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development and evaluation of an indirect enzyme immunoassay for detection of porcine antibodies to pseudorabies virus.an indirect enzyme immunoassay is described for detection of porcine serum antibody to pseudorabies virus. the analytical sensitivity of the enzyme immunoassay was found to be approximately 4.5 log 4 x 10 (5120 times) greater than the serum neutralization test, based on parallel end point titrations. the diagnostic sensitivity of the enzyme immunoassay was comparable or superior to that of the serum neutralization, based on the earliest detectable antibody after infection of swine with pseudorab ...19863017531
[electron microscopy of aujeszky's disease virus in explants of gasser's ganglion from pigs with a latent infection].different developmental stages of the aujeszky's disease virus were demonstrated by electron microscopy in the ultra-thin slices by the cultivated fragments of the gasserian ganglion (g. g.) of two pigs latently infected with the aujeszky's disease virus (adv). in a pig vaccinated with the inactivated vaccine against the disease, the virus was detected in the g. g. cells 186 days after virus challenge, the reactivation of latency being obtained after immunosuppression with dexamethasone. in the ...19863020761
dot-enzyme immunoassay for visual detection of antibodies to pseudorabies virus in swine serum.a modified solid-phase enzyme immunoassay (eia) is described for the visual detection of anti-pseudorabies virus (anti-prv) antibody in porcine serum. dots of prv antigens were adsorbed to nitrocellulose paper (hence the name dot-eia), and the remaining nonspecifically reactive sites were blocked with bovine serum albumin or skim milk powder. after immersion in test serum, bound antibodies were reacted with a peroxidase-conjugated anti-porcine immunoglobulin g (h & l). positive reactions were ea ...19863007569
characterization and mapping of a nonessential pseudorabies virus glycoprotein.antigenic variants of pseudorabies virus (prv) containing mutations in a viral glycoprotein with a molecular weight of 82,000 (giii) were isolated by selecting for resistance to a complement-dependent neutralizing monoclonal antibody (mca82-2) directed against giii. these mutants were completely resistant to neutralization with mca82-2 in the presence of complement. two mutants selected for further studies either did not express giii or expressed an improperly processed form of the glycoprotein. ...19863005646
[induction of biological protection in pigs against infection with aujeszky disease virus by vaccination with large doses of live or inactivated vaccines].pigs were inoculated against the aujeszky's disease twice in a four-week interval. the dose of the live vaccine was 10(6) tkid50 and the titres of neutralizing antibodies were 1 : 16 to 1 : 128 in blood serum. two weeks later the pigs were exposed to contact infection. primary multiplication of the virus was observed on the mucous membranes of the nose and oropharynx and the virus was detected on the nasal mucous membrane within one to five days, the maximum infection titre values being 10(1.3) ...19863008403
control of aujeszky's disease. 19863010537
[comparative studies of the detection of aujeszky virus from filtered and unfiltered study samples]. 19863011385
differentiation of serum antibodies from pigs vaccinated or infected with aujeszky's disease virus by a competitive enzyme immunoassay.a competitive enzyme immunoassay was developed to detect antibodies to a glycoprotein (gi) of aujeszky's disease virus. infected cell monolayers were used as antigen and a monoclonal antibody directed against an epitope of gi as indicator antibody. it was demonstrated that pigs vaccinated with the bartha, buk or nia-4 strains did not produce antibody to the epitope of gi, whereas all wild-type viruses tested did induce this antibody. the antibody to the gi epitope persisted for at least 15 weeks ...19863011974
vaccine engineering. violation of rules alleged. 19863012349
aujeszky's disease: blocking elisa for the detection of serum antibodies.a blocking elisa for the detection of serum antibodies to aujeszky's disease virus has been developed. the test was designed in particular with a view to examining large numbers of blood samples. it has been found to be sensitive, specific and precise. in comparison with the serum neutralization test it was superior in detecting low levels of antibodies in pig sera. the blocking elisa gave higher titre values in serum samples taken early after experimental infection of pigs with aujeszky's disea ...19863016016
pseudorabies virus gene encoding glycoprotein giii is not essential for growth in tissue culture.we have established that in the becker strain of pseudorabies virus (prv), the glycoprotein giii gene is not essential for growth in cell culture. this was accomplished by construction and analysis of viral mutants containing two defined deletion mutations affecting the giii gene. these mutations were first constructed in vitro and introduced into escherichia coli expression plasmids to verify structure and protein production. each mutation was then crossed onto prv by cotransfection of plasmid ...19863016326
phagocytosis and intracellular killing of pasteurella multocida by porcine alveolar macrophages after infection with pseudorabies virus.the purpose of this study was to determine if pseudorabies virus (prv) interfered with normal alveolar macrophage phagocytic functions. porcine alveolar macrophages (pam) obtained by pulmonary lavage were exposed to prv. at 1 hour postinfection, cells were challenged with pasteurella multocida labeled with 3[h] thymidine. the phagocytosis assay was performed by measuring total radioactivity 1 hour after pm challenge in a soft-beta spectrophotometer. intracellular killing was measured by counting ...19863020772
researcher reprimanded for pseudorabies test. 19863022375
[use of immunoenzyme (elisa) diagnosis of aujeszky's disease in pigs during the recovery period].samples of blood and blood serums of pigs were examined for the presence of antibodies to the aujeszky's disease virus. the virus-neutralizing (vn) test and the enzymoimmunologic (elisa) method were used for this examination. as indicated by comparison of the average titres of antiviral antibodies determined by both methods, the elisa method is 60 to 600 times more sensitive than the vn test. the high sensitivity of the elisa method enabled to detect antiviral antibodies even in samples consider ...19863022451
