ДОСЛІДЖЕННЯ РОБОТИ КРОКОВОГО ДВИГУНА ПРИЛАДІВ ОБЛІКУ ЕЛЕКТРИЧНОЇ ЕНЕРГІЇ ПІД ВПЛИВОМ ДІЇ ЗОВНІШНЬОГО ПОСТІЙНОГО МАГНІТНОГО ПОЛЯ, УТВОРЕНОГО З МЕТОЮ БЕЗОБЛІКОВОГО СПОЖИВАННЯ ЕЛЕКТРИЧНОЇ ЕНЕРГІЇ

Research on facts and circumstances of electrical energy uncounted consumption in the practice of conducting electrical engineering forensic examination is one of the most common. Study of the influence of a permanent magnetic field on operation of the electromechanical electricity meters is one of the areas of electrical engineering research, where scientific and practical analysis is absent in electrical engineering forensic examination. The tasks solved by electrical engineering forensic examination of electricity meters subjected to interference in their work due to the influence of an external permanent magnetic field are still being solved indirectly, mainly by examining the state of indicators of the effect of a magnetic field. The Article purpose is to determine the mechanism of interference in the operation of a stepper motor of electromechanical electricity meters of energy accounting meters under the influence of an external magnetic field artificially developed to disregard the consumption of electric power. The article examines the structure of a stepper motor of electronic-mechanical devices metering electric power. A research model of a stepper motor is built. The analysis of distribution of force magnetic lines in the magnetic system and in the magnetic shield of a stepper motor as a result of influence of an external magnetic field artificially created for the purpose of uncounted consumption of electric power in the absence of such an effect on the basis of modeling with the use of software and a mathematical apparatus: the finite element method. The mechanism of interference in the regular operation of a stepper motor of electricity meter is determined when approaching the metering device of an external permanent magnet with a high value of maximum specific energy in order to consume electric power negligently.За конструктивною будовою крокового двигуна електромеханічних рахункових механізмів приладів обліку (далі – ПО) електричної енергії побудовано дослідницьку модель. Механізм втручання в роботу крокового двигуна приладу обліку від дії зовнішнього магнітного поля, штучно утвореного з метою безоблікового споживання електричної енергії, досліджено на моделі порівняння штатного режиму роботи та роботи під дією зовнішнього магнітного поля. Проаналізовано розподілення силових магнітних ліній у магнітопроводі та магнітному екрані крокового двигуна від дії зовнішнього магнітного поля, утвореного від наближення до приладу обліку зовнішнього постійного магніту з високими значенням максимальної питомої енергії. Визначено механізм перешкоджання штатній роботі крокового двигуна рахункового механізму

Analysis of genetic relationships of genotypes of the genus Rosa L. from the collection of Nikita Botanical Gardens using ISSR and IRAP DNA markers

In connection with the development of breeding and the creation of new plant varieties, the problem of their genotyping and identification is becoming increasingly important, therefore the use of molecular methods to identify genetic originality and assess plant genetic diversity appears to be relevant. As part of the work performed, informative ISSR and IRAP DNA markers promising for the study of genetic diversity of the Rosa L. genus were sought and applied to analysis of genetic relationships among 26 accessions of the genus Rosa L. from the gene pool collection of Nikita Botanical Gardens. They included 18 cultivated varieties and 8 accessions of wild species. The species sample included representatives of two subgenera, Rosa and Platyrhodon. The subgenus Platyrhodon was represented by one accession of the species R. roxburghii Tratt. Cultivated roses were represented by varieties of garden groups hybrid tea, floribunda, and grandiflora. The tested markers included 32 ISSRs and 13 IRAPs. Five ISSR markers (UBC 824, ASSR29, 3A21, UBC 864, and UBC 843) and three IRAPs (TDK 2R, Сass1, and Сass2) were chosen as the most promising. They were used for genotyping the studied sample of genotypes. In general, they appeared to be suitable for further use in studying the genetic diversity of the genus Rosa L. The numbers of polymorphic fragments ranged from 12 to 31, averaging 19.25 fragments per marker. For markers UBC 864 and UBC 843, unique fingerprints were identified in each accession studied. The genetic relationships of the studied species and varieties of roses analyzed by the UPGMA, PCoA, and Bayesian methods performed on the basis of IRAP and ISSR genotyping are consistent with their taxonomic positions. The genotype of the species R. roxburghii of the subgenus Platyrhodon was determined genetically as the most distant. According to clustering methods, the representative of the species R. bengalensis did not stand out from the group of cultivated varieties. When assessing the level of genetic similarity among the cultivated varieties of garden roses, the most genetically isolated varieties were ‘Flamingo’, ‘Queen Elizabeth’, and ‘Kordes Sondermeldung’; for most of the other varieties, groups of the greatest genetic similarity were identified. This assessment reflects general trends in phylogenetic relationships, both among the studied species of the genus and among cultivated varieties

