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The goal of the studies was to evaluate the protective value of vaccines against pasteurellosis in rabbits. The vaccines comprised antigens to serotypes 3 and 12 of Pasteurella multocida with two different adjuvants: emulsigen and aluminium hydroxide gel. The two vaccines given subcutaneusly either once or twice at a dose of 1 ml protected rabbits markedly against intranasal infection with the virulent strains of examined serotypes. A substantial efficacy of these vaccines was supported by the occurrence of specific precipitins against somatic antigens of serotypes 3 and 12 present in the sera of immunised rabbits even 5 weeks after vaccination
Prosthetic joint infections due to Pasteurella multocida are rarely but increasingly reported but no data on production of biofilm are available. We report the case of a woman with a late, haematogenous peri-prosthetic infection of cemented total knee arthroplasty caused by a strain of P. multocida identified by pyrosequencing and unable to produce biofilm. Comparison of clinical and laboratory findings with those reported in other patients evidenced differences mainly in the period of symptoms' onset and in the behaviour of some inflammatory markers.
Medycyna Weterynaryjna
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2010
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tom 66
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nr 08
s.512-515,rys.,bibliogr.
The present study describes the role of Pasteurella (P.) multocida, in the multifactorial etiology of the porcine respiratory disease complex (PRDC). The losses due to PRDC are significant, particularly among weaners and finishers in middle-sized and large farms. They are connected with retarded growth and the necessity of eliminating some percentage of animals before the completion of the finishing process. The primary etiological factors of PRDC are: the porcine respiratory and reproductive syndrome virus (PRRSV), Mycoplasma hyopneumoniae, the swine influenza virus (SIV), Actinobacillus pleuropneumoniae (APP), Streptococcus suis, type 2, and the pseudorabies virus. One of the most important secondary etiological factors of PRDC is P. multocida. That is why the mechanism of the pathogenicity of this facultatively pathogenic microorganism is described here. The capsular and somatic antigens, which characterize the most important pathogenic serotypes, i.e. A:3, A;5, and D:3, are discussed. However, even representatives of these serotypes do not demonstrate pathogenicity without other factors weakening the innate immunity of swine. These immunosuppressive factors include environmental deficiencies which decrease the welfare of the swine population, and the above-mentioned pathogens, which are the primary etiological agents of PRDC. Despite controversial results concerning the importance of toxins of the P. multocida strains isolated from swine lungs, their contribution to the pathogenesis of PRDC can not be excluded. The role of the bacterial capsule and the ability of P. multocida (serotypes A and D) to attach themselves even to ciliated epithelial cells of the respiratory tract is of minor importance in explaining the participation of these microorganisms in the pathogenesis of PRDC, and further research is needed. The study comments on the tests used for the identification of serotypes of P. multocida, important in the etiology of PRDC, the indirect, passive haemagglutination test being “the golden standard”. However, at present this method is being increasingly replaced by PCR. Molecular typing of P. multocida strains is also performed by restriction enzyme digestion with or without subsequent hybridization with a standard probe or the sequencing of multiple loci of predominantly house-keeping genes. These modern methods contributed to a new perspective on the role of P. multocida in swine pneumonia: it came to be perceived as its secondary pathogenic agent rather than a major etiological factor. During the last decade these tests have also enabled the discovery of other, more important microorganisms, which would not have been possible earlier, when only classical diagnostic tests were used for identifying fenotypic properties of microorganisms. Segregated early weaning is the recommended method of preventing PRDC.
Evaluation of the immunogenicity of the vaccine against respiratory tract infections in calves caused by Pasteurella multocida, and prepared from antigen of a local strain of serotype 3 with oil adjuvant addition, was the object of the prescnt studies. Two experiments were carried out using calves. Vaccine was given them at a dose of 2 ml i.m., twice every 14 days. In experiment 1, sera were obtained before vaccination, 2 and 5 weeks after the first vaccination, in experiment 2 - before vaccination, 2 weeks, 1 and 2 months after the first vaccination. lmmunogenicity of the vaccine was evaluated by means of an agar gel immunodiffusion (AGID) test and an ELISA test. The carrier-state of Pasteurella multocida on mucous membrane of nasal cavity was examined. lt was found that immunisation stimulated the production of the specific precipitins for serotype 3 and it caused the increase of IgG level found using ELISA test with microplate coated with whole-bacterium antigen or LPS of that serotype. The investigation confirms the good immunogenicity of the vaccine.