herpesvirus (pseudorabies virus) latency in swine: occurrence and physical state of viral dna in neural tissues.the occurrence of the pseudorabies virus (prv, herpes suis 1) genome in various neural tissues of latently infected pigs was investigated. during the latent phase of infection, between 7 and 52 weeks p.i., the average amount of prv dna ranged between 0.3 and 0.05 genome copies per cell. the results obtained by in situ cytohybridization and reassociation kinetic experiments indicated that each latently infected cell harbored at least 30 viral genome copies. prv dna could be demonstrated in simila ...19863024403
detection of latent pseudorabies virus in porcine tissue, using a dna hybridization dot-blot assay.a dna-hybridization dot-blot technique was developed to detect the presence of pseudorabies virus (prv) dna in porcine tissue. seven 32p-nick translated probes of high specific activity were prepared from transformed escherichia coli plasmids into which bacillus amyloliquefaciens h (bam hi) restriction fragments of prv-dna had been inserted. samples of dna that had been extracted from porcine tissue or from prv grown in tissue culture were transferred to nitrocellulose paper, using a microsample ...19863024534
the properties of aujeszky's disease (pseudorabies) virus after serial passages in chick-embryo cell cultures in the presence of ethyl p-chlorphenoxyisobutyrate (cpib). 19863031907
antiviral effectiveness of butylated hydroxytoluene against pseudorabies (aujeszky's disease) virus in cell culture, mice, and swine.butylated hydroxytoluene (bht) was evaluated for antiviral effectiveness on pseudorabies virus (prv) in cell culture, mice, and swine. when relatively small amounts of bht were mixed with prv and incubated at 37 c for 30 or 60 minutes before inoculation into cell cultures, the cell cultures did not become infected with virus. the prv was not infectious when the virus was treated with bht and then inoculated intraperitoneally into mice, but was infectious when bht and prv were inoculated simultan ...19863021025
evaluation of a diagnostic antigen for the detection of aujeszky's disease virus-infected subunit-vaccinated pigs.an early virus protein complex that is found in the maintenance medium of aujeszky's disease (ad) virus-infected cells was evaluated as a subunit diagnostic antigen (suda) in the enzyme-linked immunosorbent assay (elisa). this antigen was found in purer form and in larger quantities for up to 12 h post-infection in the maintenance medium of ad virus-infected mdbk cell cultures than in the maintenance medium of virus-infected porcine fallopian tube (pft) and pk1a cell cultures. the suda was shown ...19863010548
proteins specified by the short unique region of the genome of pseudorabies virus play a role in the release of virions from certain cells.two pseudorabies virus vaccine strains (bartha and norden) that have a similar deletion in the short unique (us) region of the genome have been identified previously (b. lomniczi, m. l. blankenship, and t. ben-porat, j. virol. 49:970-979, 1984). these strains do not code for the glycoprotein gi, a glycoprotein that has been mapped on the wild type virus genome by t. c. mettenleiter, n. lukacs, and h. j. rziha (j. virol. 53:52-57, 1985) to the sequences deleted from the vaccine strain. restoratio ...19863001344
induction and characterization of swine beta interferon.newcastle disease virus (ndv) strain "h" and polyinosinic-polycytidylic acid (poly i:c) were used for interferon (ifn) induction in secondary pig kidney cells. a functional ifn system was detected and characterized. a wide similarity with the correspondent human and bovine systems was appreciated, with particular regard to the kinetics of synthesis. a glycosylated protein was essential for activity in bovine cells, but not in swine cells. poly i:c proved to be a very weak inducer, even in condit ...19873034503
restriction endonuclease analysis of aujeszky's disease viruses isolated in japan. 19873035261
local humoral and cellular responses in aujeszky's disease virus infection in pigs.mucosal and tracheal washings from pigs vaccinated parenterally and intranasally with aujeszky's disease virus were tested for specific anti-aujeszky's disease virus responses. antibody tests included complement dependent antibody lysis, antibody dependent cellular cytotoxicity, virus neutralisation, and anti-aujeszky's disease virus iga and igg levels. there was no correlation between the levels of these antibodies and protection from subsequent challenge. direct lymphocyte cytotoxicity against ...19873035662
genetic control of immune response to pseudorabies and atrophic rhinitis vaccines: i. heterosis, general combining ability and relationship to growth and backfat.data from 988 pigs from 119 litters farrowed in two seasons of a three-breed diallel crossbreeding experiment were analyzed to estimate general combining abilities of breeds and heterosis for humoral immune response to pseudorabies virus and atrophic rhinitis vaccines. twenty purebred boars and 85 sows of the duroc, landrace and yorkshire breeds were mated to provide the nine breed-of-sire and breed-of-dam combinations. immune response was measured after vaccination. a modified-live pseudorabies ...19873558146
genetic control of immune response to pseudorabies and atrophic rhinitis vaccines: ii. comparison of additive direct and maternal genetic effects.data from 52 litters farrowed in two seasons of a cross-fostering experiment were analyzed to estimate variances and covariances for additive direct and maternal genetic effects on immune response to pseudorabies virus and b. bronchiseptica vaccine. twenty purebred boars and 44 sows of the duroc, landrace and yorkshire breeds were used. immune response was measured after vaccine challenge. a modified-live pseudorabies (pr) vaccine was administered to piglets at 28 d of age; response was measured ...19873558147
effects of experimental pseudorabies virus infection on vaccinated pregnant sows.in regard to field problems, a study was done to determine the effects of an infection with virulent pseudorabies virus (prv) on pregnant sows vaccinated with an inactivated virus vaccine. three routes of viral inoculation have been tested: intranasal, intra-uterine and intra-fetal. the nasal infection did not allow to induce pregnancy disorders observed on the field on pregnant sows. after insemination with semen mixed with prv, abortion was observed on one of the two immune sows. in this one, ...19873426109
recurrent viruses in a singapore intensive pig farming estate.the ponggol intensive pig farming estate was conceived approximately 10 years ago to accommodate pig farms resettled from water catchment areas. initially stocking density of the estate was 1300-1500 pigs per hectare (ha) and the total pig population in the estate was 200,000. over the past 10 years the numbers of pigs have increased to 400,000 and the stocking density of the big commercial units have increased to 1500-2500 per ha. with such intensive methods of husbandry environmental problems ...19873446006
