Virulence as a Side Effect of Interspecies Interaction in Vibrio Coral Pathogens

The increase in prevalence and severity of coral disease outbreaks produced by Vibrio pathogens, and related to global warming, has seriously impacted reef-building corals throughout the oceans. The coral Oculina patagonica has been used as a model system to study coral bleaching produced by Vibrio infection. Previous data demonstrated that when two coral pathogens (Vibrio coralliilyticus and Vibrio mediterranei) simultaneously infected the coral O. patagonica, their pathogenicity was greater than when each bacterium was infected separately. Here, to understand the mechanisms underlying this synergistic effect, transcriptomic analyses of monocultures and cocultures as well as experimental infection experiments were performed. Our results revealed that the interaction between the two vibrios under culture conditions overexpressed virulence factor genes (e.g., those encoding siderophores, the type VI secretion system, and toxins, among others). Moreover, under these conditions, vibrios were also more likely to form biofilms or become motile through induction of lateral flagella. All these changes that occur as a physiological response to the presence of a competing species could favor the colonization of the host when they are present in a mixed population. Additionally, during coral experimental infections, we showed that exposure of corals to molecules released during V. coralliilyticus and V. mediterranei coculture induced changes in the coral microbiome that favored damage to coral tissue and increased the production of lyso-platelet activating factor. Therefore, we propose that competition sensing, defined as the physiological response to detection of harm or to the presence of a competing Vibrio species, enhances the ability of Vibrio coral pathogens to invade their host and cause tissue necrosis.This research was supported in part by the EU-H2020 MetaFluidics project with grant agreement number 685474 (to J.A.) and NSF-PIRE grant number OISE1243541 (to F.R.). E.R.-P. was funded by the postdoctoral program Vali+d (GVA) (grant number APOSTD-2016-091). A.M.C.-R. and P.C.D. were supported by the National Sciences Foundation grant IOS-1656481

Mapeo de áreas regadas usando datos geoespaciales y teledetección en el municipio de Caudete de las Fuentes (Valencia)

Las políticas de control del uso agrícola de aguas subterráneas mediante la inspección de contadores se han demostrado caras y poco eficientes, mientras que en algunos estudios se ha obtenido resultados prometedores mediante la teledetección. El rápido progreso de las tecnologías de teledetección ha hecho posible su aplicación para la identificación de áreas regadas, y los nuevos sensores y técnicas de inteligencia artificial abren nuevas oportunidades a mejorar su eficacia y precisión. Nuestro trabajo propone una metodología de bajo coste y eficiente para detectar viña en riego a escala de parcela con el fin de mejorar la gestión colectiva de aguas subterráneas. A partir de información oficial se ha distinguido la superficie regada con técnicas de análisis de aprendizaje automático, empleando variables que condicionan el estado hídrico de la planta para la temporada de riego 2019. La metodología calcula la humedad del suelo con el método OPTRAM (OPtical TRApezoid Model) de análisis multitemporal de imágenes procedentes de plataformas satelitales. Estos datos son integrados en un SIG junto a información climática, topográfica e información propia del cultivo. Finalmente, en base a inventarios de verdad-terreno se aplica un clasificador de aprendizaje automático para estimar la superficie regada con agua procedente del acuífero. Los resultados obtenidos presentan una precisión general del 94.7%. Su evaluación aporta un error medio cuadrático de 0.163 y R-cuadrado de 0.874. La alta precisión y los bajos niveles de error obtenidos permiten validar la metodología empleada, que presenta potencial de mejora mediante una mayor alimentación del proceso de aprendizaje automático, que se aplicará en breve a otros cultivos leñosos

Immunotherapy moves to the early-stage setting in non-small cell lung cancer: emerging evidence and the role of biomarkers

