Enfermedades del frijol

Diseases are one of the limiting factors to bean production in L.A. The prevalency and severity of the disease depends on the quantity of inoculum existing in the region, environmental conditions and the quality of the seed used. Data are given on geographic distribution, favorable climatic conditions for development, symptomatology, vectors, type of damage caused and control measures, including var. resistant to (1) fungal diseases, the most numerous and causing the most damage: rust, anthracnose, angular leaf spot, root rot, web blight, gray spot, powdery mildew; (2) virus diseases, some of economic importance transmitted by aphids (BCMV, BYMV); transmitted by whiteflies (BGMV, bean chlorotic mottle, euphorbia mosaic); transmitted by chrysomelids (BRMV, pod mottle, BSMV, yellow mottle); (3) bacterial diseases are few but can be a serious limitation to the crop: common and fuscous blights, halo blight; and (4) nematodes: Meloidogyne sp., Trichodorus spp., Pratylenchus spp., Heterodera spp. (CIAT

Difusão de fosfina no interior de cupinzeiros de Cornitermes cumulans (Kollar) (Isoptera: Termitidae).

Aspectos relacionados à difusão da fosfina dentro de cupinzeiros de C. cumulans foram estudados, em condições naturais, em Piracicaba-SP. Concluiu-se que as paredes externas dos montículos, construídas com partículas de latossol e cimentadas com saliva dos insetos, não eram totalmente impermeáveis à fumaça da queima da celulose existente em seu interior que fluía, com relativa facilidade, para o ambiente externo, sem o auxílio de qualquer pressão artificial interna. Medições periódicas das concentrações de fosfina em diferentes localizações internas nos montículos, através de "Multi Gás Detector DRAGER", indicaram uma perda total do gás, num intervalo de seis a trinta horas desde a introdução de quantidades variáveis de comprimidos de fosfina nos termiteiros. A mortalidade dos insetos nunca foi total, mesmo quando se aplicaram oito drágeas por montículo, encontrando-se sempre nas regiões mais baixas da câmara de celulose, pelo menos cerca de 20% de insetos vivos e em condições de reconstruírem o ninho. Mortalidade de 100% foram obtidas acima da linha do solo e para dosagens maiores que quatro comprimidos por ninho, independentemente do local de sua deposição no interior dos montículos

Supplementary report to the final report of the coral reef expert group: S6. Novel technologies in coral reef monitoring

[Extract] This report summarises a review of current technological advances applicable to coral reef monitoring, with a focus on the Great Barrier Reef Marine Park (the Marine Park). The potential of novel technologies to support coral reef monitoring within the Reef 2050 Integrated Monitoring and Reporting Program (RIMReP) framework was evaluated based on their performance, operational maturity and compatibility with traditional methods. Given the complexity of this evaluation, this exercise was systematically structured to address the capabilities of technologies in terms of spatial scales and ecological indicators, using a ranking system to classify expert recommendations.An accessible copy of this report is not yet available from this repository, please contact [email protected] for more information

Paleoenvironmental Changes at ODP Site 702 (South Atlantic): Anatomy of the Middle Eocene Climatic Optimum

The Middle Eocene Climatic Optimum (MECO) was an unusual global warming event that interrupted the long-term Eocene cooling trend ca. 40 Ma. Here we present new high-resolution bulk and benthic isotope records from South Atlantic ODP Site 702 to characterize the MECO at a high latitude setting. The MECO event, including early and peak warming as well as recovery to background levels, had an estimated ~300 Kyr duration (~40.51 to ~40.21 Ma). Cross-plots (delta O-18 vs. delta C-13) suggest that the mechanisms driving coupled changes in O and C isotope values across the MECO were weaker or absent before the event. The paleoecological response has been evaluated by quantitative analysis of calcareous nannofossils and benthic foraminifera assemblages. We document a shift in the biogeographical distribution of warm and temperate calcareous nannoplankton taxa, which migrated toward higher latitudes due to increased temperatures during the MECO. Conversely, changes in the organic matter flux to the seafloor appear to have controlled benthic foraminifera dynamics at Site 702. Benthic phytodetritus exploiting taxa increased in abundance coinciding with a positive delta C-13 excursion, ~150 Kyr before the start of the delta O-18 negative excursion that marks the start of MECO warming. Our data suggest that paleoecological disturbance in the deep sea predates MECO delta O-18 excursion and that it was driven by changes in the type and/or amount of organic matter reaching the seafloor rather than by increased temperature