aujeszky's disease vaccination and infection of pigs with maternal immunity: effects on cell- and antibody-mediated immunity.scc, adv-scc, adv-adcc and adv-lyst as well as nd50-titres of neutralizing serum antibodies were examined in 36 passively immune pigs, 25 of which were vaccinated at 3 weeks of age and partly revaccinated 3 weeks later. twenty-five vaccinated animals and 8 non-immune control pigs were challenged with infectious adv. independent of the state of maternal immunity the cytotoxic response of the white blood cells from all the animals was low at wpp 3 but rose with increasing age. adv-lyst occurred on ...19873026291
genome location and identification of functions defective in the bartha vaccine strain of pseudorabies virus.we have shown previously (lomniczi et al., j. virol. 52:198-205, 1984) that the bartha vaccine strain of pseudorabies virus has a deletion in the short unique (us) region of its genome--a deletion that is related to the absence of virus virulence. this strain is, however, also defective in other genes involved in virulence. we show here that virulence can be restored by marker rescue of the bartha strain to which an intact us has been restored (but not to the parental bartha strain) by sequences ...19873027406
construction and characterization of deletion mutants of pseudorabies virus: a new generation of 'live' vaccines.various deletions were introduced into a cloned subgenomic fragment (bamhi-7), located in the unique short (us) region of the dna from the virulent northern ireland aujeszky-3 (nia-3) strain of pseudorabies virus (prv). in the cloned hindiii-b fragment, the mlui-bglii fragment was replaced by different mlui-bglii fragments of the deleted bamhi-7 clones. transfection of the deleted hindiii-b fragments together with the hindiii-a fragment of either the nia-3 or the non-virulent nia-4 strain yielde ...19873029289
intranasal vaccination of pigs against aujeszky's disease: comparison with one or two doses of attenuated vaccines in pigs with high maternal antibody titres.ten-week-old pigs with high levels of maternally derived antibody (mda) against aujeszky's disease virus (adv) were given either a single intranasal vaccination or one or two doses (with an interval of three weeks) of commercially available attenuated adv vaccines intramuscularly. the pigs did not produce a clear neutralising antibody response to adv. however, pigs vaccinated intranasally and pigs given two doses of attenuated adv vaccines were protected against intranasal challenge with virulen ...19873029845
[comparison of the biological properties of various strains of aujeszky's disease viruses].we compared three strains of aujeszky's disease virus that had been isolated from slaughter pigs from the dormant foci of aujeszky's disease, with the known virulent strain cvos and top. no significant differences were found out in the following characters: titer value on tissue cultures from chick embryonal cells (keb) and cellular line mdbk at the temperatures of 37 degrees c and 40 degrees c, cytopathogenic effect (cpe) in the hela cells, plaque formation in the keb tissue culture, pruritus r ...19873031866
four-layer enzyme immunoassay (eia) detection of differences in igg, igm and iga antibody response to aujeszky's disease virus in infected and vaccinated pigs.the use of the four-layer enzyme immunoassay (eia) for the detection of igg, igm and iga antibodies against aujeszky's disease virus in blood and oropharyngeal swabs of infected and vaccinated pigs is described. mean antibody titres obtained using the four-layer eia were 6.1 and 3829 times higher compared with the indirect enzyme-linked immunosorbent assay (elisa) and virus neutralization (vn) test, respectively. the vn test detected mainly igg antibodies, while the igm antibodies did not react. ...19873031872
swine antibody-dependent cellular cytotoxicity against pseudorabies virus-infected cells.in pseudorabies virus (prv) infection of pigs, antibody-dependent cellular cytotoxicity (adcc) may be an early defense mechanism. peripheral blood leukocytes (pbl) and pulmonary macrophages mediate adcc activity. antibody-dependent cellular cytotoxicity against prv-infected target cells was assessed, and the effect of infection of cells having an adcc-effector function was determined. although pulmonary lavage cells (plc) had adcc activity, in vitro infection of plc led to prv replication, loss ...19873032027
a necrotizing pneumonia in lambs caused by pseudorabies virus (aujesky's disease virus).an outbreak of pseudorabies occurred in sheep housed with swine in the same building. although the sheep and swine were not in physical contact, the lambs and ewes were exposed to air from the sows' section. three dead lambs were submitted to the iowa state university veterinary diagnostic laboratory for necropsy. grossly there were pulmonary congestion and multifocal pulmonary hemorrhages. microscopic lesions were severe acute multifocal necrotizing bronchopneumonia with necrotizing vasculitis ...19873032388
evolution of pseudorabies virions containing genomes with an invertible long component after repeated passage in chicken embryo fibroblasts.the genome of pseudorabies virus consists of two components, short (s) and long (l). only the s component is bracketed by inverted repeats, and only the s component inverts itself relative to the l component, giving rise to two isomeric forms of the genome. an attenuated vaccine strain of pseudorabies virus (norden), however, has a genome which is found in four isomeric forms (b. lomniczi, m. l. blankenship, and t. ben-porat, j. virol. 49:970-979, 1984). to determine the basis for the atypical s ...19873033309
the role of acute and latent virus infections in the pathogenesis of inner ear disturbances.the possible role of herpesviral infections of the inner ear in suddenly appearing inner ear disturbances was investigated. experimental pseudorabies virus (prv, herpes sui 1) infection of mice and swine was used as a model system. infected mice represented the productive cycle of prv infection (acute phase), whereas the latent phase of infection could be tested in swine. from the acutely infected mice the virus could be reisolated from perilymphatic fluid and various parts of the brain. massive ...19873035932
