The multilayer growth of epithelium-like ESK cells in perfused cultures]

The multilayer growth of an epithelium-like ESK [correction of SPEV] cell culture was achieved under condition of culture medium perfusion. The growth of the ESK [correction of SPEV] cells is described under conditions excluding medium movement above the cells in the chamber with a semipermeable membrane separating the cells from the perfused medium. Under these conditions the multilayer (30-40 layers) growth of culture was observed. The data observed are in favour of our suggestion that it is the diffusional limitations in mass exchange, rather than intracellular interaction contacts, that may be responsible for cell growth in culture. A dependence of culture growth on the initial inoculation density, under condition of medium perfusion immediately above the cells, was determined. The dependence of the multilayer saturation density on the perfusion rate and on the complete replacement of the perfused medium is discussed. The existence of a limiting saturation density of perfused culture was shown.     

Cytotoxic effect of dihydroquercetin and its derivatives in liposomal form and in the form of fat nanoscale emulsions

We studied cytotoxic effects of dihydroquercetin (DHQ) and its derivatives, penta-O-acetylsalicylate dihydroquercetin (PAS DHQ), penta-O-acetate dihydroquercetin (PA DHQ), and penta-O-benzoate dihydroquercetin (PB DHQ), in aqueous solutions, liposomal form, and in the form of fat emulsions, on cultured tumor cells HL-60 and HEp-2. Solubility of the DHQ derivatives in aqueous solutions was much lower than that of DHQ. Modification of DHQ either did not alter its toxicity (PAS DHQ) or significantly reduced the cytotoxic effect of DHQ on tumor cells (PA DHQ, PB DHQ). DHQ and its derivative PAS DHQ were more toxic when dissolved in an aqueous solution than in the form of liposomes. Cytotoxic effect of DHQ applied in the form of fat emulsion was significantly higher than in the liposomal form and was close to the activity of DHQ in a solution. These results can be implicated for the development of new anticancer drugs based on liposomal and fat emulsions.     

Phage typing and lysogen typing of Staphylococcus aureus]

A comparison was made between the results of phage and lysogenic typing of S. aureus strains isolated during several outbreaks of staphylococcal infection and S. aureus cultures isolated from the same carriers at different periods. The study of the groups of strains having the same origin showed that the differences in the number of reactions were more pronounced in lysogenic typing than in phage typing. For this reason lysogenic typing can be recommended only for the identification of those strains which cannot be identified with the use of the phages of the International Basic Set. The results of the experiments with induced phages proliferating in a restriction-defective strain indicated that restriction and modification were mainly responsible for the specificity of lytic reactions.     

Experimental phages for differentiating nontypable methicillin-resistant Staphylococcus aureus

The possibility of using phages, isolated from the lysogenic cultures of methicillin-resistant staphylococci and modified in methicillin-resistant cultures of phage 85, for the differentiation of nontypable staphylococcal strains has been studied. The variants of phage 85 cannot be used for the determination of differences between the strains of methicillin-resistant cultures; they are not suited for typing. For this purpose the collection of phages isolated from lysogenic methicillin-resistant cultures should be used.     

Species characteristics of coagulase-negative staphylococci of animal origin

The specific identification of 271 strains of coagulase-negative staphylococci isolated from different animals (cows, sheep, swine, hens, monkeys, minks, sables, foxes, etc.) was carried out according to the scheme of Akatov--Devriese. Species could be determined in 77.5% of the strains. The representatives of S. sciuri (55.5%) and S. xylosus (11.4%), very seldom occurring in humans, prevailed among the identified cultures. In 31.4% of coagulase-negative strains of animal origin the presence of protein A was established. The study of the time of glucose fermentation in the cultures and the type of colonies formed on agar with crystalline violet permitted the additional characterization of the majority of the strains of coagulase-negative staphylococci. Only in 4.8% of cases the strains under study could be lyzed by typing phages Holmberg and belonged to 6 phage types; of these, 117 A was the most numerous one (7 out of 13 typed cultures). No relationship between the phage type and the species of the strains was established.