Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 14 de 14
Filter
Add more filters










Publication year range
1.
Acta Virol ; 64(2): 216-225, 2020.
Article in English | MEDLINE | ID: mdl-32551789

ABSTRACT

Currently, Slovakia is a rabies-free country, but the epizootiological situation of rabies was not always favorable. The main reservoir species of rabies virus in the first half of the last century was the domestic dog. Since 1906, hundreds of cases were reported, of which approximately 90% were infected dogs. The disease had a typical urban character. Since 1929, the number of rabid domestic animals decreased due to the implementation of dog vaccination campaigns in particular parts of Slovakia. From the second half of 1950s, red foxes (Vulpes vulpes) have become an important reservoir of the RABV. In this time period urban rabies in Slovakia changed into sylvatic form. One effective method of prevention and control of wildlife rabies is an oral rabies vaccination of red foxes. It is carried out in Slovakia since 1993. A detailed development of the rabies epizootiological situation on the territory of the Slovak Republic until the application of oral antirabies immunisation of foxes and the current situation after its performance is the main object of this review. Keywords: rabies; Lyssavirus; red fox; incidence; oral vaccination.


Subject(s)
Rabies Vaccines , Rabies virus , Rabies , Animals , Animals, Wild , Dogs/virology , Foxes/virology , Rabies/epidemiology , Rabies/prevention & control , Rabies/veterinary , Slovakia/epidemiology , Vaccination/veterinary
2.
Bratisl Lek Listy ; 101(10): 565-8, 2000.
Article in Slovak | MEDLINE | ID: mdl-11218947

ABSTRACT

The authors followed the influence of the arrangement of measured and control samples on microtitration plate on the ELISA test results by quantitative evaluation of rabies antibodies titres in human blood serum. They performed the test under identical conditions in all microtitration plate wells. They calculated the result according to five calibration curves--four of them were obtained by different positioning of the control positive and negative sera and the fifth curve was obtained from average values. The results from the four various positional calibration curves were significantly statistically different from the average. However, the average calibration curve--obtained from four measurements--led to identical value of rabies antibodies in cases with different dilutions of sera. The authors propose to follow some principles of measured and control samples arrangement on microtitration plates in order to minimalize the errors, caused by their dishomogeneity. (Tab. 2, Fig. 3, Ref. 10.)


Subject(s)
Antibodies, Viral/blood , Enzyme-Linked Immunosorbent Assay/methods , Rabies virus/immunology , Calibration , Diagnostic Errors , Enzyme-Linked Immunosorbent Assay/standards , Humans
3.
Vet Med (Praha) ; 42(2): 51-6, 1997 Feb.
Article in English | MEDLINE | ID: mdl-9127580

ABSTRACT

The authors prepared an experimental, inactivated, concentrated and highly purified rabies vaccine from the strain Vnukovo-32/107. The purification and concentration (simultaneous--in one operation) was carried out by affinity chromatography. The content of rabies antigen in the vaccine was 4.256 UE/cm3 (determined by ELISA method). The authors used their own lipoid adjuvant--type oil in water--to resolve lyophilized vaccine to original volume. It is based on esters of fatty the acids. The effectiveness--immunogenic activity--of the experimental preparation was compared with that of commercial rabies vaccines and the reference vaccine by means of the NIH and NRLR methods. The results obtained (2.826 units/cm3 by the NIH and 3.085 units/cm3 by the NRLR method) confirmed that the method of affinity chromatography could be used to prepare a rabies vaccine, exhibiting effectiveness superior to commercial preparations available, and complying with the WHO criteria.


Subject(s)
Rabies Vaccines/immunology , Rabies/veterinary , Animals , Mice , Rabies/prevention & control , Vaccines, Inactivated/immunology
4.
Vet Med (Praha) ; 42(2): 57-60, 1997 Feb.
Article in Slovak | MEDLINE | ID: mdl-9148571

ABSTRACT

The study was aimed at isolation and subsequent identification of strains of rabies virus by means of monoclonal antibodies from foxes killed in the vaccination zone within the complex preliminary monitoring of oral antirabies vaccination. The results obtained indicate that the vaccines for oral antirabies vaccination used in Slovakia did not contain any vaccination strain pathogenic to the extremely sensitive target species-the fox (Vulpes vulpes).