second-generation pseudorabies virus vaccine with deletions in thymidine kinase and glycoprotein genes.a modified-live pseudorabies virus (prv) vaccine, designated prv(dlg92/d1tk), with deletions in the thymidine kinase (tk) and glycoprotein-giii (g92) genes, was derived from the prv (bucharest [buk]-d13) vaccine strain. the vaccine virus also contained a deletion in glycoprotein gi. despite 3 deletions, prv(dlg92/d1tk) replicated to high titers in cell culture from 30 c to 39.1 c. enzyme assays and autoradiography revealed that prv(dlg92/d1tk) did not induce a functional tk activity in infected ...19873035972
[the effect of colostral immunity on the active formation of antibodies in pigs after the administration of inactivated vaccine against aujeszky's disease].in a large herd of pigs where a trial was performed to cure the animals from aujeszky's disease (ad) by applying to all animals an inactivated vaccine, a post-vaccination antibody response was studied in piglets coming from the sows that were vaccinated several times. when the piglets were vaccinated at the age of eight weeks (the average virus-neutralizing titer (vnt) of colostral antibodies was 1:11.4) and revaccinated at the age of 11 weeks, 73% of the forty-five animals (examined at the age ...19873037756
pathological changes in hpcd pigs with prednisolone induced recrudescence of pseudorabies virus.in hpcd pigs inoculated with prv, latent prv could be reactivated in-vivo by the administration of large doses of prednisolone 3 months after the primary infection. in two pigs, virus shedding was without clinical signs of disease, whereas depression of circulating lymphocytes was prominent. reactivation of prv was also demonstrated by cultivation of the brain cortex on the 7th day and the mandibular lymph node on the 9th day after the prednisolone began treatment. coincident with the virus isol ...19873038971
evaluation of an enzyme immunoassay for detection of antibodies to pseudorabies virus in porcine field sera.the performance of an indirect enzyme-linked immunosorbent assay and the standard serum neutralization test for detection of antibodies to pseudorabies virus in porcine field sera were compared, using 304 sera from pseudorabies-free pigs in canada, and 1082 and 580 swine sera from the usa and england, respectively. the sensitivity and specificity of the elisa relative to the serum neutralization test were in the order of 97 to 98%, with the higher agreement between the tests when a 1:40 dilution ...19872839277
production of aujeszky vaccine by the microcarrier technology "from the ampoule to the 500 litre fermentor".a process for the production of aujeszky vaccine on microcarrier cultures in large fermentors is described. the nlst cells are routinely produced in fermentors of 150 litres; cell density reaches 0.7-0.8 10(6)/ml. the authors describe the method used to obtain those results. the different parameters used in fermentors are discussed and especially po2 regulation. a study of subculturing method is being carried out to reach a volume of 500 litres. the comparison between stationary culture and micr ...19872438178
[lyophilized combined live vaccine against swine fever and aujeszky's disease]. 19872831830
failure to induce aujeszky's disease in cattle by intranasal administration of high doses of vaccine virus. 19872820109
vaccination of mice and swine with a pseudorabies virus mutant lacking thymidine kinase activity.a thymidine kinase deficient mutant of the indiana-funkhauser strain of pseudorabies virus was tested for its ability to stimulate protective immunity in mice and young pigs. mice vaccinated intraperitoneally were protected from morbidity and mortality when challenged with 50 ld50 of virulent pseudorabies virus. eight week old pigs were protected from serious morbidity and mortality when challenged with virulent pseudorabies virus. the thymidine kinase mutant was not shed from the nasal passages ...19872820561
antigenically important proteins of aujeszky's disease (pseudorabies) virus identified by immunoblotting.immunoblotting was used to identify those aujeszky's disease virus proteins which elicited major antibody responses in naturally and experimentally infected pigs. although some proteins comprising purified virus preparations reacted nonspecifically, proteins with mol. wts. of 120 k, 90 k, 71 k and 60 k were antigenically important. these corresponded in size to the virus glycoproteins identified by 3h-glucosamine labelling. glycoproteins isolated by affinity chromatography from infected pk 15 ce ...19872821962
activation of a ribosomal protein s6 kinase in mouse fibroblasts during infection with herpesvirus.if confluent fibroblasts are infected with the swine alpha-herpes virus, pseudorabies virus, ribosomal protein s6 becomes phosphorylated after a lag of approximately 2 h. when cell-free extracts were prepared from such cells in the presence of glycerol 2-phosphate and egta, a ribosomal protein s6 kinase activity was found to appear at approximately the same time as the phosphorylation in vivo. this protein kinase was similar to that activated in the same cells by replenishing the nutrient medium ...19872822412
multiple defects in the genome of pseudorabies virus can affect virulence without detectably affecting replication in cell culture.several independently isolated vaccine strains of pseudorabies virus were studied to identify the functions that play a role in the expression of virulence of this virus. all the strains that were studied grew well in three different cell types. no differences that could be correlated with avirulence could be detected either in the virus yield produced by the cells or in the length of the eclipse phases. all the attenuated strains, however, had lost their ability to replicate efficiently in the ...19872823461
specificity of the indirect enzyme-linked immunosorbent assay for detection of pseudorabies virus antibodies in pigs exposed to bovine herpesvirus-1.six 5-week-old pigs were inoculated intranasally (in) with 10(7.6) tcid50 of bovine herpesvirus-1 (bhv-1). three of the pigs also were inoculated iv with a similar dose of bhv-1. clinical responses were not observed in these 6 pigs before oronasal challenge exposure with 10(7.8) tcid50 of virulent pseudorabies virus (prv) at postinoculation day 42. two pigs inoculated in with bhv-1 and challenge exposed with prv remained healthy, whereas the remaining 4 pigs developed severe clinical signs of ps ...19872823651
evaluation of pseudorabies virus glycoprotein gp50 as a vaccine for aujeszky's disease in mice and swine: expression by vaccinia virus and chinese hamster ovary cells.pseudorabies virus (prv) is an alphaherpesvirus which causes an economically important disease of swine. one of the prv glycoproteins, gp50, was previously identified as the sequence homolog of herpes simplex virus glycoprotein gd (e.a. petrovskis, j.g. timmins, m.a. armentrout, c.c. marchioli, r.j. yancey, jr., and l.e. post, j. virol. 59:216-223, 1986). gp50 was evaluated as a prv subunit vaccine candidate. gp50 protected mice from prv-induced mortality either when delivered via infection with ...19872824827
