ABSTRACT
PURPOSE: To construct a three-dimensional (3D) culture model of adenovirus in vitro using the nanoself-assembling peptide RADA16-I as a 3D cell culture scaffold combined with virology experimental technology to provide a novel research method for virus isolation and culture, pathogenesis research, antiviral drug screening and vaccine preparation. METHODS: The nanoself-assembling peptide RADA16-I was used as a 3D scaffold material for 293T cell culture, and adenovirus was cultured in the cells. The growth, morphological characteristics and pathological effects of 3D-cultured 293T cells after adenovirus infection were observed with an inverted microscope and MTS. The proliferation of adenovirus in 293T cells was observed by TEM and detected by qPCR. The levels of TNF-α and IL-8 secreted by adenovirus-infected 293T cells in the RADA16-I 3D culture system were detected by ELISA. RESULTS: The 293T cells grew well in the RADA16-I 3D culture system for a prolonged period of time. The adenovirus infection persisted for a long time with multiple proliferation peaks, which closely resembled those of in vivo infections. The adenovirus virions amplified in the 3D system remained infectious. There were multiple secretion peaks of TNF-α and IL-8 secretion levels in adenovirus-infected 293T cells cultured in 3D culture systems. CONCLUSION: The nanoself-assembling peptide RADA16-I can be used as a 3D scaffold for adenovirus isolation, culture and research. The 3D culture system shows more realistic in vivo effects than two-dimensional (2D) culture.
Subject(s)
Adenoviridae Infections/virology , Adenoviridae/physiology , Cell Culture Techniques/methods , Nanoparticles/chemistry , Peptides/chemistry , Adenoviridae/growth & development , Adenoviridae/ultrastructure , Cell Proliferation/drug effects , Cytokines/metabolism , HEK293 Cells , Humans , Virion/ultrastructureABSTRACT
Interferon-inducible transmembrane protein 3 (IFITM3) inhibits the replication of multiple pathogenic viruses by blocking their entry. In this study, we constructed a shuttle plasmid, harboring human IFITM3. Thereafter, recombinant adenovirus rAd5-IFITM3 was obtained by co-transfection of the linearized viral backbone vector pAd5 and the shuttle plasmid. The results showed that human IFITM3 did not affect the assembly and morphogenesis of progeny adenovirus. Human IFITM3 can be expressed in both A549 and MDCK cells in a time dependent manner. Furthermore, cells infected with rAd5-IFITM3 at a multiplicity of infection (MOI) of 100 for 24â¯h were challenged with avian influenza virus (AIV) H5N1 at an MOI of 1 for 6, 12 and 24â¯h. Rates of H5N1 infection in rAd5-IFITM3 cells were significantly decreased at 24â¯h post-infection (hpi), in a time dependent manner, compared with that of wild type wtAd5-infected cells. The expressions of viral genes were significantly inhibited at transcriptional and translational levels at 6 and 12â¯hpi. These results suggest that IFITM3 can suppress H5N1 replication in the early stage of the infection, which may be used as a promise agent against H5N1 infection in vivo.
Subject(s)
Adenoviridae/genetics , Cloning, Molecular , Gene Expression , Genetic Vectors/genetics , Membrane Proteins/genetics , RNA-Binding Proteins/genetics , Adenoviridae/ultrastructure , Animals , Cell Line , Dogs , Gene Order , Humans , Influenza A Virus, H5N1 Subtype , Madin Darby Canine Kidney Cells , Membrane Proteins/metabolism , RNA-Binding Proteins/metabolismABSTRACT
Recent developments in tumour treatment had focused on virotherapies that were currently revolutionising new innovated treatment pathways. This study focused on the fabrication of oncolytic adenoviral vector (Ad) nanosphere that self-targeted at lung tumour cells (A549), utilising the immune response for upper respiratory tract infection, caused by the Ad infection. This system was dependent upon T-cell immune response, surface charge and blood metabolism. Oncolytic Ad attacked lung A549 tumour cells by incorporated its own DNA to replace A549's, the triggered immune response generated T-cells also further attack A549. Direct Ad injection was demonstrated to be lethal and prohibited in vivo. In this research a multifunctional principal using polyprotein surface precipitation technique (PSP) whist maintaining biological controls for self-assembly polyprotein Ad nanosphere both biocompatible and reproducible, was demonstrated as a result of the enhanced transfection efficiency and a successful multifunctional drug delivery system for virotherapy.
