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[new immunization schedule against equine influenza]. 1975166531
studies on the multiplication of the equine arteritis virus using the fluorescent antibody technique. 1975172683
studies on equine viral arteritis. i. characterization of the virus and trial survey on antibody with vero cell cultures. 1975172689
the genome of equine arteritis virus. 1975173077
activation of influenza a viruses by trypsin treatment. 1975173078
immunofluorescent studies on the multiplication of equine arteritis virus in vero and e. derm (nbl-6) cells. 1975176497
growth of equine arteritis virus in cells derived from infectious canine hepatitis virus-induced hamster tumor and transformed cells. 1976181624
studies on equine viral arteritis. ii. a serological survey of equine viral arteritis in horses imported in 1973/74. 1976181627
studies on two viral strains isolated from the outbreak of equine influenza in japan. 1975183035
studies on a test vaccine for equine influenza virus. i. production of a test vaccine. 1975183036
studies on a test vaccine for equine influenza virus. ii. field trials. 1975183037
[purification of equine influenza virus a/equi-2/w/9/69 by the sucrose step density gradient ultracentrifugation]. 1978213662
prevalence of antibodies to equine viruses in the netherlands.the prevalence of antibodies to various viruses was investigated in a series of serum samples collected from horses in the netherlands between 1963 and 1966 and from 1972 onwards. neutralizing antibodies to equine rhinopneumonitis virus, equine arteritis virus and to equine rhinovirus types 1 and 2 were detected in respectively 76%, 14%, 66% and 59% of the equine serum samples tested. the observed incidence of serum samples positive to equine adenovirus in the complement fixation test was 39%. p ...1979219560
viral respiratory disease. 1979228463
the 5' end of the equine arteritis virus replicase gene encodes a papainlike cysteine protease.the presence of a papainlike cysteine protease (pcp) domain in the n-terminal region of the equine arteritis virus (eav) replicase, which had been postulated on the basis of limited sequence similarities with cellular and viral thiol proteases, was confirmed by in vitro translation and mutagenesis studies. the eav protease was found to direct an autoproteolytic cleavage at its c terminus which leads to the production of an approximately 30-kda n-terminal replicase product (nsp1) containing the p ...19921331507
lactate dehydrogenase-elevating virus (ldv): subgenomic mrnas, mrna leader and comparison of 3'-terminal sequences of two ldv isolates.the 3'-terminal 1314 nucleotides of the genome of one isolate of lactate dehydrogenase-elevating virus, ldv-p, has been derived by sequence analyses of cdnas from several genomic libraries and compared to that of another ldv isolate, ldv-c (godeny et al. (1990) virol. 177, 768-771). the 3'-non-coding segment of 80 nucleotides of the two ldv genomes is identical, whereas marked, but varying nucleotide and amino acid divergence is apparent in the three upstream overlapping open reading frames (orf ...19921604932
arteritis in equine fetuses aborted due to equine viral arteritis. 19911650052
[virologico-serologic studies in horses with respiratory tract diseases].of 1081 acute and chronically respiratory diseased as well as clinically normal horses 824 sera and 257 paired serum samples collected 1986 and 1987 were tested for antibodies against several different respiratory viruses such as influenza virus a/equi 1 and 2 (influenza 1 a. 2), equine herpesvirus type 1/4 (ehv 1/4), mammalian reovirus type 1-3 (reovirus 1-3), equine rhinovirus type 1 (erv 1), equine adenovirus type 1 (eadv 1), and equine arteritis virus (eav). the investigations resulted in an ...19921558530
genomic variability among globally distributed isolates of equine arteritis virus.equine arteritis virus (eav), a non-arthropod borne togavirus, has been shown to have a global distribution. to date, no major antigenic variation has been demonstrated between eav isolates from different geographic origins. in this study, the genomic rna of eav isolates obtained from horses of different breeds in various countries around the world was oligonucleotide fingerprinted. comparisons of these fingerprints were used to determine the extent of genomic variation among such isolates. comp ...19921332249
structural proteins of equine arteritis virus.we have recently shown that the genome of equine arteritis virus (eav) contains seven open reading frames (orfs). we now present data on the structural proteins of eav and the assignment of their respective genes. virions are composed of a 14-kda nucleocapsid protein (n) and three membrane proteins designated m, gs, and gl. m is an unglycosylated protein of 16 kda, and gs and gl are n-glycosylated proteins of 25 and 30 to 42 kda, respectively. the broad size distribution of gl results from heter ...19921328669