role of a structural glycoprotein of pseudorabies in virus virulence.the virulence of deletion mutants of pseudorabies virus defective in the expression of glycoprotein gi, gp63, or both was tested in 1-day-old chickens and young pigs. in the absence of expression of gi, the virulence of a fully virulent laboratory strain, prv(ka), for 1-day-old chickens was reduced approximately fourfold. inactivation of glycoprotein gp63 appeared also to affect the virulence of prv(ka) only slightly, as did inactivation of both gi and gp63. the level of reduction in virulence, ...19872824832
diagnosis of pseudorabies virus infection in pigs with specific dna probes.two dna probes directed against pseudorabies virus dna were developed for use in a dot hybridisation to detect the presence of pseudorabies virus in infected tissues. the specificity of the probes and their sensitivity were analysed. there was a strong correlation between the results obtained by dot hybridisation and those obtained by conventional methods of virus isolation from the same tissue specimens.19872825308
effect of intratesticular inoculation with aujeszky's disease virus on genital organs of boars.ten 8-10-month-old belgian landrace boars were intratesticularly inoculated with 500 tcid50 of a virulent belgian aujeszky's disease virus (adv) isolate (75v19) in 0.1 ml volume. one control boar was similarly inoculated with phosphate-buffered saline solution. the genital organs of six inoculated boars were examined by virus isolation and immunofluorescence. in spite of high virus titers, the fluorescence in the testicles remained limited to a few small foci in the interstitial connective tissu ...19872825399
an elisa to distinguish between aujeszky's disease vaccinated and infected pigs. 19872827365
restriction fragment pattern (rfp) analysis of genomes from danish isolates of suid herpesvirus 1 (aujezsky's disease virus).purified dna from 42 isolates of suid herpesvirus 1 (shv-1) collected during 1985 from clinical outbreaks of aujezsky's disease on danish farms was compared by restriction fragment pattern (rfp) analysis. the bamhi generated rfps were found to be distinguishable, thus confirming rfp analysis as a potential epidemiological tool. however, because of variations within labile genome regions of epidemiologically closely related isolates, it was concluded that comparisons of rfps should be interpreted ...19872827607
susceptibility of various cell culture systems to pseudorabies virus.a comparative study was carried out to determine the susceptibility of five different cell lines to pseudorabies virus (prv), a herpes virus of pigs. the cell systems tested were swine testicle (st), mink lung (ml), equine dermal (ed), porcine kidney (pk15), and bovine turbinate (bt) cells. virus titers obtained were 10(4.88), 10(4.38), 10(3.75), 10(2.63), and 10(0.25) for ml, st, pk15, bt and ed cells, respectively indicating that ml, st, and pk15 are optimal cell lines for the growth of prv wh ...19872827945
comparison of three serotests for the detection of pseudorabies antibodies in pigs.the serum-neutralization test (sn), enzyme-linked immunosorbent assay (elisa) and the radial immunodiffusion enzyme assay (ridea) were compared for the detection of pseudorabies (prv) antibodies in swine sera. a total of 1285 serum samples were tested. all three tests were considered useful in determining the prv antibody status of swine on a herd basis, but available evidence supports the continued use of sn as the definitive test because of possible false positive reactions associated with eli ...19872827946
vaccines against aujeszky's disease: comparison of efficacy, dna fingerprints and antibody response to glycoprotein i.the efficacy of two inactivated and three attenuated aujeszky's disease virus (adv) vaccines was compared in pigs in a standardised test. after vaccination, excretion of attenuated vaccine viruses was not detected. all vaccines were capable of preventing mortality, but none conferred complete protection against challenge with a virulent strain of adv 3 months after the first vaccination. after a single vaccination, no large differences in vaccine efficacy were observed. revaccination markedly en ...19872829410
relative rates of aujeszky's disease virus attenuation, as assessed in mice.field strains of aujeszky's disease virus (adv) were attenuated by heat treatment and serial passage at sub-optimal growth temperatures in chicken embryo fibroblasts (cef). at chosen passage levels, virus was titrated in cell culture and in mice. for each strain, the pathogenicity was expressed as a mouse lethal index (mli), defined as the inverse of the log10 (ccid50:ld50). mlis determined for field strains displayed a wide range of comparatively high values. the attenuation of field strains wa ...19872829412
aujeszky's disease in pigs diagnosed by a simple method of nucleic acid hybridization. 19872829469
a vaccine strain of pseudorabies virus with deletions in the thymidine kinase and glycoprotein x genes.a pseudorabies virus (prv) mutant with deletions in genes for glycoprotein x (gx) and thymidine kinase, designated delta gx delta tk, was constructed and evaluated as a vaccine for protecting swine against prv-induced mortality. doses greater than or equal to 10(3) plaque-forming units (pfu) of this strain given to mice provided protection from challenge exposure with virulent prv. sera tested from mice inoculated with delta gx delta tk had high titers of neutralizing antibody to prv, but reacti ...19872829665
severe pleuritis associated with certain strains of pasteurella multocida in swine.pasteurella multocida was isolated from 2 farms on which grower or finisher pigs had problems of severe emaciation and high death loss (greater than 5%). at necropsy, the pigs had extensive suppurative pleuritis and pericarditis, with adhesions over the lung surface. on one farm, the pigs also had multiple lung abscesses. histologic findings included polymorphonuclear cell infiltration in bronchial and alveolar spaces, thickening of alveolar walls, pleuritis, and in some cases, abscesses. from a ...19873679971
