Publications
Title | Abstract | Year Filter | PMID(sorted ascending) Filter |
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strategies for purifying variants of human rhinovirus 14 2c protein. | the positive strand rna genome of picornaviruses, including human rhinovirus (hrv), poliovirus (pv) and foot-and-mouth disease virus, is translated immediately into a polyprotein that is cleaved by virally encoded proteinases into 10-13 mature proteins. these include the four proteins required to assemble the viral particle as well as 3d(pol) (the viral rna polymerase) and 2c, an atpase and putative helicase. 2c is a protein which is responsible, together with 2b and 3a, for anchoring the replic ... | 2014 | 24316192 |
molecular modeling and analysis of hepatitis e virus (hev) papain-like cysteine protease. | the biochemical or biophysical characterization of a papain-like cysteine protease in hev orf1-encoded polyprotein still remains elusive. very recently, we have demonstrated the indispensability of orf1 protease-domain cysteines and histidines in hev replication, ex vivo (parvez, 2013). in this report, the polyprotein partial sequences of hev strains and genetically-related rna viruses were analyzed, in silico. employing the consensus-prediction results of rubv-p(150) protease as structural-temp ... | 2014 | 24321124 |
collection of oral fluids using cotton ropes as a sampling method to detect foot-and-mouth disease virus infection in pigs. | in high-density farming practices, it is important to constantly monitor for infectious diseases, especially diseases that have the potential to spread rapidly between holdings. pigs are known to amplify foot-and-mouth disease (fmd) by excreting large amounts of virus, and it is therefore important to detect the virus quickly and accurately to minimize the spread of disease. ropes were used to collect oral fluid samples from pigs, and each sample was compared to saliva samples collected from ind ... | 2015 | 24325543 |
accuracy of traditional and novel serology tests for predicting cross-protection in foot-and-mouth disease vaccinated cattle. | foot-and-mouth disease virus (fmdv) antigenic-match between vaccine and field viruses has traditionally been estimated in vitro by computing the r1 value using virus neutralization test (vnt) or elisa titers. in this study we compared the accuracy in predicting cross-protection between the r1 value estimated by vnt and two recently developed tests that measure igg subtypes and avidity. data analyzed consisted of 64 serum samples from fmdv a24/cruzeiro vaccinated bovines challenged with the heter ... | 2014 | 24342253 |
evaluation of cross-protection against three topotypes of serotype o foot-and-mouth disease virus in pigs vaccinated with multi-epitope protein vaccine incorporated with poly(i:c). | epitope-based vaccines are always questioned for their cross-protection against the antigenically variable foot-and-mouth disease virus (fmdv). in this study, we proved the cross-protection effect of a multi-epitope vaccine incorporated with poly(i:c) against three topotypes of o type fmdv. a total of 45 naïve pigs were vaccinated with different doses of multi-epitope protein vaccine incorporated with poly(i:c). at 28 days post-vaccination, 45 vaccinated and 6 unvaccinated control pigs (two pigs ... | 2014 | 24345411 |
interaction of foot-and-mouth disease virus nonstructural protein 3a with host protein dctn3 is important for viral virulence in cattle. | nonstructural protein 3a of foot-and-mouth disease virus (fmdv) is a partially conserved protein of 153 amino acids in most fmdvs examined to date. the role of 3a in virus growth and virulence within the natural host is not well understood. using a yeast two-hybrid approach, we identified cellular protein dctn3 as a specific host binding partner for 3a. dctn3 is a subunit of the dynactin complex, a cofactor for dynein, a motor protein. the dynactin-dynein duplex has been implicated in several su ... | 2014 | 24352458 |
an increase in acid resistance of foot-and-mouth disease virus capsid is mediated by a tyrosine replacement of the vp2 histidine previously associated with vp0 cleavage. | the foot-and-mouth disease virus (fmdv) capsid is highly acid labile, but introduction of amino acid replacements, including an n17d change in vp1, can increase its acid resistance. using mutant vp1 n17d as a starting point, we isolated a virus with higher acid resistance carrying an additional replacement, vp2 h145y, in a residue highly conserved among picornaviruses, which has been proposed to be responsible for vp0 cleavage. this mutant provides an example of the multifunctionality of picorna ... | 2014 | 24352460 |
identification of cytotoxic t lymphocyte epitopes on swine viruses: multi-epitope design for universal t cell vaccine. | classical swine fever (csf), foot-and-mouth disease (fmd) and porcine reproductive and respiratory syndrome (prrs) are the primary diseases affecting the pig industry globally. vaccine induced cd8(+) t cell-mediated immune response might be long-lived and cross-serotype and thus deserve further attention. although large panels of synthetic overlapping peptides spanning the entire length of the polyproteins of a virus facilitate the detection of cytotoxic t lymphocyte (ctl) epitopes, it is an exc ... | 2013 | 24358361 |
genetic diversity of serotype a foot-and-mouth disease viruses in kenya from 1964 to 2013; implications for control strategies in eastern africa. | serotype a is the most genetically and antigenically diverse of the foot-and-mouth disease virus (fmdv) serotypes. records of its occurrence in kenya date back to 1952 and the antigenic diversity of the outbreak viruses in this region is reflected by the current use of two different vaccine strains (k5/1980 and k35/1980) and previous use of two other strains (k18/66 and k179/71). this study aimed at enhancing the understanding of the patterns of genetic variation of serotype a fmdv in kenya. the ... | 2014 | 24368254 |
adjuvant effect enhancement of porcine interleukin-2 packaged into solid lipid nanoparticles. | in this paper, we investigated the enhancement of adjuvant effects of porcine il-2 (pil-2) by packaging it into a solid lipid nanoparticle (sln) delivery system. sln-pil-2 was prepared using hydrogenated castor oil and polylactide-co-glycolide by double emulsion solvent evaporation methods (w/o/w). in animal trials, balb/c mice were immunized with inactivated foot and mouth disease virus (fmdv) antigen combined with the sln-pil-2 adjuvant on days 0 and 14. antibody titer, splenocyte proliferatio ... | 2014 | 24374120 |
design and synthesis of irreversible inhibitors of foot-and-mouth disease virus 3c protease. | foot-and-mouth disease virus (fmdv) causes a highly infectious and economically devastating disease of livestock. the fmdv genome is translated as a single polypeptide precursor that is cleaved into functional proteins predominantly by the highly conserved viral 3c protease, making this enzyme an attractive target for antiviral drugs. a peptide corresponding to an optimal substrate has been modified at the c-terminus, by the addition of a warhead, to produce irreversible inhibitors that react as ... | 2014 | 24374278 |
influence of hydrophilic amino acids and gc-content on expression of recombinant proteins used in vaccines against foot-and-mouth disease virus in escherichia coli. | epitope-based protein expression in escherichia coli can be improved by adjusting its amino acid composition and encoding genes. to that end, we analyzed 24 recombinant epitope proteins (reps) that carry multiple epitopes derived from vp1 protein of foot-and-mouth disease virus. high level expression of the reps was attributed to a high content of arg, asn, asp and thr, a low content of gln, pro and lys, a high content of hydrophilic amino acids and a higher isoelectric point value resulting fro ... | 2014 | 24375229 |