Despite numerous advances in targeted therapy and immunotherapy in the last decade, lung cancer continues to present the highest mortality rate of all cancers. Targeted therapy based on specific genomic alterations, together with PD-1 and CTLA-4 axis blocking-based immunotherapy, have significantly improved survival in advanced non-small cell lung cancer (NSCLC) and both therapies are now well-established in this clinical setting. However, it is time for immunotherapy to be applied in patients with early-stage disease, which would be an important qualitative leap in the treatment of lung cancer patients with curative intent. Preliminary data from a multitude of studies are highly promising, but therapeutic decision-making should be guided by an understanding of the molecular features of the tumour and host. In the present review, we discuss the most recently published studies and ongoing clinical trials, controversies, future challenges and the role of biomarkers in the selection of best therapeutic options

Helios modulates the maturation of a CA1 neuronal subpopulation required for spatial memory formation

Currently, molecular, electrophysiological and structural studies delineate several neural subtypes in the hippocampus. However, the precise developmental mechanisms that lead to this diversity are still unknown. Here we show that alterations in a concrete hippocampal neuronal subpopulation during development specifically affect hippocampal-dependent spatial memory. We observed that the genetic deletion of the transcription factor Helios in mice, which is specifically expressed in developing hippocampal calbindin-positive CA1 pyramidal neurons (CB-CA1-PNs), induces adult alterations affecting spatial memory. In the same mice, CA3-CA1 synaptic plasticity and spine density and morphology in adult CB-CA1-PNs were severely compromised. RNAseq experiments in developing hippocampus identified an aberrant increase on the Visinin-like protein 1 (VSNL1) expression in the hippocampi devoid of Helios. This aberrant increase on VSNL1 levels was localized in the CB-CA1-PNs. Normalization of VSNL1 levels in CB-CA1-PNs devoid of Helios rescued their spine loss in vitro. Our study identifies a novel and specific developmental molecular pathway involved in the maturation and function of a CA1 pyramidal neuronal subtype

PRAXIS: el Pràcticum al Grau de Pedagogia: mapa, simulació i immersió. (continuació).

El projecte d’innovació docent que presentem és la continuïtat del que es va atorgar el curs 2012-2013. Consta de la continuïtat en la implementació i anàlisi de la proposta d’innovació fonamentalment metodològica del Pràcticum al grau de Pedagogia, en les tres assignatures obligatòries que es troben coordinades sota una lògica de progressiva immersió en una institució de pràctiques. Així, la innovació que presentem per al present curs 2013-2014 es troba fonamentalment en la darrera assignatura de Pràctiques Externes, i alhora, dotant de coherència global en coordinació amb les altres dues assignatures. Durant el projecte PID anterior es van engegar les pràctiques externes, amb una mirada transdisciplinar, opten, per una part, per la immersió de l’alumnat en una organització, entesa la immersió com l'exposició intensiva d’aquest, a una organització. És una perspectiva sistèmica que considera les organitzacions com a sistemes complexos i holística perquè condueix a la integració unitària i globalitzadora de tots els coneixements de la persona. Per altra part, opten per sessions de pràctica reflexiva entre l’alumnat i el tutor de la universitat que han de permetre la transferència de coneixement, la reflexió al voltant de la relació existent entre el saber teòric i el saber experiencial en la vida professional. El tutor de la universitat i l’alumnat es reuniran per analitzar la pràctica, i les experiències de l’escenari professional. Durant aquest curs passat es va pilotar en dos tutores el portafolis digital per a l’avaluació de competències. La continuïtat pel proper curs ha estat d’implementar aquesta eina avaluativa a bona part del tutors. L’avaluació de les pràctiques es farà mitjançant la realització d’un portafolis digital, i implicarà l’autoavaluació de l’alumnat, la del tutor de l’organització de pràctiques, així com la del tutor de la universitat. També ens proposem, la sistematització i millora de les sessions de pràctica reflexiva, quant a la proposta temàtica relacionada amb els blocs de contingut i articulades al voltant de les diverses competències, tot donat continuïtat a les millores realitzades en el projecte d’innovació docent anterior. L’equip de coordinació del pràcticum i l’equip docent de l’assignatura de Pràctiques Externes ens proposem sistematitzar aquestes experiències i avaluar-les tot analitzant el seu potencial en l’alumnat pel desenvolupament de les competències que es plantegen en el pràcticum. També considerem fonamental donar continuïtat a les coordinacions de tot el conjunt del pràcticum implicant les altres dues assignatures: professionalització i sortides laborals i pràctiques d’iniciació professional. Donada la necessitat i valoracions rebudes entre els tres equips docents, pensem que s’ha de seguir apostant per aquesta via. En aquest sentit, l’aplicació de l’avaluació de competències transversals mitjançant el portafolis digital que aquest curs ho pilotarem a molts més grups de Pràctiques Externes, tenim la intencionalitat que en un futur sigui un recurs que acompanyi l’estudiantat en les tres assignatures. Finalment, consolidar la missió de constituir-nos com agents de transferència de coneixement. Actualment amb la programació d’una sèrie d’activitats institucionals que representaran l’inici d’una nova visió del Pràcticum de la Facultat de Pedagogia de la Universitat de Barcelona ho hem iniciat, però cal avançar més en aquesta direcció. És així com adquireix el sentit principal de seguir contribuint al ple desenvolupament com a persones, ciutadans i professionals dels nostres estudiants i a la millora de la competitivitat de les nostres empreses en un nou país més cohesionat, just i sostenible dins d’un món global i orientat al coneixement i la revalorització dels valors humans més fonamentals

