Novel broadside trisection filters employing nonresonating nodes

This work presents novel filter topologies implemented in microstrip technology. The topologies combine printed line resonators with non resonating nodes (NRN) to implement transmission zeros in a very flexible way. Depending on the number of resonators and NRN, the filtering response exhibits a single transmission zero either below or above the passband, or two transmission zeros, one at each side of the passband. Several examples are designed and validated, using the new proposed structures.The authors thank Ministerio de Educación y Ciencia of Spain, which has supported this work under Grant TEC2007- 67630-C03-02

An interpolated spatial images method for the analysis of multilayered shielded microwave circuits

In this paper, an efficient interpolation method is presented in order to compute the Green’s function associated to electrical sources, when they are placed inside cylindrical cavities. The interpolation scheme is formulated in the frame of the spatial images technique recently developed. The original idea was to calculate, for every location of a point electric source, the complex values of the electric dipole and charge images, placed outside the cavity, to impose the appropriate boundary conditions for the potentials. In order to considerably reduce the computational cost of the original technique, a simple interpolation method is proposed to obtain the complex values of the images for any source location. To do that, a rectangular spatial subdivision inside the cavity is proposed. Each new sub-region is controlled by means of the exact images values obtained when the source is placed at the four corners of the region. The key idea is to use a bilinear interpolation to obtain the images complex values when the source is located anywhere inside this sub-region. The interpolated images provide the Green’s functions of the new source positions fast, and with high accuracy. This new approach can be directly applied to analyze printed planar filters. Two examples with CPU time comparisons are provided, showing the high accuracy and computational gain achieved with the technique just derived.This work was partially supported by the Spanish Ministry of Education and Science under Grant FPU-AP2006-015 and with the Project TEC2007-67630-C03-02

Nuclear DNA fragmentation in boar spermatozoa: measurement methods and reproductive performance implications

The aim of this research was to compare the different techniques to measure sperm nuclear DNA fragmentation (sDF) and to check its relations to boar reproductive value, classical spermiogram parameters, and reproductive results of the doses in sows. Sperm chromatin stability assay (SCSA), terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay, and sperm chromatin dispersion test (SCD, Halomax®) results were compared, finding a statistically significant correlation only between SCSA and TUNEL results. The fertility direct boar effect (DBE) index, calculated from the whole productive life of the boar, was not correlated (p > 0.05) with sDF (measured by any technique). Total or progressive sperm motility was not correlated with sDF, while it found a positive correlation between TUNEL measure and abnormal acrosomes (%) and between SCD measure and total sperm morphological abnormalities (%). No significant correlations were obtained between fertility or prolificacy results and sDF results with the different techniques. However, in the case of total born and SCSA measure, the correlation was close to significance (r partial = -0.095; p = 0.066), appointing to a tendency; as SCSA increases, the number of total piglets born decreases. In conclusion, although the different techniques for the sDF seem not to target exactly the same DNA events and the relationship between their values and the reproductive results and the classical spermiogram results is still to be elucidated, the studied sDF techniques may offer extra information that could be useful for the management of AI studs. Copyright © 2022 Ausejo, Martínez, Mendoza, Bolarin, Tejedor and Falceto

Estrogen-related genes and postmenopausal osteoporosis risk

Background To date, more than 150 candidate genes related to osteoporosis have been described, but osteoporosis has increasingly been considered a polygenic disease modulated by environmental factors. It is thought that osteoporosis predisposition, pathology, and treatment response depend on the interaction between different genes or between genes and environmental factors. Objective The aim of this study was to evaluate the relationship between the presence of single nucleotide polymorphisms (SNPs) in the estrogen metabolic pathway and the development of osteoporosis and to determine whether this relationship is monogenic or whether interactions between genes exist. Materials and methods A multicentric study with 1980 postmenopausal Spanish women in fi ve Spanish communities was conducted. The women completed a specifi c questionnaire that inquired about risk factors for osteoporosis. Data on participants ’ bone mineral density were obtained with dual-energy X-ray densitometers, and genetic data were obtained from frozen peripheral blood. Results The digenic protection combinations indicated involvement of the wild-type genotype (WT) of the 3 UTR marker for the CYP19A1 gene, the IVS4 marker of the same gene, and the BMP15 and FSHR genes. Among patients who carried two or more of the genotypes considered ‘ risky ’ , the triple combination among markers of the ESR2 and NRIP1 genes with any of the two mutations of the analyzed markers of the BMP15 gene gave a mean T -score value of 2.32 0.91 ( p 0.02). Conclusion Variants of the new candidate genes ( NRIP and BMP15 ) can predispose patients to osteoporosis

Development and characterisation of highly antibiotic resistant Bartonella bacilliformis mutants