Some groups of Toll-like receptor gene polymorphisms and their clinical and pathogenetic manifestations in children with bronchial asthma

The prevalence of bronchial asthma has shown its steady increase in the world in recent years. Despite all the achievements of Allergology, control of the disease can be achieved only in two-thirds of patients even if all social risk factors and the influence of concomitant diseases are excluded. Thus, it is necessary to study endogenous factors that modify the pathogenesis of the disease. Toll-like receptors are the main molecules for recognizing pathogenic patterns in the human immune system. Since any Allergy is a recognition error, mutation of the genes of the recognizing molecules can have a direct and multidirectional effect on the nature of the inflammation and its clinical manifestations in bronchial asthma (BA). To detect this effect, 65 patients with BA were examined, and mutations of Toll-like receptor genes were detected: TLR2-Arg753Glu, TLR4- Asp299Gly, TLR4-Ghr399Ile, TLR9-T1237C, TLR9-A2848G, lymphocyte subpopulations CD3, CD19, CD4, CD8, CD16, phagocytosis indicators, levels of IgA, IgM, IgG, IgE and IL-6, IL-7, IL-9. The assessment of the severity of asthma and its level of control were conducted according to clinical recommendations of the Ministry of health of the Russian Federation in 2019 criteria. We have shown characteristic clinical manifestations of the studied mutations. A lighter course of the disease, more complete control over it and a better response to therapy were found in single-nucleotide substitutions in the Toll-like receptor 4 and 9 (TLR4-Asp299Gly, TLR4-Ghr399Ile, TLR9-T1237C, TLR9-A2848G). On the contrary, a heavier course and a worse response to therapy were detected in the TLR2 mutation with Arg753Glu replacement. In the studied groups, the features of immunity indicators characteristic of genotypes with a lighter and more controlled course of BA were determined: a higher absolute number of T-helpers, with multidirectional changes in the number of T-killers, but with invariably preserved higher ratio of CD4/CD8 in such genotypes. Higher levels of phagocytosis indicators (primarily characterizing chemotaxis) and IL-7, IL-9 were also detected. The exception is the TLR9-A2848G mutation, in which greater disease control and better response to therapy are combined with no changes in the studied laboratory characteristics. At the same time, a specific feature of the genotype of the studied patients with BA was revealed – a combination of Toll-like receptors 4 and 9 mutations. This suggests the presence of genetic patterns that characterize groups of patients with BA that differ in severity, response to therapy, and degree of control, which makes it possible to personalize approaches to diagnosis, prevention, and therapy of the disease

IRAP-analysis for evaluating the genetic stability of endemic and endangered species of the Western Caucasus flora in the collection in vitro

The characterization of genetic diversity is one of the main components of the genetic resources collection and management. Molecular markers are the most effective tool for characterizing and assessing genetic diversity in plant collections. IRAP (inter-retrotransposons amplified polymorphism) markers have proven to be some of the most effective for characterizing and evaluating germplasm, confirming the genetic fidelity of in vitro preserved cultivars and species. In this regard, the aim of this work is to test several IRAP primers to identify genetic polymorphism and study the genetic fidelity of three rare and endemic flora species of the Western Caucasus during in vitro conservation. Approbation of 16 IRAP-primers on the investigated species was carried out for Eryngium maritimum L., Galanthus woronowii Losinsk. and Campanula sclerophylla Kolak. The results made it possible to select the most efficient of them for genetic fidelity analysis of micropropagated plants. Out of 16 IRAP primers 8 amplified PCR products in Eryngium maritimum. In Galanthus woronowii as well 8 of 16 IRAP primers resulted in the amplification with the number of DNA fragments ranging from 2 to 12. In Campanula sclerophylla 9 of 16 IRAP primers amplified 1 to 11 fragments, depending on the marker. The results of the genotyping of regenerants were compared with data on stock in situ plants, which were the source of explants for in vitro conservation. In total, 60 regenerants for each species of the natural flora of the Western Caucasus were involved in the study. The results obtained demonstrated no genetic changes of the regenerants in all the studied species. These results were confirmed using ISSR analysis of an extended sample set of microplants for each species. The results obtained can serve as evidence of a low probability of genetic disorders during in vitro propagation and conservation of the species Eryngium maritimum L., Galanthus woronowii Losinsk. and Campanula sclerophylla Kolak