pneumonia in pigs induced by intranasal challenge exposure with pseudorabies virus and pasteurella multocida.the interaction between pseudorabies virus (prv) and pasteurella multocida was investigated to determine whether single or combined infections result in pneumonia in 6- to 7-week-old pigs. the effect of the prv-p multocida challenge exposure on feed consumption, rate of gain, and extent of pneumonic lesions appeared dependent on the prv dose; however, pneumonic lesions were of bacterial pneumonia. pigs inoculated with a virulent strain of prv plus p multocida developed severe pneumonia, whereas ...19873674553
porcine effector mechanisms: antibody-dependent cell-mediated cytotoxicity of pseudorabies-infected target cells.antibody-dependent cell-mediated cytotoxicity (adcc) against pseudorabies virus (prv)-infected cells was determined in neonatal porcine pulmonary washout cells and in partially purified blood-derived leukocytes. the adcc assays were performed at approximately 1, 2, 3 and 11 days after birth. it was found that pulmonary-derived cells had a low level of cytolytic activity against the prv-infected target cells at about 1 day of age. this activity increased sharply during the next 2 days of age, but ...19873590615
transcription from the pseudorabies virus genome during latent infection. brief report.trigeminal ganglia from swine latently infected with pseudorabies virus (prv) were examined for the presence of prv nucleic acids by in situ hybridization. both viral dna and rna were detectable in latently infected neurons, indicating that the prv genome is transcriptionally active during the latent phase of infection.19882829800
flow cytometric analysis of porcine peripheral blood leukocytes infected with pseudorabies virus.the susceptibility of fractionated porcine peripheral blood leukocytes (pbl) to pseudorabies virus (prv) was studied by flow cytometry and defined by viral antigen expression. viral antigens on the surface of infected cells and cell viability were evaluated by forward angle light scatter (fals), 90-degree light scatter (90ls), green fluorescence (fitc-anti-prv), and red fluorescence (propidium iodide). approximately 10% of infected mononuclear cells from healthy pigs expressed cell-surface prv a ...19882830358
subclinical aujeszky's disease virus infection in a pig herd and the characterisation of the strain of virus isolated.the spread of antibody to aujeszky's disease virus through a susceptible pig herd was monitored after the probable introduction of infection by a recently purchased boar. the infection spread slowly through the herd but no clinical signs of aujeszky's disease were seen. the strain of virus isolated was designated nia-6. it has been characterised by a series of experimental infections and extends the known range of virulence of isolates of aujeszky's disease virus made in northern ireland. the st ...19882832999
reduced yield of infectious pseudorabies virus and herpes simplex virus from cell lines producing viral glycoprotein gp50.pseudorabies virus (prv) glycoprotein gp50 is the homolog of herpes simplex virus (hsv) glycoprotein d. several cell lines that constitutively synthesize gp50 were constructed. vero cells, hela cells, and pig kidney (mvpk) cells that produce gp50 all gave reduced yields of prv and hsv progeny viruses when compared with the parent cell line or the same cell line transfected to produce a different protein. the reduction in virus yield was greatest at low multiplicities of infection. the vero and h ...19882835521
glycoprotein giii of pseudorabies virus is multifunctional.one of the major glycoproteins of pseudorabies virus, giii, is nonessential for growth in cell culture. mutants defective in giii, however, consistently yield lower titers of infectious virus (3- to 20-fold) than does wild-type virus. the interactions of giii- mutants with their host cells were compared with those of wild-type virus in an attempt to uncover the functions of giii. we show that giii plays a major role in the stable adsorption of the virus to its host cell; in the absence of giii, ...19882836609
[a method for distinguishing infected from vaccinated pigs as a basis for the control of aujeszky's disease].vaccination against aujeszky's disease (ad) does not lead to eradication of the disease. nevertheless, to reduce the economic losses, vaccination against ad is widely practised in many countries. with regard to control of ad, a method to distinguish infected from vaccinated pigs is a prerequisite in those countries. this paper deals with such a method. the assay (gi-elisa) makes use of 2 monoclonal antibodies directed against 2 different epitopes on glycoprotein i (gi) of ad virus (adv), and det ...19882829384
propagation and quantitation of animal herpesviruses in eight cell culture systems.a comparative study was carried out to determine the relative sensitivities of eight different cell culture systems to six different herpesviruses of animals. the cells used were: ofl (ovine fetal lung), ml (mink lung), fk (ferret kidney), ptk-2 (potoroo kidney), tek (turkey embryo kidney), ed (equine dermal), bt (bovine turbinate), and pk15 (porcine kidney). the viruses tested were: prv (pseudorabies) of swine, cphv (caprine herpesvirus), ibrv (infectious bovine rhinotracheitis virus), dn-599 s ...19882846231
aujeszky's disease: vaccines and diagnostics. 19882837863
serological investigations for some bacterial and viral pathogens in fallow deer (cervus dama) and wild boar (sus scrofa) of the san rossore preserve, tuscany, italy.sera of 43 fallow deer (cervus dama) of the san rossore preserve (tuscany, italy) were examined for antibodies against eight pathogens; one proved positive for brucella sp., 21 for listeria monocytogenes, 34 for chlamydia psittaci, three for coxiella burnetii, one for infectious bovine rhinotracheitis virus, 11 for parainfluenza-3 virus, 25 for bovine viral diarrhea virus and six for bovine respiratory syncytial virus. no age and sex difference in the positivity rates and titers was evidenced, w ...19882832622
host cell-specific growth advantage of pseudorabies virus with a deletion in the genome sequences encoding a structural glycoprotein.several attenuated strains of pseudorabies virus contain genomes that carry a deletion in their short unique (us) component. the sizes of the deletions are different in the various attenuated strains; the deletions may include part of one of the inverted repeats as well as part of the us region of the genome. in most cases, the deletion includes the gene encoding the glycoprotein gi. the attenuated strains with a deletion in their s component have a common history of having been cultivated in ch ...19882824839