Subject(s)
Adenoviridae/metabolism , Chemical Precipitation , Nanospheres/chemistry , Oncolytic Virotherapy , Oncolytic Viruses/metabolism , Polyproteins/metabolism , Transfection , A549 Cells , Adenoviridae/ultrastructure , Humans , Nanospheres/ultrastructure , Oncolytic Viruses/ultrastructure , Surface Properties , UltrasonicsABSTRACT
Adenoviruses (Ads) subvert MHC class I Ag presentation and impair host anti-Ad cellular activities. Specifically, the Ad-encoded E3-19K immunomodulatory protein targets MHC class I molecules for retention within the endoplasmic reticulum of infected cells. We report the x-ray crystal structure of the Ad type 4 (Ad4) E3-19K of species E bound to HLA-A2 at 2.64-Å resolution. Structural analysis shows that Ad4 E3-19K adopts a tertiary fold that is shared only with Ad2 E3-19K of species C. A comparative analysis of the Ad4 E3-19K/HLA-A2 structure with our x-ray structure of Ad2 E3-19K/HLA-A2 identifies species-specific features in HLA-A2 recognition. Our analysis also reveals common binding characteristics that explain the promiscuous, and yet high-affinity, association of E3-19K proteins with HLA-A and HLA-B molecules. We also provide structural insights into why E3-19K proteins do not associate with HLA-C molecules. Overall, our study provides new information about how E3-19K proteins selectively engage with MHC class I to abrogate Ag presentation and counteract activation of CD8(+) T cells. The significance of MHC class I Ag presentation for controlling viral infections, as well as the threats of viral infections in immunocompromised patients, underline our efforts to characterize viral immunoevasins, such as E3-19K.
Subject(s)
Adenoviridae/immunology , Adenoviridae/ultrastructure , Adenovirus E3 Proteins/immunology , Adenovirus E3 Proteins/ultrastructure , Adenovirus E3 Proteins/chemistry , Amino Acid Sequence , Animals , Antigen Presentation/immunology , Conserved Sequence , Crystallography, X-Ray , HLA-A2 Antigen/chemistry , HLA-A2 Antigen/immunology , HLA-A2 Antigen/ultrastructure , Humans , Protein Conformation , Species SpecificityABSTRACT
Every year brings another round of zoonotic viral infections. Usually they fall under the radar, but the occasional lethal epidemic brings another scare to the public and new urgency to the medical community. The types of these viruses (DNA vs. RNA genomes, enveloped vs. proteinaceous) as well as the preceding host(s) vary. Over the last 20 years, bats have been identified as an enigmatic carrier for several pathogens that have jumped the species barrier and infected humans. Factors that favour the emergence of zoonotic pathogens include the increasing overlap of the human and animal habitats, cultural activities, and the host reservoir. In this context, we asked whether bat and/or nonhuman primate adenoviruses are a risk for human health.
Subject(s)
Adenoviridae Infections/epidemiology , Zoonoses/epidemiology , Zoonoses/virology , Adenoviridae/physiology , Adenoviridae/ultrastructure , Animals , Humans , Risk AssessmentABSTRACT
Electrostatics is one of the fundamental driving forces of the interaction between biomolecules in solution. In particular, the recognition events between viruses and host cells are dominated by both specific and non-specific interactions and the electric charge of viral particles determines the electrostatic force component of the latter. Here we probe the charge of individual viruses in liquid milieu by measuring the electrostatic force between a viral particle and the Atomic Force Microscope tip. The force spectroscopy data of co-adsorbed Ï29 bacteriophage proheads and mature virions, adenovirus and minute virus of mice capsids is utilized for obtaining the corresponding density of charge for each virus. The systematic differences of the density of charge between the viral particles are consistent with the theoretical predictions obtained from X-ray structural data. Our results show that the density of charge is a distinguishing characteristic of each virus, depending crucially on the nature of the viral capsid and the presence/absence of the genetic material.
