Search results for "Nucleopolyhedrovirus"

showing 10 items of 19 documents

Co-infection with iflaviruses influences the insecticidal properties of Spodoptera exigua multiple nucleopolyhedrovirus occlusion bodies: Implication…

2017

Biological insecticides based on Spodoptera exigua multiple nucleopolyhedrovirus (SeMNPV) can efficiently control S. exigua larvae on field and greenhouse crops in many parts of the world. Spanish wild populations and laboratory colonies of S. exigua are infected by two iflaviruses (SeIV-1 and SeIV-2). Here we evaluated the effect of iflavirus co-infection on the insecticidal characteristics of SeMNPV occlusion bodies (OBs). Overall, iflavirus co-inoculation consistently reduced median lethal concentrations (LC50) for SeMNPV OBs compared to larvae infected with SeMNPV alone. However, the speed of kill of SeMNPV was similar in the presence or absence of the iflaviruses. A reduction of the we…

0106 biological sciences0301 basic medicineLife CyclesInsecticidesPhysiologyBiosecuritySeMNPV occlusion bodieslcsh:MedicineInsectPathogenesisPathology and Laboratory MedicineWeight Gain01 natural sciencesIflavirus co-infectionLarvaeInvertebrate GenomicsMedicine and Health Scienceslcsh:Sciencemedia_commonLarvaMultidisciplinaryCoinfectionAgricultureGenomicsInsectsPhysiological ParametersAgrochemicalsResearch ArticleArthropodamedia_common.quotation_subjectBiologySpodopteraSpodopteraMicrobiologyLepidoptera genitalia03 medical and health sciencesExtraction techniquesExiguaGeneticsAnimalsPest Control BiologicalBiological InsecticidesInoculationlcsh:RfungiBody WeightOrganismsBiology and Life SciencesPesticidebiology.organism_classificationInvertebratesRNA extractionNucleopolyhedrovirusesResearch and analysis methods010602 entomology030104 developmental biologyBiological insecticidesAnimal Genomicslcsh:QDevelopmental BiologyPLoS ONE
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Improved display of synthetic IgG-binding domains on the baculovirus surface.

2004

Improved display of foreign protein moieties in combination with beneficial alteration of the viral surface properties should be of value for targeted and enhanced gene delivery. Here, we describe a vector based on Autographa californica multiple nucleopolyhedrovirus (AcMNPV) displaying synthetic IgG-binding domains (ZZ) of protein A fused to the transmembrane anchor of vesicular stomatitis virus (VSV) G protein. This display vector was equipped with a GFP/EGFP expression cassette enabling fluorescent detection in both insect and mammalian cells. The virus construct displayed the biologically active fusion protein efficiently and showed increased binding capacity to IgG. As the display is …

0301 basic medicineCancer ResearchvirusesRecombinant Fusion Proteins030106 microbiologyGenetic VectorsGene deliveryBiologySpodopteraVesicular stomatitis Indiana virusViral vectorCell Line03 medical and health sciencesViral Envelope ProteinsViral entryCricetinaeAnimalsMembrane GlycoproteinsImmune SerafungiGenetic Therapybiology.organism_classificationMolecular biologyFusion proteinNucleopolyhedroviruses030104 developmental biologyOncologyIgG bindingVesicular stomatitis virusImmunoglobulin Gbiology.proteinExpression cassetteBinding Sites AntibodyRabbitsProtein ABaculoviridaeTechnology in cancer researchtreatment
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A novel baculovirus-derived promoter with high activity in the baculovirus expression system

2016

The baculovirus expression vector system (BEVS) has been widely used to produce a large number of recombinant proteins, and is becoming one of the most powerful, robust, and cost-effective systems for the production of eukaryotic proteins. Nevertheless, as in any other protein expression system, it is important to improve the production capabilities of this vector. The orf46 viral gene was identified among the most highly abundant sequences in the transcriptome of Spodoptera exigua larvae infected with its native baculovirus, the S. exigua multiple nucleopolyhedrovirus (SeMNPV). Different sequences upstream of the orf46 gene were cloned, and their promoter activities were tested by the expr…

