Publications
| Title | Abstract | Year(sorted ascending) Filter | PMID Filter |
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| fusion activation by a headless parainfluenza virus 5 hemagglutinin-neuraminidase stalk suggests a modular mechanism for triggering. | the paramyxoviridae family of enveloped viruses enters cells through the concerted action of two viral glycoproteins. the receptor-binding protein, hemagglutinin-neuraminidase (hn), h, or g, binds its cellular receptor and activates the fusion protein, f, which, through an extensive refolding event, brings viral and cellular membranes together, mediating virus-cell fusion. however, the underlying mechanism of f activation on receptor engagement remains unclear. current hypotheses propose conform ... | 2012 | 22949640 |
| role of ubiquitin in piv5 particle formation. | ubiquitin is important for the budding of many retroviruses and other enveloped viruses, but the precise role for ubiquitin in virus budding remains unclear. here, we characterized ubiquitination of the matrix (m) protein of a paramyxovirus, parainfluenza virus 5 (piv5). piv5 m protein (but not piv5 nucleocapsid protein) was found to be targeted for monoubiquitination in transfected mammalian cells. major sites of ubiquitin attachment identified by mass spectrometry analysis were lysine residues ... | 2012 | 22258249 |
| The chicken chorioallantoic membrane tumor assay as model for qualitative testing of oncolytic adenoviruses. | Oncolytic adenoviruses are promising anticancer agents. To study and optimize their tumor-killing potency, genuine tumor models are required. Here we describe the use of the chicken chorioallantoic membrane (CAM) tumor model in studies on oncolytic adenoviral vectors. Suspensions of human melanoma, colorectal carcinoma and glioblastoma multiforme cell lines were grafted on the CAM of embryonated chicken eggs. All cell lines tested formed 5-10?mm size tumors, which recapitulated hallmarks of corr ... | 2012 | 22015640 |
| a novel rabies vaccine based on a recombinant parainfluenza virus 5 expressing rabies virus glycoprotein. | untreated rabies virus (rabv) infection leads to death. vaccine and postexposure treatment have been effective in preventing rabv infection. however, due to cost, rabies vaccination and treatment have not been widely used in developing countries. there are 55,000 human death caused by rabies annually. an efficacious and cost-effective rabies vaccine is needed. parainfluenza virus 5 (piv5) is thought to contribute to kennel cough, and kennel cough vaccines containing live piv5 have been used in d ... | 2012 | 23269806 |
| evaluating a parainfluenza virus 5-based vaccine in a host with pre-existing immunity against parainfluenza virus 5. | parainfluenza virus 5 (piv5), formerly known as simian virus 5 (sv5), is a paramyxovirus often referred to as canine parainfluenza virus (cpi) in the veterinary field. piv5 is thought to be a contributing factor to kennel cough. kennel cough vaccines containing live piv5 have been used in dogs for many decades. piv5 is not known to cause any diseases in humans or other animals. piv5 has been used as a vector for vaccine development for humans and animals. one critical question concerning the use ... | 2012 | 23185558 |
| isg56/ifit1 is primarily responsible for interferon-induced changes to patterns of parainfluenza virus type 5 transcription and protein synthesis. | interferon (ifn) induces an antiviral state in cells that results in alterations of the patterns and levels of parainfluenza virus type 5 (piv5) transcripts and proteins. this study reports that ifn-stimulated gene 56/ifn-induced protein with tetratricopeptide repeats 1 (isg56/ifit1) is primarily responsible for these effects of ifn. it was shown that treating cells with ifn after infection resulted in an increase in virus transcription but an overall decrease in virus protein synthesis. as ther ... | 2012 | 23052390 |
| pathogens of wild maned wolves (chrysocyon brachyurus) in brazil. | the maned wolf, chrysocyon brachyurus, is an endangered neotropical canid that survives at low population densities. diseases are a potential threat for its conservation but to date have been poorly studied. we performed clinical evaluations and investigated the presence of infectious diseases through serology and coprologic tests on maned wolves from galheiro natural private reserve, perdizes city, minas gerais state, southeastern brazil. fifteen wolves were captured between 2003 and 2008. we f ... | 2012 | 23060508 |
| [metagenomics-based detection of swine viruses]. | extreme varieties of viruses exist in the environment and animals, some of which are unknown. however, many unknown viruses are barely detected by means of conventional virus isolation and pcr assay. | 2013 | 23627112 |
