Search PubMed⌕ Search

Biomedical subjects

T S Il'ina

Publications and source records attributed to T S Il'ina.

At least 19 recordsLinked to original sources
PubMed2006

[Communication systems in bacteria and their role in pathogenicity].

A review of the literature about the bacterial systems of regulation of expression of the genes controlled by signals generated by the bacteria themselves is given. Three types of presently known Quorum sensing systems contributing to the expression of the pathogenicity factors, infection process, and formation of biofilms by pathogenic bacteria are described. Possible mechanisms of enhanced resistance of bacteria in films to antibacterial preparations and factors of immune protection of human body are discussed. The perspectives of the development of new approaches to treatment of chronic diseases caused by the pathogens producing bacterial films are considered.

Animals↗
PubMed2006

[Wild small mammals are the reservoir hosts of the Bartonella genus bacteria in the south of Moscow region].

A total of 103 blood samples collected from wild small mammals captured in the Prioksko-Terrasny Reserve on the south of Moscow region were studied to determine the bartonellae prevalence. The examined species were the yellow-necked mice Apodemus flavicollis (35 samples), the European wood mouse Apodemus uralensis (10 samples), the bank vole Clethrionomys glareolus (51 samples), the house mouse Mus musculus (3 samples), the common vole Microtus arvalis (2 samples), and the shrew Sorex araneus (2 samples). Initially, we obtained 76 bacterial Bartonella-like isolates after plating onto the surface of the solid nutrient media. 66 of them were PCR-positive at least for three of four targets, gltA, ftsZ, ribC and 16S RNA. Thus, the percentage of the infection in the studied community was 64%. Subsequent RFLP assay showed that obtained isolates belonged to the Bartonella grahamii and/or B. taylorii species. In 7 cases we found both bartonellae species in one animal. These data were confirmed by direct sequencing of four ftsZ, four ribC and two gltA amplicons. According to our data, there is no any marked host specificity for these bartonellae species. Now we have laid the bartonellae strain collection consisting of 31 isolates. To our knowledge, this is the first investigation of the bartonellae prevalence in wild small mammals performed in Russia. The comparison of our data with those obtained by European researchers and issues of coinfection by different bartonellae species and host specificity are discussed.

Animals↗
PubMed2006

[Bacterial superintegrons, a source of new genes with adaptive functions].

Data on the structural organization of the platform of integrons, gene cassettes, and integrons with integrated cassettes of genes encoding drug resistance are briefly summarized. Data obtained during recent years about superintegrons or chromosomal integrons, characteristics of their organization, the presence of genes with known adaptive and unidentified functions in them, as well as data on the differences between superintegrons and previously described multiple resistance integrons, are considered in more detail. Studies that provide evidence for translocations of gene cassettes from stationary chromosomal integrons into integrons associated with mobile elements resulting in gene flows in natural bacterial populations, which favors their survival and adaptation to changing environment, are also reviewed.

Adaptation, Biological↗
PubMed2004

[Bacteria of Bartonella genus: characteristics, pathogenicity factors and methods of molecular-genetic investigation].

Bartonella bacteria are an agent of a variety of human and animal diseases whose etiology used to be unknown. The survey contains a description of the above bacteria with the established pathogenicity factors and with the molecular and genetic approaches to studies of genes' functions and of their regulation being in the focus of attention. Modern methods related with the genus-specific and species-specific determination and identification of Bartonella bacteria are discussed.

Animals↗
PubMed2004

[Biofilms as a mode of existence of bacteria in external environment and host body: the phenomenon, genetic control, and regulation systems of development].

Studies of the last decade have shown that most bacteria exist in natural ecosystems as specifically organized, attached to substrates biofilms rather than as freely floating plankton cells. The formation of these biofilms is a complex and highly regulated process. The development of biofilm communities is a primary strategy of bacterial survival not only in the external environment but also in the bodies of infected macroorganisms. In these organisms, bacteria are joined by complicated cell-cell associations, which makes them functionally similar to multicellular organisms. In the present review, we consider the structural organization of biofilms, factors affecting initiation of the biofilm formation, differential expression of bacterial genes at various stages of the biofilm development and their regulation. The significance of studies in this field for medicine, in particular, for prevention and protection against pathogenic bacteria, is discussed.

Bacteria↗
PubMed2001

[Structural organization and mechanisms of mobility of the gene cassette coding for resistance to antibiotics and bacterial virulence factors].

The review is focussed on two types of gene cassettes which are significant in bacterial variability. The first type are cassettes with antibiotic resistance genes; these are the smallest mobile genetic elements including a gene (most commonly an antibiotic resistance gene) and a short sequence acting as a recombination site. Sometimes these cassettes contain genes not responsible for antibiotic resistance but their functions are not yet known. The second type contains large clusters of genes coding for bacterial virulence factors. They were termed "pathogenicity islands" due to their difference in the percentage of G-C pairs in comparison with bacterial chromosomes, in which they are contained. The structural organization and mechanisms of mobility of various types of gene cassettes are discussed.

Bacteria↗
PubMed2001

[Mobile genetic elements and their role in evolution of pathogenic bacteria].

