Verticillium wilt of olive in the Guadalquivir Valley (southern Spain): relations with some agronomical factors and spread of Verticillium dahliae

Verticillium wilt of olive (VWO) is now the most destructive olive disease in the Guadalquivir valley in Andalucía (southern Spain). Disease surveys, conducted to assess the association of agronomical and geographical factors with the current spread of the disease, have shown that VWO is widespread in the valley, with a mean disease incidence (DI) in infested plots reaching 20.4%  (9000 inspected trees), but with significant differences among the provinces surveyed (25.7, 23.7 and 12%, for Jaén, Córdoba and Seville, respectively). The DI was significantly higher in irrigated (20.7%) than in dry-farming (18.3%) orchards, and also higher in non-tilled orchards (25.6%) than in regularly-tilled orchards (16.3%). The DI was likewise significantly lower for tree densities above 200 trees ha-1; and it was higher (21.5%) when the orchards were located near areas where other V. dahliae host plants were cultivated, than if the orchards were surrounded by non-host plants (11.9%). Lastly, the DI was significantly higher in plots where the tree were less than 25 year old and in plantations close to the Guadalquivir River (less than 10 km). ‘Picual’ was the cultivar most often affected with the disease, reaching a DI of 41.9% in orchards where this cultivar was grown. Highly virulent defoliating (D) isolates in the plantation surveyed were significantly more common (67.7%) than non-defoliating (ND) isolates (32.3%). These factors could explain the substantial increase in incidence and severity of VWO seen in the valley during the last decade

Parallelisms between sea surface temperature changes in the western tropical Atlantic (Guiana Basin) and high latitude climate signals over the last 140 000 years

Sea surface temperatures (SST) in the Guiana Basin over the last 140 ka were obtained by measuring the C37 alkenone unsaturation index Uk'37 in the sediment core MD03-2616 (7° N, 53° W). The resulting data set is unique in the western tropical Atlantic region for this period. The SSTs range from 25.1 to 28.9 °C, i.e. glacial-interglacial amplitude of 3.8 °C, which is in the range of change of other tropical areas. During the last two interglacial stages (marine isotope stages; MIS1 and MIS5e) and warm long interstadials (MIS5d-a), a rapid transmission of climate variability from Arctic-tropical latitudes is recorded. During these periods, the MD03-2616 SSTs show a conspicuous parallelism with temperature changes observed in Greenland and SST records of North Atlantic mid-latitude cores (Iberian Margin 38° N, Martrat et al., 2007). The last deglaciation in the Guiana Basin is particularly revealing. MIS2 stands out as the coldest period of the interval analysed. The events recorded in Guiana parallel northern latitude events such as the Bølling-Allerød warming and the Younger Dryas cooling which ensued. These oscillations were previously documented in the δ18O of the Sajama tropical ice core (Bolivia) and are present in Guiana, with rates of ca. 6 °C ka-1 and changes of over 2 °C. During the glacial interval, significant abrupt variability is observed, e.g. oscillations of 0.5-1.2 °C during MIS3, which is about 30 % of the maximum glacial-interglacial SST change. In the MD03-2616 record, it is possible to unambiguously identify either the Dansgaard-Oeschger oscillations described in northern latitudes or the SST drops associated with the Heinrich events characteristic of North Atlantic records. Although these events form the background of the climate variability observed, what truly shapes SSTs in the Guiana Basin is a long-term tropical response to precessional changes, which is modulated in the opposite way to Northern Hemisphere variability. This lack of synchrony is consistent with other tropical records in locations to the north or south of the Guiana Basin and evidences an Arctic-tropical decoupling when a substantial reduction in the Atlantic meridional overturning circulation (AMOC) takes place. © Author(s) 2015. CC Attribution 3.0 License.Peer reviewe

Omentin: a biomarker of cardiovascular risk in individuals with axial spondyloarthritis

ABSTRACT: Cardiovascular (CV) disease is the main cause of mortality in axial spondyloarthritis (axSpA). CV risk is enhanced by dysregulation of adipokines. Low omentin levels were associated with metabolic dysfunction and CV disease in conditions different from axSpA. Accordingly, we evaluated the genetic and functional implication of omentin in CV risk and subclinical atherosclerosis in a cohort of 385 axSpA patients. Subclinical atherosclerosis was evaluated by carotid ultrasound. Omentin rs12409609, in linkage disequilibrium with a polymorphism associated with CV risk, was genotyped in 385 patients and 84 controls. Serum omentin levels were also determined. omentin mRNA expression was assessed in a subgroup of individuals. Serum and mRNA omentin levels were lower in axSpA compared to controls. Low serum omentin levels were related to male sex, obesity, inflammatory bowel disease (IBD) and high atherogenic index. rs12409609 minor allele was associated with low omentin mRNA expression in axSpA. No association was observed with subclinical atherosclerosis at the genetic or functional level. In conclusion, in our study low omentin serum levels were associated with CV risk factors in axSpA. Furthermore, rs12409609 minor allele may be downregulating the expression of omentin. These data support a role of omentin as a CV risk biomarker in axSpA.We wish to thank all the patients and controls that participated in this study. This work was supported by funds of a NEXT-VAL grant (NVAL17/10) (Instituto de Investigación Sanitaria IDIVAL) awarded to FG. SR-M is supported by funds of the RETICS Program (RD16/0012/0009) from the ‘Instituto de Salud Carlos III´ (ISCIII), co-funded by the European Regional Development Fund (ERDF). VP-C is supported by a pre-doctoral grant from IDIVAL (PREVAL 18/01). VM is supported by funds of a Miguel Servet type I programme (grant CP16/00033) (ISCIII, co-funded by the European Social Fund (ESF)). LL-G is supported by funds of PI18/00042 (ISCIII, co-funded by ERDF). RL-M is a recipient of a Miguel Servet type I programme fellowship from the ISCIII, co-funded by the ESF (grant CP16/00033)

