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Yeast like fungi of Malassezia pachydermatis species are numbered among the opportunistic agents accounting for acute dermatoses or even systemic infections in people and animals. They exhibit the clear heterogeneity pertaining to the phenotypic traits and growth requirements. The objective of the present study was to determine the degree of variation as well as the biochemical profiles of M. pachydermatis strains. The studies were conducted on 40 strains isolated from the auditory canal of healthy dogs and those with otitis externa symptoms recognized. An assessment was conducted of the traits of fungus morphology (size and shape of cells and colony type), expression of extracellular hydrolases (API-ZYM) and the activity of catalase, urease, caseinase, beta-glucosidase, phospholipase and Tween hydrolases: 20, 40, 60 and 80. The obtained results made it possible to determine the general metabolism pattern for this species: no fermentability or capacity for assimilation of most carbohydrates, poor proteolytic properties, high activity of enzymes from the phosphatase and lipolytic enzymes groups. On the grounds of the statistical analysis, the examined strains were classified into 7 separate groups of congenial morphology and a determined level of enzymatic activity. Biotype I includes large, smooth and creamy-white colonies of high metabolic activity; moreover, they exhibit high sensitivity to the inhibitory operation of Tween 20 and Cremophor EL; biotype II exhibits a rough type of colony growth, the lowest metabolic activity and a lack of expression of lipase C14 and enzymes from the arylamidase group; biotype III comprises the strains of large, smooth colonies, poor total enzymatic activity and with no activity of cystynic arylamidase; biotype IV includes the strains of small and smooth colonies, average metabolic activity but with optimal usability of Tween 40 and 60 hydrolysis products for growth; biotype V groups the strains of the average metabolic activity and without phospholipase activity recorded; biotype VI comprises the strains of smooth, large or medium-sized colonies and a relatively high enzymatic activity as well as the highest level for alkaline phosphatase and valine arylimidase, phospholipase, catalase, caseine, Tween 80 hydrolase; biotype VII is characterized by the highest total enzymatic activity, high capacity for eskulin break-down, Tween 40, 60 and 80 hydrolysis. Further studies are needed to demonstrate a correlation between the strain classification into a defined biotype and its ecologic or clinical status.
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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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