Subject(s)
Foxes/virology , Lyssavirus/isolation & purification , Rabies Vaccines/administration & dosage , Administration, Oral , Animals , Rabies/prevention & control , Rabies/veterinary , Rabies virus/isolation & purification , Slovakia
5.
Zentralbl Veterinarmed B ; 43(3): 129-35, 1996 May.
Article in English | MEDLINE | ID: mdl-8928572

ABSTRACT

The effect of fungal and yeast glucan on different immune functions in mice was examined and compared. The simultaneous administration of glucan and a sensitizing dose of DNFB on the different sites significantly stimulated delayed-type hypersensitivity (DTH) response only when using fungal glucan. Both glucans tested, when administered before sensitization, significantly increased DTH response, but with a significantly higher level at the beginning of the investigation (on day 7) when using fungal glucan. The increase in phagocytic activity by the blood leucocytes started in the 1st week after fungal-glucan treatment, and in the 2nd week after yeast-glucan treatment, and took longer after administration of fungal glucan. The values of the phagocytic-activity index were significantly influenced only after fungal-glucan injection. The results of the study indicate that fungal glucan isolated from Pleurotus ostreatus could be a prospective immunomodulating substance.


Subject(s)
Glucans/pharmacology , Hypersensitivity, Delayed/immunology , Leukocytes/drug effects , Phagocytosis/drug effects , Polyporaceae/immunology , Animals , Dinitrofluorobenzene/toxicity , Drug Hypersensitivity/immunology , Female , Glucans/immunology , Hypersensitivity, Delayed/chemically induced , Leukocytes/immunology , Male , Mice , Specific Pathogen-Free Organisms
6.
Vet Med (Praha) ; 40(3): 87-96, 1995 Mar.
Article in English | MEDLINE | ID: mdl-7762124

ABSTRACT

The immunogenic and antigenic activity of an experimental live oral rabies vaccine prepared from the strain Vnukovo-32/107 was evaluated on the basis of results obtained in 3 sets of experiments. These were carried out as model experiments on white mice, then on target animals--red foxes (Vulpes vulpes) and a related species--farm-bred polar foxes (Alopex lagopus). For quantitative determination of the immunogenic activity of the orally or subcutaneously administered rabies vaccines in model experiments on mice a method was used that had been developed in our laboratory. Antibodies were detected and quantified by an ELISA kit that had also been developed in our lab. Tenacity of the experimental vaccine (infectious tissue culture medium after yolk addition) was verified at different temperatures; the effects of storage temperature upon virus titre and immunogenic activity were investigated. An important part of the experiments--evaluation of the antigenic and immunogenic activity of the live vaccine at oral vaccination (vaccination baits, conditions simulating field vaccination) was carried out in foxes. The immunogenic activity (challenge experiments with a street virus on day 180 and 360 after vaccination) was evaluated in common foxes (Vulpes vulpes). The results document a high immunogenic and antigenic activity of the experimental live oral rabies vaccine. The strain Vnukovo-32/107 is suitable for the industrial manufacturing of vaccination baits. In the target species--common foxes challenged on day 180 after primovaccination an 83% protection was observed. Challenge on day 180 after revaccination (or day 360 after primovaccination), the orally immunized foxes proved to be 100% protected. For parallel evaluation of the immunogenic activity of an oral vaccine and for antibody titration it is recommended to employ the quantitative mice test and an ELISA technique, respectively.