Cardiovascular events in Systemic Lupus Erythematosus: a nationwide study in Spain from the RELESSER Registry

This article estimates the frequency of cardiovascular (CV) events that occurred after diagnosis in a large Spanish cohort of patients with systemic lupus erythematosus (SLE) and investigates the main risk factors for atherosclerosis. RELESSER is a nationwide multicenter, hospital-based registry of SLE patients. This is a cross-sectional study. Demographic and clinical variables, the presence of traditional risk factors, and CV events were collected. A CV event was defined as a myocardial infarction, angina, stroke, and/or peripheral artery disease. Multiple logistic regression analysis was performed to investigate the possible risk factors for atherosclerosis. From 2011 to 2012, 3658 SLE patients were enrolled. Of these, 374 (10.9%) patients suffered at least a CV event. In 269 (7.4%) patients, the CV events occurred after SLE diagnosis (86.2% women, median [interquartile range] age 54.9 years [43.2-66.1], and SLE duration of 212.0 months [120.8-289.0]). Strokes (5.7%) were the most frequent CV event, followed by ischemic heart disease (3.8%) and peripheral artery disease (2.2%). Multivariate analysis identified age (odds ratio [95% confidence interval], 1.03 [1.02-1.04]), hypertension (1.71 [1.20-2.44]), smoking (1.48 [1.06-2.07]), diabetes (2.2 [1.32-3.74]), dyslipidemia (2.18 [1.54-3.09]), neurolupus (2.42 [1.56-3.75]), valvulopathy (2.44 [1.34-4.26]), serositis (1.54 [1.09-2.18]), antiphospholipid antibodies (1.57 [1.13-2.17]), low complement (1.81 [1.12-2.93]), and azathioprine (1.47 [1.04-2.07]) as risk factors for CV events. We have confirmed that SLE patients suffer a high prevalence of premature CV disease. Both traditional and nontraditional risk factors contribute to this higher prevalence. Although it needs to be verified with future studies, our study also shows-for the first time-an association between diabetes and CV events in SLE patients

Predictores de riesgo en una cohorte española con cardiolaminopatías. Registro REDLAMINA