[three cases of virus isolation from horse fetuses diagnosed with equine arteritis virus (eav) abortion from stud farms with different breeds].three cases of abortions were diagnosed as caused by equine arteritis virus (eav) by isolation and typing of this virus from the respective fetuses. all 3 abortions were single cases, one occurring on a stud with iceland ponies, one with warmbloods, one with lipizzaner horses. on each stud horses of the respective breed were kept exclusively, therefore there existed no epidemiologic link. by means of seroneutralization tests performed on in contact horses it could be shown, that eav had only bee ...19921323268
multiple complex families of endogenous retroviruses are highly conserved in the genus gallus.we have analyzed the genome of the domestic chicken for the presence of genetic sequences related to the envelope protein-encoding genes of avian sarcoma/leukosis retroviruses to determine the organization, structure, potential functionality, and distribution of such sequences. we have previously identified in the genus gallus an extensive group of endogenous avian retroviruses termed eav-0. southern blot and sequence analysis presented here of eav-0 elements revealed that the majority of the ea ...19921321278
equine arteritis virus: an overview.the causative agent of the respiratory disease equine viral arteritis is a small, single-stranded rna virus with a genome organization and replication strategy related to that of coronaviruses and toroviruses. clinical signs of infection in horses vary widely and severe infection can lead to pregnant mares aborting. infected horses generally make good recoveries but stallions may become semen shedders of equine arteritis virus (eav). these carrier stallions play an important role in the dissemin ...19921319787
equine viral arteritis: how serious is the threat to the british horse population? 19921319786
fatal, congenitally acquired infection with equine arteritis virus in a neonatal thoroughbred. 19921316264
venereal disease.equine venereal infections of concern in the united states include ehv-3, t. equigenitalis, p. aeruginosa, and k. pneumoniae. stallions may also harbor eav in the genital tract and transmit the virus to mares during coitus. with the exception of ehv-3, the stallion generally remains asymptomatic while transmitting infections to mares during breeding. methods for diagnosis, treatment, and control of these infections are discussed.19921315616
lactate dehydrogenase-elevating virus, equine arteritis virus, and simian hemorrhagic fever virus: a new group of positive-strand rna viruses. 19921315480
art-ch, a new chicken retroviruslike element.a 3' region of a previously unknown retroviruslike element named art-ch (avian retrotransposon from chicken genome) was obtained in the course of polymerase chain reaction-mediated cloning of avian leukosis virus long terminal repeats (ltrs) from dnas of infected chicken cells. about 50 copies of art-ch are present in the genome of chickens of different breeds. art-ch is not found in dna of quails, ducks, turkeys, or several other birds tested. the art-ch element is about 3 kb in size, including ...19921310773
isolation of c1q-binding immune complexes by affinity chromatography and desorption with a diaminoalkyl compound.the applicability of affinity chromatography to the isolation of c1q-binding immune complexes (ic) in sera was explored. purified human c1q was covalently coupled to agarose or adsorbed to igg-agarose resins. sera containing preformed virus-antibody complexes or rheumatoid arthritis (ra) sera were passed through the columns and c1q-bound ic, eluted off with 1,4-diaminobutan at mild basic conditions, were analysed by immunodiffusion, crossed immunoelectrophoresis, gel filtration and electron micr ...1976773099
epidemiology of equine upper respiratory tract disease on standardbred racetracks.the outbreaks of upper respiratory tract infections in horses at standardbred racetracks were investigated over a three year period. the most serious epidemics of respiratory disease occurred in the winter and spring seasons. both influenza viruses and equine herpesvirus 1 were shown to be present in the horse population. the herpesvirus was associated with respiratory disease particularly in the winter but the equine influenza viruses apparently were responsible for the major epidemics of respi ...1979218705