resiquimod and polyinosinic-polycytidylic acid formulation with aluminum hydroxide as an adjuvant for foot-and-mouth disease vaccine. | toll-like receptor (tlr) agonists reportedly have potent antiviral and antitumor activities and may be a new kind of adjuvant for enhancing immune efficacy. resiquimod (r848) is an imidazoquinoline compound with potent antiviral activity and functions through the tlr7/tlr8 myd88-dependent signaling pathway. polyinosinic-polycytidylic acid [poly(i:c)] is a synthetic analog of double-stranded rna that induces the production of pro-inflammatory cytokines by the activation of nf-κb through tlr3. thi ... | 2014 | 24386990 |
multiple micrornas targeted to internal ribosome entry site against foot-and-mouth disease virus infection in vitro and in vivo. | foot-and-mouth disease virus (fmdv) causes a severe vesicular disease in domestic and wild cloven-hoofed animals. because of the limited early protection induced by current vaccines, emergency antiviral strategies to control the rapid spread of fmd outbreaks are needed.here we constructed multiple micrornas (mirnas) targeting the internal ribosome entry site (ires) element of fmdv and investigated the effect of ires-specific mirnas on fmdv replication in baby hamster kidney (bhk-21) cells and su ... | 2014 | 24393133 |
detection and seroprevalence of foot and mouth disease in sheep and goats in punjab, pakistan. | foot and mouth disease (fmd) is a highly contagious disease of ruminants that causes huge economic losses around the globe. however, the prevalence of fmdv in small ruminants has been overlooked in pakistan. a seroepidemiological study was conducted in chakwal, faisalabad and khanewal districts of punjab, pakistan to determine the prevalence of fmd in sheep and goats. a total 1200 serum samples were collected from sheep (n = 180) and goats (n = 920) and were subjected to 3abc non-structural prot ... | 2014 | 24393420 |
application of a cell-based protease assay for testing inhibitors of picornavirus 3c proteases. | proteolytical cleavage of the picornaviral polyprotein is essential for viral replication. therefore, viral proteases are attractive targets for anti-viral therapy. most assays available for testing proteolytical activity of proteases are performed in vitro, using heterologously expressed proteases and peptide substrates. to deal with the disadvantages associated with in vitro assays, we modified a cell-based protease assay for picornavirus proteases. the assay is based on the induction of expre ... | 2014 | 24393668 |
artificial micrornas as antiviral strategy to fmdv: structural implications of target selection. | rna interference (rnai) appears as a promising strategy to control virus replication. while the antiviral power of short-hairpin rnas or small-interfering rnas against fmdv has been demonstrated widely, safer rnai effectors such as artificial micrornas (amirs) have not been evaluated extensively. in this work, transgenic monoclonal cell lines constitutively expressing different amirs targeting fmdv 3d-coding region or 3'utr were established. certain cell lines showed an effective, sequence-speci ... | 2014 | 24406623 |
detection of antibodies specific for foot-and-mouth disease virus infection using indirect elisa based on recombinant nonstructural protein 2b. | foot-and-mouth disease (fmd) is a highly contagious viral disease of transboundary importance. in india, since the launch of the fmd control programme, there has been a substantial increase in the vaccinated bovine population. in this scenario, there is a need for additional locally developed non-structural protein (nsp)-based immnoassays for efficient identification of fmd virus (fmdv)-infected animals in the vaccinated population. the 2b nsp of fmdv, lacking the transmembrane domain (δ2b), was ... | 2014 | 24420160 |
peptides as viral vaccines: lessons from experiments with foot-and-mouth disease virus. | the highly variable sequence encompassing amino acids 141-160 of vp1, one of the four capsid proteins of foot-and-mouth disease virus, elicits neutralizing antibodies in a range of experimental animals. the sequence has been synthesized chemically by merrifield's solid phase method and biochemically as part of different fusion proteins. by incorporating the peptide into the core protein of hepatitis b virus, particles are produced which elicit levels of neutralizing antibody approaching those ob ... | 1991 | 24424921 |
development of porcine respiratory and reproductive syndrome virus replicon vector for foot-and-mouth disease vaccine. | foot-and-mouth disease (fmd) is an economically important global animal disease. to control fmd virus (fmdv) outbreaks, a lot of different novel approaches have been attempted. in this study, we proposed a novel porcine reproductive and respiratory syndrome virus (prrsv) as a replicon vector to express fmdv structural protein. | 2014 | 24427767 |
development of loop-mediated isothermal amplification assay for specific and rapid detection of differential goat pox virus and sheep pox virus. | capripox viruses are economically important pathogens in goat and sheep producing areas of the world, with specific focus on goat pox virus (gtpv), sheep pox virus (sppv) and the lumpy skin disease virus (lsdv). clinically, sheep pox and goat pox have the same symptoms and cannot be distinguished serologically. this presents a real need for a rapid, inexpensive, and easy to operate and maintain genotyping tool to facilitate accurate disease diagnosis and surveillance for better management of cap ... | 2014 | 24438089 |
characteristics of a foot-and-mouth disease virus with a partial vp1 g-h loop deletion in experimentally infected cattle. | previous work in cattle illustrated the protective efficacy and negative marker potential of a a serotype foot-and-mouth disease virus (fmdv) vaccine prepared from a virus lacking a significant portion of the vp1 g-h loop (termed a(-)). since this deletion also includes the arginine-glycine-aspartate (rgd) motif required for virus attachment to the host cell in vivo, it was hypothesised that this virus would be attentuated in naturally susceptible animals. the a(-) virus was passaged three times ... | 2014 | 24438986 |
a serological survey for antibodies against foot-and-mouth disease virus (fmdv) in domestic pigs during outbreaks in kenya. | foot-and-mouth disease (fmd) is endemic in kenya and has been well studied in cattle, but not in pigs, yet the role of pigs is recognised in fmd-free areas. this study investigated the presence of antibodies against fmd virus (fmdv) in pigs sampled during a countrywide random survey for fmd in cattle coinciding with sat 1 fmdv outbreaks in cattle. a total of 191 serum samples were collected from clinically healthy pigs in 17 districts. forty-two of the 191 sera were from pigs vaccinated against ... | 2014 | 24442573 |
evolution of serotype a foot-and-mouth disease virus capsid under neutralizing antibody pressure in vitro. | in this study, the indian foot-and-mouth disease virus (fmdv) vaccine strain (a ind 40/2000) was passaged under homologous bovine convalescent serum (bcs) pressure to gain insight into the evolutionary dynamics of the antigenic sites. a considerable drop in the neutralization titres of the bcs for the isolated variants as compared to the parental population in either virus neutralization or plaque reduction neutralization test was observed. t143k substitution preceding the integrin binding 'rgd' ... | 2014 | 24452141 |
ribavirin-resistant variants of foot-and-mouth disease virus: the effect of restricted quasispecies diversity on viral virulence. | mutagenic nucleoside analogues can be used to isolate rna virus high-fidelity rna-dependent rna polymerase (rdrp) variants, the majority of which are attenuated in vivo. however, attenuated foot-and-mouth disease virus (fmdv) high-fidelity rdrp variants have not been isolated, and the correlations between rdrp fidelity and virulence remain unclear. here, the mutagen ribavirin was used to select a ribavirin-resistant population of fmdv, and 4 amino acid substitutions (d5n, a38v, m194i, and m296v) ... | 2014 | 24453363 |