| single-dose vaccination of a recombinant parainfluenza virus 5 expressing np from h5n1 virus provides broad immunity against influenza a viruses. | influenza viruses often evade host immunity via antigenic drift and shift despite previous influenza virus infection and/or vaccination. vaccines that match circulating virus strains are needed for optimal protection. development of a universal influenza virus vaccine providing broadly cross-protective immunity will be of great importance. the nucleoprotein (np) of influenza a virus is highly conserved among all strains of influenza a viruses and has been explored as an antigen for developing a ... | 2013 | 23514880 |
| efficacy of parainfluenza virus 5 mutants expressing hemagglutinin from h5n1 influenza a virus in mice. | parainfluenza virus 5 (piv5) is a promising viral vector for vaccine development. piv5 is safe, stable, efficacious, cost-effective to produce and, most interestingly, it overcomes preexisting antivector immunity. we have recently reported that piv5 expressing the hemagglutinin (ha) from highly pathogenic avian influenza (hpai) virus h5n1 (piv5-h5) provides sterilizing immunity against lethal doses of hpai h5n1 infection in mice. it is thought that induction of apoptosis can lead to enhanced ant ... | 2013 | 23804633 |
| recombinant parainfluenza virus 5 vaccine encoding the influenza virus hemagglutinin protects against h5n1 highly pathogenic avian influenza virus infection following intranasal or intramuscular vaccination of balb/c mice. | new approaches for vaccination to prevent influenza virus infection are needed. emerging viruses, such as the h5n1 highly pathogenic avian influenza (hpai) virus, pose not only pandemic threats but also challenges in vaccine development and production. parainfluenza virus 5 (piv5) is an appealing vector for vaccine development, and we have previously shown that intranasal immunization with piv5 expressing the hemagglutinin from influenza virus was protective against influenza virus challenge (s. ... | 2013 | 23077318 |
| recombinant parainfluenza virus 5 expressing hemagglutinin of influenza a virus h5n1 protected mice against lethal highly pathogenic avian influenza virus h5n1 challenge. | a safe and effective vaccine is the best way to prevent large-scale highly pathogenic avian influenza virus (hpai) h5n1 outbreaks in the human population. the current fda-approved h5n1 vaccine has serious limitations. a more efficacious h5n1 vaccine is urgently needed. parainfluenza virus 5 (piv5), a paramyxovirus, is not known to cause any illness in humans. piv5 is an attractive vaccine vector. in our studies, a single dose of a live recombinant piv5 expressing a hemagglutinin (ha) gene of h5n ... | 2013 | 23077314 |
| point mutations in the paramyxovirus f protein that enhance fusion activity shift the mechanism of complement-mediated virus neutralization. | parainfluenza virus 5 (piv5) activates and is neutralized by the alternative pathway (ap) in normal human serum (nhs) but not by heat-inactivated (hi) serum. we have tested the relationship between the fusion activity within the piv5 f protein, the activation of complement pathways, and subsequent complement-mediated virus neutralization. recombinant piv5 viruses with enhanced fusion activity were generated by introducing point mutations in the f fusogenic peptide (g3a) or at a distal site near ... | 2013 | 23785199 |
| structure of the parainfluenza virus 5 (piv5) hemagglutinin-neuraminidase (hn) ectodomain. | paramyxoviruses cause a wide variety of human and animal diseases. they infect host cells using the coordinated action of two surface glycoproteins, the receptor binding protein (hn, h, or g) and the fusion protein (f). hn binds sialic acid on host cells (hemagglutinin activity) and hydrolyzes these receptors during viral egress (neuraminidase activity, na). additionally, receptor binding is thought to induce a conformational change in hn that subsequently triggers major refolding in homotypic f ... | 2013 | 23950713 |
| mutations in the parainfluenza virus 5 fusion protein reveal domains important for fusion triggering and metastability. | paramyxovirus membrane glycoproteins f (fusion protein) and hn, h, or g (attachment protein) are critical for virus entry, which occurs through fusion of viral and cellular envelopes. the f protein folds into a homotrimeric, metastable prefusion form that can be triggered by the attachment protein to undergo a series of structural rearrangements, ultimately folding into a stable postfusion form. in paramyxovirus-infected cells, the f protein is activated in the golgi apparatus by cleavage adjace ... | 2013 | 24089572 |