a herpesvirus vector for expression of glycosylated membrane antigens: fusion proteins of pseudorabies virus giii and human immunodeficiency virus type 1 envelope glycoproteins.we describe experiments using the swine herpesvirus, pseudorabies virus (prv), as a vector for expression of hybrid membrane protein genes. in particular, we present the construction and analysis of three infectious prv mutants expressing chimeric viral membrane proteins composed of portions of the prv envelope glycoprotein giii and of the human retrovirus, human immunodeficiency virus type 1 (hiv-1), envelope glycoproteins gp120 and gp41. all of the chimeric genes contain the transcription cont ...19882459411
[the antigenic effect of pseudorabies virus after inactivation by gamma irradiation]. 19882840048
protection of mice and swine from pseudorabies virus-induced mortality by administration of pseudorabies virus-specific mouse monoclonal antibodies.hybridomas were selected for secretion of monoclonal antibodies directed against pseudorabies virus (prv) glycoproteins. each monoclonal antibody was capable of neutralizing prv in vitro in the presence of complement. this panel of antibodies was used in passive immunization studies to protect mice and swine from prv-induced mortality. the most protective antibody in mice was 3a4, specific for prv glycoprotein gp50, which afforded as high as 100% protection. although antibody 3a4 was partially p ...19882840843
rapid detection of aujeszky's disease (pseudorabies) virus infection of pigs by direct filter hybridisation of nasal and tonsillar specimens.a direct filter hybridisation method has been developed to diagnose acute aujeszky's disease in live pigs. the advantages of the method are easy, fast sample processing; no dna-purification is needed, and the hybridisation itself is simplified. the direct filter hybridisation method has been tested on pseudorabies virus infected cultured cells, experimentally infected pigs and on specimens from an outbreak of aujeszky's disease. virus isolation and filter hybridisation gave comparable results, i ...19882841732
induction of antibodies to glycoprotein i in pigs exposed to different doses of a mildly virulent strain of aujeszky's disease virus.it has recently been shown that the antibody response to glycoprotein i (gi) of aujeszky's disease virus can be used to distinguish infected from vaccinated pigs. to examine whether pigs exposed to low doses of a mildly virulent strain of aujeszky's disease virus produce antibody to gi four groups of four pigs were inoculated intranasally with 10, 10(2), 10(3) or 10(4) plaque forming units (pfu) of the sterksel strain. two unvaccinated pigs and two pigs vaccinated intranasally with bartha's k st ...19882841789
detection of antibody to pseudorabies virus in swine sera by indirect immunoperoxidase plaque staining.a new method for the detection of pseudorabies antibody in swine sera was developed by use of the indirect immunoperoxidase plaque staining test. the indirect immunoperoxidase plaque staining test demonstrated serologic responses in pigs that were subcutaneously infected with pseudorabies virus. the test had a sensitivity and a specificity comparable to those of the complement-dependent neutralization test and appeared to be somewhat more sensitive than the neutralization test and the enzyme-lin ...19882830301
pseudorabies virus glycoprotein giii is required for efficient virus growth in tissue culture.glycoprotein giii of pseudorabies virus is a major antigen found in the envelopes of virus particles as well as in and on the surfaces of infected cells. it is not an essential gene product for virus growth in tissue culture. in this report, we provide evidence that, although it is not essential, the giii protein is required for efficient virus growth and that giii mutants are quickly outgrown by wild-type virus in mixed infections.19882836630
studies of transplacental and perinatal infection with two clones of a single aujeszky's disease (pseudorabies) virus isolate.the effect of aujeszky's disease virus (adv) infection in the last third of gestation was studied using two clones from an adv isolate. twelve sows were infected with one or other clone at 85 +/- 1 days of gestation. the dose of infection was 5 x 10(6) tcid50 per sow. the clinical and serological responses to the infection were different. one clone, ls-1, produces a severe and acute illness. the course of the disease went from 9 to 14 days while the other clone, ls-2, caused a mild or silent inf ...19882836996
susceptibility of mitogen and non-mitogen treated pig lymphocytes to four strains of pseudorabies virus (prv).an in vitro study was carried out to determine the susceptibility of pig lymphocytes to infection by 4 strains of pseudorabies virus (prv) and the response of the cells to 3 different mitogens. the prv strains used were usda, 13-1, 3-1 and norden, while the mitogens were phytohemagglutinin (pha) concanavalin (con a) and lipopolysaccharide s (lps). the susceptibility of lymphocytes was evaluated by accessing the viral end point dilution, at which cytopathogenic effects (cpe) were achieved, when i ...19882845230
some immune reactions induced in pigs by an attenuated aujeszky's disease vaccine. 19882849291
detection of antibodies to aujeszky's disease virus by enzyme-linked immunosorbent assay in pigs. 19882850390
development of an elisa for detection of antibodies to glycoprotein i of aujeszky's disease virus: a method for the serological differentiation between infected and vaccinated pigs.a blocking elisa was developed to distinguish between aujeszky's disease virus (adv)-infected and vaccinated pigs, on the basis of presence or absence of serum antibodies to glycoprotein i (gi) of adv. the gi-elisa detects antibodies that block the reaction of monoclonal antibodies to one or two epitopes on gi of adv. the adv-gi antibody response appeared between one and two weeks post-infection and persisted at a high level for at least seven months. five of the nine adv-vaccine strains examine ...19882851599
studies on the ability of a 98-kilodalton pseudorabies virus diagnostic antigen to detect latent infections induced by low-dose exposure to the virus.the effect of low-dose challenge of immunity with pseudorabies virus (prv) on subunit-vaccinated pigs was studied in 2 experiments. in the first experiment, we studied the effect of challenge dose on the antibody response to an early excreted 98-kilodalton prv-glycoprotein that was used as a diagnostic antigen in the elisa. in the second experiment, we studied the effect of low doses of virus on the establishment of latent infections in subunit-vaccinated pigs. the relationship of virus exposure ...19882851953