Massive deworming, nutritional status and learning capacity in school children in a rural community

one hundred and ninety eight children of a rural village school were studied for parasitological variables, nutritional status (anthropometric variables and blood parameters) and assessment of their learning capacity. the study was designed as a baseline study and included both massive anthelminthic treatment and follow-up of the reinfection process. the initial prevalence of infection by soil helminths was: ascaris lumbricoides 36,4 %, trichuris trichiura 34.8%, hookworm 18,2 % and strongyloides stercoralis 4,5 %. 53,1 % of children were under risk of malnutrition and the values of hematocrit and hemoglobin concentration were below normal in 83 % and 55 % respectively. an important deficit in all the learning capacity tests was observed. some relationship was found between these results and infection by parasites.Se estudiaron 198 niños de 5 a 15 años de una comunidad escolar rural en variables parasitológicas, estado nutricional (antropometría y parámetros en sangre) y evaluación de la capacidad de aprendizaje. El estudio se diseño como línea de base e incluyó tratamiento masivo y seguimiento al proceso de reinfección. La prevalencia inicial de helmintos fue: Ascaris lumbricoides 36,4 %, Trichuris trichiura 34,8 %, Uncinaria 18,2 % y Strongyloides stercoralis 4,5 %. El 53,1 % de los niños estaban en riesgo de desnutrición y los valores del hematocrito y de la hemoglobina estaban por debajo de lo normal en el 83 y 55 % respectivamente. Así mismo, se detectó un importante déficit en todas las pruebas de capacidad de aprendizaje. Se encontraron algunas relaciones entre los resultados anteriores y la presencia de parásitos

Tamizaje de cardiopatías congénitas

Congenital heart diseases are structural anomalies of the heart characterized by being the most frequent malformations in addition to being an important cause of infant and prenatal mortality. There is solid evidence that has shown pulse oximetry to be an effective tool for early recognition in critical cases after 24 hours of birth and before 48 hours; increasing the possibility of a clinical evolution to improve the patient, this test has been recognized as "neonatal screening for congenital heart disease".Las cardiopatías congénitas son anomalías estructurales del corazón caracterizadas por ser las malformaciones más frecuente además de constituir una importante causa de mortalidad infantil y prenatal.  Existen evidencias solidas que han demostrado la realización de pulsioximetria como una herramienta efectiva para su reconocimiento temprano en casos críticos después de 24 horas de nacido y antes de 48 horas; incrementando la posibilidad de una evolución clínica a mejoría del paciente, dicha prueba ha sido reconocida como “tamizaje neonatal de cardiopatías congénitas”

Informe de la salud visual y ocular de los países que conforman la Red Epidemiológica Iberoamericana para la Salud Visual y Ocular (REISVO), 2009 y 2010

Según las estimaciones más recientes de la Organización Mundial de la Salud (OMS), cerca de 314 millones de personas en el mundo presentan discapacidad visual, debido a enfermedades oculares o a errores de refracción no corregidos. De estas personas, 45 millones son ciegos y el 90 % vive en países con ingresos bajos. Las principales causas de ceguera son catarata (39 %), errores refractivos no corregidos (18 %), glaucoma (10 %), degeneración macular asociada a la edad (7 %), opacidad corneal (4 %), retinopatía diabética (4 %), tracoma (3 %), afecciones oculares infantiles (3 %) y oncocercosis (0,7 %)

Vaspin in atherosclerotic disease and cardiovascular risk in axial spondyloarthritis: a genetic and serological study