| characterization in vitro and in vivo of a novel porcine parainfluenza virus 5 isolate in korea. | a novel porcine parainfluenza 5 (ppiv5), knu-11, in the genus rubulavirus of the subfamily paramyxovirinae, was isolated from the lung of a piglet in korea in 2011. to understand the importance of this virus as an infectious agent, in vitro and in vivo characteristics of knu-11 virus was investigated. knu-11 was remarkably cytopathogenic, showing distinct cell rounding and clumping evident in porcine alveolar macrophage (pam), porcine kidney (pk-15), and swine testicle (st) cells within 12h post ... | 2013 | 24050998 |
| complete genome sequence of a novel porcine parainfluenza virus 5 isolate in korea. | a novel cytopathogenic paramyxovirus was isolated from a lung sample from a piglet, using continuous porcine alveolar macrophage cells. morphologic and genetic studies indicated that this porcine virus (ppiv5) belongs to the species parainfluenza 5 in the family paramyxoviridae. we attempted to determine the complete nucleotide sequence of the first korean ppiv5 isolate, designated knu-11. the full-length genome of knu-11 was found to be 15,246 nucleotides in length and consist of seven nonoverl ... | 2013 | 23807746 |
| full conversion of the hemagglutinin-neuraminidase specificity of the parainfluenza virus 5 fusion protein by replacement of 21 amino acids in its head region with those of the simian virus 41 fusion protein. | for most parainfluenza viruses, a virus type-specific interaction between the hemagglutinin-neuraminidase (hn) and fusion (f) proteins is a prerequisite for mediating virus-cell fusion and cell-cell fusion. the molecular basis of this functional interaction is still obscure partly because it is unknown which region of the f protein is responsible for the physical interaction with the hn protein. our previous cell-cell fusion assay using the chimeric f proteins of parainfluenza virus 5 (piv5) and ... | 2013 | 23698295 |
| deep sequencing analysis of defective genomes of parainfluenza virus 5 and their role in interferon induction. | preparations of parainfluenza virus 5 (piv5) that are potent activators of the interferon (ifn) induction cascade were generated by high-multiplicity passage in order to accumulate defective interfering virus genomes (dis). nucleocapsid rna from these virus preparations was extracted and subjected to deep sequencing. sequencing data were analyzed using methods designed to detect internal deletion and "copyback" dis in order to identify and characterize the different dis present and to approximat ... | 2013 | 23449801 |
| membrane-dependent conformation, dynamics, and lipid interactions of the fusion peptide of the paramyxovirus piv5 from solid-state nmr. | the entry of enveloped viruses into cells requires protein-catalyzed fusion of the viral and cell membranes. the structure-function relation of a hydrophobic fusion peptide (fp) in viral fusion proteins is still poorly understood. we report magic-angle-spinning solid-state nmr results of the membrane-bound conformation, dynamics, and lipid interactions of the fp of the f protein of the paramyxovirus, parainfluenza virus 5 (piv5). (13)c chemical shifts indicate that the piv5 fp structure depends ... | 2013 | 23183373 |
| fusion activation through attachment protein stalk domains indicates a conserved core mechanism of paramyxovirus entry into cells. | paramyxoviruses are a large family of membrane-enveloped negative-stranded rna viruses causing important diseases in humans and animals. two viral integral membrane glycoproteins (fusion [f] and attachment [hn, h, or g]) mediate a concerted process of host receptor recognition, followed by the fusion of viral and cellular membranes, resulting in viral nucleocapsid entry into the cytoplasm. however, the sequence of events that closely links the timing of receptor recognition by hn, h, or g and th ... | 2014 | 24453369 |
| probing the paramyxovirus fusion (f) protein-refolding event from pre- to postfusion by oxidative footprinting. | to infect a cell, the paramyxoviridae family of enveloped viruses relies on the coordinated action of a receptor-binding protein (variably hn, h, or g) and a more conserved metastable fusion protein (f) to effect membrane fusion and allow genomic transfer. upon receptor binding, hn (h or g) triggers f to undergo an extensive refolding event to form a stable postfusion state. little is known about the intermediate states of the f refolding process. here, a soluble form of parainfluenza virus 5 f ... | 2014 | 24927585 |
| stability of the parainfluenza virus 5 genome revealed by deep sequencing of strains isolated from different hosts and following passage in cell culture. | the strain diversity of a rubulavirus, parainfluenza virus 5 (piv5), was investigated by comparing 11 newly determined and 6 previously published genome sequences. these sequences represent 15 piv5 strains, of which 6 were isolated from humans, 1 was from monkeys, 2 were from pigs, and 6 were from dogs. strain diversity is remarkably low, regardless of host, year of isolation, or geographical origin; a total of 7.8% of nucleotides are variable, and the average pairwise difference between strains ... | 2014 | 24453358 |