Subject(s)
Adenoviridae , Bacillus Phages , Minute Virus of Mice , Virion , Adenoviridae/chemistry , Adenoviridae/ultrastructure , Animals , Bacillus Phages/chemistry , Bacillus Phages/ultrastructure , Mice , Microscopy, Atomic Force , Minute Virus of Mice/chemistry , Minute Virus of Mice/ultrastructure , Static Electricity , Virion/chemistry , Virion/ultrastructureABSTRACT
The field of structural virology developed in parallel with methodological advances in X-ray crystallography and cryo-electron microscopy. At the end of the 1970s, crystallography yielded the first high resolution structure of an icosahedral virus, the T=3 tomato bushy stunt virus at 2.9Å. It took longer to reach near-atomic resolution in three-dimensional virus maps derived from electron microscopy data, but this was finally achieved, with the solution of complex icosahedral capsids such as the T=25 human adenovirus at â¼3.5Å. Both techniques now work hand-in-hand to determine those aspects of virus assembly and biology that remain unclear. This review examines the trajectory followed by EM imaging techniques in showing the molecular structure of icosahedral viruses, from the first two-dimensional negative staining images of capsids to the latest sophisticated techniques that provide high resolution three-dimensional data, or snapshots of the conformational changes necessary to complete the infectious cycle.
Subject(s)
Adenoviridae/ultrastructure , Capsid/ultrastructure , Cryoelectron Microscopy/methods , Tombusvirus/ultrastructure , Adenoviridae/physiology , Capsid/physiology , Crystallography, X-Ray , Humans , Molecular Structure , Tombusvirus/physiologyABSTRACT
Genome packing in adenovirus has long evaded precise description, since the viral dsDNA molecule condensed by proteins (core) lacks icosahedral order characteristic of the virus protein coating (capsid). We show that useful insights regarding the organization of the core can be inferred from the analysis of spatial distributions of the DNA and condensing protein units (adenosomes). These were obtained from the inspection of cryo-electron tomography reconstructions of individual human adenovirus particles. Our analysis shows that the core lacks symmetry and strict order, yet the adenosome distribution is not entirely random. The features of the distribution can be explained by modeling the condensing proteins and the part of the genome in each adenosome as very soft spheres, interacting repulsively with each other and with the capsid, producing a minimum outward pressure of â¼0.06 atm. Although the condensing proteins are connected by DNA in disrupted virion cores, in our models a backbone of DNA linking the adenosomes is not required to explain the experimental results in the confined state. In conclusion, the interior of an adenovirus infectious particle is a strongly confined and dense phase of soft particles (adenosomes) without a strictly defined DNA backbone.
Subject(s)
Adenoviridae/ultrastructure , DNA, Viral/ultrastructure , Viral Core Proteins/ultrastructure , Virion/ultrastructure , Electron Microscope Tomography , Molecular Dynamics SimulationABSTRACT
Acute gastroenteritis accounts for a significant burden of medically attended illness in children under the age of five. For this study, four multiplex reverse transcription PCR assays were used to determine the incidence of adenovirus, astrovirus, coronavirus, norovirus GI and GII, rotavirus, and sapovirus in stool samples submitted for viral electron microscopy (EM) to the Children's Hospital Colorado. Of 1105 stool samples available, viral RNA/DNA was detected in 247 (26.2%) of 941 pediatric samples (median age = 2.97 years, 54% male) with 28 (3.0%) positive for more than one virus. Adenovirus, astrovirus, norovirus GI, norovirus GII, rotavirus, and sapovirus were detected in 95 (10.0%), 33 (3.5%), 8 (0.9%), 90 (9.6%), 49 (5.2%), and 2 (0.2%) of the pediatric samples, respectively. No coronaviruses were identified. Sequencing of norovirus positive samples indicated an outbreak of norovirus strain GII.4 in 2006 with evidence of numerous circulating strains. Multiple samples from the same immunocompromised patients demonstrated symptomatic shedding of norovirus for up to 32 weeks and astrovirus for 12 weeks. RT-PCR detected 99 of 111 (89%) adenovirus-positive samples versus 12 (11%) by EM, and 186 of 192 (97%) sapovirus/astrovirus/norovirus-positive samples versus 21 (11%) by EM. Noroviruses and adenoviruses are common causes of gastroenteritis in children. Immunocompromised patients can be infected with multiple viruses and shed viruses in their stools for prolonged periods. This data support the superiority of RT-PCR compared to EM for diagnosis of viral gastroenteritis.