Assessment of breeding lines of rice (Oryza sativa L.) carrying the Pi-40 gene for resistance to rice blast strains from Krasnodar region

Blast caused by fungal pathogen Magnaporthe oryzae B.C. Couch, 2002, is one of the most harmful diseases of rice (Oryza sativa L.), and so the development of resistant varieties is important in rice breeding. Evaluation of the efficiency of blast resistance genes against local populations of the blast pathogen is an important preliminary stage in the formation of the breeding program. In the course of the study, the level of resistance to blast pathogen was estimated for hybrid lines BC1F3 derived from local rice variety Khazar and containing the Pi-40 gene. Plants carrying the dominant allele of the Pi-40 gene in the homozygous state were used in the study. A synthetic population of Magnaporthe oryzae consists of six strains selected at different rice-growing regions in the Krasnodar territory and Rostov region in the season with epiphytotic development of blast disease was used for phytopathological evaluation. Resistance to neck and panicle blast was estimated. Phytopathological testing revealed that the disease had high prevalence in domestic rice varieties Diamant, Courage and Khazar (74.4 %, 57.9 % and 83.3 %, respectively). Khazar/IR 83260-2-10-5-2-1-B hybrid plants from population BC1F3 carrying the target gene showed a high level of resistance (7.6 % prevalence). They are valuable for breeding blast resistant varieties. These findings confirmed a wide spectrum of blast resistance of the Pi-40 gene and promise for use for development of rice cultivars resistant to the population of Magnaporthe oryzae common in the Krasnodar territory

Genetic diversity analysis of apricots from Dagestan using SSR markers

Background. This publication presents the results of a study into the genetic structure of apricot genotypes from Dagestan using the SSR genotyping technique. The importance of the study is seen in the still underexplored gene pool of Dagestani apricot at the genetic level. With this in view, an assessment of the Dagestani apricot genetic diversity, followed by an analysis of its genetic structure, is of theoretical and practical interest.Materials and methods. The study included 27 apricot genotypes of Dagestani origin: 9 advanced contemporary cultivars and hybrids, 15 seed selections and landraces, and 3 wild forms. Eight SSR markers were used for the genetic diversity analysis: H1-3, A1-91, H2-79, H1-26-2, H2-16, A1-17, RPPG1-032, and RPPG3-026.Results. The UPGMA and NJ dendrogram construction techniques revealed the genetic similarity among the Dagestani apricots, confirmed by a low level of cluster significance. The tendency towards setting apart the genotypes of hybrid origin (obtained from free pollination of introduced cultivars) from the locally selected cultivars was observed by comparing the results of Bayesian analysis and the K-means approach using the Structure and Statistica software. Such isolation is partial, being obviously affected by constant integration of new apricot genotypes into the local gene pool and its enrichment with new alleles at the genetic level.Conclusion. The contemporary assortment of apricots in Dagestan was formed on the basis of both the local autochthonous gene pool and Central Asian and European cultivars introduced into this area. The obtained data will enrich the knowledge about the genetic diversity of apricots in Dagestan and serve as the platform for further studies into the florigenetic links of the North Caucasus with other regions

Complex estimation of mitochondrial changes of immunocompetent blood cells in pregnant women with urgent and premature birth