results of an epidemiological investigation on viral arteritis in france and some other european and african countries.an original microplate seroneutralization technique was developed in order to study the existence of antibodies against equine viral arteritis. the technique involves a high amount of complement, and has allowed to demonstrate antibodies in 18.5% out of 4,037 horses examined. titers varied not or little during periods as long as 6 years. among 3,324 sera samples from french horses, a 15.2% frequency of antibodies was shown. the infection level was not very different between breeds, which is diff ...1978213008
[serologic follow-up studies of viral arteritis in horses at a stud farm]. 19872823506
a serologic survey on equine influenza for the past ten years. 1978212632
structural polypeptides of equine arteritis virus. 19872824911
serological studies concerning equine arteritis virus infection in the german democratic republic. 19882840046
complement-fixation reactions in equine viral arteritis. 1977202179
[influenza a/equine 2: example for an atypical course in a group of 21 horses]. 1976188127
the structural proteins of equine arteritis virus. 1976183352
viral respiratory infections. 1976177853
efficacy of 9-beta-d-arabinofuranosylhypoxanthine 5'-monophosphate in therapy of equine abortion virus-induced hepatitis in hamsters.equine abortion virus (eav)-induced hepatitis in hamsters presents an interesting animal model for the evaluation of drugs possessing anti-deoxyribonucleic acid virus activity. these experiments demonstrate that 9-beta-d-arabinofuranosylhypoxanthine 5'-monophosphate (ara-hxmp), a new synthetic, water-soluble, antiviral agent, effectively controls this disease in hamsters with a therapeutic index of approximately 60. ara-hxmp prevented hepatitis-associated deaths in hamsters, reduced the titer of ...1975172009
antigenic relationship between the surface antigens of avian and equine influenze viruses.influenza virus equine 1 (a/equine/prague/56) has a hemagglutinin which is antigenically related to the hemagglutinin of fowl plague virus strain rostock (fpv) and a neuraminidase which cross-reacts with the enzyme of virus n (a/chick/germany/49). after a single injection of chickens with equine 1 virus no hemagglutination inhibiting (hi) and neutralizing antibodies against fpv can be demonstrated, although the birds are fully protected against a lethal dose of fpv. hi and neutralizing antibodie ...197553781
hemagglutination by equine infectious anemia virus.equine infectious anemia (eia) virus which was propagated on an equine dermal cell line agglutinated guinea pig erythrocytes. viral fluids containing about 10(7.5) mean tissue culture infective doses/ml showed hemagglutinating (ha) titers ranging from 16 to 32 units/0.05 ml. results of cesium chloride equilibrium density gradient centrifugation revealed that the hemagglutinin was inseparable from the virus particles. the hemagglutination reaction persisted over a wide range of temperature and ph ...19769361
reverse transcription and cdna amplification by the polymerase chain reaction of equine arteritis virus (eav).a technique is described for the amplification and specific identification of equine arteritis virus (eav) nucleotide sequences. the polymerase chain reaction (pcr) was evaluated initially by amplification of cloned virus specific cdna sequences prior to amplification of single-stranded (ss) cdna produced by reverse transcription (rt) of viral genomic rna. three separate primer pairs were used for rt/pcr of eav genomic rna, each pair producing only one band in agarose gels of the predicted size ...19901702094
viral respiratory disease of the horse.the diagnosis of any viral respiratory disease relies on laboratory procedures to isolate the virus and demonstrate a significant rise in serum antibody titers. to isolate viruses from the upper respiratory tract, it is imperative that nasopharyngeal swabs are obtained from animals in the early acute stage of illness, i.e., during the pyrexic phase when the virus is replicating. nasopharyngeal swabs must be placed in a virus transport medium and forwarded immediately to the laboratory at refrige ...19911647261
detection of cattle infected with bovine viral diarrhea virus using nucleic acid hybridization.a ribonucleic acid (rna) hybridization assay to identify cattle infected by bovine viral diarrhea virus (bvdv) is described. the rna probe was derived from the coding region at the 3' end of the genome of the nadl strain of bvdv. total rna from infected cell cultures or peripheral blood leukocytes from suspect animals was extracted and applied to nylon membranes with a slot blot apparatus. peripheral blood leukocytes were tested concurrently for bvdv by virus isolation. the results of hybridizat ...19911645592