| rig-i-like receptors evolved adaptively in mammals, with parallel evolution at lgp2 and rig-i. | rig-i-like receptors (rlrs) are nucleic acid sensors that activate antiviral innate immune response. these molecules recognize diverse non-self rna substrates and are antagonized by several viral inhibitors. we performed an evolutionary analysis of rlr genes (rig-i, mda5, and lgp2) in mammals. results indicated that purifying selection had a dominant role in driving the evolution of rlrs. however, application of maximum-likelihood analyses identified several positions that evolved adaptively. po ... | 2014 | 24211720 |
| mutations in the fpiv motif of newcastle disease virus matrix protein attenuate virus replication and reduce virus budding. | the fpiv-like late domains identified in the matrix (m) proteins of parainfluenza virus 5 and mumps virus have been demonstrated to be critical for virus budding. in this study, we found that the same fpiv sequence motif is present in the n-terminus of the newcastle disease virus (ndv) m protein. mutagenesis experiments demonstrated that mutation of either phenylalanine (f) or proline (p) to alanine led to a more obvious decrease in viral virulence and replication and resulted in poor budding of ... | 2014 | 24477785 |
| paramyxovirus v protein interaction with the antiviral sensor lgp2 disrupts mda5 signaling enhancement but is not relevant to lgp2-mediated rlr signaling inhibition. | the interferon antiviral system is a primary barrier to virus replication triggered upon recognition of nonself rnas by the cytoplasmic sensors encoded by retinoic acid-inducible gene i (rig-i), melanoma differentiation-associated gene 5 (mda5), and laboratory of genetics and physiology gene 2 (lgp2). paramyxovirus v proteins are interferon antagonists that can selectively interact with mda5 and lgp2 through contact with a discrete helicase domain region. interaction with mda5, an activator of a ... | 2014 | 24829334 |
| a respiratory syncytial virus (rsv) vaccine based on parainfluenza virus 5 (piv5). | human respiratory syncytial virus (rsv) is a leading cause of severe respiratory disease and hospitalizations in infants and young children. it also causes significant morbidity and mortality in elderly and immune compromised individuals. no licensed vaccine currently exists. parainfluenza virus 5 (piv5) is a paramyxovirus that causes no known human illness and has been used as a platform for vector-based vaccine development. to evaluate the efficacy of piv5 as a rsv vaccine vector, we generated ... | 2014 | 24717150 |
| the neutralizing capacity of antibodies elicited by parainfluenza virus infection of african green monkeys is dependent on complement. | the african green monkey (agm) model was used to analyze the role of complement in neutralization of parainfluenza virus. parainfluenza virus 5 (piv5) and human parainfluenza virus type 2 were effectively neutralized in vitro by naïve agm sera, but neutralizing capacity was lost by heat-inactivation. the mechanism of neutralization involved formation of massive aggregates, with no evidence of virion lysis. following inoculation of the respiratory tract with a piv5 vector expressing hiv gp160, ag ... | 2014 | 25010267 |
| activation of paramyxovirus membrane fusion and virus entry. | the paramyxoviruses represent a diverse virus family responsible for a wide range of human and animal diseases. in contrast to other viruses, such as hiv and influenza virus, which use a single glycoprotein to mediate host receptor binding and virus entry, the paramyxoviruses require two distinct proteins. one of these is an attachment glycoprotein that binds receptor, while the second is a fusion glycoprotein, which undergoes conformational changes that drive virus-cell membrane fusion and viru ... | 2014 | 24530984 |
| viral aetiology and clinical outcomes in hospitalised infants presenting with respiratory distress. | to determine the prevalence of various types of viruses in infants hospitalised due to respiratory distress, compare molecular diagnostic tests and evaluate symptom severity. | 2014 | 24606114 |
| efficacy of a parainfluenza virus 5 (piv5)-based h7n9 vaccine in mice and guinea pigs: antibody titer towards ha was not a good indicator for protection. | h7n9 has caused fatal infections in humans. a safe and effective vaccine is the best way to prevent large-scale outbreaks in the human population. parainfluenza virus 5 (piv5), an avirulent paramyxovirus, is a promising vaccine vector. in this work, we generated a recombinant piv5 expressing the ha gene of h7n9 (piv5-h7) and tested its efficacy against infection with influenza virus a/anhui/1/2013 (h7n9) in mice and guinea pigs. piv5-h7 protected the mice against lethal h7n9 challenge. interesti ... | 2015 | 25803697 |