Inflammation is among the factors promoting development of premature rupture of the membranes (PPROM). Upon the conditions of physiological immune imbalance in pregnancy, inflammation modifies its course and can even change the immune response. Appropriate indexes may be quantitative and functional. We used a marker of mitochondrial membrane potential (MPM, Ay) as an integral index of the functional state of immunocompetent blood cells (IBC) in 159 women who were examined at 8-14 weeks of gestation; they were observed up to 34-36 weeks. Of these cohort, 121 women were referred to a comparison group. The main group (n = 46) consisted of pregnant women with PPROM at the term of 28-33 weeks. The examination was carried out according to current medical standards, with informed consent, being approved by the Ethics committee at the Khabarovsk branch of Far Eastern Scientific Centre of Physiology and Pathology of Respiration — Research Institute of Maternity and Childhood Protection. Additionally, MPM and lymphocyte populations were determined by flow cytometry. The degree of disturbed energy supply in the IBC was based on the data of simultaneous determination of lymphocyte, granulocyte and monocyte numbers with reduced MPM values (application for invention No. 2020115963), thus revealing 3 degrees of energy deficiency: 1st degree, monovariant IBC composition with reduced MPM; 2nd degree, bivariant composition, 3rd degree, total changes. A relative and absolute decrease in CD3 (72% vs 78% and 1624 vs 1980), CD8 (28% vs 33% and 651 vs 851), an increase in CD19 (14% vs 9% and 304 vs 219) were revealed in pregnant women with PPROM. When assessing MPM values in the IBC populations, a decreased proportion of women without energy deficiency from the 1st to the 2nd trimester (from 41% to 30%), due to the 3rd degree of energy deficiency (from 17% to 26%) was detected. A shift of affected pools at the 2nd degree of energy deficiency in favor of lymphocytic-granulocytic association (from 7% to 25%) from lymphocytic-monocytic compartment (from 73% to 50%) was found. From the 2nd to 3rd trimester, we have detected redistribution of granulocyte pools at the 1st degree (0 to 8%) and from the lymphocytic-granulocytic association (25% and 5%) to monocytic-granulocytic (25% and 40%). In the group with PPROM, there was a decreased proportion of pregnant women without energy deficiency (13% and 27%), as well as with the 1st and 2nd degrees (17% vs 31% and 9% vs 17%), due to the 3rd degree of energy deficiency (61% and 26 %), relative to the comparison group. The IBC pools of in the main group were redistributed at the 1st degree in favor of granulocytes (25% and 8%), at the 2nd, in favor of the lymphocytic-monocytic association (100% and 55%) from the granulocytic-monocytic (0% and 40%). Such imbalance of bioenergetic processes in the IBC can be an important factor of pathologically ongoing inflammation. These changes could be caused by both higher incidence of infections in such patients and by alloimmune interactions between mother and fetus. However, they may also determine the pathological course of inflammation. Preterm birth, which is usually caused by PPROM, is a multifactorial pathological condition. However, independent on specific triggers, the changes in energy supply of IBC, at least, may serve as a significant biomarker of probability for this disorder

Identification of apple genes <i>Md-Exp7</i> and <i>Md-PG1</i> alleles in advanced selections resistant to scab

The creation of apple varieties with a high level of flesh firmness and long shelf life is one of the important goals in breeding. Among the genes controlling these traits, the role of the endogenous ethylene biosynthesis control gene, Md-ACS1, the expansin gene, Md-Exp7, and the polygalacturonase gene, Md-PG1, has been established. The use of DNA marker analysis to solve problems in breeding for fruit quality traits allows one not only to track several target genes simultaneously, but also to cull plants with undesirable alleles at the early stages of development. In order to select complex donors of breeding traits, molecular genetic identification of the genes that determine the quality traits of apple fruits Md-Exp7 and Md-PG1 was performed in 256 breeding selections carrying the scab resistance gene Rvi6 and valuable allelic variants of the Md-ACS-1 gene, which determines the endogenous synthesis of ethylene in fruits: 90 samples with the Md-ACS1 allele (2/2) and 166 samples with Md-ACS1 (1/2). As a result of the study, an allelic combination for the Md-Exp7 and Md-PG1 genes was established. Analysis of the parental cultivars (Renet Simirenko, Modi, Smeralda, Renoir, Fulzhion and Granny Smith) used to obtain hybrid selections revealed three alleles 198, 202, 214 bp according to the DNA marker of the Md-Exp7 gene. The SSR marker for the Md-PG1 gene amplified three alleles (289, 292, 298 bp) on the abovementioned cultivars. Within the 256 breeding selections samples that have the most priority for breeding alleles of the desired genes in combination with the Rvi6 gene and/or with selection-priority allelic variants of the Md-ACS-1 gene were identified. Of the most valuable for breeding, 46 accessions carrying the combination Md-Exp7 (202:202) + Md-ACS1 (2/2) were distinguished. Hybrids with alleles Md-PG1 (292:292) + Md-ACS1 (2/2) are also most valuable for use in breeding and as donors of selection-valuable alleles; 21 samples were identified. Accessions with a complex of breeding-valuable target alleles are valuable complex donors, as well as valuable breeding material for creating varieties with improved fruit quality characteristics and scab resistance

