory syndrome (SARS) CoV-2 is currently based on the experimental administration of HIV antiviral drugs, such as lopinavir, ritonavir, and remdesivir (a nucleotide analogue used for Ebola infection). This work proposes a repurposing process using a database containing approximately 8000 known drugs in synergy structure- and ligand-based studies by means of the molecular docking and descriptor-based protocol. The proposed in silico findings identified new potential SARS CoV-2 main protease (MPRO) inhibitors that fit in the catalytic binding site of SARS CoV-2 MPRO. Several sel…

Models Molecular0301 basic medicineAgingmedicine.medical_treatmentcoronaviruslcsh:QR1-502Viral Nonstructural Proteinsmedicine.disease_causelcsh:Microbiology0302 clinical medicineSettore BIO/10 - BiochimicaCoronavirus 3C ProteasesCoronavirusvirus diseasesLopinavirHypothesisMolecular Docking SimulationCysteine EndopeptidasesDrug repositioningInfectious Diseases030220 oncology & carcinogenesisCoronavirus InfectionsOxidation-Reductionmedicine.drugDNA damageIn silicoPneumonia ViralBiologyAntiviral AgentsHIV-proteaseBetacoronavirus03 medical and health sciencesSARS-CoV-2 main proteaseVirologymedicineHumansComputer SimulationProtease InhibitorsPandemicsBinding SitesProteaseSARS-CoV-2Drug RepositioningCOVID-19HIV Protease InhibitorsDRUDIT web servicemolecular dockingNADbiology.organism_classificationVirologySettore CHIM/08 - Chimica FarmaceuticaCOVID-19 Drug Treatmentcoronaviru030104 developmental biologyNADHRitonavirBetacoronavirusDNA Damage
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Membrane Integration of Poliovirus 2B Viroporin

2011

Virus infections can result in a variety of cellular injuries, and these often involve the permeabilization of host membranes by viral proteins of the viroporin family. Prototypical viroporin 2B is responsible for the alterations in host cell membrane permeability that take place in enterovirus-infected cells. 2B protein can be localized at the endoplasmic reticulum (ER) and the Golgi complex, inducing membrane remodeling and the blockade of glycoprotein trafficking. These findings suggest that 2B has the potential to integrate into the ER membrane, but specific information regarding its biogenesis and mechanism of membrane insertion is lacking. Here, we report experimental results of in vi…

Models MolecularFarmacologiaVesicle-associated membrane protein 8MedicinaMolecular Sequence DataImmunologyPorinsViral Nonstructural ProteinsEndoplasmic ReticulumModels BiologicalMicrobiologyAmino acid sequencesymbols.namesakeMolecular sequence dataCricetinaeVirologyAnimalsAmino Acid SequenceIntegral membrane proteinCells CulturedSequence DeletionHost cell membranebiologyMembrane transport proteinEndoplasmic reticulumGolgi apparatusBiología y Biomedicina / BiologíaVirusVirus-Cell InteractionsCell biologyPoliovirusMembraneBiochemistryCytoplasmInsect Sciencesymbolsbiology.proteinJournal of Virology
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