| analysis of cathepsin and furin proteolytic enzymes involved in viral fusion protein activation in cells of the bat reservoir host. | bats of different species play a major role in the emergence and transmission of highly pathogenic viruses including ebola virus, sars-like coronavirus and the henipaviruses. these viruses require proteolytic activation of surface envelope glycoproteins needed for entry, and cellular cathepsins have been shown to be involved in proteolysis of glycoproteins from these distinct virus families. very little is currently known about the available proteases in bats. to determine whether the utilizatio ... | 2015 | 25706132 |
| influenza a virus uses intercellular connections to spread to neighboring cells. | in the extracellular environment, cell-free virions seek out naive host cells over long distances and between organisms. this is the primary mechanism of spread for most viruses. here we provide evidence for an alternative pathway previously undescribed for orthomyxoviruses, whereby the spread of influenza a virus (iav) infectious cores to neighboring cells can occur within intercellular connections. the formation of these connections requires actin dynamics and is enhanced by viral infection. c ... | 2015 | 25428869 |
| the nectin-4/afadin protein complex and intercellular membrane pores contribute to rapid spread of measles virus in primary human airway epithelia. | the discovery that measles virus (mv) uses the adherens junction protein nectin-4 as its epithelial receptor provides a new vantage point from which to characterize its rapid spread in the airway epithelium. we show here that in well-differentiated primary cultures of airway epithelial cells from human donors (hae), mv infectious centers form rapidly and become larger than those of other respiratory pathogens: human respiratory syncytial virus, parainfluenza virus 5, and sendai virus. while visi ... | 2015 | 25926640 |
| molecular characteristics of canine parainfluenza viruses type 5 (cpiv-5) isolated in korea. | three canine parainfluenza viruses type 5 (cpiv-5) were isolated from lung tissues of 3 korean dogs with mild pneumonia between 2008 and 2009. the isolates were fully sequenced and compared with published reference sequences. the size of the genome was 15 246 nucleotides long and no remarkable differences were found when compared with previously published reference sequences. in phylogenetic analysis based on the f and p genes, parainfluenza virus 5 (piv-5) strains were divided into at least 3 s ... | 2015 | 25673911 |
| rnasek is required for internalization of diverse acid-dependent viruses. | viruses must gain entry into cells to establish infection. in general, viruses enter either at the plasma membrane or from intracellular endosomal compartments. viruses that use endosomal pathways are dependent on the cellular factors that control this process; however, these genes have proven to be essential for endogenous cargo uptake, and thus are of limited value for therapeutic intervention. the identification of genes that are selectively required for viral uptake would make appealing drug ... | 2015 | 26056282 |
| structure of the paramyxovirus parainfluenza virus 5 nucleoprotein-rna complex. | parainfluenza virus 5 (piv5) is a member of the paramyxoviridae family of membrane-enveloped viruses with a negative-sense rna genome that is packaged and protected by long filamentous nucleocapsid-helix structures (rnps). these rnps, consisting of ∼2,600 protomers of nucleocapsid (n) protein, form the template for viral transcription and replication. we have determined the 3d x-ray crystal structure of the nucleoprotein (n)-rna complex from piv5 to 3.11-å resolution. the structure reveals a 13- ... | 2015 | 25831513 |
| on the stability of parainfluenza virus 5 f proteins. | the crystal structure of the f protein (prefusion form) of the paramyxovirus parainfluenza virus 5 (piv5) wr isolate was determined. we investigated the basis by which point mutations affect fusion in piv5 isolates w3a and wr, which differ by two residues in the f ectodomain. the p22 stabilizing site acts through a local conformational change and a hydrophobic pocket interaction, whereas the s443 destabilizing site appears sensitive to both conformational effects and amino acid charge/polarity c ... | 2015 | 25589638 |
