Caracterización simbiótica y filogenética de rizobios que nodulan la nueva especie Lupinus mariae-josephi

Una nueva especie de altramuz, Lupinus mariae-josephi, ha sido identificado recientemente en Valencia (Pascual, H.). Esta especie, a diferencia de las descritas en la Península ibérica y en el viejo mundo, no crece en suelos ácidos sino en suelos alcalinos y con alto contenido en calcio. El objetivo general de este proyecto es investigar si existen diferencias fenotípicas y genéticas entre los rizobios que nodulan Lupinus mariae-josephi y lupinos de suelos ácidos nativos de la Península Ibérica (Lupinus angustifolius, L.luteus y otras cuatro especies). En este proyecto se han aislado bacterias (rizobios) de nódulos de L. maria-josephi a partir de suelos básicos de Valencia (localidad de LLombai) y se está realizando su caracterización a nivel morfológico, nutricional, simbiótico y molecular. A nivel molecular se han comparado los genes “housekeeping” 16S rRNA, recA, atpD, gln2 y el simbiótico, nodC de diversas cepas que nodulan L. mariae-josephi y con cepas de otras especies de rizobios. Por otra parte, también se está evaluando la capacidad de L. mariae-josephi de ser nodulada por diferentes rizobios bajo condiciones bacteriológicamente controladas

Second-Generation Objects in the Universe: Radiative Cooling and Collapse of Halos with Virial Temperatures Above 10^4 Kelvin

The first generation of protogalaxies likely formed out of primordial gas via H2-cooling in cosmological minihalos with virial temperatures of a few 1000K. However, their abundance is likely to have been severely limited by feedback processes which suppressed H2 formation. The formation of the protogalaxies responsible for reionization and metal-enrichment of the intergalactic medium, then had to await the collapse of larger halos. Here we investigate the radiative cooling and collapse of gas in halos with virial temperatures Tvir > 10^4K. In these halos, efficient atomic line radiation allows rapid cooling of the gas to 8000 K; subsequently the gas can contract nearly isothermally at this temperature. Without an additional coolant, the gas would likely settle into a locally gravitationally stable disk; only disks with unusually low spin would be unstable. However, we find that the initial atomic line cooling leaves a large, out-of-equilibrium residual free electron fraction. This allows the molecular fraction to build up to a universal value of about x(H2) = 10^-3, almost independently of initial density and temperature. We show that this is a non--equilibrium freezeout value that can be understood in terms of timescale arguments. Furthermore, unlike in less massive halos, H2 formation is largely impervious to feedback from external UV fields, due to the high initial densities achieved by atomic cooling. The H2 molecules cool the gas further to about 100K, and allow the gas to fragment on scales of a few 100 Msun. We investigate the importance of various feedback effects such as H2-photodissociation from internal UV fields and radiation pressure due to Ly-alpha photon trapping, which are likely to regulate the efficiency of star formation.Comment: Revised version accepted by ApJ; some reorganization for clarit

Neutrino Halos in Clusters of Galaxies and their Weak Lensing Signature

We study whether non-linear gravitational effects of relic neutrinos on the development of clustering and large-scale structure may be observable by weak gravitational lensing. We compute the density profile of relic massive neutrinos in a spherical model of a cluster of galaxies, for several neutrino mass schemes and cluster masses. Relic neutrinos add a small perturbation to the mass profile, making it more extended in the outer parts. In principle, this non-linear neutrino perturbation is detectable in an all-sky weak lensing survey such as EUCLID by averaging the shear profile of a large fraction of the visible massive clusters in the universe, or from its signature in the general weak lensing power spectrum or its cross-spectrum with galaxies. However, correctly modeling the distribution of mass in baryons and cold dark matter and suppressing any systematic errors to the accuracy required for detecting this neutrino perturbation is severely challenging.Comment: 13 pages, 11 figures. Submitted to JCA

Paper-based chromatic toxicity bioassay by analysis of bacterial ferricyanide reduction

Water quality assessment requires a continuous and strict analysis of samples to guarantee compliance with established standards. Nowadays, the increasing number of pollutants and their synergistic effects lead to the development general toxicity bioassays capable to analyse water pollution as a whole. Current general toxicity methods, e.g. Microtox®, rely on long operation protocols, the use of complex and expensive instrumentation and sample pre-treatment, which should be transported to the laboratory for analysis. These requirements delay sample analysis and hence, the response to avoid an environmental catastrophe. In an attempt to solve it, a fast (15 min) and low-cost toxicity bioassay based on the chromatic changes associated to bacterial ferricyanide reduction is here presented. E. coli cells (used as model bacteria) were stably trapped on low-cost paper matrices (cellulose-based paper discs, PDs) and remained viable for long times (1 month at -20 °C). Apart from bacterial carrier, paper matrices also acted as a fluidic element, allowing fluid management without the need of external pumps. Bioassay evaluation was performed using copper as model toxic agent. Chromatic changes associated to bacterial ferricyanide reduction were determined by three different transduction methods, i.e. (i) optical reflectometry (as reference method), (ii) image analysis and (iii) visual inspection. In all cases, bioassay results (in terms of half maximal effective concentrations, EC50) were in agreement with already reported data, confirming the good performance of the bioassay. The validation of the bioassay was performed by analysis of real samples from natural sources, which were analysed and compared with a reference method (i.e. Microtox). Obtained results showed agreement for about 70% of toxic samples and 80% of non-toxic samples, which may validate the use of this simple and quick protocol in the determination of general toxicity. The minimum instrumentation requirements and the simplicity of the bioassay open the possibility of in-situ water toxicity assessment with a fast and low-cost protocolPostprint (author's final draft

