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Biomedical subjects

V S Lebedev

Publications and source records attributed to V S Lebedev.

At least 19 recordsLinked to original sources

[Origin of the house mice (superspecies complex Mus musculus sensu lato) from the Transcaucasian region: A new look at dispersal routes and evolution].

We analyzed our results and literature evidence on variability of nuclear protein genes in 39 populations of eight synanthropic and wild species of house mice (superspecies complexes Mus musculus and M. spicilegus) from Transcaucasia, Eastern and Western Europe, Near and Middle East, Central, South, and East Asia, and Cuba. These data were for the first time ever combined into a single database by unification of nomenclature of 21 loci examined by different authors in 39 populations. Analysis of geographical allele distribution have shown that populations of domestic Transcaucasian mice are close to Indo-Pakistani populations of form oriental of the species M. castaneus, which preserved a high level of ancestral polymorphism. We concluded that a very heterogeneous, rich gene pool of house mice from Transcaucasia could not develop only by secondary contacts of differentiated M. musculus s. str. and M. domesticus forms, since it is similar to the ancestral gene pool of the superspecies complexes M. musculus and M. spicilegus. In this context, unique characteristics of some Central Asian populations were examined; these populations may have served as a "transit station" in the dispersal of synanthropic house mice forms. We suggest that the Transcaucasian populations are genealogically closely related to an early Near East form of M. musculus, which, as M. domesticus and M. castaneus, split from the common ancestor and preserved nondifferentiated pool of ancestral alleles of protein genes. This hypothesis admits the involvement of differentiated species M. musculus s. str. and M. domesticus in the ultimate formation of the gene pool of Transcaucasian house mice. Apparently, these populations resulted from alternation and (or) "overlapping" of different evolutionary processes. A scenario suggesting that hybrid events having occurred in Transcaucasia at different times, were "superposed" on the gene pool of the ancient autochtonous population of house mice from this region seems most plausible. Analysis of allozyme variability in the modern Transcaucasian Mus populations could not always distinguish between ancestral polymorphism and hybridization consequences.

Alleles↗

[Determination of the antigenic activity of diphtheria anatoxin in liquid and sorbed preparations using an erythrocyte diphtheria antigen (anatoxin) diagnostic agent].

On the basis of the experimentally established dependence of the degree of binding of diphtheria toxoid with standard diphtheria antitoxin on the duration of their joint incubation with the maximum binding occurring in 3-4 hours of incubation at 37 degrees C, the method of the in vitro determination of the antigenic activity of diphtheria toxoid in liquid and adsorbed preparations is proposed. The method is based on the principle of double binding with the use of diphtheria antigenic (toxoid) erythrocyte diagnosticum. The antigenic activity of diphtheria toxoid, evaluated by the degree of its maximum binding with diphtheria antitoxin, correlated with its antitoxin-binding activity in animal experiments and did not correlate with its flocculating activity. The antigenic activity of diphtheria toxoid in adsorbed preparations, evaluated by their maximum binding with standard diphtheria antitoxin, was shown to be closely related to the immunogenic potency of these vaccines in animals.

Adsorption↗

[Antitoxic properties of monoclonal antibodies against diphtheria toxin].

Antitoxin properties of monoclonal antibodies to diphtheria toxin were studied in chick fibroblast culture and during the dermonecrotic tests in guinea pigs. Antitoxic properties were shown for antibodies specific to B subunit of the toxin but not for the ones specific to a subunit. The mixture of monoclonal B subunit specific antibodies reveals a higher neutralizing activity as compared with the activity produced by any single monoclonal antibody tested. The protective activity demonstrated by antibodies is connected with the preventing of toxin molecules fixation on the cellular receptors.

Animals↗

[Relationship of the sensitizing and protective properties of pertussis antigens].