b epitope multiplicity and b/t epitope orientation influence immunogenicity of foot-and-mouth disease peptide vaccines. | synthetic peptides incorporating protective b- and t-cell epitopes are candidates for new safer foot-and-mouth disease (fmd) vaccines. we have reported that dendrimeric peptides including four copies of a b-cell epitope (vp1 136 to 154) linked to a t-cell epitope (3a 21 to 35) of fmd virus (fmdv) elicit potent b- and t-cell specific responses and confer protection to viral challenge, while juxtaposition of these epitopes in a linear peptide induces less efficient responses. to assess the relevan ... | 2013 | 24454475 |
molecular characterization of foot-and-mouth disease viruses collected in tanzania between 1967 and 2009. | this paper describes the molecular characterization of foot-and-mouth disease viruses (fmdv) recovered from outbreaks in tanzania that occurred between 1967 and 2009. a total of 44 fmdv isolates, containing representatives of serotypes o, a, sat 1 and sat 2 from 13 regions of tanzania, were selected from the fao world reference laboratory for fmd (wrlfmd) virus collection. vp1 nucleotide sequences were determined for rt-pcr amplicons, and phylogenetic reconstructions were determined by maximum l ... | 2015 | 24460931 |
interconversion between parallel and antiparallel conformations of a 4h rna junction in domain 3 of foot-and-mouth disease virus ires captured by dynamics simulations. | rna junctions are common secondary structural elements present in a wide range of rna species. they play crucial roles in directing the overall folding of rna molecules as well as in a variety of biological functions. in particular, there has been great interest in the dynamics of rna junctions, including conformational pathways of fully base-paired 4-way (4h) rna junctions. in such constructs, all nucleotides participate in one of the four double-stranded stem regions, with no connecting loops. ... | 2014 | 24461020 |
immunogenicity of the capsid precursor and a nine-amino-acid site-directed mutant of the 3c protease of foot-and-mouth disease virus coexpressed by a recombinant goatpox virus. | the myristoylated capsid precursor mp1-2a of foot-and-mouth disease virus (fmdv), when expressed in mammalian cells and processed by the fmdv 3c protease, can self-assemble into virus-like particles (vlps). in the present study, nine amino acids of the 3c protease were replaced by site-directed mutagenesis to create a mutant 3c protease, 9m3c. to coexpress mp1-2a and 9m3c and test the resulting proteolytic processing and vlp assembly, two recombinant goatpox viruses (rgtpvs) were constructed by ... | 2014 | 24473707 |
a recombinant adenovirus bicistronically expressing porcine interferon-α and interferon-γ enhances antiviral effects against foot-and-mouth disease virus. | foot-and-mouth disease (fmd) is a virulent and economically costly disease in domestic livestock. since the current vaccine available against fmd provides no protection until 7days postvaccination, the only alternative method to halt the spread of the fmd virus (fmdv) during outbreaks is by the application of anti-viral agents. the combination of recombinant adenovirus expressing type i interferon (ifn-α) and adenovirus expressing type ii ifn (ifn-γ) has been reported to be an effective anti-vir ... | 2014 | 24485895 |
complete genome sequence of foot-and-mouth disease virus serotype o isolated from bangladesh. | foot-and-mouth disease (fmd) is a highly infectious enzootic disease caused by fmd virus. the complete genome sequence of a circulatory fmd virus (fmdv) serotype o isolated from natore, bangladesh, is reported here. genomic analysis revealed antigenic heterogeneity within the vp1 region, a fragment deletion, and insertions at the 5' untranslated region (utr) and 3a region compared to the genome of the available vaccine strain. | 2014 | 24503997 |
neutralizing antibody responses to foot-and-mouth disease quadrivalent (type o, a, c and asia 1) vaccines in growing calves with pre-existing maternal antibodies. | the presence of maternal antibodies is a major obstacle for eliciting protective immune responses to foot-and-mouth disease (fmd) vaccines in young, growing animals. in this report, we analyzed the ability of inactivated quadrivalent oil emulsified and aluminium hydroxide adjuvanted fmd vaccines to elicit neutralizing antibody responses in growing calves that had maternal antibodies. our results demonstrate that oil emulsified vaccines but not aluminium hydroxide adjuvanted fmd vaccines could su ... | 2014 | 24508311 |
infection dynamics of foot-and-mouth disease virus in pigs using two novel simulated-natural inoculation methods. | in order to characterize foot-and-mouth disease virus (fmdv) infection dynamics in pigs, two simulated-natural inoculation systems were developed and evaluated. intra-oropharyngeal (iop) and intra-nasopharyngeal (inp) inoculation both enabled precise control of dose and timing of inoculation while simulating field exposure conditions. there were substantial differences between outcomes of infections by the two routes. iop inoculation resulted in consistent and synchronous infection, whereas inp ... | 2014 | 24548596 |
3cpro of foot-and-mouth disease virus antagonizes the interferon signaling pathway by blocking stat1/stat2 nuclear translocation. | foot-and-mouth disease virus (fmdv) causes a highly contagious, debilitating disease in cloven-hoofed animals with devastating economic consequences. to survive in the host, fmdv has evolved to antagonize the host type i interferon (ifn) response. previous studies have reported that the leader proteinase (l(pro)) and 3c(pro) of fmdv are involved in the inhibition of type i ifn production. however, whether the proteins of fmdv can inhibit type i ifn signaling is less well understood. in this stud ... | 2014 | 24554650 |
the expression of il6 and 21 in crossbred calves upregulated by inactivated trivalent fmd vaccine. | foot and mouth disease (fmd) is an economically important disease and a whole-virus inactivated trivalent virus vaccine is the mainstay for controlling the disease in india. the protective humoral immune response to fmd vaccination is a complex, but, tightly regulated process mediated by the interplay of interleukins (il). based on the specific role of il6 and 21 in adaptive immune response, we hypothesized that inactivated trivalent fmd vaccine would stimulate il6 and 21 expression in the circu ... | 2014 | 24555796 |
in vitro surrogate models to aid in the development of antivirals for the containment of foot-and-mouth disease outbreaks. | foot-and-mouth disease virus (fmdv) is a highly pathogenic member of the genus aphthovirus (family picornaviridae) that is only to be manipulated in high-containment facilities, thus complicating research on and discovery of antiviral strategies against the virus. bovine rhinitis b virus (brbv) and equine rhinitis a virus (erav), phylogenetically most closely related to fmdv, were explored as surrogates for fmdv in antiviral studies. although no efficient cell culture system has been reported so ... | 2014 | 24583031 |
novel antibody binding determinants on the capsid surface of serotype o foot-and-mouth disease virus. | five neutralizing antigenic sites have been described for serotype o foot-and-mouth disease viruses (fmdv) based on monoclonal antibody (mab) escape mutant studies. however, a mutant virus selected to escape neutralization of mab binding at all five sites was previously shown to confer complete cross-protection with the parental virus in guinea pig challenge studies, suggesting that amino acid residues outside the mab binding sites contribute to antibody-mediated in vivo neutralization of fmdv. ... | 2014 | 24584474 |