Subject(s)
Antibodies, Viral/analysis , Foxes/immunology , Rabies Vaccines/immunology , Administration, Oral , Animals , Enzyme-Linked Immunosorbent Assay , Mice , Rabies Vaccines/administration & dosage , Rabies virus/immunology , Temperature , Vaccination/veterinary , Vaccines, Attenuated/immunology
7.
Vet Med (Praha) ; 40(2): 53-64, 1995 Feb.
Article in English | MEDLINE | ID: mdl-7740717

ABSTRACT

The present work summarizes the results of 11 groups of experiments carried out with the aim to complexly quantify the residual virulence of a cold mutant of the Vnukovo-32/107 rabies virus vaccination strain intended for the preparation of an oral rabies vaccine (Kamark) for the immunization of free-living carnivores. According to WHO prescriptions, residual virulence was quantified in experiments on carnivores, mainly red foxes (Vulpes vulpes)--the presumed target species, and farm-bred polar foxes (Alopex lagopus)--a related species. Further experiments were carried out in cats, dogs, non-target autochthonous micromammals, predatory birds (Microtus arvalis, Apodemus flavicollis, Falco tinnunculus) and in a large number of laboratory animals--white mice. At oral administration (including extremely high doses) the strain Vnukovo-32/107 proved to be apathogenic to the target carnivores--Vulpes vulpe and Alopex lagopus as well as cats, dogs and the autochthonous micromammals. For Falco tinnunculus the strain proved to be apathogenic even at intramuscular and intracerebral administration. The residual virulence of the Vnukovo-32/107 vaccination strain, also quantified by comprehensive model experiments on white mice of different weight categories that had been infected orally, subcutaneously, intramuscularly, intracerebrally, by contact, with ingestion of rabic material or by modelled immune suppression, proved to be extremely low-levelled. The strain under investigation revealed a high level of attenuation and a low level of residual virulence and proved to be suitable for the preparation of non-reactogenic oral vaccine intended for foxes, an extremely susceptible target species.


Subject(s)
Rabies Vaccines/adverse effects , Rabies/veterinary , Administration, Oral , Animals , Cat Diseases/prevention & control , Cats , Dog Diseases/prevention & control , Dogs , Foxes , Mice , Rabies/prevention & control , Rabies Vaccines/administration & dosage , Rabies virus/pathogenicity , Virulence
8.
Bratisl Lek Listy ; 95(2): 73-7, 1994 Feb.
Article in Slovak | MEDLINE | ID: mdl-7922630

ABSTRACT

The authors developed a kit for the purpose of assessment of anti-rabies antibodies by the ELISA immunoenzymatic method in human immunized sera. The results of the detection and quantification of anti-rabies antibodies acquired by the ELISA method were compared with those originating from classical procedures (virusneutralizing test on mice, indirect hemagglutination test), and a sufficient correlation and sensitivity of the immunoenzymatic method were detected. By means of the developed test it is possible to detect the particular level of anti-rabies virusneutralizing IgG antibodies. (Tab. 2, Fig. 1, Ref. 25).


Subject(s)
Antibodies, Viral/blood , Rabies Vaccines/immunology , Rabies virus/immunology , Vaccination , Enzyme-Linked Immunosorbent Assay , Hemagglutination Tests , Humans , Neutralization Tests , Rabies/prevention & control
9.
Vet Med (Praha) ; 37(12): 675-85, 1992 Dec.
Article in Slovak | MEDLINE | ID: mdl-1297245