the role of the housefly, musca domestica, in the spread of aujeszky's disease (pseudorabies).starved houseflies were held over a suspension of aujeszky's virus (prv-1) for 24-48 h. one group was rinsed in 70% ethanol to kill virus attached to the body surface. no virus was isolated from this group. for the other group the titre of virus decreased more rapidly on the body surface of flies than in the environment. model experiments demonstrated that the aujeszky's virus cannot survive in the body of the housefly but the body surface may be contaminated for a period of time depending on th ...19882856539
programs for the elimination of pseudorabies virus from large herds of swine. 19883403349
introduction of foreign strains of suid herpesvirus 1 (aujeszky's disease virus) documented by restriction fragment pattern (rfp) analysis.six isolates of suid herpesvirus 1 (shv-1) collected from clinical outbreaks of aujeszky's disease (ad) in jutland in january-february, 1985, were compared by restriction fragment pattern (rfp) analyses with older shv-1 isolates from jutland as well as with shv-1 isolates from different parts of west germany and ireland. the rfp analysis indicated that the outbreaks were caused by shv-1 isolates introduced from abroad.19882898930
the effect of human recombinant interleukin-2 on the porcine immune response to a pseudorabies virus subunit vaccine.the effect of human recombinant interleukin-2 (ril-2) as an immune enhancing agent was evaluated in pigs vaccinated with a pseudorabies virus subunit vaccine (sv). two groups of three pigs received two 25 micrograms doses of sv given 3 weeks apart. one group received 10(5) kg-1 day-1 of ril-2 subcutaneously over two 5-day periods beginning on the day of the first and second vaccine inoculation. six other pigs were immunized with two 5 micrograms doses of sv. three of these pigs were treated as a ...19892626820
detection of pseudorabies virus transcripts in trigeminal ganglia of latently infected swine.two pseudorabies virus (prv) poly(a)+ rnas, 2.0 and 0.95 kilobases, were detected in the trigeminal ganglia of latently infected pigs. these rnas were partially colinear at the 3' end. they were located in the bamhi j fragment (0.706 to 0.737 map units), 3' of the prv immediate-early gene. a potential polyadenylation signal was also identified in bamhi-j. the direction of transcription of the latency-associated rnas was antiparallel (i.e., opposite in polarity) to that of the prv immediate-early ...19892470921
in vitro comparison between four variants of aujeszky's disease virus.four aujeszky's disease (pseudorabies) virus variants were characterized in vitro by investigation of their resistance to heat at 48 degrees c, sensitivity to trypsin and ability to replicate in pig alveolar macrophages, two of these variants (ls-1 and ls-2) were cloned previously from a single isolate of virus and showed differing pathogenicity for pigs; the virulent stanley strain; and the non-virulent nia-4 strain were included for comparison. heat treatment produced slight decreases in infec ...19892555108
influence of isoprinosine on lymphocyte function in virus-infected feeder pigs.pseudorabies is a porcine herpesvirus of major importance in the swine industry. isoprinosine is an immunomodulating drug that has been shown to be beneficial in treating herpesvirus infections. twenty-four 7-week-old pigs were allotted within litters to 1 of 4 groups: control, isoprinosine (iso), pseudorabies virus (prv), or isoprinosine and pseudorabies virus (iso-prv). isoprinosine was administered daily for 16 days to the iso and iso-prv groups (75 mg/kg of body weight/day, po). immunity in ...19892478051
neuropathogenesis of pseudorabies: leakage of anti-viral antibody and serum constituents into cerebrospinal fluid of infected pigs.antibody levels to pseudorabies virus (prv) in cerebrospinal fluid (csf) were compared to serum levels from immunized and infected pigs. antibody was measured by single-dilution indirect solid-phase radioimmunoassay (iria). there was significantly higher csf anti-prv igg relative to serum anti-prv igg (anti-prv index, %) from infected pigs (1.390%, n = 14) than from vaccinated ones (0.141-0.149%, n = 5 and 7). the index from vaccinated and challenged pigs was intermediate (0.627%, n = 16), sugge ...19892535701
the potency testing of pseudorabies vaccines in pigs. a proposal for a quantitative criterion and a minimum requirement.a criterion for the potency testing of pseudorabies vaccine based on the difference between the mean weight gain during the seven days after pathogenic challenge of vaccinated or control piglets is proposed. this criterion, termed delta g7, has been studied as a function of initial weight variation of the animals, different challenge strains and the period between challenge and the end of the test. the statistical analysis of results optimizes the experimental parameters and gives rise to a quan ...19892537829
immunohistologic study of pulmonary and lymphatic tissues from gnotobiotic pigs inoculated with ara-t-resistant strain of pseudorabies virus.ara-t-resistant strain of pseudorabies virus (prv) was inoculated intranasally into six 2-week-old gnotobiotic pigs. five inoculated pigs were sneezing and coughing. in pigs 1 to 4 killed on postinoculation days (pid) 3, 5, 7, and 9, respectively, prv antigen was detected in respiratory epithelial cells, and pigs had severe pneumonitis. in pigs 5 and 6 killed on pid 11 and 13, respectively, prv antigen was localized in macrophages in alveoli and necrotizing nodules. immunoglobulin-containing cel ...19892559633
aujeszky's disease. 19892559694
interactions of pseudorabies virus with swine alveolar macrophages i: virus replication.the replication of pseudorabies virus (prv) in cultured swine alveolar macrophages (am) was studied using 6 different virus strains. am were highly permissive to prv infection, with progeny virus titres of 10(7) tcid50/ml from some strains. virus progeny titres were higher in cultures infected with the field strains s-62 and 4892 than in cultures infected with the strains bartha or prv-c. virus replication, viral dna synthesis and the concomitant cell damage were dependent upon virus input m.o.i ...19892538108
rapid diagnosis of aujeszky's disease in pigs by improved in situ hybridization using biotinylated probes on paraffin-embedded tissue sections.a practical in situ hybridization (ish) method has been developed for the rapid diagnosis of pseudorabies virus (prv) infection in pigs. the method utilizes routine formalin fixed and paraffin-embedded tissue sections, non radioactive biotin-labelling, simple hybridization procedure and diaminobenzidine (dab) silver enhancement detection system. the rapid (ish) method showed concordance with the direct filter hybridization (dfh) and with the peroxidase-antiperoxidase (pap) assays. by the simplif ...19892538976
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