Why a pregnant age can be the risk factor in chronic obstructive pyelonephritis?

The aim of the study was to identify possible mechanisms that could reproduce the recurrence of CVD in older men against the background of non-steroidal anti-inflammatory drugs and antibiotics, thereby justifying why age and sex may be risk factors for acute pyelonephritis in urolithiasis. Material and methods. The results of a study of 88 men with chronic obstructive pulmonary disease, including 45 patients over 65 years of age (mean age 74.0 ± 1.3 years) and 43 patients in the age range of 55-65 years (mean age of patients 61.0 ± 0, 8 year). In the phase of remission of CVD, 48 patients were examined and in the phase of relapse-40 patients. The study included patients who took non-steroidal anti-inflammatory drugs (NSAIDs) and antibiotics in a standard dose of at least 5-10 days before hospitalization. From the peripheral blood by centrifugation, plasma-enriched plasma was isolated. Platelet content in 1 μl was 200,000 ± 20,000. To stimulate platelets, adrenaline and ADP (Sigma, USA) were used at an effective concentration (EC50) of 5 μM, which caused platelet aggregation (ATC) in healthy individuals (10 donors) at the level of 50 ± 5%. The aggregation of Tc was evaluated on a Chrono log analyzer (USA). The formation of platelet-leukocyte aggregates (TPA) was modeled in vitro by incubation of stimulated platelets (epinephrine at a concentration of EC50) and intact leukocytes isolated from the peripheral blood of patients with CVD. The number of intact TL was assessed after the color of blood smears according to the Romanovsky-Giemsa method. Results. In the phase of remission of CVD on the background of the appointment of NSAIDs and antibiotics, in patients of the two age groups studied, it was not possible to detect differences in the response of leukocytes. Recurrence of CVD in patients age range 55-65 years was characterized by leukocytosis, neutrophilocytosis, increased ESR (

Band alignment and interlayer hybridisation in transition metal dichalcogenide/hexagonal boron nitride heterostructures

In van der Waals heterostructures, the relative alignment of bands between layers, and the resulting band hybridisation, are key factors in determining a range of electronic properties. This work examines these effects for heterostructures of transition metal dichalcogenides (TMDs) and hexagonal boron nitride (hBN), an ubiquitous combination given the role of hBN as an encapsulating material. By comparing results of density functional calculations with experimental angle-resolved photoemission spectroscopy (ARPES) results, we explore the hybridisation between the valence states of the TMD and hBN layers, and show that it introduces avoided crossings between the TMD and hBN bands, with umklapp processes opening `ghost' avoided crossings in individual bands. Comparison between DFT and ARPES spectra for the MoSe$_2$/hBN heterostructure shows that the valence bands of MoSe$_2$ and hBN are significantly further separated in energy in experiment as compared to DFT. We then show that a novel scissor operator can be applied to the hBN valence states in the DFT calculations, to correct the band alignment and enable quantitative comparison to ARPES, explaining avoided crossings and other features of band visibility in the ARPES spectra

Results from the Baksan Experiment on Sterile Transitions (BEST)