[serological studies of the recent infections of austrian horses with the equine arteritis virus].944 serum samples of horses, collected in 1988 and 1989, were examined for the occurrence of antibodies against equine arteritis virus by a microneutralizations test. in 10.9% of all sera reactors could be found. the distribution of seropositive horses varied from 4.6% (salzburg) to 15.7% (lower austria). from tyrol and vorarlberg no samples could be obtained. it was not possible, to correlate clinical symptoms (infertility, respiratory symptoms, fever and edema) with the infection. it is assume ...19911851082
equine arteritis virus is not a togavirus but belongs to the coronaviruslike superfamily.the nucleotide sequence of the genome of equine arteritis virus (eav) was determined from a set of overlapping cdna clones and was found to contain eight open reading frames (orfs). orfs 2 through 7 are expressed from six 3'-coterminal subgenomic mrnas, which are transcribed from the 3'-terminal quarter of the viral genome. a number of these orfs are predicted to encode structural eav proteins. the organization and expression of the 3' part of the eav genome are remarkably similar to those of co ...19911851863
a nested set of eight rnas is formed in macrophages infected with lactate dehydrogenase-elevating virus.total rna was extracted from primary cultures of mouse macrophages isolated from 10-day-old mice 6 to 12 h postinfection with lactate dehydrogenase-elevating virus (ldv). poly(a)+ rna was extracted from spleens of 18-h ldv-infected mice. the rnas were analyzed by northern (rna) blot hybridization with a number of ldv-specific cdnas as probes. a cdna representing the nucleocapsid protein (vp-1) gene located at the 3' terminus of the viral genome (e. k. godeny, d. w. speicher, and m. a. brinton, v ...19911870216
equine viral arteritis. 19901963771
morphological studies on equine arteritis virus. 19704195609
the occurrence of equine arteritis virus in australia.this paper reports the first isolation of equine arteritis virus (eav) in australia and serological evidence of exposure to eav in australian horses. twelve standardbred stallions imported from north america were found to shed eav in semen. one hundred and seven stallions were tested for serum antibodies to eav and 73% of standardbred stallions tested were seropositive as compared to 8% of thoroughbred stallions. serum antibody was detected in 71% of standardbred mares, 6% of standardbred raceho ...19901963772
all subgenomic mrnas of equine arteritis virus contain a common leader sequence.during the replication of equine arteritis virus (eav) six subgenomic mrnas are synthesized. we present evidence that the viral mrnas form a 3'-coterminal nested set and contain a common leader sequence of 208 nucleotides which is encoded by the 5'-end of the genome. the leader is joined to the bodies of mrna 5 and 6 at positions defined by the sequence 5' ucaac 3'. the part of the leader sequence flanking the ucaac motif is very similar to the 5'-splice site of the tetrahymena pre-rrna. a possi ...19902162519
induction of immune response and protection from equine viral arteritis (eva) by formalin inactivated-virus vaccine for eva in horses.thirty-nine horses included 3 pregnant mares were examined by inoculating with formalin inactivated-virus vaccine for eva. antibody response of horses after one dose vaccination was somewhat poor and 50% effective inoculum dose of the vaccine should be included 10(8.4) pfu of virus before inactivation. after 2 doses given at an interval of 4 weeks, the horses developed such high titer of sn antibody as up to 1:5,120. the sn titer declined rather rapidly, but supplemental administration of the va ...19902163579
further properties of equine arteritis virus. 19664293706
kinetics of viral deoxyribonucleic acid, protein, and infectious particle production and alterations in host macromolecular syntheses in equine abortion (herpes) virus-infected cells.infection of exponential-phase suspension cultures of mouse fibroblast cells (l-m) with equine abortion virus (eav) resulted in inhibition of cell growth and marked alterations in host metabolic processes. the synthesis of deoxyribonucleic acid (dna) and ribonucleic acid was inhibited within 4 hr after infection and was suppressed by more than 90% by the time of maximal virus replication (14 to 18 hr). the overall rate of protein synthesis, however, was similar in uninfected and virus-producing ...19684302745