Mononuclear Pd(II) and Pt(II) complexes with an α-N-heterocyclic thiosemicarbazone: Cytotoxicity, solution behaviour and interaction: Versus proven models from biological media

Two Pd(ii) and Pt(ii) complexes with two pyrrol-2-carbaldehyde N-p-chlorophenylthiosemicarbazone ligands are designed and characterized showing mononuclear structures. An important pharmacological property for both compounds is the high selectivity for tumor cells and a lack of activity in healthy cells. The Pd(ii) compound shows a higher antitumor activity and selectivity than the Pt(ii) compound. Both complexes present a variety of biological interactions: with DNA models (pBR322 and CT DNA), proteins (lysozyme and RNase) and other biological targets like proteosome. Our results show that the Pd(ii) complex is a more interesting candidate for potential anticancer therapies than the Pt(ii) complex, and we provide new insight into the design and synthesis of palladium compounds as potential antitumor agents.This work was supported by the following grants for the Spanish MINECO: SAF-2012-34424, CTQ2015-68779R and CTQ2015-70371-RED

Progressive Shifts in the Gut Microbiome Reflect Prediabetes and Diabetes Development in a Treatment-Naive Mexican Cohort.

Type 2 diabetes (T2D) is a global epidemic that affects more than 8% of the world\u27s population and is a leading cause of death in Mexico. Diet and lifestyle are known to contribute to the onset of T2D. However, the role of the gut microbiome in T2D progression remains uncertain. Associations between microbiome composition and diabetes are confounded by medication use, diet, and obesity. Here we present data on a treatment-naive cohort of 405 Mexican individuals across varying stages of T2D severity. Associations between gut bacteria and more than 200 clinical variables revealed a defined set of bacterial genera that were consistent biomarkers of T2D prevalence and risk. Specifically, gradual increases in blood glucose levels, beta cell dysfunction, and the accumulation of measured T2D risk factors were correlated with the relative abundances of four bacterial genera. In a cohort of 25 individuals, T2D treatment-predominantly metformin-reliably returned the microbiome to the normoglycemic community state. Deep clinical characterization allowed us to broadly control for confounding variables, indicating that these microbiome patterns were independent of common T2D comorbidities, like obesity or cardiovascular disease. Our work provides the first solid evidence for a direct link between the gut microbiome and T2D in a critically high-risk population. In particular, we show that increased T2D risk is reflected in gradual changes in the gut microbiome. Whether or not these T2D-associated changes in the gut contribute to the etiology of T2D or its comorbidities remains to be seen

Transcriptional silencing of the Dickkopfs-3 (Dkk-3) gene by CpG hypermethylation in acute lymphoblastic leukaemia

Dkk-3 is a newly characterised mortalisation-related gene and an antagonist of the Wnt oncogenic signalling pathway whose expression is decreased in a variety of cancer cell lines, suggesting that the Dkk-3 gene, located at chromosome 11p15.1, functions as a tumour suppressor gene. Although 11p15 is a ‘hot spot’ for methylation in acute lymphoblastic leukaemia (ALL), the role of Dkk-3 abnormalities has never been evaluated in this disease. We analysed CpG island methylation of the Dkk-3 promoter in six ALL cell lines and 183 ALL patients. We observed Dkk-3 hypermethylation in all cell lines and in cells from 33% (60/183) of ALL patients. Moreover, Dkk-3 methylation was associated with decreased Dkk-3 mRNA expression and this expression was restored after exposure to the demethylating agent 5-AzaC. Clinical features did not differ between hypermethylated and unmethylated patients. Estimated disease-free survival (DFS) and overall survival at 10 and 11 years, respectively, were 49.8 and 45.6% for normal patients and 10.5 and 15.1% for hypermethylated patients (P¼0.001 and 0.09). Multivariate analysis demonstrated that Dkk-3 methylation was an independent prognostic factor predicting DFS (P¼0.0009). Our data suggest that Dkk-3 methylation occurs at an early stage in ALL pathogenesis and probably influences the clinical behaviour of the disease