The Baksan Experiment on Sterile Transitions (BEST) was designed to investigate the deficit of electron neutrinos, $\nu_{e}$, observed in previous gallium-based radiochemical measurements with high-intensity neutrino sources, commonly referred to as the \textit{gallium anomaly}, which could be interpreted as evidence for oscillations between $\nu_e$ and sterile neutrino ($\nu_s$) states. A 3.414-MCi \nuc{51}{Cr} $\nu_e$ source was placed at the center of two nested Ga volumes and measurements were made of the production of \nuc{71}{Ge} through the charged current reaction, \nuc{71}{Ga}($\nu_e$,e$^-$)\nuc{71}{Ge}, at two average distances. The measured production rates for the inner and the outer targets respectively are (54.9^{+2.5}_{-2.4}(\mbox{stat})\pm1.4 (\mbox{syst})) and (55.6^{+2.7}_{-2.6}(\mbox{stat})\pm1.4 (\mbox{syst})) atoms of \nuc{71}{Ge}/d. The ratio ($R$) of the measured rate of \nuc{71}{Ge} production at each distance to the expected rate from the known cross section and experimental efficiencies are $R_{in}=0.79\pm0.05$ and $R_{out}= 0.77\pm0.05$. The ratio of the outer to the inner result is 0.97$\pm$0.07, which is consistent with unity within uncertainty. The rates at each distance were found to be similar, but 20-24\% lower than expected, thus reaffirming the anomaly. These results are consistent with $\nu_e \rightarrow \nu_s$ oscillations with a relatively large $\Delta m^2$ ($>$0.5 eV$^2$) and mixing sin$^2 2\theta$ ($\approx$0.4).Comment: Paper updated to final versio

Oxidation behavior of graphene-coated copper at intrinsic graphene defects of different origins

The development of ultrathin barrier films is vital to the advanced semiconductor industry. Graphene appears to hold promise as a protective coating; however, the polycrystalline and defective nature of engineered graphene hinders its practical applications. Here, we investigate the oxidation behavior of graphene-coated Cu foils at intrinsic graphene defects of different origins. Macro-scale information regarding the spatial distribution and oxidation resistance of various graphene defects is readily obtained using optical and electron microscopies after the hot-plate annealing. The controlled oxidation experiments reveal that the degree of structural deficiency is strongly dependent on the origins of the structural defects, the crystallographic orientations of the underlying Cu grains, the growth conditions of graphene, and the kinetics of the graphene growth. The obtained experimental and theoretical results show that oxygen radicals, decomposed from water molecules in ambient air, are effectively inverted at Stone-Wales defects into the graphene/Cu interface with the assistance of facilitators

Probing the Thermal Deoxygenation of Graphene Oxide using High Resolution In Situ X-Ray based Spectroscopies

Despite the recent developments in Graphene Oxide due to its importance as a host precursor of Graphene, the detailed electronic structure and its evolution during the thermal reduction remain largely unknown, hindering its potential applications. We show that a combination of high resolution in situ X-ray photoemission and X-ray absorption spectroscopies offer a powerful approach to monitor the deoxygenation process and comprehensively evaluate the electronic structure of Graphene Oxide thin films at different stages of the thermal reduction process. It is established that the edge plane carboxyl groups are highly unstable, whereas carbonyl groups are more difficult to remove. The results consistently support the formation of phenol groups through reaction of basal plane epoxide groups with adjacent hydroxyl groups at moderate degrees of thermal activation (~400 {\deg}C). The phenol groups are predominant over carbonyl groups and survive even at a temperature of 1000 {\deg}C. For the first time a drastic increase in the density of states (DOS) near the Fermi level at 600 {\deg}C is observed, suggesting a progressive restoration of aromatic structure in the thermally reduced graphene oxideComment: Pagona Papakonstantinou as Corresponding author, E-mail: [email protected]

The Complete Genome of Propionibacterium freudenreichii CIRM-BIA1T, a Hardy Actinobacterium with Food and Probiotic Applications