When comparing delayed hypersensitivity (DN) to B. pertussis corpuscular antigens with the agglutinogenic composition of B. pertussis, as well as to its histamine-sensitizing, leukocyte-sensitizing, adjuvant and hemagglutinating activity, no correlation was detected between the specific sensitizing properties of these antigens and the serotype and studied nonspecific properties of B. pertussis. The DH level correlated with the protective activity of B. pertussis corpuscular antigens and the ultrasonic fractions of B. pertussis. The close correlation of these two phenomena suggest that DH-inducing and protective B. pertussis antigens are identical, though their action has different manifestations, depending on the method of administration of the antigen preparation. On these grounds a new method for evaluating the immunogenicity of B. pertussis antigens is proposed. This method consists in comparing the sensitizing activity of the antigen under test and that of the national standard.

Animals↗

[Modification of the agarose drop micromethod for studying mouse macrophage migration inhibition factor].

A modification of the drop agarose micromethod for the study of the factor inhibiting the migration of mouse macrophages is proposed. The syngeneic system was used instead of type RPMI-1640 complex culture media and calf embryonal serum, commonly used in the work with mouse macrophages. The production of the factor inhibiting the migration of macrophages by sensitized lymphocytes from mice of different strains has been shown to occur in vitro under the influence of pertussis corpuscular antigen. The method of obtaining supernatant containing macrophage migration inhibiting factor, from immune mouse lymphocyte culture is proposed. This supernatant may be used for, the analysis of the above-mentioned factor and other lymphokins.

Animals↗

[Cu2+-induced permeability of the Escherichia coli cytoplasmic membrane].

Cu(2+)-induced permeability of cytoplasmic membranes of Escherichia coli for different cations and neutral molecules of saccharose was estimated by studying their effect on cell plasmolysis during uncharged exchange of cytoplasmic K+ ions by periplasmic space cations. The addition of copper resulted in the exchange of K+ ions by periplasmic Na+, Tris+, streptomycin2+, Cu2+, Ca2+, Mg2+, Cd2+, and Mn2+. It is concluded that Cu(2+)-induced conducting pathways in bacterial membranes are hydrophilic channels with a radius of approximately 0.5 nm and a nonselective permeability for different cations.

Cell Membrane↗

[Reducing centers on the surface of Escherichia coli bacteria and their role in copper-induced plasma membrane permeability].

The reducing properties of Escherichia coli and their role in the induction of nonselective cationic permeability of plasma membrane by the action of Cu2+ ions were studied. The ability of cells to reduce exogenous dithiopyridine was shown to be maximal in freshly collected culture and to decrease upon starvation or exhaustion of bacteria by dinitrophenol, in the presence of other oxidants of cell thiols in the medium, and after the disturbance of the barrier properties of membrane by tetrachloracetic acid or butanol. The alkylation of cell thiols accessible for N-ethyl maleimide completely disrupted the reducing activity of bacteria. These data are consistent with the conception that the reduction of dithiopyridine and Cu2+ ions by bacteria occurs on the thiol-containing centers of the cell surface, which are continuously reduced by the transfer of cell reducing equivalents from the inner to the outer surface of plasma membrane. The analysis of data on the effect of external oxidizing and reducing agents on the copper-induced plasmolysis of bacteria showed that the induction of membrane permeability by the action of copper can occur upon interaction with critical targets on the surface of Cu+ ions formed in the periplasmic space in the reaction of Cu2+ ions with reducing centers.

Cell Membrane↗

[The role of reactive oxygen species in copper-induced permeability of plasma membranes in Escherichia coli].

The role of active oxygen species in the induction of nonselective cationic permeability of the plasma membrane of bacteria Escherichia coli B by the action of Cu2+ ions was studied. It was found that the increase in the amount of active oxygen species in the suspension after treating cells with copper occurred synchronously with the leakage of K+ cations from them. Evidence is presented that active oxygen species formed during the interaction of copper ions with bacteria under aerobic conditions are not involved in the induction of channel conductivity in the membrane. Moreover, the ability of oxygen to protect the membrane from the toxic action of copper was shown, and the activation of membrane damage by external reductants was confirmed. These data suggest that the barrier properties of the membrane are disturbed during the interaction of Cu+ ions with critical targets on the surface, the concentration of Cu+ being determined by all redox processes in the near-membrane space.