redistribution of demethylated rna helicase a during foot-and-mouth disease virus infection: role of jumonji c-domain containing protein 6 in rha demethylation. | previously, rna helicase a (rha) re-localization from the nucleus to the cytoplasm in foot-and-mouth disease virus (fmdv) infected cells was shown to coincide with loss of rha methylated arginine residues at its c-terminus. the potential interaction between rha and jumonji c-domain (jmjc) protein 6 (jmjd6) arginine demethylase in infected cells was investigated. treatment with n-oxalylglycine (nog) inhibitor of jmjc demethylases prevented fmdv-induced rha demethylation and re-localization, and a ... | 2014 | 24606677 |
foot-and-mouth disease virus virulence in cattle is co-determined by viral replication dynamics and route of infection. | early events in the pathogenesis of foot-and-mouth disease virus (fmdv) infection in cattle were investigated through aerosol and intraepithelial lingual (iel) inoculations of a cdna-derived fmdv-a24 wild type virus (fmdv-wt) or a mutant derived from the same clone (fmdv-mut). after aerosolization of fmdv-wt, primary infection sites had significantly greater quantities of fmdv, viral rna, and type i/iii interferon (ifn) activity compared to corresponding tissues from cattle infected with fmdv-mu ... | 2014 | 24606678 |
determination of cattle foot-and-mouth disease virus by micro-elisa method. | the development of foot-and-mouth disease virus (fmdv) detection methods is crucial for animal food security, tackling regional fmdv epidemic, and global fmdv prognostic control. for these purposes, a fast and sensitive analysis method is required. in this study, we developed a microchip-based elisa (enzyme-linked immunosorbent assay), micro-elisa, to realize fmdv detection. nickel(ii) chelating chemistry was utilized to immobilize recombinant protein (antigen) on polystyrene micro-beads in orde ... | 2014 | 24614730 |
comparison of test methodologies for foot-and-mouth disease virus serotype a vaccine matching. | vaccination has been one of the most important interventions in disease prevention and control. the impact of vaccination largely depends on the quality and suitability of the chosen vaccine. to determine the suitability of a vaccine strain, antigenic matching is usually studied by in vitro analysis. in this study, we performed three in vitro test methods to determine which one gives the lowest variability and the highest discriminatory capacity. binary ethylenimine inactivated vaccines, prepare ... | 2014 | 24623625 |
emergence of antigenic variants of foot-and-mouth disease virus serotype o in ecuador and preliminary evaluation of a field strain as a vaccine candidate. | foot-and-mouth disease virus serotype o has been circulating regularly throughout most provinces of ecuador, one of the two south american countries that still remain endemic, although satisfactory vaccination coverage was reported. this study concentrates in the characterization of isolates collected during 2008-2011, focusing particularly on the antigenic and immunogenic relationships of the field viruses with the o1/campos vaccine strain in use in the region and with an experimental vaccine f ... | 2014 | 24625343 |
early protection against foot-and-mouth disease virus in cattle using an inactivated vaccine formulated with montanide essai ims d 12802 vg pr adjuvant. | foot and mouth disease is an acute disease of cattle with a broad distribution around the world. due to the fast spread of fmdv infections, control measures must be applied immediately after an outbreak, such as the use of vaccines that induce fast protection. previously, it was shown that mice vaccinated with fmd inactivated virus (ifmdv) formulated with montanide™ essai ims d 12802 vg pr adjuvant (802-ifmdv) were protected when they were challenged 4 and 7 days post-vaccination (dpv) with homo ... | 2014 | 24631088 |
immunological evaluation of mannosylated chitosan nanoparticles based foot and mouth disease virus dna vaccine, pvac fmdv vp1-ompa in guinea pigs. | a dna vaccine for foot and mouth disease (fmd) based on mannosylated chitosan nanoparticles was evaluated in guinea pigs. the dna construct was comprised of fmd virus full length-vp1 gene and outer membrane protein a (omp a) gene of salmonella typhimurium as a toll-like receptor (tlr)-ligand in pvac vector. groups of guinea pigs immunized either intramuscularly or intra-nasally were evaluated for induction of virus neutralizing antibodies, th1(igg2) and th2 (igg1) responses, lymphocyte prolifera ... | 2014 | 24656961 |
the leader proteinase of foot-and-mouth disease virus: structure-function relationships in a proteolytic virulence factor. | the leader proteinase (lpro) of the foot-and-mouth disease virus inhibits the host innate immune response by at least three different mechanisms. the most well-characterised of these is the prevention of the synthesis of cytokines such as interferons immediately after infection, brought about by specific proteolytic cleavage of the eukaryotic initiation factor 4g. this prevents the recruitment of capped cellular mrna; however, the viral rna can be translated under these conditions. the two other ... | 2014 | 24670358 |
hsv-1 amplicon vectors as genetic vaccines. | hsv-1 amplicon vectors have been used as platforms for the generation of genetic vaccines against both dna and rna viruses. mice vaccinated with such vectors encoding structural proteins from both foot-and-mouth disease virus and rotavirus were partially protected from challenge with wild-type virus (d'antuono et al. vaccine 28: 7363-7372, 2010; laimbacher et al. mol ther 20: 1810-1820, 2012), indicating that hsv-1 amplicon vectors are attractive tools for the development of complex and safe gen ... | 2014 | 24671679 |
identification and analysis of differential mirnas in pk-15 cells after foot-and-mouth disease virus infection. | the alterations of micrornas(mirnas) in host cell after foot-and-mouth disease virus (fmdv) infection is still obscure. to increase our understanding of the pathogenesis of fmdv at the post-transcriptional regulation level, solexa high-throu micrornas (mirnas) play an important role both in the post-transcriptional regulation of gene expression and host-virus interactions. despite investigations of mirna expression ghput sequencing and bioinformatic tools were used to identify differentially exp ... | 2014 | 24675746 |
development of anti-bovine iga single chain variable fragment and its application in diagnosis of foot-and-mouth disease. | recombinant antibody fragments like single chain variable fragments (scfvs) represent an attractive yet powerful alternative to immunoglobulins and hold great potential in the development of clinical diagnostic/therapeutic reagents. structurally, scfvs are the smallest antibody fragments capable of retaining the antigen-binding capacity of whole antibodies and are composed of an immunoglobulin (ig) variable light (vl) and variable heavy (vh) chain joined by a flexible polypeptide linker. in the ... | 2014 | 24678404 |
establishment and evaluation of stable cell lines inhibiting foot-and-mouth disease virus by rna interference. | rna interference (rnai) has been proved to be a powerful tool for foot-and-mouth disease virus fmdv inhibition in vitro and in vivo. we established five stable baby hamster kidney 21 cell lines (bhk-21) containing five short hairpin rnas (shrnas) expression plasmids (p3d1shrna, p3d2shrna, p3d3shrna, p3d4shrna, and p3d5shrna) targeting 3d gene of fmdv. immunofluorescent assay, virus titration, and real-time quantitative reverse transcription polymerase chain reaction (q-rt-pcr) were conducted to ... | 2014 | 24683539 |