| parainfluenza virus 5 expressing the g protein of rabies virus protects mice after rabies virus infection. | rabies remains a major public health threat around the world. once symptoms appear, there is no effective treatment to prevent death. in this work, we tested a recombinant parainfluenza virus 5 (piv5) strain expressing the glycoprotein (g) of rabies (piv5-g) as a therapy for rabies virus infection: we have found that piv5-g protected mice as late as 6 days after rabies virus infection. piv5-g is a promising vaccine for prevention and treatment of rabies virus infection. | 2015 | 25552723 |
| efficacy of parainfluenza virus 5 (piv5)-based tuberculosis vaccines in mice. | mycobacterium tuberculosis, the etiological agent of tuberculosis (tb), is an important human pathogen. bacillus calmette-guérin (bcg), a live, attenuated variant of mycobacterium bovis, is currently the only available tb vaccine despite its low efficacy against the infectious pulmonary form of the disease in adults. thus, a more-effective tb vaccine is needed. parainfluenza virus 5 (piv5), a paramyxovirus, has several characteristics that make it an attractive vaccine vector. it is safe, inexpe ... | 2015 | 26552000 |
| regulation of viral rna synthesis by the v protein of parainfluenza virus 5. | paramyxoviruses include many important animal and human pathogens. the genome of parainfluenza virus 5 (piv5), a prototypical paramyxovirus, encodes a v protein that inhibits viral rna synthesis. in this work, the mechanism of inhibition was investigated. using mutational analysis and a minigenome system, we identified regions in the n and c termini of the v protein that inhibit viral rna synthesis: one at the very n terminus of v and the second at the c terminus of v. furthermore, we determined ... | 2015 | 26378167 |
| viral fusion protein transmembrane domain adopts β-strand structure to facilitate membrane topological changes for virus-cell fusion. | the c-terminal transmembrane domain (tmd) of viral fusion proteins such as hiv gp41 and influenza hemagglutinin (ha) is traditionally viewed as a passive α-helical anchor of the protein to the virus envelope during its merger with the cell membrane. the conformation, dynamics, and lipid interaction of these fusion protein tmds have so far eluded high-resolution structure characterization because of their highly hydrophobic nature. using magic-angle-spinning solid-state nmr spectroscopy, we show ... | 2015 | 26283363 |
| identification of two essential aspartates for polymerase activity in parainfluenza virus l protein by a minireplicon system expressing secretory luciferase. | gene expression of nonsegmented negative-strand rna viruses (nsnsvs) such as parainfluenza viruses requires the rna synthesis activity of their polymerase l protein; however, the detailed mechanism of this process is poorly understood. in this study, a parainfluenza minireplicon assay expressing secretory gaussia luciferase (gluc) was established to analyze large protein (l) activity. measurement of gluc expression in the culture medium of cells transfected with the minigenome and viral polymera ... | 2015 | 26446904 |
| parainfluenza virus 5 as possible cause of severe respiratory disease in calves, china. | 2015 | 26583313 | |
| characterization of the variability of epstein-barr virus genes in nasopharyngeal biopsies: potential predictors for carcinoma progression. | epstein-barr virus (ebv) infection is a significant factor in the pathogenesis of nasopharyngeal carcinoma, especially in the undifferentiated carcinoma of nasopharyngeal type (ucnt, world health organization type iii), which is the dominant histopathological type in high-risk areas. the major ebv oncogene is latent membrane protein 1 (lmp1). lmp1 gene shows variability with different tumorigenic and immunogenic potentials. ebv nuclear antigen 1 (ebna1) regulates progression of ebv-related tumor ... | 2016 | 27071030 |
| exploring the virome of cattle with non-suppurative encephalitis of unknown etiology by metagenomics. | non-suppurative encephalitis is one of the most frequent pathological diagnosis in cattle with neurological disease, but there is a gap in the knowledge on disease-associated pathogens. in order to identify viruses that are associated with non-suppurative encephalitis in cattle, we used a viral metagenomics approach on a sample set of 16 neurologically-diseased cows. we detected six virus candidates: parainfluenza virus 5 (piv-5), bovine astrovirus ch13/neuros1 (boastv-ch13/neuros1), bovine poly ... | 2016 | 26994586 |
| solid-state nuclear magnetic resonance investigation of the structural topology and lipid interactions of a viral fusion protein chimera containing the fusion peptide and transmembrane domain. | the fusion peptide (fp) and transmembrane domain (tmd) of viral fusion proteins play important roles during virus-cell membrane fusion, by inducing membrane curvature and transient dehydration. the structure of the water-soluble ectodomain of viral fusion proteins has been extensively studied crystallographically, but the structures of the fp and tmd bound to phospholipid membranes are not well understood. we recently investigated the conformations and lipid interactions of the separate fp and t ... | 2016 | 27766858 |