Background: Propionibacterium freudenreichii is essential as a ripening culture in Swiss-type cheeses and is also considered for its probiotic use [1]. This species exhibits slow growth, low nutritional requirements, and hardiness in many habitats. It belongs to the taxonomic group of dairy propionibacteria, in contrast to the cutaneous species P. acnes. The genome of the type strain, P. freudenreichii subsp. shermanii CIRM-BIA1 (CIP 103027T), was sequenced with an 11-fold coverage. Methodology/Principal Findings: The circular chromosome of 2.7 Mb of the CIRM-BIA1 strain has a GC-content of 67% and contains 22 different insertion sequences (3.5% of the genome in base pairs). Using a proteomic approach, 490 of the 2439 predicted proteins were confirmed. The annotation revealed the genetic basis for the hardiness of P. freudenreichii, as the bacterium possesses a complete enzymatic arsenal for de novo biosynthesis of aminoacids and vitamins (except panthotenate and biotin) as well as sequences involved in metabolism of various carbon sources, immunity against phages, duplicated chaperone genes and, interestingly, genes involved in the management of polyphosphate, glycogen and trehalose storage. The complete biosynthesis pathway for a bifidogenic compound is described, as well as a high number of surface proteins involved in interactions with the host and present in other probiotic bacteria. By comparative genomics, no pathogenicity factors found in P. acnes or in other pathogenic microbial species were identified in P. freudenreichii, which is consistent with the Generally Recognized As Safe and Qualified Presumption of Safety status of P. freudenreichii. Various pathways for formation of cheese flavor compounds were identified: the Wood-Werkman cycle for propionic acid formation, amino acid degradation pathways resulting in the formation of volatile branched chain fatty acids, and esterases involved in the formation of free fatty acids and esters. Conclusions/Significance: With the exception of its ability to degrade lactose, P. freudenreichii seems poorly adapted to dairy niches. This genome annotation opens up new prospects for the understanding of the P. freudenreichii probiotic activity

Evidence for Reductive Genome Evolution and Lateral Acquisition of Virulence Functions in Two Corynebacterium pseudotuberculosis Strains

Ruiz JC, D'Afonseca V, Silva A, et al. Evidence for Reductive Genome Evolution and Lateral Acquisition of Virulence Functions in Two Corynebacterium pseudotuberculosis Strains. PLoS ONE. 2011;6(4): e18551.Background: Corynebacterium pseudotuberculosis, a Gram-positive, facultative intracellular pathogen, is the etiologic agent of the disease known as caseous lymphadenitis (CL). CL mainly affects small ruminants, such as goats and sheep; it also causes infections in humans, though rarely. This species is distributed worldwide, but it has the most serious economic impact in Oceania, Africa and South America. Although C. pseudotuberculosis causes major health and productivity problems for livestock, little is known about the molecular basis of its pathogenicity. Methodology and Findings: We characterized two C. pseudotuberculosis genomes (Cp1002, isolated from goats; and CpC231, isolated from sheep). Analysis of the predicted genomes showed high similarity in genomic architecture, gene content and genetic order. When C. pseudotuberculosis was compared with other Corynebacterium species, it became evident that this pathogenic species has lost numerous genes, resulting in one of the smallest genomes in the genus. Other differences that could be part of the adaptation to pathogenicity include a lower GC content, of about 52%, and a reduced gene repertoire. The C. pseudotuberculosis genome also includes seven putative pathogenicity islands, which contain several classical virulence factors, including genes for fimbrial subunits, adhesion factors, iron uptake and secreted toxins. Additionally, all of the virulence factors in the islands have characteristics that indicate horizontal transfer. Conclusions: These particular genome characteristics of C. pseudotuberculosis, as well as its acquired virulence factors in pathogenicity islands, provide evidence of its lifestyle and of the pathogenicity pathways used by this pathogen in the infection process. All genomes cited in this study are available in the NCBI Genbank database (http://www.ncbi.nlm.nih.gov/genbank/) under accession numbers CP001809 and CP001829

Mineral–Polymer Composites Based on Hydroxyapatite and Polyvinylpyrrolidone for Medical Applications

© 2019, Pleiades Publishing, Ltd. Abstract: Hydroxyapatite (HA)–polyvinylpyrrolidone (PVP) nanocomposites with the HA/PVP ratio of 3.6–14.5 were synthesized by chemical precipitation from solutions of calcium nitrate and ammonium hydrogen phosphate in a PVP solution. The phase composition, size of coherent scattering regions, and size and morphology of HA particles were determined after heat treatment of the products of synthesis. The chemical interaction of the composite components was established by ESR spectroscopy on exposure to laser radiation at 355 nm