0301 basic medicineInsect virusviruseslcsh:MedicineSpodopteraGeneral Biochemistry Genetics and Molecular Biology03 medical and health sciencesNucleopolyhedrovirusVirologyExiguaPolyhedrinInsect virusGeneMolecular BiologySf21biologyGeneral Neurosciencelcsh:RfungiPromoterGeneral Medicinebiology.organism_classificationMolecular biologyAutographa californica030104 developmental biologyProtein expressionGeneral Agricultural and Biological SciencesBiotechnologyPeerJ
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New Isolate ofMalacosoma neustriaNuclear Polyhedrosis Virus in Latvia

1998

AnimalsNuclear Polyhedrosis VirusMothsMalacosoma neustriaBiologybiology.organism_classificationVirologyNucleopolyhedrovirusesEcology Evolution Behavior and SystematicsVirusJournal of Invertebrate Pathology
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Baculovirus entry into human hepatoma cells.

2005

ABSTRACT Autographa californica multiple nucleopolyhedrovirus (AcMNPV), a prototype member of the Baculoviridae family, has gained increasing interest as a potential vector candidate for mammalian gene delivery applications. AcMNPV is known to enter both dividing and nondividing mammalian cell lines in vitro, but the mode and kinetics of entry as well as the intracellular transport of the virus in mammalian cells is poorly understood. The general objective of this study was to characterize the entry steps of AcMNPV- and green fluorescent protein-displaying recombinant baculoviruses in human hepatoma cells. The viruses were found to bind and transduce the cell line efficiently, and electron …

BaculoviridaeCarcinoma HepatocellularEndosomeImmunoelectron microscopyvirusesImmunologyGenetic VectorsGreen Fluorescent ProteinsEndosomesBiologySpodopteraEndocytosisVirus ReplicationMicrobiologyClathrinCell Linesymbols.namesakeViral entryVirologyAnimalsHumansPinocytosisVirionGolgi apparatusbiology.organism_classificationNucleopolyhedrovirusesCell biologyVirus-Cell InteractionsInsect Sciencebiology.proteinsymbolsHepatocytesJournal of virology
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Host-range expansion of Spodoptera exigua multiple nucleopolyhedrovirus to Agrotis segetum larvae when the midgut is bypassed.

2010

Given the high similarity in genome content and organization between Spodoptera exigua multiple nucleopolyhedrovirus (SeMNPV) and Agrotis segetum nucleopolyhedrovirus (AgseNPV), as well as the high percentages of similarity found between their 30 core genes, the specificity of these NPVs was analysed for the respective insect hosts, S. exigua and A. segetum. The LD(50) for AgseNPV in second-instar A. segetum larvae was 83 occlusion bodies per larva and the LT(50) was 8.1 days. AgseNPV was orally infectious for S. exigua, but the LD(50) was 10 000-fold higher than for SeMNPV. SeMNPV was not infectious for A. segetum larvae when administered orally, but an infection was established by injecti…

BaculoviridaeLaboratory of VirologyMothsSpodopterain-vivoheliothis-virescens larvaeLaboratorium voor VirologiebaculovirusBeet armywormVirologyExiguaparasitic diseasescalifornica-m-nucleopolyhedrovirusAnimalsPeritrophic matrixRNA MessengerLarvabiologyReverse Transcriptase Polymerase Chain ReactionfungiNuclear Polyhedrosis VirusMidgutocclusion-derived virusbiology.organism_classificationPE&RCVirologyNucleopolyhedrovirusesperitrophic matrixIntestinesAutographa californicacell-linesbeet armywormautographa-californicanuclear polyhedrosis-virusLarvaThe Journal of general virology
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Enhancing the multiplication of nucleopolyhedrovirus in vitro by manipulation of the pH

2009

Insect nucleopolyhedroviruses (NPVs) are studied widely as agents for biological control, as expression vectors for the production of heterologous proteins, and as transduction vectors for gene therapy applications. Most of these applications rely on the existence of cell lines that allow in vitro multiplication of the virus. The influence of pH in the medium culture on the multiplication of SeMNPV, HearSNPV and AcMNPV in different cell culture lines was investigated. The study showed a strong influence of the medium pH on the virus multiplication with the best results at pH 6.5, about half pH unit above the pH of insect culture media used most commonly. Additional experiments using a recom…