MICROSATELLITES-BASED EVALUATION OF THE PEAR CULTIVARS SELECTED FROM NIKITSKY BOTANICAL GARDENS GERMPLASM BY THEIR ECONOMICALLY VALUABLE CHARACTERISTICS

Mobilization and preservation of genetic sources of diversity of the cultivated pear varieties and their wild relatives is one of the main aspects of new cultivars breeding for modern intensive horticulture. The crucial matter during a new cultivar creation goes to the selection of parental pairs, which obtain a complex of positive features. The aim of this work is to study the Gene Fund collection of pear plantings from Nikitsky Botanical Gardens in accordance with the main economically important traits and to select the most valuable genotypes for using them in breeding programs as a starting material, as well as to conduct a DNA-fingerprinting and the analyses of genetic polymorphism of promising cultivars from the collection of pear with implementing of microsatellite analyses. As a result of long-term studies the following cultivars were selected in accordance with the complex of features promising for the breeding program: Gvardeiskaya Zimnyaya, Izuminka Kryma, Izumrudnaya, Kelmenchanka, Krymskaya Aromatnaya, Krymskaya Medovaya, Lazurnaya, Maria, Mriya, Nadezhda Stepi, Nezabudka, Novosadovskaya, Oreanda Kryma, Otechestvennaya, Tauschaya, Yakimovskaya. The samples of these cultivars were forwarded for genotyping. For the genetic polymorphism analyses of the studied cultivars, seven microsatellite DNA-markers – EMPc108, EMPc117, EMPc115, CH04e03 and CH01d09, CH01f07a, CH01d08 – grouped into 2 multiplex sets were used. The SSR-markers were significantly different according to their level of polymorphism – from 3 (CH04e03 marker) to 11 (EMPc115) alleles per a gene locus were revealed, the effective number of alleles varying from 1.37 to 4.65. Based on SSR-markers polymorphism analysis data, the rate of genetic similarity of the studied pear cultivars was estimated. This evaluation research helped estimate genetic relations inside the studied sample collection of genotypes. The SSR-fingerprints of the cultivars obtained will be used as a starting material for the creation of DNA-passports database of the “NBG – NSC” Gene Fund collection of pear cultivars

Ultrastructural changes in the chorioretinal complex of the rat after inducing form-deprivation axial myopia only, diabetic retinopathy only and diabetic retinopathy in the presence of myopia

Purpose: To determine the features of the microstructure of choreoretinal complex in rats with diabetes induced by streptozotocin in the presence of axial myopia. Material and Methods: Fifty-five Wistar rats (110 eyes; age, 2 weeks to 14 weeks) were used in experiments. Four groups were formed: group 1 (axial myopia only); group 2 (diabetes only); group 3 (both myopia and diabetes); and group 4 (controls; intact animals). High form-deprivation myopia was produced in two-week animals by surgically fusing the eyelids of both eyes and these animals were maintained under conditions of reduced illumination for two weeks to induce a more intense myopization of the globe. Eyelid sutures were removed on completion of these two weeks. Two weeks thereafter, type 2 diabetes mellitus was induced in rats with induced axial myopia and intact rats. A 50 mg/kg intraperitoneal streptozotocin injection for 5 days was used for this purpose. Elongated axial length and increased anterior chamber depth as measured by in vivo ultrasound were an objective criterion of the development of myopia in experimental animals. A glucose level of ≥ 4.5 mmol/L was a criterion of the development of diabetes. Two months after inducing diabetes, 14-week rats were sacrificed, and their eye tissue samples were processed by a routine method and assessed by electron microscopy. Ultrastructure of the choroid, RPE, and retinal photoreceptor cells were examined. Ultra-thin sections were cut, stained with lead citrate according to the procedure described by Reynolds, and observed with a PEM-100-01 Transmission Electron Microscope. Results: Our ultrastructural study found that myopization of the rat globe with elongation of the axial length somewhat reduced the severity of some ultrastructural changes in the choreoretinal complex in induced type 2 diabetes due to reduced choroidal swelling and dominance of compensatory processes with increased energy producing, protein synthesis and other functions in the endothelial vessels and choriocapillaries as well as RPE cells. Out findings seem to corroborate the concept that myopized eyes have capacity to somewhat buffer the development of severe diabetic retinopathy, likely due to some compensatory-and-restorative processes