equine abortion (herpes) virus: strain differences in susceptibility to inactivation by dithiothreitol.the infectivity of equine abortion (herpes) virus (eav) was inactivated by treatment with reduced dithiothreitol (dtt). according to their susceptibility to dtt, the eav strains could be divided into three groups. the vaccine strain rac-h (419) proved to be more resistant to dtt than all of the other 14 strains tested. the hemagglutinin of eav was also inactivated by dtt; no strain differences were observed in this respect.19724339509
[route of inoculation and aluminium hydroxide influences in the immunological response of horses vaccinated against equine influenza (author's transl)]. 19734377407
failure to propagate equine arteritis virus in an aedine and an anopheline mosquito species. 19724402402
the mechanisms of neutralization of sensitized equine arteritis virus by complement components. 19744474357
[equine viral arteritis].equine viral arteritis (eva) caused by the equine arteritis virus, member of the genus arterivirus within the family of togaviridae was recently isolated from the seminal plasma of two stallions indicating that the virus infection is also prevalent in the federal republic of germany despite the apparent lack of acute clinical symptoms in the horse population. these findings are further supported by data from serological screenings. out of 739 horse sera, 28 (3.8%) were found to have eva virus-sp ...19902165641
phylogenetic distribution of the novel avian endogenous provirus family eav-0.a new family of related endogenous proviruses, existing at 50 to 100 copies per haploid genome and distinguishable by remarkably short long terminal repeats, has been described for domestic chickens (gallus gallus subsp domesticus). in this communication, by using southern blot analysis and probes derived from both internal viral sequences and locus-specific, cellular flanking sequences, we studied the genetic distribution of this family of moderately repetitive avian endogenous retroviruses wit ...19902398526
equine arteritis virus-induced polypeptide synthesis.intracellular virus-specific proteins induced by equine arteritis virus (eav) have been compared with in vitro translation products of virion and intracellular eav rnas. in infected bhk-21 cells, the two major virion proteins (c and e1) and polypeptides with mol. wt. of 60,000 (p60), 42,000 (p42) and 30,000 (p30) were found. there were no indications that the viral proteins were processed from a larger precursor as shown by pulse-chase, amino acid analogue and protease inhibitor experiments. the ...19862426393
[properties of the equine arteritis virus]. 19654956350
identification and antigenic comparison of equine arteritis virus isolated from an outbreak of epidemic abortion of mares. 19862431561
buoyant density studies on equine arteritis virus. 19704989678
neutralization of equine arteritis virus: enhancing effect of guinea pig serum. 19704993579
[complement dependent neutralization of equine arteritis virus. brief report]. 19714996685
temporal distribution of equine arteritis virus in respiratory mucosa, tissues and body fluids of horses infected by inhalation. 19714999643
aetiology of kawasaki disease.thirteen serum samples from nine children with kawasaki disease and 23 control samples gave negative results on screening for antibodies to hog cholera virus, border disease of sheep, bovine diarrhoea virus, and equine arteritis virus. the sera from two children with kawasaki disease were cytotoxic; a possible link with cytotoxin from propionibacterium acnes is considered.19892539788
the effects of vaccination with tissue culture-derived viral vaccines on detection of antibodies to equine arteritis virus by enzyme-linked immunosorbent assay (elisa).an enzyme-linked immunosorbent assay (elisa) was developed for the detection of serum antibodies to equine arteritis virus (eav). results from this assay produced a good correlation with results from virus neutralisation tests in horses which had not been regularly vaccinated with commercially available mammalian tissue culture-derived viral vaccines. vaccination of some horses with tissue culture-derived vaccines induced the formation of antibodies to bovine serum. these antibodies reacted with ...19892773278
[equine viral arteritis: detection of antibodies of horses in argentina]. 19846091374
the carrier state in equine arteritis virus infection in the stallion with specific emphasis on the venereal mode of virus transmission.the carrier state has been confirmed virologically in thoroughbred and non-thoroughbred stallions naturally infected with equine arteritis virus (eav). short-term or convalescent and long-term carriers occur. the frequency rate of the long-term carrier state in thoroughbreds was high, averaging 33.9% among the three groups of stallions under study. while the convalescent carrier state only lasted a few weeks after clinical recovery, the long-term carrier state could persist for years. there was ...19872824772