sequence variability in the structural protein-encoding region of foot-and-mouth disease virus serotype a and o of ethiopian isolates. | a total of 13 serotype o and 5 serotype a fmd ethiopian isolates and some isolates from other countries (six for serotype a and four for serotype o) were sequenced on the structural protein (p1) coding region. the deduced amino acid sequences were aligned and investigated in an attempt to determine the amino acid variation. differences were observed at 115 (15.6%) and 119 (16.1%) amino acid positions for serotype o and serotype a, respectively. the variation in the derived amino acid sequences i ... | 2014 | 24684893 |
dietary germanium biotite supplementation enhances the induction of antibody responses to foot-and-mouth disease virus vaccine in pigs. | we evaluated the potential ability of germanium biotite (gb) to stimulate the production of antibodies specific for foot-and-mouth disease virus (fmdv). to this aim, we measured the total fmdv-specific antibody responses and igm production after vaccination against fmd both experimentally and in the field. gb supplementation with fmdv vaccination stimulated the production of anti-fmdv antibodies, and effectively increased ifn-γ and tnf-α levels. these results suggest that gb may be a novel alter ... | 2014 | 24690605 |
a reverse transcription loop-mediated isothermal amplification assay to rapidly diagnose foot-and-mouth disease virus c. | a reverse transcription loop-mediated isothermal amplification (rt-lamp) assay was developed to rapidly detect foot-and-mouth disease virus serotype c (fmdv c). by testing 10-fold serial dilutions of fmdv c samples, sensitivity of the fmdv c rt-lamp was found to be 10 times higher than that of conventional reverse transcription- pcr (rt-pcr). no cross-reactivity with a, asia 1, or o fmdv or swine vesicular disease virus (svdv) indicated that fmdv c rt-lamp may be an exciting novel method for det ... | 2014 | 24690607 |
construction of self-replicating subgenomic dengue virus 4 (denv4) replicon. | dengue virus serotypes 1-4 are members of mosquito-borne flavivirus genus of flaviviridae family that encode one long open reading frame (orf) that is translated to a polyprotein. both host and virally encoded proteases function in the processing of the polyprotein by co-translational and posttranslational mechanisms to yield 10 mature proteins prior to viral rna replication. to study cis- and trans-acting factors involved in viral rna replication, many groups [1-8] have constructed cdnas encodi ... | 2014 | 24696335 |
first isolation and molecular characterization of foot-and-mouth disease virus in benin. | foot-and-mouth disease (fmd) is a highly contagious viral disease of cloven-hoofed animals. it is one of the most economically devastating diseases affecting livestock animals. in west africa, where constant circulation of fmd virus (fmdv) is assumed, very few studies on the characterization of circulating strains have been published. this study describes the first isolation and characterization of fmdv in benin. fmdv was isolated from 42 samples. antigen capture elisa (ag-elisa) and vp1 coding ... | 2014 | 24720890 |
genome sequences of foot-and-mouth disease virus o/me-sa/ind-2001 lineage from outbreaks in libya, saudi arabia, and bhutan during 2013. | the complete genomes of foot-and-mouth disease (fmd) viruses recovered in libya and saudi arabia in 2013 are described here. these viruses belong to an fmd virus lineage (ind-2001, topotype middle east-south asia, serotype o) which is normally endemic in the indian subcontinent. a contemporary virus sequence from bhutan is also reported here. | 2014 | 24723708 |
serotype diversity of foot-and-mouth-disease virus in livestock without history of vaccination in the far north region of cameroon. | little information is available about the natural cycle of foot-and-mouth disease (fmd) in the absence of control measures such as vaccination. cameroon presents a unique opportunity for epidemiological studies because fmd vaccination is not practiced. we carried out a prospective study including serological, antigenic and genetic aspects of fmd virus (fmdv) infections among different livestock production systems in the far north of cameroon to gain insight into the natural ecology of the virus. ... | 2016 | 24735162 |
evaluation of monoclonal antibody-based sandwich direct elisa (msd-elisa) for antigen detection of foot-and-mouth disease virus using clinical samples. | a monoclonal antibody-based sandwich direct elisa (msd-elisa) method was previously developed for foot-and-mouth disease (fmd) viral antigen detection. here we evaluated the sensitivity and specificity of two fmd viral antigen detection msd-elisas and compared them with conventional indirect sandwich (is)-elisa. the msd-elisas were able to detect the antigen in saliva samples of experimentally-infected pigs for a longer term compared to the is-elisa. we also used 178 rt-pcr-positive field sample ... | 2014 | 24736560 |
single amino acid substitution of vp1 n17d or vp2 h145y confers acid-resistant phenotype of type asia1 foot-and-mouth disease virus. | infection by foot-and-mouth disease virus (fmdv) is triggered by the acidic ph in endosomes after virus uptake by receptor-mediated endocytosis. however, dissociation of the fmdv 146s particle in mildly acidic conditions renders inactivated foot-and-mouth disease (fmd) vaccines much less effective. type asia1 fmdv mutants with increased resistance to acid inactivation were selected to study the molecular basis of viral resistance to acid-induced disassembly and improve the acid stability of fmdv ... | 2014 | 24752763 |
exploration of sequence space as the basis of viral rna genome segmentation. | the mechanisms of viral rna genome segmentation are unknown. on extensive passage of foot-and-mouth disease virus in baby hamster kidney-21 cells, the virus accumulated multiple point mutations and underwent a transition akin to genome segmentation. the standard single rna genome molecule was replaced by genomes harboring internal in-frame deletions affecting the l- or capsid-coding region. these genomes were infectious and killed cells by complementation. here we show that the point mutations i ... | 2014 | 24757055 |
diagnostic potential of recombinant nonstructural protein 3b to detect antibodies induced by foot-and-mouth disease virus infection in bovines. | detection of antibodies to nonstructural proteins (nsp) of foot-and-mouth disease virus is the preferred diagnostic method to differentiate infected from vaccinated animals. in india, an endemic region practising preventive biannual vaccination, 3ab3 indirect elisa (r3ab3 i-elisa) has been employed as the primary screening test for serosurveillance. however, because of the variability observed in the immune response to the nsps, the likelihood of detecting or confirming an infected animal is inc ... | 2014 | 24777827 |
pathogens in water deer (hydropotes inermis) in south korea, 2010-12. | water deer (hydropotes inermis) are among the most common wildlife to approach farmhouses and livestock barns in korea. we collected 305 water deer from gangwon (n=168), south chungcheong (n=89), and gyeongsang (n=48) provinces in 2010-12 and used pcr and serologic tests to screen the deer for pathogens. in 2010, tests for bovine viral diarrhea virus (bvdv), rotavirus, and brucella abortus were positive in 8% (5/60), 2% (1/60), and 59% (33/56) of the animals, respectively. in 2010, the water dee ... | 2014 | 24779466 |
orientation of llama antibodies strongly increases sensitivity of biosensors. | sensitivity of biosensors depends on the orientation of bio-receptors on the sensor surface. the objective of this study was to organize bio-receptors on surfaces in a way that their analyte binding site is exposed to the analyte solution. vhh proteins recognizing foot-and-mouth disease virus (fmdv) were used for making biosensors, and azides were introduced in the vhh to function as bioorthogonal reactive groups. the importance of the orientation of bio-receptors was addressed by comparing sens ... | 2014 | 24793095 |
