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Autor przedstawił działalność przemysłu gorzelniczego w Polsce od 1918 r. do 1995 r. oraz produkcję i kierunki zużycia spirytusu w Polsce.
Rhodococcosis is known largely as an infectious disease of young foals that causes losses in the horse breeding industry. Besides in animals, the infection can also be a significant diagnostic, clinical and therapeutic problem in human medicine. The aim of the paper is to present the zoonotic aspect of rhodococcosis, including basic data about pathogen, epidemiology, pathogenesis, clinical picture, pathology, diagnosis and therapy of the disease. R. equi was isolated for the first time in 1923 by Magnusson in Sweden from a dead foal with the signs of pyogranulomatous pneumonia. The first case of human R. equi infection has been described in 1967 in a 29-year-old man subjected to immunosuppressive therapy. Hundreds of new cases of human rhodococcosis have been described since that time all over the world. The majority of human cases of R. equi infections concern patients immunodeppressed during the course of different diseases or treated with immunosuppressive drugs. However, 10-15% of cases concern fully immunocompetent patients. The role of farm animals as a primary source of infection to people has not been proved, but the importance of a contaminated environment seems to be evident. Molecular studies of human R. equi strains revealed that only 21% of isolates contained the typical for foal strains VapA plasmid. This suggests that the pathogenesis of the disease in humans may be different from that described in animals. Immunological investigations supporting the role of cell-mediated immunity in R. equi infections explain why AIDS patients with confirmed CD4+ lymphocytes deficiency and decreasing ability of INF gamma synthesis are more susceptible to infection in comparison to immunocompetent people. The clinical course of rhodococcosis in humans is varied, but in 80% of cases the process is localized in the respiratory tract. The mortality rate in immunosuppressed patients ranges between 20-55%. Diagnosis of rhodococcosis in humans is based on the isolation and identification of the pathogen in antemortem collected biological material. Radiology and CT may also be helpful. Myc. tuberculosis and Nocardia spp. infections should be included as a differential diagnosis. Treatment of rhodococcosis in humans, similarly to animals, usually requires a several-week course of a combination of 2-3 antibiotics. In practice intravenous application of vancomycin, carbapenem or aminoglycosides combined with oral administration of azithromycin and/or rifampin is used. In apparently cured individuals relapses occur frequently in which pathological changes are localized in primarily involved or in other tissues and organs.
The experiment was carried out on 72 fattening pigs divided into 4 experimental groups. The control mixture /I/ comprised soybean meal. The mixtures given in II, III and IV group contained repeseed meal supplemented with 3 and 6% of pea in II and III group respectively. Wheat meal in groups III and IV was replaced by rye meal. The other components of mixtures were the same. Weight gain of fattening pigs in groups II, III, IV was nearly the same and only slightly lower then that in the control /P < 0.05/. In the groups given mixtures supplemented with ground pea increase of feed intake per kg of weight gain was noted. The presence of rapeseed meal in the mixtures resulted in increasing of thyroid gland weight /P < 0.05/. The results of the carcass evaluation did not differ significantly between the groups. In group IV the digestibility coefficient of nitrogen components was 6% lower compared with that in other groups but it did not effect nitrogen retention. Rapeseed meal combined with ground pea in the mixtures resulted in the increase of apparent digestibility and retention of Ca. The data demonstrated that rapeseed meal can replace soybean meal in concentrate mixtures for fattening pigs.
The digestibility of Italian rye-grass /Lotos, Kroto, Telga and GOH varieties/ and three mixtures of Meadow fescue with red clover /75:25, 50:50, 25:75/ was evaluated by two in vitro techniques - standard method of Tilley and Terry or by modified method in which samples were incubated in the nylon bags and washed out in the washing-machine. It was found out that in vitro digestibility coefficients of forages were significantly correlated with the in vivo results /P ≤ 0,01/. Digestibility of organic dry matter obtained by the modified in vitro method appeared to be better correlated with in vivo data as compared to the standard in vitro technique. Both in vitro methods, standard and modified, appeared to be less suitable for estimation of the crude protein dogestlbillty in the green forages.
The aim of the studies was to evaluate the usefulness of determining the level of haptoglobin, IgG and lysozyme in sera for monitoring the state of health of breeding polar foxes of different behavior at the preparturient period. It was found that in determining the physiological parameters of unspecific humoral immunity, the behavior of the animals should be borne in mind. Significant differences exist in the examined parameters of unspecific immune responses and behavior of foxes. The highest and statistically significant level of haptoglobin, IgG and lysozyme was noted in fearful foxes in comparison to aggressive and confident animals. It can be assumed that lower phagocytic and bactericidal activity noted in the fearful foxes in comparison to that in the aggressive and confident animals is compensated by a higher bacteriolytic activity of lysozyme and a higher level of serum IgG.
T. pyogenes belongs to Gram-positive, facultative anaerobic, pleomorphic, non-spore forming microorganisms, currently classified as a representative of the genus Trueperella. Species from this genus have been separated from Arcanobacterium to constitute a new taxonomic unit. The primary basis for the reclassification of these microorganisms was provided by the results of investigations concerning the presence and types of isoprenoid quinones in the bacterial cell wall. Biochemical studies were subsequently extended to include the analyses of the 16S rRNA gene sequence, the peptidoglycan structure, the G+C content in the DNA strand, the profile of lipid acids, the cell wall sugar composition, the type of muramyl acyl groups, the polar lipid profile, and the menaquinone composition. Owing to a variety of virulence factors, T. pyogenes is able to colonise many tissues, causing clinical symptoms in various organs and systems. The main virulence factor in T. pyogenes is pyolysin (PLO), an intracellular toxin with cytolytic activity against various types of cells, particularly neutrophils and macrophages. The microorganism also exhibits the ability to adhere to host cells, which ensures its persistence and survival on the mucous membrane surface. The main role in the adhesion process of T. pyogenes is played by the neuraminidases NanH and NanP. Additionally, with their ability to attach to the components of the extracellular matrix (ECM) of the host cell, surface proteins also serve as an adhesion factor. Fimbriae are an important virulence factor of T. pyogenes. The function of the hitherto recognized fimbrial proteins FimB, FimA, and StrA consists in facilitating bacterial penetration through the cell membrane. During infections caused by T. pyogenes a characteristic bacterial growth is observed, known as biofilm formation, which results in resistance to antibacterial agents and mechanisms of anti-infective host immune response, including phagocytosis. Virulence factors of T. pyogenes also include specific calcium-dependent proteins exhibiting proteolytic activity, which play a significant role in the infectious process and tissue damage, microbial escape from the host’s immune defence, and the modulation of the immune system during infectious and inflammatory processes. The identification of the types and mechanisms of action of individual virulence factors of T. pyogenes at the molecular level will provide a basis for the development of a rational veterinary medical strategy for the treatment of animals infected with these microorganisms.
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