Catalase↗

[Structural modifications of the surface of Escherichia coli bacteria and copper-induced permeability of plasma membrane].

The effect of Cu2+ on the structural organization of the cell surface of Escherichia coli bacteria during the induction of conductivity of a plasma membrane was studied. A fluorescent study did not reveal any substantial changes in the microviscosity of lipids by the action of copper ions. At the same time, a substantial reorganization of membrane proteins during plasmolysis was observed. A model of the copper-induced structural reorganization of membrane lipids was constructed, according to which the reorganization leads to the opening in the membrane of channels of nonspecific conductivity for cations. The opening of conductivity channels results from the break of disulfide bonds in critical membrane proteins during the interaction with Cu+, which form either due to the reduction of Cu2+ on specific sites of cell surface or by means of external reducing agents.

Bacterial Proteins↗

[Analysis of the binding site of copper with intact and Escherichia coli bacteria modified by N-ethylmaleimide by ESR].

Characteristics of copper binding sites in the bacteria E. coli were studied using ESR spectroscopy. It was found that these cations had high local density on the strong binding range represented by the two type sites. The former include nitrogen and oxygen ligands and the second ones--sulfur of the thiol biomolecules. The weak coupling Cu(II) sites of E. coli represent more polar nitrogen-oxygen environment. Blocking SH-groups by N-ethylmaleimide makes them inaccessible for copper ligation, sharply increases the percentage of ESR-detectable copper of the strong-binding sites and prevents the membrane breakdown by these cations. The results suggest that the Cu(2+)-induced membrane damage is the effect of Cu2+ binding with the SH-containing sites of the bacterial membrane.

Binding Sites↗

[The copper-dependent accumulation of magnesium in Escherichia coli].

Cu2(+)-induced accumulation of Mg ions by E. coli cells has been studied. The accumulation was demonstrated to take place only when the cell had endogenous energetic resources. The data obtained and their correlation with the data on Cu2+ binding by bacterial cells and Cu2(+)-dependent streptomycin accumulation allowed to conclude that copper induced nonspecific potential-dependent influx of cations into cells.

Copper↗

[The role of oxygen in the inhibition of Escherichia coli respiration by copper ions].

Effect of Cu2+ on E. coli respiration and the role of oxygen in toxic action of copper has been studied. Stimulation of respiration is observed at initial time after introduction of Cu2+. It is based on a nonspecific cell response to membrane damage. After finishing of transitory processes, Cu2+ influenced respiration by noncompetitive inhibition, i.e. copper-sensitive enzyme can be oxygenated or nonoxygenated, and only the latter form of the enzyme is inhibited.

Copper↗

[Characteristics of the toxic action of a highly disperse copper powder on the energy processes in Escherichia coli B].

The role of changes in incubation medium, connected with electrochemical dissolution of fine copper powder (FCP), in efficiency of copper inhibition of energy-dependent proton efflux from E. coli was studied. In conditions of aeration of bacterial suspension in water, toxic properties of FCP can be modelled by dispersed hydrogen peroxide. Addition of hydrogen peroxide to bacteria does not influence their sensitivity to copper chloride. Transfer of the bacteria to anaerobic conditions leads to complete inhibition of energy-dependent proton efflux from E. coli by various copper-containing compounds. The data obtained suggest that the higher efficiency of FCP action on energy processes in E. coli as compared to copper chloride is determined by alkalinization of medium and oxygen absorption in the process of electrochemical dissolution of the metal.

Copper↗

[The role of surface and transmembrane potentials in copper binding by Escherichia coli cells].

Cu2+-induced accumulation of Mg2+ ions by E. coli cells has been studied. The accumulation was demonstrated to take place only when the cell had endogenous energy resources. The data obtained and their correlation with the data on Cu2+ binding by bacterial cells and Cu2+-dependent streptomycin accumulation allowed to conclude that copper induced nonspecific potential-dependent influx of cations into cell.

Binding Sites↗