Immunodominant proteins α-1 giardin and β-giardin are expressed in both assemblages A and B of Giardia lamblia

<p>Abstract</p> <p>Background</p> <p>To date, eight assemblages of <it>Giardia lamblia </it>have been described, but only assemblages A and B are known to infect humans. Despite the fact that the genomic, biological, and clinical differences found between these two assemblages has raised the possibility that they may be considered different species, there is relatively limited information on their phenotypic differences. In the present study, we developed monoclonal antibodies against alpha-1 and beta giardin, two immunodominant proteins produced during <it>G. lamblia </it>infection, and studied their expression and localization in WB (assemblage A) and GS trophozoites (assemblage B).</p> <p>Results</p> <p>The polyclonal antibodies generated against WB trophozoites, particularly those recognizing intracellular proteins as well as the proteins present at the plasma membrane (variable-specific surface proteins), showed cross-reactivity with intracellular proteins in GS trophozoites. The use of monoclonal antibodies against beta giardin indicated ventral disc localization, particularly at the periphery in WB trophozoites. Interestingly, although beta giardin was also restricted to the ventral disc in GS trophozoites, the pattern of localization clearly differed in this assemblage. On the other hand, monoclonal antibodies against alpha-1 giardin showed plasma membrane localization in both assemblages with the bare area of GS trophozoites also being distinguished. Moreover, the same localization at the plasma membrane was observed in Portland-1 (Assemblage A) and in P15 (Assemblage E) trophozoites.</p> <p>Conclusions</p> <p>We found differences in localization of the beta giardin protein between assemblages A and B, but the same pattern of localization of alpha-1 giardin in strains from Assemblages A, B and E. These findings reinforce the need for more studies based on phenotypic characteristics in order to disclose how far one assemblage is from the other.</p

Gestational hypothyroxinemia affects its offspring with a reduced suppressive capacity impairing the outcome of the experimental autoimmune encephalomyelitis

Indexación: Scopus.Hypothyroxinemia (Hpx) is a thyroid hormone deficiency (THD) condition highly frequent during pregnancy, which although asymptomatic for the mother, it can impair the cognitive function of the offspring. Previous studies have shown that maternal hypothyroidism increases the severity of experimental autoimmune encephalomyelitis (EAE), an autoimmune disease model for multiple sclerosis (MS). Here, we analyzed the immune response after EAE induction in the adult offspring gestated in Hpx. Mice gestated in Hpx showed an early appearance of EAE symptoms and the increase of all parameters of the disease such as: the pathological score, spinal cord demyelination, and immune cell infiltration in comparison to the adult offspring gestated in euthyroidism. Isolated CD4+CD25+ T cells from spleen of the offspring gestated in Hpx that suffer EAE showed reduced capacity to suppress proliferation of effector T cells (TEff) after being stimulated with anti-CD3 and anti-CD28 antibodies. Moreover, adoptive transfer experiments of CD4+CD25+ T cells from the offspring gestated in Hpx suffering EAE to mice that were induced with EAE showed that the receptor mice suffer more intense EAE pathological score. Even though, no significant differences were detected in the frequency of Treg cells and IL-10 content in the blood, spleen, and brain between mice gestated in Hpx or euthyroidism, T cells CD4+CD25+ from spleen have reduced capacity to differentiate in vitro to Treg and to produce IL-10. Thus, our data support the notion that maternal Hpx can imprint the immune response of the offspring suffering EAE probably due to a reduced capacity to trigger suppression. Such "imprints" on the immune system could contribute to explaining as to why adult offspring gestated in Hpx suffer earlier and more intense EAE. © 2018 Haensgen, Albornoz, Opazo, Bugueño, Jara Fernández, Binzberger, Rivero-Castillo, Venegas Salas, Simon, Cabello-Verrugio, Elorza, Kalergis, Bueno and Riedel.https://www.frontiersin.org/articles/10.3389/fimmu.2018.01257/ful