| parainfluenza virus 5 upregulates cd55 expression to produce virions with enhanced resistance to complement-mediated neutralization. | many enveloped rna viruses recruit host cell proteins during assembly as a mechanism to limit antiviral effects of complement. using viruses which incorporated cd46 alone, cd55 alone or both cd46 and cd55, we addressed the role of these two host cell regulators in limiting complement-mediated neutralization of parainfluenza virus 5 (piv5). piv5 incorporated functional forms of both cd55 and cd46 into virions. piv5 containing cd55 was highly resistant to complement-mediated neutralization, wherea ... | 2016 | 27505156 |
| immobilization of the n-terminal helix stabilizes prefusion paramyxovirus fusion proteins. | parainfluenza virus 5 (piv5) is an enveloped, single-stranded, negative-sense rna virus of the paramyxoviridae family. piv5 fusion and entry are mediated by the coordinated action of the receptor-binding protein, hemagglutinin-neuraminidase (hn), and the fusion protein (f). upon triggering by hn, f undergoes an irreversible atp- and ph-independent conformational change, going down an energy gradient from a metastable prefusion state to a highly stable postfusion state. previous studies have high ... | 2016 | 27335462 |
| genome sequence of the parainfluenza virus 5 strain that persistently infects ags cells. | we have sequenced the parainfluenza virus 5 strain that persistently infects the commonly used ags human cell line without causing cytopathology. this virus is most closely related to human strains, indicating that it may have originated from biopsy material or from laboratory contamination during generation of the cell line. | 2016 | 27445371 |
| c-terminal dxd-containing sequences within paramyxovirus nucleocapsid proteins determine matrix protein compatibility and can direct foreign proteins into budding particles. | paramyxovirus particles are formed by a budding process coordinated by viral matrix (m) proteins. m proteins coalesce at sites underlying infected cell membranes and induce other viral components, including viral glycoproteins and viral ribonucleoprotein complexes (vrnps), to assemble at these locations from which particles bud. m proteins interact with the nucleocapsid (np or n) components of vrnps, and these interactions enable production of infectious, genome-containing virions. for the param ... | 2016 | 26792745 |
| structure and stabilization of the hendra virus f glycoprotein in its prefusion form. | hendra virus (hev) is one of the two prototypical members of the henipavirus genus of paramyxoviruses, which are designated biosafety level 4 (bsl-4) organisms due to the high mortality rate of nipah virus (niv) and hev in humans. paramyxovirus cell entry is mediated by the fusion protein, f, in response to binding of a host receptor by the attachment protein. during posttranslational processing, the fusion peptide of f is released and, upon receptor-induced triggering, inserts into the host cel ... | 2016 | 26712026 |
| flexibility of the head-stalk linker domain of paramyxovirus hn glycoprotein is essential for triggering virus fusion. | the paramyxoviridae comprise a large family of enveloped, negative-sense, single-stranded rna viruses with significant economic and public health implications. for nearly all paramyxoviruses, infection is initiated by fusion of the viral and host cell plasma membranes in a ph-independent fashion. fusion is orchestrated by the receptor binding protein hemagglutinin-neuraminidase (hn; also called h or g depending on the virus type) protein and a fusion (f) protein, the latter undergoing a major re ... | 2016 | 27489276 |
| human ifit1 inhibits mrna translation of rubulaviruses but not other members of the paramyxoviridae family. | we have previously shown that ifit1 is primarily responsible for the antiviral action of interferon (ifn) alpha/beta against parainfluenza virus type 5 (piv5), selectively inhibiting the translation of piv5 mrnas. here we report that while piv2, piv5, and mumps virus (muv) are sensitive to ifit1, nonrubulavirus members of the paramyxoviridae such as piv3, sendai virus (sev), and canine distemper virus (cdv) are resistant. the ifit1 sensitivity of piv5 was not rescued by coinfection with an ifit1 ... | 2016 | 27512068 |
