PubMed Health⌕ Search

Biomedical subjects

V I Tynianova

Publications and source records attributed to V I Tynianova.

12 recordsLinked to original sources

[Possible mechanisms of implementation of toxic potential of lipopolysaccharides of pathogenic bacteria].

The significance of variability of biological properties of lipopolysaccharides (LPS) is discussed in the paper within the pathogenesis of infectious process. On the basis of an analysis of published data and of results of independent research of two microorganisms (Yersinia pestis and Francisella tularensis) a conclusion is made on that a biologically inert LPS form (with a weak cytokine-inducing ability, apirogenicity and non-toxicity etc.) is typical of highly pathogenic bacteria. It is suggested that the above phenomenon is biologically expedient. Presumably, the inert LPS transforms to the active form inside a sensitive host and, according to an infection stage, each of them being functionally significant. It is the inert status of LPS that enables the pathogens, at the initial stages, to surmount freely the humoral and cell barriers of host. As the infection progressively aggravates and the proliferation of bacteria modifies itself due to LPS micro- and macroorganisms, its chemical structure and biopolymer conformation change. Both modification mechanisms enhance the LPS toxic potential. In case of a sensitive host, such variations transform the biologically inert LPS into a toxically active form with its function of endotoxin being realized. There is no LPS modification in a host insensitive to such infection, which entails either recovery or prolonged persistence of the pathogen inside the microorganism.

Cytokines↗

[The utilization of heme iron by Yersinia pestis in human blood and blood sera].

Y. pestis, the causative agents of plague, have been found to be incapable of using heme iron bound to haptoglobin and hemopexin complexes in human blood and blood serum, and protein components of the serum are not the factors inhibiting this process. At the same time iron of free hemoglobin can be successfully utilized by Y. pestis in the systems used in this study. On the contrary, hemin not only produces any stimulating effect on the growth of Y. pestis in blood serum, but leads to the death of these bacteria [correction of lasteria].

Drug Resistance, Microbial↗

[Utilization of hemoglobin by the plague microbe].

Hemin and hemoglobin are found to be adequate sources of iron for growth of Yersinia pestis. The mechanism of their assimilation is similar and consists of absorbtion of the free intact hem molecule.

Electrophoresis, Polyacrylamide Gel↗

[Comparison of specific recognition sites of adenine and cytosine DNA-methylase of Yersinia Pestis EV 76 C dam and dcm by Escherichia coli methylases].

Using enzymatic modelling of in vitro methylation of chromosome DNAs from Yersinia pestis EV 76, E. coli 834 and E. coli C600 RII by DNA methylases of Eco RII and Eco dam as well as of DNA hydrolysis of plasmid pBR 322 from the cells of Y. pestis EV 76, E. coli C600 and E. coli 834 by restrictases of Eco RII and Cfu I, it was found that cytosine DNA methylase from plague bacteria does not correspond to the type of RII methylases of E. coli. Adenyl DNA methylase is related to E. coli methylases type dam and modifies adenine in the nucleotide sequence of GATC.

Base Sequence↗

[DNA-methyltransferase of the plague microbe].

DNA-methyltransferases of Yersinia pestis EV, plague agent bacteria were isolated by P-II phosphocellulose chromatography. The methylating activity is eluated by two fractions at the 0.47 M and 0.53 M NaCl concentrations. Methylases of the plague microbe are specific with respect to two bases (adenine and cytosine) and are capable of modifying both native and denaturated form of DNA.

Chromatography, Affinity↗

[An increase in the virulence of Yersinia pestis bacteria when the cells are incubated in hemolyzed human erythrocytes].

The incubation of Y. pestis, the causative agent of plague, in hemolyzed human red blood cells at 37 degrees C for 3 hours enhanced the virulence of vaccine strain EV76 in white mice and guinea pigs and decreased the LD50 of attenuated strains. The phenomenon of increased virulence has been observed only in case of the combined injection of bacteria with the incubation medium. The virulence of Y. pestis cells, introduced alone after such treatment, has proved to remain at the same level.

Animals↗

[The activation of Yersinia pestis "murine" toxin and endotoxin by hemolyzed erythrocytes from mammalian blood].

Y. pestis "mouse" toxin and endotoxin have been found to be capable of being activated with hemolyzed mammalian red blood cells. The LD50 of the activated endotoxin decreases 5-10 times in comparison with the initial preparation. The LD50 of the activated "mouse" toxin decreases 5 times. As revealed in this study, the joint introduction of nonlethal doses of "mouse" toxin and endotoxin is highly toxic for white mice and guinea pigs. The presence of both "mouse" toxin and endotoxin in the toxic mixture is an essential factor for these two species of animals.

Animals↗