The API 20E test and standard methods were applied to examine biochemical features of P. multocida strains. All tested isolates decomposed glucose, mannitol and saccharose. Sorbitol and arabinose were fermented by 82% and 43% of the strains, respectively. Xylose, trehalose, and dulcitol were fermented by 30%, 13% and 4% of isolates, respectively. All the tested strains produced catalase, ornithine decarboxylase, cytochrome-oxidase, indole, and reduced nitrates to nitrites. Moreover, the strains did not reveal motility and did not grow on MacConkey agar and failed to ferment maltose. Our findings enabled the recognition of ten distinct biochemical types, termed biovars I to X, and permitted the assignation of the strains into 3 subspecies. Of the isolates tested, 78% were identified as P. multocida subsp. multocida, 8.1 % as P. multocida subsp. septica, and 4% as P. multocida subsp. gallicida according to Mutters et al. ( 12). On the other hand, 9.7% of the strains were not classified as one of the three subspecies.
The goal of the study was to evaluate under field conditions the protective value of the vaccines comprising antigens to serotypes 3 and 12 of P. multocida with emulsigen (Cunipastivac E) and aluminium hydroxide gel (Cunipastivac A) against pasteurellosis in rabbits. Both vaccines were given subcutaneously at a dose of 1 ml. This study revealed: 1) No harmful effects of these vaccines and a beneficial influence on body weight gains, 2) An effective protection of rabbits against the acute form of pasteurellosis in a rabbitry with a high mortality rate resulting from this disease.
The ELISA was used to measure anti-Pasteurella multocida IgG levels in the serum of 30 geese collected randomly from a 300-goose flock aged 2 months and vaccinated against pasteurellosis with the Pastivac E vaccine comprising Polish isolates of serotypes 1 and 3 with oil adjuvant. The blood was sampled every 14 days for 2 months from two groups of 10 birds each vaccinated singly and doubly and from non-vaccinated considered the controls. The ELISA kits were prepared by the author's procedure because no commercial kits for goose blood were available. An increase in anti-P. multocida IgG level was found after each vaccination.
Prevalence of Pasteurella multocida toxinogenic strains in pigs in the South-East of Poland Prevalence of Pasteurella multocida toxinogenic strains in pigs in the South-East of Poland was investigated. Nasal swabs from 355 pigs aged 7 weeks to 4 months were taken and examinations were done using ELISA. Toxinogenic strains of P. multocida were identified in nasal swabs of 91 (25%) of pigs. The highest percentage of positive results (64%) was noted on a farm where pigs suffered from typical symptoms of infectious atrophic rhinitis.
It is assumed that rT3 (3,3’,5’-triiodothyronine) antagonized the effect of 3.3’,5-triiodothyronine (T₃) and thyroxine (T₄). Non-thyroidal illnesses are associated with „low T₃ syndrome” and higher гТ₃ plasma levels. The aim of this preliminary investigation was to discover if rТ₃, which acts hypometabolically may have an attenuating effect on mice infected with Pasteurella multocida (P.M.). A dose of about 20 thousand of P. multocida bacteria per animal i.p. at a volume of 0.1 ml was applied. Reverse T₃ or T₄ were applied s.c. at a dose of 10 or 2 µg/animal, respectively, at 12 h after bacteria infection, and at 12 h intervals for 3 consecutive days. The survival time was measured 10 days after infection of P. multocida. The mean survival time was 75.6 ± 5.9, 92.4 ± 11.6 and 117.6 ± 16.2 h for animals receiving T₄ + P.m. (n=10), 0.9% NaCl + P.m. (n=10) or rT₃ + P.m. (n=15), respectively. Two mice treated with rT₃ survived. A significant differences (P≤0.05) was obtained only in groups treated with T₄ and rT₃. The results have shown that in comparison with T₄, rT₃ prolonged the survival time of mice infected with P. multocida. These results also confirm a different action of rT₃ and T₄.
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