Photoreceptor perturbation around subretinal drusenoid deposits as revealed by adaptive optics scanning laser ophthalmoscopy

PURPOSE: To describe the microscopic structure of photoreceptors impacted by subretinal drusenoid deposits, also called pseudodrusen, an extracellular lesion associated with age-related macular degeneration (AMD), using adaptive optics scanning laser ophthalmoscopy (AOSLO). DESIGN: Observational case series. METHODS: We recruited 53 patients with AMD and 10 age-similar subjects who had normal retinal health. All subjects underwent color fundus photography, infrared reflectance, red-free reflectance, autofluorescence, and spectral-domain optical coherence tomography (OCT). Subretinal drusenoid deposits were classified by a 3-stage OCT-based grading system. Lesions and surrounding photoreceptors were examined by AOSLO. RESULTS: Subretinal drusenoid deposits were found in 26 eyes of 13 patients with AMD and imaged by AOSLO and spectral-domain OCT in 18 eyes (n = 342 lesions). Spectral-domain OCT showed subretinal drusenoid deposits as highly reflective material accumulated internal to the retinal pigment epithelium. AOSLO revealed that photoreceptor reflectivity was qualitatively reduced by stage 1 subretinal drusenoid deposits and was greatly reduced by stage 2. AOSLO presented a distinct structure in stage 3, a hyporeflective annulus consisting of deflected, degenerated or absent photoreceptors. A central core with a reflectivity superficially resembling photoreceptors is formed by the lesion material itself. A hyporeflective gap in the photoreceptor ellipsoid zone on either side of this core shown in spectral-domain OCT corresponded to the hyporeflective annulus seen by AOSLO. CONCLUSIONS: AOSLO and multimodal imaging of subretinal drusenoid deposits indicate solid, space-filling lesions in the subretinal space. Associated retinal reflectivity changes are related to lesion stages and are consistent with perturbations to photoreceptors, as suggested by histology

The genetic contribution of the NO system at the glutamatergic post-synapse to schizophrenia : further evidence and meta-analysis

NO is a pleiotropic signaling molecule and has an important role in cognition and emotion. In the brain, NO is produced by neuronal nitric oxide synthase (NOS-I, encoded by NOS1) coupled to the NMDA receptor via PDZ. interactions; this protein-protein interaction is disrupted upon binding of NOS1 adapter protein (encoded by NOS1AP) to NOS-I. As both NOS1 and NOS1AP were associated with schizophrenia, we here investigated these genes in greater detail by genotyping new samples and conducting a meta-analysis of our own and published data. In doing so, we confirmed association of both genes with schizophrenia and found evidence for their interaction in increasing risk towards disease. Our strongest finding was the NOS1 promoter SNP rs41279104, yielding an odds ratio of 1.29 in the meta-analysis. As findings from heterologous cell systems have suggested that the risk allele decreases gene expression, we studied the effect of the variant on NOS1 expression in human post-mortem brain samples and found that the risk allele significantly decreases expression of NOS1 in the prefrontal cortex. Bioinformatic analyses suggest that this might be due the replacement of six transcription factor binding sites by two new binding sites as a consequence of proxy SNPs. Taken together, our data argue that genetic variance in NOS1 resulting in lower prefrontal brain expression of this gene contributes to schizophrenia liability, and that NOS1 interacts with NOS1AP in doing so. The NOS1-NOS1AP PDZ interface may thus well constitute a novel target for small molecules in at least some forms of schizophrenia. PostprintPeer reviewe