[Abstract] Introduction and objectives. According to sudden cardiac death guidelines, an implantable cardioverter-defibrillator (ICD) should be considered in patients with LMNA-related dilated cardiomyopathy (DCM) and ≥ 2 risk factors: male sex, left ventricular ejection fraction (LVEF) < 45%, nonsustained ventricular tachycardia (NSVT), and nonmissense genetic variants. In this study we aimed to describe the clinical characteristics of carriers of LMNA genetic variants among individuals from a Spanish cardiac-laminopathies cohort (REDLAMINA registry) and to assess previously reported risk criteria. Methods. The relationship between risk factors and cardiovascular events was evaluated in a cohort of 140 carriers (age ≥ 16 years) of pathogenic LMNA variants (54 probands, 86 relatives). We considered: a) major arrhythmic events (MAE) if there was appropriate ICD discharge or sudden cardiac death; b) heart failure death if there was heart transplant or death due to heart failure. Results. We identified 11 novel and 21 previously reported LMNA-related DCM variants. LVEF < 45% (P = .001) and NSVT (P < .001) were related to MAE, but not sex or type of genetic variant. The only factor independently related to heart failure death was LVEF < 45% (P < .001). Conclusions. In the REDLAMINA registry cohort, the only predictors independently associated with MAE were NSVT and LVEF < 45%. Therefore, female carriers of missense variants with either NSVT or LVEF < 45% should not be considered a low-risk group. It is important to individualize risk stratification in carriers of LMNA missense variants, because not all have the same prognosis.[Resumen] Introducción y objetivos. Según las guías de muerte súbita, se debe considerar un desfibrilador automático implantable (DAI) para los pacientes con miocardiopatía dilatada debida a variantes en el gen de la lamina (LMNA) con al menos 2 factores: varones, fracción de eyección del ventrículo izquierdo (FEVI) < 45%, taquicardia ventricular no sostenida (TVNS) y variantes no missense. Nuestro objetivo es describir las características clínicas de una cohorte española de pacientes con cardiolaminopatías (registro REDLAMINA) y evaluar los criterios de riesgo vigentes. Métodos. Se evaluó la relación entre factores de riesgo y eventos cardiovasculares en una cohorte de 140 portadores de variantes en LMNA (54 probandos, 86 familiares, edad ≥ 16 años). Se consideró: a) evento arrítmico mayor (EAM) si hubo descarga apropiada del DAI o muerte súbita, y b) muerte por insuficiencia cardiaca, incluidos los trasplantes. Resultados. Se identificaron 11 variantes nuevas y 21 previamente publicadas. La FEVI < 45% (p = 0,001) y la TVNS (p < 0,001) se relacionaron con los EAM, pero no el sexo o el tipo de variante (missense frente a no missense). La FEVI < 45% (p < 0,001) fue el único factor relacionado con la muerte por insuficiencia cardiaca. Conclusiones. En el registro REDLAMINA, los únicos 2 predictores asociados con EAM fueron la TVNS y la FEVI < 45%. No se debería considerar grupo de bajo riesgo a las portadoras de variantes missense con TVNS o FEVI < 45%. Es importante individualizar la estratificación del riesgo de los portadores de variantes missense en LMNA, porque no todas tienen el mismo pronóstico.This study received a grant from the Proyecto de investigación de la Sección de Insuficiencia Cardiaca 2017 from the Spanish Society of Cardiology and grants from the Instituto de Salud Carlos III (ISCIII) [PI14/0967, PI15/01551, AC16/0014] and ERA-CVD Joint Transnational Call 2016 (Genprovic). Grants from the ISCIII and the Ministerio de Economía y Competitividad de España (Spanish Department of Economy and Competitiveness) are supported by the Plan Estatal de I+D+i 2013-2016: Fondo Europeo de Desarrollo Regional (FEDER) “Una forma de hacer Europa”

Association of a single nucleotide polymorphism combination pattern of the Klotho gene with non-cardiovascular death in patients with chronic kidney disease