The objective was to develop and characterise in vitro Bartonella bacilliformis antibiotic resistant mutants. Three B. bacilliformis strains were plated 35 or 40 times with azithromycin, chloramphenicol, ciprofloxacin or rifampicin discs. Resistance-stability was assessed performing 5 serial passages without antibiotic pressure. MICs were determined with/without Phe-Arg-beta-Napthylamide and artesunate. Target alterations were screened in the 23S rRNA, rplD, rplV, gyrA, gyrB, parC, parE and rpoB genes. Chloramphenicol and ciprofloxacin resistance were the most difficult and easiest (>37.3 and 10.6 passages) to be selected, respectively. All mutants but one selected with chloramphenicol achieved high resistance levels. All rifampicin, one azithromycin and one ciprofloxacin mutants did not totally revert when cultured without antibiotic pressure. Azithromycin resistance was related to L4 substitutions Gln-66 --> Lys or Gly-70 --> Arg; L4 deletion Delta62-65 (Lys-Met-Tyr-Lys) or L22 insertion 83::Val-Ser-Glu-Ala-His-Val-Gly-Lys-Ser; in two chloramphenicol-resistant mutants the 23S rRNA mutation G2372A was detected. GyrA Ala-91 --> Val and Asp-95 --> Gly and GyrB Glu474 --> Lys were detected in ciprofloxacin-resistant mutants. RpoB substitutions Gln-527 --> Arg, His-540 --> Tyr and Ser-545 --> Phe plus Ser-588 --> Tyr were detected in rifampicin-resistant mutants. In 5 mutants the effect of efflux pumps on resistance was observed. Antibiotic resistance was mainly related to target mutations and overexpression of efflux pumps, which might underlie microbiological failures during treatments

Detection and analysis of tumour biomarkers to strengthen the diagnosis of acute and chronic leukaemias

AbstractMolecular markers in leukaemia are essential to diagnose, establish prognosis factors and determine the correct treatment of patients; therefore, it is imperative to include molecular biology studies, so that, combined with cytomorphology and immunophenotyping studies, they constitute the differential diagnosis of these neoplasias. It is extremely important to implement a panel of molecular markers that allows us to detect oncogenes derived from chromosomal translocations, genes derived from epigenetic alterations and drug-resistant genes.A panel of molecular markers that included 11 genes derived from chromosomal translocations BCR-ABL major and minor breakpoints, E2A-PBX1, MLL-AF4, TEL-AML1, PML-RARα, AML1-ETO was standardised; cancer testis antigens (CTA) derived from NY-ESO1 and MAGE-A3 epigenetic alterations and multi-drug-resistant genes ABCB1 and ABCG2. 30 patients diagnosed with leukaemia from Mexico's General Hospital (Hospital General de Mexico) were included. They suffered from acute lymphoblastic leukaemia (ALL) and acute myeloblastic leukaemia (AML); bone marrow mononuclear cells were used, from which RNA was extracted for the synthesis of cDNA and RT-PCR for each of the markers. In acute lymphoblastic leukaemia (ALL), BCR-ABL biomarkers expressed under 30% (3/10), E2A-PBX1 10% (1/10), ABC-B1 80% (8/10), and ABC-G2 60% (6/10). Patients with acute myeloblastic leukaemia (AML) expressed 30% PML-RARα (3/10), 40% ABC-B1 (4/10), and 10% ABC-G2 (1/10). Lastly, in patients with chronic myeloid leukaemia (CML), BCR-ABL was over 100% (10/10), ABC-B1 20% (2/10), and ABC-G2 50% (5/10). The presence of transcripts from chimeric genes minor BCR-ABL and E2A-PBX1 in ALL; PML-RARα in AML; and major BCR-ABL in CML, confirms the importance that the panel of molecular markers has in strengthening the diagnosis and prognosis of these conditions

Aprovechamiento del bagazo de piña para obtener celulosa y bioetanol

Actualmente se están buscando nuevas alternativas energéticas a partir de biomasa, recursos renovables y desechos agroindustriales, para desarrollar nuevas tecnologías y procesos en la obtención de biocombustibles. El objetivo fue obtener celulosa y bio-etanol del bagazo de piña (desecho agrícola). El aprovechamiento de este bagazo evitará el consumo de cultivos destinados a la alimentación, evitando el uso excesivo de tierras y el empleo de residuos orgánicos agroindustriales. Además, el producto obtenido tiene un valor agregado y podría convertirse en un beneficio para los productores de piña. La finalidad fue estudiar un proceso para extraer celulosa del bagazo de piña, y mediante hidrólisis ácida de celulosa y bagazo se obtuvo glucosa. Esta glucosa se neutralizó a pH de 5 y se realizó la fermentación en un medio anaeróbico, utilizando el microorganismo Saccharomyces cerevisiae, variando tiempos de fermentación (36, 40, 48 y 72 h) y manteniendo la temperatura a 30ºC. La celulosa obtenida presentó una conversión del 60% y mediante FTIR se corroboró que la celulosa fue tipo II. Se obtuvo bio-etanol mediante destilación, presentando un rendimiento del 35% con bagazo y del 57% con celulosa con un tiempo de fermentación de 48 y 72 h, respectivamente