cpg odn nanorings induce ifnα from plasmacytoid dendritic cells and demonstrate potent vaccine adjuvant activity. | cpg oligodeoxynucleotides (odn) are short single-stranded synthetic dna molecules that activate the immune system and have been found to be effective for preventing and treating infectious diseases, allergies, and cancers. structurally distinct classes of synthetic odn expressing cpg motifs differentially activate human immune cells. k-type odn (k-odn), which have progressed into human clinical trials as vaccine adjuvants and immunotherapeutic agents, are strong activators of b cells and trigger ... | 2014 | 24807558 |
potential applications for antiviral therapy and prophylaxis in bovine medicine. | viral disease is one of the major causes of financial loss and animal suffering in today's cattle industry. increases in global commerce and average herd size, urbanization, vertical integration within the industry and alterations in global climate patterns have allowed the spread of pathogenic viruses, or the introduction of new viral species, into regions previously free of such pathogens, creating the potential for widespread morbidity and mortality in naïve cattle populations. despite this, ... | 2014 | 24810855 |
determining the epitope dominance on the capsid of a serotype sat2 foot-and-mouth disease virus by mutational analyses. | monoclonal-antibody (mab)-resistant mutants were used to map antigenic sites on foot-and-mouth disease virus (fmdv), which resulted in the identification of neutralizing epitopes in the flexible βg-βh loop in vp1. for fmdv sat2 viruses, studies have shown that at least two antigenic sites exist. by use of an infectious sat2 cdna clone, 10 structurally exposed and highly variable loops were identified as putative antigenic sites on the vp1, vp2, and vp3 capsid proteins of sat2/zimbabwe (zim)/7/83 ... | 2014 | 24829347 |
transmission of foot-and-mouth disease virus from experimentally infected indian buffalo (bubalus bubalis) to in-contact naïve and vaccinated indian buffalo and cattle. | this study investigated the transmission of foot-and-mouth disease virus (fmdv) from experimentally infected indian buffalo to in-contact naïve and vaccinated cattle and buffalo. in each of six rooms, two donor buffalo that had been inoculated with fmdv were housed for five days with four recipient animals, comprising one vaccinated buffalo, one vaccinated calf, one unvaccinated buffalo and one unvaccinated calf. vaccination was carried out with current indian vaccine strain (o/ind/r2/75) and ch ... | 2014 | 24837776 |
the use of an adeno-associated viral vector for efficient bicistronic expression of two genes in the central nervous system. | recombinant adeno-associated viral (aav) vectors are one of the most promising therapeutic delivery systems for gene therapy to the central nervous system (cns). preclinical testing of novel gene therapies requires the careful design and production of aav vectors and their successful application in a model of cns injury. one major limitation of aav vectors is their limited packaging capacity (<5 kb) making the co-expression of two genes (e.g., from two promoters) difficult. an internal ribosomal ... | 2014 | 24838969 |
evaluation of a 3a-truncated foot-and-mouth disease virus in pigs for its potential as a marker vaccine. | foot-and-mouth disease (fmd) is a highly contagious and economically devastating disease of cloven-hoofed animals in the world. the disease can be effectively controlled by vaccination of susceptible animals with the conventional inactivated vaccine. however, one major concern of the inactivated fmd virus (fmdv) vaccine is that it does not allow serological discrimination between infected and vaccinated animals, and therefore interferes with serologic surveillance and the epidemiology of disease ... | 2014 | 24885414 |
estimation of the transmission of foot-and-mouth disease virus from infected sheep to cattle. | the quantitative role of sheep in the transmission of foot-and-mouth disease virus (fmdv) is not well known. to estimate the role of sheep in the transmission of fmdv, a direct contact transmission experiment with 10 groups of animals each consisting of 2 infected lambs and 1 contact calf was performed. secretions and excretions (oral swabs, blood, urine, faeces and probang samples) from all animals were tested for the presence of fmdv by virus isolation (vi) and/or rt-pcr. serum was tested for ... | 2014 | 24886222 |
foot-and-mouth disease virus low-fidelity polymerase mutants are attenuated. | previous studies have shown that rna viruses can be attenuated by either increased or decreased viral polymerase replication fidelity. although foot-and-mouth disease virus (fmdv) high-fidelity rna-dependent rna polymerase (rdrp) variants with an attenuated phenotype have been isolated using mutagens, no fmdv mutant with a low-fidelity polymerase has been documented to date. here, we describe the generation of several fmdv rdrp mutants using site-directed mutagenesis via a reverse genetic system ... | 2014 | 24888311 |
induction of protective immune response against both pprv and fmdv by a novel recombinant pprv expressing fmdv vp1. | peste des petits ruminants (ppr) and foot-and-mouth disease (fmd) are both highly contagious diseases of small domestic and wild ruminants caused by the ppr virus (pprv) and the fmd virus (fmdv). in this study, a recombinant pprv expressing the fmdv vp1 gene (rpprv/vp1) was generated and fmdv vp1 expression did not impair replication of the recombinant virus in vitro and immunogenicity in inducing neutralizing antibody against ppr in goats. vaccination with one dose of rpprv/vp1 induced fmdv neu ... | 2014 | 24898430 |
assessing the potential spread and maintenance of foot-and-mouth disease virus infection in wild ungulates: general principles and application to a specific scenario in thrace. | foot-and-mouth disease (fmd), due to infection with serotype o virus, occurred in wild boar and within eleven outbreaks in domestic livestock in the south-east of bulgaria, thrace region, in 2011. hence, the issue of the potential for the spread and maintenance of fmd virus (fmdv) infection in a population of wild ungulates became important. this assessment focused on the spread and maintenance of fmdv infection within a hypothetical wild boar and deer population in an environment, which is char ... | 2016 | 24903641 |
intratypic heterologous vaccination of calves can induce an antibody response in presence of maternal antibodies against foot-and-mouth disease virus. | maternal antibodies can interfere with foot-and-mouth disease vaccination. in this study we determined whether intratypic heterologous vaccination could help to improve herd immunity. | 2014 | 24906852 |
complex assembly, crystallization and preliminary x-ray crystallographic analysis of the bovine cd8αα-bola-2*02201 complex. | in order to clarify the structural characteristics of the bovine mhc class i molecule (bola-i) complexed with cd8αα (cd8αα-bola-i), bovine cd8αα, bola-i (bola-2*02201) and β2m were expressed and purified, and were then assembled with a peptide derived from foot-and-mouth disease virus (fmdv-vp1yy9) and crystallized. the crystal diffracted to 1.7 å resolution and belonged to space group p21, with unit-cell parameters a=53.9, b=103.8, c=61.8 å, α=γ=90, β=96°. the asymmetric unit contained one comp ... | 2014 | 24915083 |
rapeseed oil and ginseng saponins work synergistically to enhance th1 and th2 immune responses induced by the foot-and-mouth disease vaccine. | previous investigations demonstrated that saponins isolated from the root of panax ginseng c. a. meyer (i.e., ginseng root saponin [gs-r]) had adjuvant activity. in the present study, the combined effects of rapeseed oil (ro) and gs-r on the immune responses elicited by foot-and-mouth disease (fmd) vaccine were investigated by measuring fmd virus (fmdv)-specific antibody levels, cytokine levels, lymphocyte proliferation, and long-lived igg-secreting plasma cells from bone marrow in a mouse model ... | 2014 | 24920601 |