Subject(s)
Adenoviridae Infections/epidemiology , Adenoviridae/isolation & purification , Adenovirus Infections, Human/epidemiology , Caliciviridae Infections/epidemiology , Enterovirus Infections/epidemiology , Gastroenteritis/epidemiology , Gastroenteritis/virology , Rotavirus Infections/epidemiology , Adenoviridae/genetics , Adenoviridae/ultrastructure , Child , Child, Preschool , Colorado/epidemiology , Coronavirus/isolation & purification , Coronavirus/ultrastructure , Disease Outbreaks , Feces/virology , Female , Gastroenteritis/etiology , Humans , Infant , Male , Microscopy, Electron , Multiplex Polymerase Chain Reaction , Norovirus/isolation & purification , Norovirus/ultrastructure , RNA Viruses/genetics , RNA Viruses/isolation & purification , RNA Viruses/ultrastructure , RNA, Viral/genetics , RNA, Viral/isolation & purification , Rotavirus/genetics , Rotavirus/isolation & purification , Sapovirus/isolation & purification , Sapovirus/ultrastructure , Time Factors , Virus SheddingABSTRACT
Disinfection by low-pressure monochromatic ultraviolet (UVC) radiation (253.7 nm) became an important technique to sanitize drinking water and also wastewater in tertiary treatments. In order to prevent the transmission of waterborne viral diseases, the analysis of the disinfection kinetics and the quantification of infectious viral pathogens and indicators are highly relevant and need to be addressed. The families Adenoviridae and Polyomaviridae comprise human and animal pathogenic viruses that have been also proposed as indicators of fecal contamination in water and as Microbial Source Tracking tools. While it has been previously suggested that dsDNA viruses may be highly resistant to UVC radiation compared to other viruses or bacteria, no information is available on the stability of polyomavirus toward UV irradiation. Here, the inactivation of dsDNA (HAdV2 and JCPyV) and ssRNA (MS2 bacteriophage) viruses was analyzed at increasing UVC fluences. A minor decay of 2-logs was achieved for both infectious JC polyomaviruses (JCPyV) and human adenoviruses 2 (HAdV2) exposed to a UVC fluence of 1,400 J/m(2), while a decay of 4-log was observed for MS2 bacteriophages (ssRNA). The present study reveals the high UVC resistance of dsDNA viruses, and the UV fluences needed to efficiently inactivate JCPyV and HAdV2 are predicted. Furthermore, we show that in conjunction with appropriate mathematical models, qPCR data may be used to accurately estimate virus infectivity.