ABSTRACT

The level of cell-mediated immune response in vivo was investigated using the test of delayed hypersensitive reaction (DHR) to DNFB, along with the phagocytic activity (PA) of blood leucocytes in mice after subcutaneous implantation of fungal and yeast glucan and levamisol in dependence on the dose and administration schedule. The soluble form of fungal glucan (Pleurotus ostreatus) potentiated the DHR significantly at a dose of 10 mg/kg (but not at a dose of 50 mg/kg) while it was administered during DNFB sensitization (P < 0.05)-Tab. I and when its pre-medication effect was investigated (days -7 and -14; P < 0.05) with regard to the time of sensitization (Tab. II). The identical dose of glucan also had a positive effect (P < 0.05 or 0.01) on the percentual proportion of phagocytic cells (PC) reaching the maximum in the 2nd and 3rd week of investigation, as well as on the phagocytic activity index (P < 0.05; 3rd week) and percentage of neutrophil granulocytes (P < 0.05; 2nd week)-Tab. III. Yeast glucan (Saccharomyces cerevisiae) showed a potentiating effect on the DHR to DNFB only in the case of its pre-medication use; its soluble form was effective at both doses (10 mg and 50 mg/kg) in days -7 and -14 (P < 0.05), and its corpuscular form at a dose of 50 mg/kg on days -7, -14 and -21 (P < 0.05 or 0.01)-Tab. II. PA parameters of blood leucocytes displayed a stimulative effect only on the PC percentage. The most significant effects in this case were observed in the soluble form (both doses) in the 2nd and 3rd week (P < 0.01 and 0.05, resp.) and in the insoluble form (both doses) in the 3rd and 4th week of observation (P < 0.05 and 0.01, resp.). An increase in the number of neutrophil granulocytes was significant in the 2nd (P < 0.05 or 0.01; corpuscular form) and 3rd week of the experiment (P < 0.01; soluble form)-Tab. III. Levamisol affected both investigated parameters (DHR and PA) only at a dose 20 mg/kg (10 mg/kg-no effect). Its potentiating effect on the DHR level was observed both for its administration at the time of sensitization (P < 0.05) and for its administration on days 7 (P < 0.05) and 14 (P < 0.01) before DNFB sensitization (Tabs. I and II). A statistically significant increase in PC was recorded in weeks 2, 3 and 4 (P < 0.05 or 0.01), a statistically significant increase in the number of neutrophil granulocytes in the 3rd week of investigation (P < 0.05). The phagocytic activity index was not affected.


Subject(s)
Adjuvants, Immunologic/pharmacology , Glucans/pharmacology , Hypersensitivity, Delayed , Leukocytes/immunology , Levamisole/pharmacology , Phagocytosis/drug effects , Polyporaceae/metabolism , Animals , Dinitrofluorobenzene , Immunity, Cellular/drug effects , Mice , Saccharomyces cerevisiae/metabolism
10.
Vet Med (Praha) ; 37(4): 203-12, 1992 Apr.
Article in Slovak | MEDLINE | ID: mdl-1641950

ABSTRACT

Applicability of a skin test induced by dinitrofluorobenzene (DNFB) to quantification of the actual level of cellular immunity (CI) in vivo and its level after an experimental immunomodulation intervention were evaluated in two breeds (40 animals in each) of fattening bulls (10-11 months old). At the selected methodical procedure of intensity determination of the delayed type of hypersensitivity (DTH), its average value reached 4.5 +/- 1.5 mm in 80 animals, while in 77.5% of bulls its level ranged from 3.6 to 9.6 mm, in 18.7% from 2.0 to 3.5 mm and in 3.8% remained less than 2.0 mm. Evident expression of the reaction points to the possibility of application of the used methodical procedure of the skin test using DNFB to quantify the level of CI response in vivo in cattle. Percentual representation of animals according to the intensity of skin reaction (Tab. I) and concentration of total serum immunoglobulins (Cs-Ig) and serum IgG (Tab. II) indicates the different cellular and humoral state of animals in investigated breeds. This is also confirmed by the recorded average values of mentioned parameters which were significantly lower (P less than 0.01; or 0.05) in animals of the first breed (4.0 +/- 1.3 mm; 28.3 +/- 4.4 U ZST, 18.4 +/- 3.5 g.l-1) than in breed 2 (4.9 +/- 1.6 mm; 32.5 +/- 3.8 U ZST; 20.3 +/- 3.5 g.l-1). The animals of each breed were divided into four experimental groups with the approximately equal actual levels of DTH (Tab. III).(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Cattle/immunology , Glucans/pharmacology , Levamisole/pharmacology , Skin Tests/veterinary , Animals , Immunity, Cellular/drug effects , Immunoglobulins/analysis , Male
11.
Vet Med (Praha) ; 28(12): 717-26, 1983 Dec.
Article in Slovak | MEDLINE | ID: mdl-6426120