cellular micrornas and picornaviral infections. | micrornas (mirnas) are a subtype of short, endogenous, and non-coding rnas, which post-transcriptionally regulate gene expression. the mirna-mediated gene silencing mechanism is involved in a wide spectrum of biological processes, such as cellular proliferation, differentiation, and immune responses. picornaviridae is a large family of rna viruses, which includes a number of causative agents of many human and animal diseases viz., poliovirus, foot-and-mouth disease virus (fmdv), and coxsackievir ... | 2014 | 24921242 |
[advances in reverse genetics-based vaccines of foot and mouth disease]. | reverse-genetic engineering of foot and mouth disease virus (fmdv) can improve the productivity, antigen matching, antigen stability, immune response ability, and biological safety of vaccines, so vaccine candidates with anticipated biological characteristics can be promptly achieved. negative influence in taming of virulent strains can also be decreased or avoided. reverse genetics not only make up for deficiencies like limitation of viral nature, low success rate, and time and energy consuming ... | 2014 | 24923178 |
complete genome sequence of foot-and-mouth disease virus type a circulating in bangladesh. | the complete genome sequence of a foot-and-and mouth disease virus (fmdv) type a strain (ban/ga/sa-197/2013), isolated from gazipur in bangladesh, revealed an 84-nucleotide insertion within the 5'-untranslated region (utr), a lengthened poly(c) tract, and amino acid substitutions at the vp1 region compared to the available genome sequence of the vaccine strain (genbank accession no. hm854025). | 2014 | 24926048 |
proof of principle: non-invasive sampling for early detection of foot-and-mouth disease virus infection in wild boar using a rope-in-a-bait sampling technique. | in this study we describe the use of a rope-in-a-bait sampling method ("pswab": pathogen sampling wild animals with baits) for non-invasive saliva sampling aimed at the detection of foot-and-mouth disease (fmd) viral genome in wild boar. the pswabs are produced in the form of a standardized product by embedding a 10 cm long cotton rope in a cereal-based bait matrix. to assess the general suitability of this novel sampling technique an animal experiment was conducted to detect fmd viral genome in ... | 2014 | 24930983 |
experimental infection of cattle and goats with a foot-and-mouth disease virus isolate from the 2010 epidemic in japan. | in this study, we carried out experimental infections in cattle and goats using a foot-and-mouth disease virus (fmdv) isolate from the 2010 epidemic in japan to analyze clinical manifestations, virus-shedding patterns and antibody responses in the animals. we found that the fmdv o/jpn/2010 isolate is virulent in cattle and goats, produces clinical signs, is spread efficiently by direct contact within the same species, and is persistently infectious in cattle. quantitative analysis of levels of v ... | 2014 | 24938483 |
detection of foot-and-mouth disease virus rna and capsid protein in lymphoid tissues of convalescent pigs does not indicate existence of a carrier state. | a systematic study was performed to investigate the potential of pigs to establish and maintain persistent foot-and-mouth disease virus (fmdv) infection. infectious virus could not be recovered from sera, oral, nasal or oropharyngeal fluids obtained after resolution of clinical infection with any of five fmdv strains within serotypes a, o and asia-1. furthermore, there was no isolation of live virus from tissue samples harvested at 28-100 days post-infection from convalescent pigs recovered from ... | 2016 | 24943477 |
[progress in insertion sites for foreign sequence of foot and mouth disease virus]. | with the progess in studying gene structure and function of foot and mouth disease virus (fmdv), fmdv can express exogenous genes in different sites. through transforming and modifying fmdv can achieve different application purposes such as improving virus titer, introducing tag, improving immune responses, and reducing pathogenicity. from the perspective of fmdv receiving inserted exogenous gene, this paper mainly describes the latest relevant developments of fmdv's expression to exogenous gene ... | 2014 | 24945052 |
a pig tonsil cell culture model for evaluating oral, low-dose ifn-α treatments. | oral, low-dose ifn-α treatments proved effective in several models of viral infections and immunopathological conditions. also, they do not give rise to the serious side effects observed after parenteral inoculation of high doses (10(5)u/kg b.w. and higher). there is convincing evidence that such treatments work through an early, effective interaction with oral lymphoid tissues before the ifn-α molecules are rapidly destroyed by gut enzymes. yet, the paucity of detailed information about these c ... | 2014 | 24951265 |
magnesium-dependent folding of a picornavirus ires element modulates rna conformation and eif4g interaction. | internal ribosome entry site (ires) elements are high-order rna structures that promote internal initiation of translation to allow protein synthesis under situations that compromise the general cap-dependent translation mechanism. picornavirus ires elements are highly efficient elements with a modular rna structure organization. here we investigated the effect of mg(2+) concentration on the local flexibility and solvent accessibility of the foot-and-mouth disease virus (fmdv) ires element measu ... | 2014 | 24961997 |
influence of antibodies transferred by colostrum in the immune responses of calves to current foot-and-mouth disease vaccines. | immunity to currently used oil-adjuvanted inactivated vaccines against foot-and-mouth disease virus (fmdv) has been studied in detail in adult animals; however, the influence of maternally derived antibodies transferred through colostrum (mat-abs) in the immune responses of vaccinated calves is less clear. here, we report the anti-fmdv humoral responses elicited in calves with or without mat-abs that received one or two doses of the current tetravalent oil-adjuvanted commercial vaccine used in a ... | 2014 | 24968156 |
protection against rift valley fever virus infection in mice upon administration of interferon-inducing rna transcripts from the fmdv genome. | in this work we have addressed the effect of synthetic, non-infectious, rna transcripts, mimicking structural domains of the non-coding regions (ncrs) of the foot-and-mouth disease virus (fmdv) genome on the infection of mice with rift valley fever virus (rvfv). groups of 5 mice were inoculated intraperitoneally (i.p.) with 200 μg of synthetic rna resembling the 5'-terminal s region, the internal ribosome entry site (ires) or the 3'-ncr of the fmdv genome. rna inoculation was performed 24h befor ... | 2014 | 24973761 |
swine interferon-induced transmembrane protein, sifitm3, inhibits foot-and-mouth disease virus infection in vitro and in vivo. | the interferon-induced transmembrane protein 3 (ifitm3) is a widely expressed potent antiviral effector of the host innate immune system. it restricts a diverse group of pathogenic, enveloped viruses, by interfering with endosomal fusion. in this report, the swine ifitm3 (sifitm3) gene was cloned. it shares the functionally conserved cd225 domain and multiple critical amino acid residues (y19, f74, f77, r86 and y98) with its human ortholog, which are essential for antiviral activity. ectopic exp ... | 2014 | 24973762 |
comparative evaluation of non-structural protein-antibody detecting elisas for foot-and-mouth disease sero-surveillance under intensive vaccination. | foot-and-mouth disease is a highly infectious and contagious disease of livestock animals with transboundary and economical importance. animals in the endemic settings are regularly vaccinated in addition to intensive surveillance for control of the disease. under intensive vaccination, detection of infected animals among the vaccinated population is essential to monitor the infection and to track down the virus movement. sero-surveillance and retrospective disease diagnosis is performed primari ... | 2014 | 24996132 |