Chronic kidney disease (CKD) is associated with an elevated risk of all-cause mortality, with cardiovascular death being extensively investigated. However, non-cardiovascular mortality represents the biggest percentage, showing an evident increase in recent years. Klotho is a gene highly expressed in the kidney, with a clear influence on lifespan. Low levels of Klotho have been linked to CKD progression and adverse outcomes. Single nucleotide polymorphisms (SNPs) of the Klotho gene have been associated with several diseases, but studies investigating the association of Klotho SNPs with noncardiovascular death in CKD populations are lacking. The main aim of this study was to assess whether 11 Klotho SNPs were associated with non-cardiovascular death in a subpopulation of the National Observatory of Atherosclerosis in Nephrology (NEFRONA) study (n ¼ 2185 CKD patients). After 48 months of follow-up, 62 cardiovascular deaths and 108 non-cardiovascular deaths were recorded. We identified a high non-cardiovascular death risk combination of SNPs corresponding to individuals carrying the most frequent allele (G) at rs562020, the rare allele (C) at rs2283368 and homozygotes for the rare allele (G) at rs2320762 (rs562020 GG/AG þ rs2283368 CC/CT þ rs2320762 GG). Among the patients with the three SNPs genotyped (n ¼ 1016), 75 (7.4%) showed this combination. Furthermore, 95 (9.3%) patients showed a low-risk combination carrying all the opposite genotypes (rs562020 AA þ rs2283368 TT þ rs2320762 GT/TT). All the other combinations [n ¼ 846 (83.3%)] were considered as normal risk. Using competing risk regression analysis, we confirmed that the proposed combinations are independently associated with a higher fhazard ratio [HR] 3.28 [confidence interval (CI) 1.51-7.12]g and lower [HR 6 × 10- (95% CI 3.3 × 10--1.1 × 10-)] risk of suffering a non-cardiovascular death in the CKD population of the NEFRONA cohort compared with patients with the normal-risk combination. Determination of three SNPs of the Klotho gene could help in the prediction of non-cardiovascular death in CKD

Association of candidate gene polymorphisms with chronic kidney disease : Results of a case-control analysis in the NEFRONA cohort

Chronic kidney disease (CKD) is a major risk factor for end-stage renal disease, cardiovascular disease and premature death. Despite classical clinical risk factors for CKD and some genetic risk factors have been identified, the residual risk observed in prediction models is still high. Therefore, new risk factors need to be identified in order to better predict the risk of CKD in the population. Here, we analyzed the genetic association of 79 SNPs of proteins associated with mineral metabolism disturbances with CKD in a cohort that includes 2,445 CKD cases and 559 controls. Genotyping was performed with matrix assisted laser desorption ionization-time of flight mass spectrometry. We used logistic regression models considering different genetic inheritance models to assess the association of the SNPs with the prevalence of CKD, adjusting for known risk factors. Eight SNPs (rs1126616, rs35068180, rs2238135, rs1800247, rs385564, rs4236, rs2248359, and rs1564858) were associated with CKD even after adjusting by sex, age and race. A model containing five of these SNPs (rs1126616, rs35068180, rs1800247, rs4236, and rs2248359), diabetes and hypertension showed better performance than models considering only clinical risk factors, significantly increasing the area under the curve of the model without polymorphisms. Furthermore, one of the SNPs (the rs2248359) showed an interaction with hypertension, being the risk genotype affecting only hypertensive patients. We conclude that 5 SNPs related to proteins implicated in mineral metabolism disturbances (Osteopontin, osteocalcin, matrix gla protein, matrix metalloprotease 3 and 24 hydroxylase) are associated to an increased risk of suffering CKD

Subsurface Geophysics and Geology (GEOFSU

[EN] The geophysics line at the IGME began in 1927 as a Geophysics Sectiondedicated to subsurface exploration. During all this time, it has been developed in order to support and give expert service in all IGME’s activities both as a geological service and public research institution, as well as a research and development work itself. On the other hand, in recent years the IGME has promoted a line of research aimed at the characterization and 3D modeling of geological structures and formations, the development of dedicated software and the evolution and sophistication of computer equipment. The new scenario of incorporation of the IGME to the CSIC as a national reference center in the field of Earth Sciences has allowed the establishment of the GEOFSUB Research Group (Subsurface Geophysics and Geology). It is constituted by 21 members who had been collaborating regularly of the IGME former scientific-technic areas Geophysics and remote sensing (Área de Geofísica y Teledetección) and Subsurface geology and 3D geological modelling (Área de Geología del Subsuelo y Modelización Geológica 3D). Our main differentiating element is our extensive knowledge of geophysical and geological techniques, which allows us to characterize the subsoil in an optimal waPeer reviewe