Background: Vaspin is a novel anti-inflammatory adipokine associated with cardiovascular (CV) disease and inflammation in chronic inflammatory conditions different from axial spondyloarthritis (axSpA). Given the high incidence of CV disease (mainly due to accelerated atherosclerosis) exhibited by axSpA patients, we wondered if vaspin could also be a key molecule in this process. However, data on the role of vaspin regarding atherosclerotic disease in the context of axSpA is scarce. For this reason, we aimed to evaluate the implication of vaspin, at the genetic and serological level, in subclinical atherosclerosis and CV risk in axSpA. Methods: This study included 510 patients diagnosed with axSpA. Carotid ultrasound (US) was performed to evaluate the presence of subclinical atherosclerosis. Three vaspin gene variants (rs2236242, rs7159023, and rs35262691) were genotyped by TaqMan probes. Serum vaspin levels were assessed by enzyme-linked immunosorbent assay. Statistical analysis was performed using STATA® v.11.1. Results: Serum vaspin levels were significantly higher in female patients than in males and also in obese patients when compared to those with normal weight (p < 0.05). At the genetic level, we disclosed that the minor allele of rs2236242 (A) was associated with lower serum vaspin levels in axSpA, while the rs7159023 minor allele (A) was linked to higher serum levels (p < 0.05). When the three polymorphisms assessed were combined conforming haplotypes, we disclosed that the TGC haplotype related to high serum levels of vaspin (p = 0.01). However, no statistically significant association was observed between vaspin and markers of subclinical atherosclerosis, both at the genetic and serological level. Conclusions: Our results revealed that vaspin is linked to CV risk factors that may influence on the atherosclerotic process in axSpA. Additionally, we disclosed that serum vaspin concentration is genetically modulated in a large cohort of patients with axSpA.This work was partially supported by funds of a NEXT-VAL grant (NVAL17/10) (Instituto de Investigación Sanitaria IDIVAL) awarded to FG. RL-M is a recipient of a Miguel Servet type I programme fellowship (grant CP16/00033) from the “Instituto de Salud Carlos III” (ISCIII) and co-funded by the European Social Fund, ESF). SR-M is supported by funds of the RETICS Program (RD16/0012/0009) from ISCIII and co-funded by the European Regional Development Fund. VP-C is supported by a pre-doctoral grant from IDIVAL (PREVAL18/01). LL-G is supported by funds of a Miguel Servet type I programme fellowship from ISCIII (grant CP16/00033, co-funded by the ESF). OG is beneficiary of a grant funded by Xunta de Galicia, Consellería de Educación, Universidade e Formación Profesional and Consellería de Economía, Emprego e Industria (GAIN), GPC IN607B2019/10

Informe de la salud visual y ocular de los países que conforman la Red Epidemiológica Iberoamericana para la Salud Visual y Ocular (REISVO), 2009 y 2010

A pesar de que se han hecho importantes progresos en el cuidado de la salud ocular, la prevalencia de la ceguera evitable sigue siendo inaceptablemente alta en muchos países y comunidades (OMS, 2009). La salud visual es un tema de la agenda política en algunos países; sin embargo, aún no se cuenta con un sistema de información que permita identificar la situación de morbilidad en salud visual en Iberoamérica, para poder priorizar y planificar la orientación de los servicios de atención en optometría y oftalmología. Para que existan planes de salud, deben establecerse líneas de base a través de un diagnóstico epidemiológico y de necesidades de la población; por esta razón, REISVO ha desarrollado, en esta primera fase, una descripción retrospectiva de la frecuencia y distribución de las alteraciones visuales y oculares, para lo cual ha tenido en cuenta que los errores refractivos son la segunda causa de ceguera prevenible y la primera de las deficiencias visuales.Facultad de Ciencias Exacta

Estudio limnológico de varios sistemas lóticos y lénticos aledaños a la reserva Yotoco Valle del Cauca, Colombia

Este trabajo es un estudio limnológico básico de cinco cuerpos de agua de la cuenca alta del río Cauca. Dos de ellos fueron ambientes lénticos (la laguna de Sonso y el embalse Calima) y tres fueron lóticos (el río Calima y las quebradas La Berreadera y El Boleo). Se ubican en los municipios de Buga, Yotoco y Calima en el Valle del Cauca, Colombia. Los muestreos se hicieron los días 15 y 16 de octubre de 2016. Como principal objetivo se buscó caracterizar cada uno de los lugares de muestreo en cuanto a sus variables morfológicas, fisicoquímicas y biológicas, por medio de la evaluación de distintas variables, tanto in situ como en laboratorio. Todo lo anterior permitió determinar las características generales y algunas específicas de las condiciones actuales de cada ecosistema acuático evaluado. Tales particularidades podrían ser relevantes en estudios de línea base, impacto ambiental, bioindicación y concientización ambiental

Consenso colombiano para el manejo de pacientes con Hipofosfatasia

La hipofosfatasia (HPP) es una enfermedad metabólica, de tipo hereditario, causada por mutaciones en el gen ALPL. Teniendo en cuenta los retos del manejo adecuado de los pacientes con HPP, se realizó un consenso interdisciplinario de expertos (endocrocrinólogos pediatras, nefrólogos pediatras, ortopedistas infantiles y genetistas clínicos) con el fin de proponer recomendaciones de utilidad clínica para el diagnóstico, tratamiento y seguimiento de los pacientes colombianos con HPP. Estas sugerencias se realizan en el contexto de los diferentes tipos de presentaciones y las edades de los pacientes.Q41-7Hypophosphatasia (HPP) is a hereditary metabolic disease caused by mutations in the ALPL gene. Taking into account the challenges found in the adequate management of patients with HPP, an interdisciplinary consensus of experts (pediatric endocrinologists, pediatric nephrologists, pediatric orthopedists and clinical geneticists) was carried out, in order to propose recommendations of clinical utility for the diagnosis, treatment and follow-up of Colombian patients with HPP. These suggestions are made in the context of the different types of presentations and the ages of the patients