equine viral arteritis may have been introduced. 19882851969
preparing for equine arteritis. 19852983980
[serologic studies on the occurrence of the arteritis virus in the horse in west germany]. 19853002746
intracellular equine arteritis virus (eav)-specific rnas contain common sequences.equine arteritis virus (eav) is a nonarthropod-borne togavirus. six virus-specific rna species have been found in eav-infected cells having the following molecular weights: 4.3 x 10(6) (rna1), 1.3 x 10(6) (rna2), 0.9 x 10(6) (rna3), 0.7 x 10(6) (rna4), 0.3 x 10(6) (rna5), and 0.2 x 10(6) (rna6). rna1 comigrates with the viral genome (m. f. van berlo, m. c. horzinek, and b. a. m. van der zeijst, 1982, virology 118, 345-352). all rnas hybridized with a radio-labeled cdna probe representing rna6, i ...19863014727
stability of viability and immunizing potency of lyophilized, modified equine arteritis live-virus vaccine.the bucyrus strain of equine arteritis virus, previously modified to avirulence and vaccinal virus by 131 serial passages in primary cell cultures of horse kidney followed by 111 passages in primary cell cultures of rabbit kidney, was further passaged in cultures of the e. derm (nbl-6) cell line, a continuous diploid cell line. pools of the 16th and 25th passages of the virus in this last equine dermal cell line were lyophilized and stored in lots at 37 c, 23 to 28 c, 4c, and -20 c. the viabilit ...19816275755
equine arteritis virus-infected cells contain six polyadenylated virus-specific rnas. 19826283728
translation of equine arteritis virus rna in rabbit reticulocyte lysates. 19873035263
status of equine viral arteritis in kentucky for 1986. 19873035776
equine arteritis virus subgenomic rna transcription: uv inactivation and translation inhibition studies.the expression of the genetic information of equine arteritis virus (eav), an arterivirus, involves the synthesis of six subgenomic (sg) mrnas. these are 5' and 3' coterminal since they are composed of a leader and a body sequence, which are identical to the 5' and 3' ends of the genome, respectively. previously, it has been suggested that cis-splicing of a genome-length precursor rna is involved in their synthesis. this was reevaluated in a comparative analysis of the sg rna synthesis of eav, t ...19957491761
a 29k envelope glycoprotein of equine arteritis virus expresses neutralization determinants recognized by murine monoclonal antibodies.a panel of six neutralizing murine monoclonal antibodies (mabs) to equine arteritis virus (eav) was produced. the mabs were characterized by western immunoblotting assay and competitive elisa. the six mabs identify a single neutralization site on a 29k envelope glycoprotein. deglycosylation of viral proteins prior to immunoblotting showed that the 29k protein is the glycosylated form of a 20k protein. equine anti-eav serum also strongly bound the 29k glycoprotein, as well as an unglycosylated pr ...19937504076
status of equine viral arteritis in kentucky, 1985.clinical cases of equine arteritis virus infection have not been diagnosed in kentucky since 1984, and there has been no indication that any of the horses involved in the 1984 epizootic have since been responsible for spread of the disease to horses in other states or other countries. cases of abortion caused by naturally acquired infection with this virus have not been confirmed in 1984 or 1985. neither field nor vaccine strains of equine arteritis virus have been shown to induce teratologic ab ...19873038806
[respiratory infectious diseases in horses].among all infectious diseases affecting horses, respiratory disease pose the greatest threat to horses kept in stables, horses used for breeding and race horses. here a distinction should be made between the so-called monocausal infectious diseases (so-called henle-koch postulates) and multicausal infectious diseases which are the result of the synergistic interaction of different processes, that alone do not lead to disease. there is no clearcut distinction between the two groups. the most impo ...19873296310
equine arteritis virus: ferritin-tagging and determination of ribonucleic acid core. 19714109496
[equine arteritis virus: multiplication in bhk 21-cells buoyant density and electron microscopical demonstration]. 19704194811
the role of sensitizing antibody in the neutralization of equine arteritis virus by complement or anti-igg serum. 19734197221
the fate of sensitized equine arteritis virus following neutralization by complement of anti-igg serum. 19734197222