The review discusses a role of mobile genetic elements in the evolution of pathogenic bacteria. Particularly great emphasis is placed on two recent thoroughly studied mobile genetic elements--the islets of pathogenicity and cassettes containing antibiotic resistant genes. The matters associated with the structural organization of these types of mobile elements, mechanisms of their translocations and involvement in the production of pathogenic bacteria are considered in detail. The data on the impact of macroorganisms on the horizontal dissemination of genetic information are discussed.

Bacteria↗
PubMed1995

[Genetic study of plasmid pVM82 which contributes to the pathogenicity of the pseudotuberculosis pathogen].

The large pVM82 plasmid isolated from epidemic strains of Yersinia pseudotuberculosis includes the 25MD segment, which encodes a series of properties affecting the virulence of the bacterium. Insertion mutants of pVM82 containing transposition-defective Tn2507 with a kanamycin-resistance marker in different Hind III fragments of the 25MD segment were obtained. By recombination between two homologous pVM82 containing genetic markers in different parts, deletion derivatives of pVM82 plasmid and insertions of the plasmid segment, carrying kanamycin-resistance marker, into a chromosome were obtained. Results were obtained suggesting the presence in the plasmid 25MD segment of a transposon-like structure capable of migrating from pVM82 plasmid onto a chromosome and from a chromosome and pVM82 onto pRP1.2 plasmid of a broad host range.

Chromosomes, Bacterial↗
PubMed1991

[Phenotypic features of a strain of Yersinia pseudotuberculosis with the pVM82 plasmid, detected at pseudotuberculosis outbreak foci].

The phenotypic properties conferred to Yersinia pseudotuberculosis cells by the genetical determinants of a 25Md fragment of the plasmid pVM82 coding for the modified cellular immune response in the infected organism. The fragment was shown to determine the conjugative properties of the plasmid, the resistance of bacterial cells to a number of hydrophobic agents and cellular ability to absorb the Congo red dye. The latter confirms the presence of additional structural components in the cell wall of the strain harbouring the plasmid pVM82. The increased resistance of the plasmid-containing strain to bactericidal effect of the blood plasma was demonstrated as compared with the resistance of the strains harbouring the p57 plasmid lacking the 25Md fragment or no plasmid at all.

DNA Transposable Elements↗
PubMed1990

[Inheritance and expression of cholera toxin genes introduced into Vibrio cholerae el tor cells in a hybrid plasmid].

Two replicons, pOX38 (in F-factor derivative lacking all IS elements) and pCT105 (containing cholera toxin operon cloned in pBR322) have been fused to produce recombinant plasmid, pCO109, which was then introduced into Vibrio cholerae eltor by conjugation. Restriction analysis showed pCO109 to dissociate in V. cholerae cells at a higher frequency than in Escherichia coli strains, its pOX38 component being lost, while the pCT105 component demonstrated relative stability. V. cholerae eltor RV79 (pCT105) produced 4-5 micrograms/ml of cholera toxin. Occasional insertion of cloned vctA, B operon into RV79 chromosome was also observed.

Cholera Toxin↗
PubMed1988

[The role of the RS1 sequence of Vibrio cholerae in the amplification of a segment of plasmid DNA carrying the tetracycline resistance gene and cholera toxin genes].

The clones with 4 to 30-fold increased level of tetracycline resistance (TcR) were selected from the strain of Escherichia coli K-12 carrying the pCO107 plasmid. The plasmid is the cointegrate formed from the plasmids pOX38 (F-derivative) and pCT105 (pBR322-derivative carrying the vct operon of Vibrio cholerae eltor and the RSI sequence). pCO107 contains RSI at the junctions of two plasmid genomes. Using restriction analysis and Southern blot hybridization technique it was shown that increased tetracycline resistance is accompanied by amplification of the pCT105 segment of pCO107 and depends upon the presence of direct repeats of flanking RSI. Amplification of the pCT105 also resulted in increased production of the cholerae toxin (CT).

Base Sequence↗
PubMed1986

[Bacterial transposons and the mechanisms of their transposition].

The published data on molecular mechanisms of transposons movement inside and between genomes are reviewed. The replicative mechanism of transposition of the family of Tn3-like elements is discussed, as well as the modes of bacteriophage Mu, Tn9, Tn10, Tn903 transposition. The factors affecting the choice of transposition pathways are analysed.

Bacteria↗
PubMed1985

[Different effect of mutations in Escherichia coli K12 dna-genes on the transposition of Tn5- and Tn10-elements].

The effect of mutations in dnaA(dnaA46), dnaG(dnaG3), dnaC (dnaC1 and dnaC2) and dnaB genes on transposition of two transposons, Tn5 and Tn10, from bacteriophage lambda genome into the chromosome of host cells has been studied. Transposition was performed at permissive temperatures for the mutant recipients. The mutations in dnaA, dnaC, dnaG genes were shown to decrease the transposition of Tn10 for some orders of magnitude as compared with transposition registered in wild type cells. Independence of Tn5 transposition of the above mentioned genes was demonstrated, providing evidence on the different modes of transposition of these two Tn-elements.

Bacteriophage lambda↗