Subject(s)
Adenoviridae/radiation effects , DNA, Viral/radiation effects , Disinfection/methods , Polyomaviridae/radiation effects , RNA, Viral/radiation effects , Adenoviridae/metabolism , Adenoviridae/pathogenicity , Adenoviridae/ultrastructure , Adenoviruses, Human/metabolism , Adenoviruses, Human/pathogenicity , Adenoviruses, Human/radiation effects , Adenoviruses, Human/ultrastructure , Cell Line , DNA, Viral/metabolism , Humans , JC Virus/metabolism , JC Virus/pathogenicity , JC Virus/radiation effects , JC Virus/ultrastructure , Kinetics , Levivirus/metabolism , Levivirus/pathogenicity , Levivirus/radiation effects , Levivirus/ultrastructure , Microbial Viability/radiation effects , Microscopy, Electron, Transmission , Polyomaviridae/metabolism , Polyomaviridae/pathogenicity , Polyomaviridae/ultrastructure , RNA Stability/radiation effects , RNA, Viral/metabolism , Radiation Tolerance , Real-Time Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction , Ultraviolet Rays , Virion/metabolism , Virion/pathogenicity , Virion/radiation effects , Virion/ultrastructure , Virus Inactivation/radiation effectsABSTRACT
Rotavirus (RoV) and adenovirus (AdV) are important viral pathogens for the risk analysis of drinking water. Despite this, little is known about their retention and transport behaviors in porous media due to a lack of representative surrogates. We developed RoV and AdV surrogates by covalently coupling 70-nm sized silica nanoparticles with specific proteins and a DNA marker for sensitive detection. Filtration experiments using beach sand columns demonstrated the similarity of the surrogates' concentrations, filtration efficiencies and attachment kinetics to those of the target viruses. The surrogates showed the same magnitude of concentration reduction as the viruses. Conversely, MS2 phage (a traditional virus model) over-predicted concentrations of AdV and RoV by 1- and 2-orders of magnitude respectively. The surrogates remained stable in size, surface charge and DNA concentration for at least one year. They can be easily and rapidly detected down to a single particle. Preliminary tests suggest that they were readily detectable in a number of environmental waters and treated effluent. With up-scaling validation in pilot trials, the surrogates developed here could be a cost-effective new tool for studying virus retention and transport in porous media. Examples include assessing filter efficacy in water and wastewater treatment, tracking virus migration in groundwater after effluent land disposal, and establishing safe setback distances for groundwater protection.
Subject(s)
Adenoviridae/physiology , DNA/chemistry , Filtration/methods , Nanoparticles/chemistry , Proteins/chemistry , Rotavirus/physiology , Silicon Dioxide/chemistry , Adenoviridae/ultrastructure , Computer Simulation , Electrophoresis, Agar Gel , Hydrodynamics , Levivirus/ultrastructure , Motion , Nanoparticles/ultrastructure , Rotavirus/ultrastructure , Soil , Static ElectricityABSTRACT
An adult male domestic pigeon (Columba livia) was presented for necropsy following natural death after a period of chronic weight loss and severe intestinal ascariasis. Histopathologic examination of the liver found moderate to marked, multifocal necrotizing hepatitis with large, basophilic intranuclear inclusion bodies. Transmission electron microscopy of affected hepatocytes demonstrated numerous intra- and perinuclear icosahedral virions arranged in a lattice structure, consistent with adenoviral infection.
Subject(s)
Adenoviridae Infections/veterinary , Adenoviridae/ultrastructure , Bird Diseases/pathology , Columbidae , Hepatitis, Animal/pathology , Adenoviridae Infections/pathology , Adenoviridae Infections/virology , Animals , Bird Diseases/virology , Diagnosis, Differential , Hepatocytes/pathology , Hepatocytes/ultrastructure , Hepatocytes/virology , Inclusion Bodies, Viral/ultrastructure , Liver/pathology , Liver/virology , Male , Microscopy, Electron, Transmission/veterinaryABSTRACT
In this chapter we compile a battery of biophysical and imaging methods suitable to investigate adenovirus structural stability, structure, and assembly. Some are standard methods with a long history of use in virology, such as embedding and sectioning of infected cells, negative staining, or immunoelectron microscopy, as well as extrinsic fluorescence. The newer cryo-electron microscopy technique, which combined with advanced image processing tools has recently yielded an atomic resolution picture of the complete virion, is also described. Finally, we detail the procedure for imaging and interacting with single adenovirus virions using the atomic force microscope in liquid conditions. We provide examples of the kind of data obtained with each technique.