sequence adaptations affecting cleavage of the vp1/2a junction by the 3c protease in foot-and-mouth disease virus-infected cells. | the foot-and-mouth disease virus (fmdv) capsid protein precursor p1-2a is cleaved by the virus-encoded 3c protease to vp0, vp3, vp1 and 2a. it was shown previously that modification of a single amino acid residue (k210e) within the vp1 protein and close to the vp1/2a cleavage site, inhibited cleavage of this junction and produced 'self-tagged' virus particles. a second site substitution (e83k) within vp1 was also observed within the rescued virus [gullberg et al. (2013). j virol 87: , 11591-1160 ... | 2014 | 25000961 |
laboratory animal models to study foot-and-mouth disease: a review with emphasis on natural and vaccine-induced immunity. | laboratory animal models have provided valuable insight into foot-and-mouth disease virus (fmdv) pathogenesis in epidemiologically important target species. while not perfect, these models have delivered an accelerated time frame to characterize the immune responses in natural hosts and a platform to evaluate therapeutics and vaccine candidates at a reduced cost. further expansion of these models in mice has allowed access to genetic mutations not available for target species, providing a powerf ... | 2014 | 25000962 |
recombinant viral capsid protein vp1 suppresses lung cancer metastasis by inhibiting cox-2/pge2 and mig-7. | recombinant capsid protein vp1 (rvp1) of foot-and-mouth disease virus binds to integrins to modulate akt/gsk3-β signaling and suppress migration/invasion and metastasis of cancer cells, but the underlying molecular mechanism is unclear. here, we showed that the rvp1-mediated inhibition of akt/gsk3-β signaling and cell migration/invasion was accompanied by downregulation in phosphatidylinositol (3,4,5)-triphosphate (pip3), integrin-linked kinase (ilk) and ikk/nf-κb signaling as well as suppressio ... | 2014 | 25004182 |
spatial and temporal distribution of foot-and-mouth disease virus in the lake zone of tanzania. | this study was conducted to determine the spatiotemporal distribution of foot-and-mouth disease (fmd) virus (fmdv) serotypes and evaluate the awareness of livestock keepers about fmd in tanzania. an observational prospective study involving serological analysis, fmdv antigen detection and questionnaire survey was carried out in the lake zone of tanzania. seroprevalence of antibodies to the nonstructural protein 3abc of fmdv and serotype-specific antigen detection were investigated by using svano ... | 2014 | 25005020 |
molecular survey for foot-and-mouth disease virus in livestock in tanzania, 2008-2013. | phylogeography data are of paramount importance in studying the molecular epidemiology dynamics of foot-and-mouth disease virus (fmdv). in this study, epithelial samples and oesophageal-pharyngeal fluids were collected from 361 convalescent animals (cattle and buffaloes) in the field throughout tanzania between 2009 and 2013. the single plex real-time rt-pcr (qrt-pcr) assay for rapid and accurate diagnosis of fmdv employing the callahan 3df-2, 3df-r primers and callahan 3dp-1 probe were used. pr ... | 2014 | 25005022 |
rapid, sensitive and effective diagnostic tools for foot-and-mouth disease virus in africa. | speed is paramount in the diagnosis of highly infectious diseases, such as foot-and-mouth disease (fmd), as well as for emerging diseases; however, simplicity is required if a test is to be deployed in the field. recent developments in molecular biology have enabled the specific detection of fmd virus (fmdv) by reverse-transcription loop-mediated isothermal amplification (rt-lamp), real-time reverse-transcription polymerase chain reaction (rt-qpcr) and sequencing. rt-lamp enables amplification o ... | 2014 | 25005362 |
serosurveillance of foot-and-mouth disease virus in selected livestock-wildlife interface areas of tanzania. | foot-and-mouth disease (fmd) is caused by a virus of the genus aphthorvirus of the family picornaviridae. there is great scientific need for determining the transmission dynamics of fmd virus (fmdv) by drawing more attention to the livestock-wildlife interface areas. a variety of literature suggests that buffalo could serve as reservoir of fmdv in wildlife and cattle. however, many fmdv research studies conducted on experimentally infected cattle as carriers and groups of animal highly susceptib ... | 2014 | 25005680 |
morphologic and phenotypic characteristics of myocarditis in two pigs infected by foot-and mouth disease virus strains of serotypes o or a. | myocarditis is often cited as the cause of fatalities associated with foot-and-mouth disease virus (fmdv) infection. however, the pathogenesis of fmdv-associated myocarditis has not been described in detail. the current report describes substantial quantities of fmdv in association with a marked mononuclear inflammatory reaction, interstitial edema and cardiomyocyte degeneration in the myocardium of two pigs that died during acute infection with either of two different strains of fmdv. despite s ... | 2014 | 25015718 |
development of tailored real-time rt-pcr assays for the detection and differentiation of serotype o, a and asia-1 foot-and-mouth disease virus lineages circulating in the middle east. | rapid and accurate diagnosis is essential for effective control of foot-and-mouth disease (fmd). in countries where fmd is endemic, identification of the serotypes of the causative virus strains is important for vaccine selection and tracing the source of outbreaks. in this study, real-time reverse transcription polymerase chain reaction (rrt-pcr) assays using primer/probe sets designed from the vp1 coding region of the virus genomes were developed for the specific detection of serotype o, a and ... | 2014 | 25016065 |
induction of protection against foot-and-mouth disease virus in cell culture and transgenic suckling mice by mirna targeting integrin αv receptor. | foot-and-mouth disease virus (fmdv) is an rna virus that causes a highly contagious disease in domestic and wild cloven-hoofed animals. although vaccination has been used to protect animals against fmdv, there are shortcomings in the efficacy of the available vaccines. rna interference (rnai) is triggered by small rna molecules, including short interfering rnas and micrornas (mirnas), and the use of rnai-based methods have demonstrated promise as an alternative method of controlling the transmis ... | 2014 | 25016204 |
expression of porcine fusion protein irf7/3(5d) efficiently controls foot-and-mouth disease virus replication. | several studies have demonstrated that the delivery of type i, ii, or iii interferons (ifns) by inoculation of a replication-defective human adenovirus 5 (ad5) vector expressing ifns can effectively control foot-and-mouth disease (fmd) in cattle and swine during experimental infections. however, relatively high doses are required to achieve protection. in this study, we identified the functional properties of a porcine fusion protein, poirf7/3(5d), as a biotherapeutic and enhancer of ifn activit ... | 2014 | 25031341 |
effects of two amino acid substitutions in the capsid proteins on the interaction of two cell-adapted panasia-1 strains of foot-and-mouth disease virus serotype o with heparan sulfate receptor. | some cell-adapted strains of foot-and-mouth disease virus (fmdv) can utilize heparan sulfate (hs) as a receptor to facilitate viral infection in cultured cells. a number of independent sites on the capsid that might be involved in fmdv-hs interaction have been studied. however, the previously reported residues do not adequately explain hs-dependent infection of two cell-adapted panasia-1 strains (o/tibet/cha/6/99tc and o/fujian/cha/9/99tc) of fmdv serotype o. to identify the molecular determinan ... | 2014 | 25056022 |