BaculoviridaevirusesGreen Fluorescent ProteinsCell Culture TechniquesHeterologousSpodopteraVirus ReplicationVirusCell LineGreen fluorescent proteinTransduction (genetics)VirologyAnimalsInsect virusExpression vectorbiologyfungiHydrogen-Ion ConcentrationVirus Internalizationbiology.organism_classificationMolecular biologyNucleopolyhedrovirusesCulture MediaCell biologyMicroscopy FluorescenceCell cultureJournal of Virological Methods
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Morphological characterization of baculovirus Autographa californica multiple nucleopolyhedrovirus

2009

The budded form of baculovirus Autographa californica multiple nucleopolyhedrovirus is used widely in biotechnological applications. In this study, we observed the morphology of baculovirus in nanometer scale by atomic force microscopy. Additionally, the correlation between transduction efficiency and virus stock storage time was evaluated. By atomic force microscopy, asymmetrical baculovirus particles with enlarged head regions were detected. Observed virus stocks contained variable-length particles, 256 ± 40 nm, along with disintegrated particles and/or cellular components. Long-term storage of stocks led to virus aggregation and decreased cellular entry and transgene expression in mammal…

Cancer ResearchbiologyAtomic force microscopyvirusesTransgeneVirionVirus InternalizationMicroscopy Atomic Forcebiology.organism_classificationMolecular biologyNucleopolyhedrovirusesVirusCell biologyAutographa californicaInfectious DiseasesVirologyHumansVirus StructureParticle sizeNucleocapsidGenome sizeHeLa CellsVirus Research
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Improvement of baculovirus as protein expression vector and as biopesticide by CRISPR/Cas9 editing

2019

The clustered regularly interspaced short palindromic repeats (CRISPR) system?associated Cas9 endonuclease is a molecular tool that enables specific sequence editing with high efficiency. In this study, we have explored the use of CRISPR/Cas9 system for the engineering of baculovirus. We have shown that the delivering of Cas9-single guide RNA ribonucleoprotein (RNP) complex with or without DNA repair template into Sf21 insect cells through lipofection might be efficient to produce knockouts as well as knock-ins into the baculovirus. To evaluate potential application of our CRISPR/Cas9 method to improve baculovirus as protein expression vector and as biopesticide, we attempted to knockout se…

DNA repairvirusesBACULOVIRUSGenetic VectorsBioengineeringComputational biologyGenome ViralINGENIERÍAS Y TECNOLOGÍASBiologySpodopteraApplied Microbiology and BiotechnologyGenomelaw.inventionBiotecnología Industrial03 medical and health sciencesGenome editingGENOME EDITINGlawKNOCK-INSf9 CellsCRISPRAnimalsVector (molecular biology)Guide RNANUCLEOPOLYHEDROVIRUSPest Control BiologicalGeneCRISPR/CAS9030304 developmental biologyRibonucleoproteinGene Editing0303 health sciencesExpression vector030306 microbiologyCas93. Good healthKNOCKOUTRecombinant DNACRISPR-Cas SystemsBaculoviridaeBiotechnology
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Assembly of the Major and the Minor Capsid Protein of Human Papillomavirus Type 33 into Virus-like Particles and Tubular Structures in Insect Cells

1994

Native virions of human papillomaviruses (HPV) can be isolated from genital lesions only in very limited amounts. Recent studies have shown that virus-like particles can be obtained by expression of the capsid proteins using vaccinia virus recombinants or the baculovirus system. We now present the first detailed characterization of virus-like particles of a human papillomavirus associated with malignant genital lesions, HPV-33, produced in high yield using the baculovirus expression system. Assembly of the major capsid protein L1 alone or together with the minor capsid protein L2 has been obtained. Both spherical virus-like particles of 50-60 nm diameter and tubular structures of either 25-…

Density gradientIcosahedral symmetryvirusesImmunoelectron microscopyMolecular Sequence DataMothsBiologyNegative StainingViruschemistry.chemical_compoundCapsidVirus-like particleVirologyMorphogenesisAnimalsDisulfidesPapillomaviridaeCells CulturedBase SequenceMolecular biologyNucleopolyhedrovirusesRecombinant ProteinsMicroscopy ElectronchemistryCapsidCell cultureVacciniaVirology
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