| releasing the genomic rna sequestered in the mumps virus nucleocapsid. | in a negative strand rna virus, the genomic rna is sequestered inside the nucleocapsid when the viral rna-dependent rna polymerase uses it as the template for viral rna synthesis. it must require a conformational change in the nucleocapsid protein (np) to make the rna accessible by the viral polymerase during this process. the structure of an empty mumps virus nucleocapsid-like particle is determined to 10.4 å resolution by cryoem image reconstruction. by modeling the crystal structure of parain ... | 2016 | 27581981 |
| parainfluenza virus chimeric mini-replicons indicate a novel regulatory element in the leader promoter. | gene expression of paramyxoviruses is regulated by genome-encoded cis-acting elements; however, whether all the required elements for viral growth have been identified is not clear. using a mini-replicon system, it has been shown that human parainfluenza virus type 2 (hpiv2) polymerase can recognize the promoter elements of parainfluenza virus type 5 (piv5), but reporter activity is lower in this case. we constructed a series of luciferase-encoding chimeric piv2/5 mini-genomes that are basically ... | 2016 | 27072881 |
| enhancement of adherence of helicobacter pylori to host cells by virus: possible mechanism of development of symptoms of gastric disease. | it remains unclear why gastric disease does not develop in all cases of helicobacter pylori infection. in this study, we analyzed whether simian virus 5 (sv5) enhanced adherence of h. pylori to adenocarcinoma epithelial cells (ags). h. pylori in ags (harboring sv5) and sv5-infected vero cells, and an agglutination of h. pylori mixed with sv5 were observed by light microscopy, scanning and transmission electron microscopies. the adherent rate of h. pylori to sv5-infected vero cells and treated wi ... | 2017 | 28283804 |
| a single dose recombinant piv5 expressing respiratory syncytial virus f and g proteins protected cotton rats and african green monkeys from rsv challenge. | human respiratory syncytial virus (rsv) is a common cause of severe respiratory disease among infants, immunocompromised individuals and the elderly. no licensed vaccine is currently available. in this study, we evaluated two parainfluenza virus 5 (piv5)-vectored vaccines expressing rsv f (piv5/f) or g (piv5/g) proteins in the cotton rat and african green monkey models for their replication, immunogenicity and efficacy of protection against rsv challenge. following a single intranasal inoculatio ... | 2017 | 28298602 |
| the genetic stability of piv5-vectored rsv vaccine candidates after in vitro and in vivo passage. | human respiratory syncytial virus (rsv) is the leading etiologic agent of lower respiratory tract infections in children, but no licensed vaccine exists. previously, our laboratory developed two parainfluenza virus 5 (piv5)-based rsv vaccine candidates that protect mice against rsv challenge. piv5 was engineered to express either the rsv fusion protein (f) or the rsv major attachment glycoprotein (g) between the hn and l genes of the piv5 genome [piv5-rsv-f (hn-l) or piv5-rsv-g (hn-l)]. to inves ... | 2017 | 28747497 |
| parainfluenza virus 5 (piv5) expressing wild-type or pre-fusion respiratory syncytial virus (rsv) fusion protein protect mice and cotton rats from rsv challenge. | human respiratory syncytial virus (rsv) is the leading cause of pediatric bronchiolitis and hospitalizations. rsv can also cause severe complications in elderly and immunocompromised individuals. there is no licensed vaccine. we previously generated a piv5-vectored vaccine candidate expressing the rsv fusion protein (f) that was immunogenic and protective in mice. in this work, our goal was to improve the original vaccine candidate by modifying the piv5 vector or by modifying the rsv-f antigen. ... | 2017 | 28747496 |
| isolation and genomic characterization of a canine parainfluenza virus type 5 strain in china. | a canine parainfluenza virus type 5 strain was isolated from a lung sample from a diseased dog. the genome sequene of this isolate, named hen0718, was determined and compared tho those of other previously reported canine parainfluenza viruses. unlike previously reported viruses, the hen0718 strain contained several nucleotide mutations in the sh gene that led to a frame shift in the open reading frame. phylogenetic analysis based on the complete virus genome and the p, f, and hn genes showed tha ... | 2017 | 28455668 |
| first complete genome sequence of parainfluenza virus 5 isolated from lesser panda. | parainfluenza virus 5 (piv5) is widespread in mammals and humans. up to now, there is little information about piv5 infection in lesser pandas. in this study, a piv5 variant (named zjq-221) was isolated from a lesser panda with respiratory disease in guangzhou zoo in guangdong province, southern china. the full-length genome of zjq-221 was found to be 15,246 nucleotides and consisted of seven non-overlapping genes encoding eight proteins (i.e., np, v, p, m, f, sh, hn and l). sequence alignment a ... | 2017 | 28138777 |