ABSTRACT

Trials were conducted with young cattle to study the effect of adjuvants, applied subcutaneously and intramuscularly, upon the antigenic activity of live and inactivated cell rabies vaccine prepared from the Vnukovo -32 strain at the level of the 107th series cell passage. Cerebral vaccine of Fermi type was also used in the trials for comparison. The antibodies were parallelly titrated by four methods, three of which were conducted in vitro. The levels of antirabies antibodies indicate a possibility of fortifying the antigenic activities of inactivated vaccine by means of the Bioveta Nitra oil adjuvant and the activities of the live vaccine by means of adjuvant prepared after Buchnev . The antigenic activity of the Czechoslovak-produced cerebral rabies vaccine for veterinary use is extraordinarily low.


Subject(s)
Adjuvants, Immunologic/administration & dosage , Antibodies, Viral/biosynthesis , Rabies Vaccines/immunology , Rabies virus/immunology , Animals , Cattle , Drug Evaluation
13.
Vet Med (Praha) ; 26(5): 271-8, 1981 May.
Article in Slovak | MEDLINE | ID: mdl-6791359

ABSTRACT

The comparative experiments were carried out to study the distribution of the rabies antigen in the central nervous system (CNS) of sewer-rats and mice experimentally infected with three "hamster" strains (for comparison also with "fox" strain 1151); it was found out that with microscopical observation of preparations stained by the method of direct immunofluorescence the "hamster" strains produced a blended picture of fluorescing particles characteristic of strains with a reduced virulence and virulent strains. As for mice infected with strains 3 O and 7 E the rabies antigen was detected in all parts of CNS as early as 24 hours after infection. In this period the rabies antigen strain 9 E was not detected in lumbar spinal cord and that with strain 1151 was detected only in the Ammonian horns. After 48 hours the rabies antigen in mice was detected in all parts of CNS with all four strains used. In sewer-rats, with regard to their lower susceptibility to the rabies virus, the first detection of rabies antigen in CNS was recorded on the 6th day after infection with strains 3 O, 7 E and 1151, whereas with strain 9 E as late as the 9th day in lumbar spinal cord and not in all animals.


Subject(s)
Antigens, Viral/analysis , Central Nervous System/immunology , Rabies virus/immunology , Rabies/veterinary , Rodent Diseases/immunology , Animals , Cricetinae/microbiology , Mice , Rabies/immunology , Rabies virus/isolation & purification , Rats
14.
Vet Med (Praha) ; 26(4): 233-46, 1981 Apr.
Article in Slovak | MEDLINE | ID: mdl-6791357

ABSTRACT

All the infected foxes (9) contracted the disease and died from rabies the 20th-21st day from infection with the virus isolated from hamster. Out of the total number of 9 cats experimentally infected by intramuscular infection, seven showed symptoms of clinical disease on the 18th-34th day from infection. The infected dogs, wolves and rabbits did not show clinical disease. In the post mortem examination of eight foxes the rabies virus or rabies antigen was detected in all parts of the CNS and in n. ischiadicus. Of the extraneural organs, the virus was present, in all animals, in the pharyngeal salivary glands, and in one fox also in the tongue. The bioassay on the eye was positive in all cases. The rabies antigen was detected in 4 foxes in the thigh muscle, in liver and spleen, and in all 8 foxes in lungs and cornea, in 5 cases in kidney, and in 3 cases in heart and tongue. Seven cats were examined post mortem by the inoculation test on mice and the PMIF-staining test; it was found that the rabies virus, or rabies antigen, was distributed in the same manner as in foxes.


Subject(s)
Cat Diseases/pathology , Cricetinae/microbiology , Foxes , Rabies/veterinary , Animals , Antigens, Viral/analysis , Cat Diseases/immunology , Cats , Fluorescent Antibody Technique , Rabies/immunology , Rabies/pathology , Rabies/transmission , Rabies virus/immunology , Rabies virus/isolation & purification
SELECTION OF CITATIONS
SEARCH DETAIL
...