Subject(s)
Adenoviridae/ultrastructure , Adenoviridae/physiology , Microscopy, Atomic Force/methods , Microscopy, Electron/methods , Spectrometry, Fluorescence/methodsABSTRACT
The comparative characteristic of the reproduction of adenovirus serotypes 2 and 5 (HAdV-C2 and -C5) in the various lymphoblastoid cell lines were studied. Rapid formation of infectious viruses in Raji, MP-1, Namalwa, BJAB, MT4 and Jurkat cells was marked and it was found to be close to the level of viruses during reproduction in permissive Hep-2 epithelial cells. Yield of infective adenovirus was low in B95-8 cells, which were chronically infected with Epstein-Barr virus (EBV). This may indicate the interference of Ad with EBV during super-infection. The CEM cells produced chronically low amounts of human adenovirus serotype 2.
Subject(s)
Adenoviridae/physiology , B-Lymphocytes/virology , Virion/physiology , Virus Replication/physiology , Adenoviridae/ultrastructure , B-Lymphocytes/pathology , Cell Line, Tumor , Coinfection , Herpesvirus 4, Human/physiology , Humans , Organ Specificity , Virion/ultrastructureABSTRACT
MOTIVATION: Structural information of macromolecular complexes provides key insights into the way they carry out their biological functions. Achieving high-resolution structural details with electron microscopy requires the identification of a large number (up to hundreds of thousands) of single particles from electron micrographs, which is a laborious task if it has to be manually done and constitutes a hurdle towards high-throughput. Automatic particle selection in micrographs is far from being settled and new and more robust algorithms are required to reduce the number of false positives and false negatives. RESULTS: In this article, we introduce an automatic particle picker that learns from the user the kind of particles he is interested in. Particle candidates are quickly and robustly classified as particles or non-particles. A number of new discriminative shape-related features as well as some statistical description of the image grey intensities are used to train two support vector machine classifiers. Experimental results demonstrate that the proposed method: (i) has a considerably low computational complexity and (ii) provides results better or comparable with previously reported methods at a fraction of their computing time. AVAILABILITY: The algorithm is fully implemented in the open-source Xmipp package and downloadable from http://xmipp.cnb.csic.es.
Subject(s)
Automation, Laboratory/methods , Microscopy, Electron , Adenoviridae/ultrastructure , Algorithms , DNA Helicases/ultrastructure , Image Processing, Computer-Assisted/methods , Macromolecular Substances , Particle SizeABSTRACT
It has been well-established that chemo-immunotherapy using cytotoxic drugs and appropriate cytokines offers a promising approach for the treatment of neoplastic diseases. In view of this, to improve melanoma treatment effect, our study developed a new codelivery system (AL/Ad5/PTX) that paclitaxel (PTX) and adenovirus encoding for murine interleukin-12 (Ad5-mIL-12) were incorporated into anionic liposomes (AL). First, AL/Ad5/PTX complexes were prepared by incorporating Ad5 into anionic PTX liposomes using calcium-induced phase change. Second, the size distribution and zeta potential of AL/Ad5/PTX were investigated. Third, the results of in vitro transduction assays showed that PTX introduced into AL/Ad-luc or AL/Ad5-mIL-12 highly enhanced gene transduction efficiency in B16 cells than naked Ad5 or AL/Ad complexes while it had no comparability in A549 cells. Finally, a melanoma-bearing mouse model was established to assess the antitumor effect. Tumor growth inhibition and prolonged survival time, accompanied by increased mIL-12 or interferon-γ (IFN-γ) expression levels in serum or tumor sites, were observed in mice treated with AL/Ad5-mIL-12/PTX, as compared with those treated with either AL/Ad5-mIL-12 or AL/PTX. In conclusion, these results suggested that codelivery of Ad5-mIL-12 and PTX incorporated into AL could be a relatively efficient strategy for the treatment of melanoma.