evidence for a relationship between equine abortion (herpes) virus deoxyribonucleic acid synthesis and the s phase of the kb cell mitotic cycle.autoradiographic analyses of deoxyribonucleic acid (dna) synthesis in randomly growing kb cell cultures infected with equine abortion virus (eav) suggested that viral dna synthesis was initiated only at times that coincided with the entry of noninfected control cells into the s phase of the cell cycle. synchronized cultures of kb cells were infected at different stages of the cell cycle, and rates of synthesis of cellular and viral dna were measured. when cells were infected at different times w ...19714254680
the complement-requiring neutralization of equine arteritis virus by late antisera. 19734630828
serological study of equine viral arteritis in standard-breds in the uk. 19957645189
structural proteins of equine arteritis virus. 19734633581
equine abortion (herpes) virus: evaluation of markers in a field vaccination trial.twelve mares were vaccinated with attenuated equine abortion virus (eav) strain rac-h. two nonvaccinated mares served as controls. in at least three mares the vaccination appeared to coincide with a natural infection. this was indicated by characterization of the eav isolated from nasal secretions of six vaccinated mares, a nonvaccinated control, and also from the lung, spleen, and liver of a fetus aborted by a vaccinated mare. the relative sensitivity of the isolated eav to dithiothreitol was u ...19734796167
comparison of the structural protein coding sequences of the vr-2332 and lelystad virus strains of the prrs virus.the 3'-portion of the genome of a u.s. isolate of the porcine reproductive and respiratory syndrome (prrs) virus, atccvr-2332, was cloned and sequenced. the resultant 3358 nucleotides contain 6 open reading frames (orfs) with homologies to orfs 2 through 7 of the european strain of the prrs virus and other members of the free-standing genus of arteriviruses. both vr-2332 and the european isolate (called the lelystad virus) have been identified as infectious agents responsible for the swine disea ...19957661696
a plaque assay of equine arteritis virus in bhk-21 cells. 19694988871
mycoplasmal deoxyribonuclease activity in virus-infected l-cell cultures.cell-free extracts of mycoplasma hominis and medium from 72-hr broth cultures had deoxyribonuclease activity like that of deoxyribonuclease i. mg(++) stimulated activity, and the ph optimum was between 8.0 and 9.0. double-stranded or heatdenatured deoxyribonucleic acid (dna) served as a substrate, and oligonucleotides were produced. cell-free extracts of l cells infected with m. hominis or m. hominis plus equine abortion virus (equine herpes virus, eav) had greatly increased activity over that o ...19695782042
biological and morphological aspects of the growth of equine abortion virus.darlington, r. w. (st. jude children's research hospital, memphis, tenn.), and c. james. biological and morphological aspects of the growth of equine abortion virus. j. bacteriol. 92:250-257. 1966.-the growth of equine abortion virus (eav) was studied by bioassay and electron microscopy in l-cell monolayer and suspension cultures, and in hela and bhk 21/13 cell monolayers. results of virus assay (plaque-forming units) indicated that production of cell-associated virus (cav) began at 6 to 9 hr af ...19665941279
[current virus diseases in horses. diseases in foals and respiratory tract infections].at the moment, horse praxis is confronted by two disease complexes which are difficult to fight against as well in prophylaxis as in therapy, but which get an increasing importance. first they concern virus infections of the foals and second primary virus-caused respiratory diseases. foals get infected during the embryonal/fetal development, in the perinatal or postnatal period. normally the infection is caused by latent infected, clinical healthy mares, or in the postnatal period by ubiquitous, ...19846098971
antigenic comparison of equine arteritis virus (eav) and lactic dehydrogenase virus (ldv); binding of staphylococcal protein a to the nucleocapsid protein of eav. 19836191473
temperature-sensitive mutants of equine arteritis virus.seventeen temperature-sensitive mutants of equine arteritis virus, a nonarthropod-borne togavirus, have been isolated. 5-fluorouracil, o-methylhydroxylamine and ethyl methanesulphonate were used as mutagens. the mutants were characterized by their ability to synthesize virus rna and virus proteins at the permissive (35 degrees c) and restrictive temperature (40 degrees c) using autoradiography of cells labelled with 3h-uridine in the presence of actinomycin d and immunofluorescence respectively. ...19806252293
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