Subject(s)
Antineoplastic Agents, Phytogenic/administration & dosage , Interleukin-12/genetics , Interleukin-12/therapeutic use , Melanoma, Experimental/therapy , Paclitaxel/administration & dosage , Adenoviridae/genetics , Adenoviridae/ultrastructure , Animals , Cell Line, Tumor , Cell Survival/drug effects , Genetic Therapy , Genetic Vectors , Humans , Immunotherapy , Interferon-gamma/blood , Interferon-gamma/metabolism , Interleukin-12/metabolism , Liposomes/ultrastructure , Male , Melanoma, Experimental/genetics , Melanoma, Experimental/pathology , Mice , Mice, Inbred C57BL , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Recombinant Proteins/therapeutic use , Transduction, GeneticABSTRACT
Mucus, with its burden of inspired particulates and pathogens, is cleared from mucosal surfaces of the airways by cilia beating within the periciliary layer (PCL). The PCL is held to be "watery" and free of mucus by thixotropic-like forces arising from beating cilia. With radii of gyration ~250 nm, however, polymeric mucins should reptate readily into the PCL, so we assessed the glycocalyx for barrier functions. The PCL stained negative for MUC5AC and MUC5B, but it was positive for keratan sulfate (KS), a glycosaminoglycan commonly associated with glycoconjugates. Shotgun proteomics showed KS-rich fractions from mucus containing abundant tethered mucins, MUC1, MUC4, and MUC16, but no proteoglycans. Immuno-histology by light and electron microscopy localized MUC1 to microvilli, MUC4 and MUC20 to cilia, and MUC16 to goblet cells. Electron and atomic force microscopy revealed molecular lengths of 190-1,500 nm for tethered mucins, and a finely textured glycocalyx matrix filling interciliary spaces. Adenoviral particles were excluded from glycocalyx of the microvilli, whereas the smaller adenoassociated virus penetrated, but were trapped within. Hence, tethered mucins organized as a space-filling glycocalyx function as a selective barrier for the PCL, broadening their role in innate lung defense and offering new molecular targets for conventional and gene therapies.
Subject(s)
Glycocalyx/metabolism , Mucins/metabolism , Mucus/metabolism , Respiratory Mucosa/metabolism , Adenoviridae/metabolism , Adenoviridae/ultrastructure , Animals , Cell Culture Techniques , Cilia/ultrastructure , Dependovirus/metabolism , Dependovirus/ultrastructure , Epithelial Cells/metabolism , Glycocalyx/ultrastructure , Glycosaminoglycans/metabolism , Guinea Pigs , Humans , Keratan Sulfate/metabolism , Mucins/ultrastructure , Respiratory Mucosa/virologyABSTRACT
Biomineralization-based virus shell-engineering (BVSE) is a potential surface modification strategy to afford a biocompatible and biodegradable calcium phosphate (CaPi) shell onto single virus, allowing development of Trojan virus with enhanced infection, expanded tropism and neutralization escape, which open up the multiple applications of virus in biomedicines and materials.
Subject(s)
Adenoviridae/chemistry , Adenoviridae/genetics , Calcium Phosphates/chemistry , Capsid/chemistry , Capsid/physiology , Genetic Engineering/methods , Adenoviridae/ultrastructure , Biocompatible Materials/chemistry , Capsid/ultrastructure , Minerals/chemistry , Viral Tropism/physiologyABSTRACT
Adenovirus (Ad) cell attachment is initiated by the attachment of the fiber protein to a primary receptor (usually CAR or CD46). This event is followed by the engagement of the penton base protein with a secondary receptor (integrin) via its loop region, which contains an Arg-Gly-Asp (RGD) motif, to trigger virus internalization. To understand the well-orchestrated adenovirus cell attachment process that involves the fiber and the penton base, we reconstructed the structure of an Ad5F35 capsid, comprising an adenovirus type 5 (Ad5) capsid pseudotyped with an Ad35 fiber, at a resolution of approximately 4.2 Å. The fiber-penton base interaction in the cryo-electron microscopic (cryo-EM) structure of Ad5F35 is similar to that in the cryo-EM structure of Ad5, indicating that the fiber-penton base interaction of adenovirus is conserved. Our structure also confirms that the C-terminal segment of the fiber tail domain constitutes the bottom trunk of the fiber shaft. Based on the conserved fiber-penton base interaction, we have proposed a model for the interaction of Ad5F35 with its primary and secondary receptors. This model could provide insight for designing adenovirus gene delivery vectors.