Using plant-based preparations to protect common bean against halo blight disease: the potential of nettle to trigger the immune system

Halo blight disease of beans (Phaseolus vulgaris L.), caused by the bacterium Pseudomonas syringae pv. phaseolicola (Pph), is responsible for severe losses in crop production worldwide. As the current agronomic techniques used are not effective, it is necessary to search for new ones which may prevent disease in common bean. In this study, we challenged four plant-based preparations (PBPs), with no other agronomic uses, as they come from industrial waste (grapevine pomace (R-G) and hop residue (R-H)) or wild plants (Urtica dioica (U) and Equisetum sp. (E)), to be used as immune defense elicitors against Pph in common bean. After studying their inhibitory effect against Pph growth by bioassays, the two most effective PBPs (R-G and U) were applied in common bean plants. By measuring the total H2O2, lipid peroxidation, and antioxidant enzymatic activities, as well as the expression of six defense-related genes-PR1, WRKY33, MAPKK, RIN4, and PAL1-, it was observed that U-PBP application involved a signaling redox process and the overexpression of all genes, mostly PR1. First infection trials in vitro suggested that the application of U-PBP involved protection against Pph. The elicitation of bean defense with U-PBP involved a decrease in some yield parameters, but without affecting the final production. All these findings suggest a future use of U-PBP to diminish halo blight disease

Molecular markers applied to evaluation of environmental services in the araucaria forest in Southern Brazil.

Resumo

Epidemiologia molecular aplicada ao monitoramento de estirpes de Staphylococcus aureus na produção de queijo minas frescal.

Resumo: Foi realizado o monitoramento epidemiológico molecular de estirpes de Staphylococcus aureus potencialmente toxigênicas isoladas no processo de produção do queijo Minas frescal em micro-usina do Estado de São Paulo. Para tanto, foram realizadas seis amostragens durante o período de junho de 2008 a julho de 2009, de modo a perfazer um total de 140 amostras. Essas amostras foram colhidas da superfície dos tanques de recepção e estocagem do leite cru, da superfície do tanque de equilíbrio do leite pasteurizado, da rede de abastecimento de água, das tubulações e equipamentos, das mãos do manipulador e de queijos embalados prontos para consumo. As colônias isoladas em Agar Baird-Parker confirmadas como cocos Gram positivos e que mostravam-se positivas às provas de catalase, coagulase e da produção de acetoína, foram submetidas à extração do DNA bacteriano através da utilização do Kit Invitek - Uniscience®. A confirmação molecular da espécie dos isolados e a presença de enterotoxinas SEA, SEB, SEC, SED e da toxina TSST-1 foi realizada a partir da amplificação dos fragmentos de DNA cromossômico específico. Entre as 74 estirpes de estafilococos coagulase positivos isoladas, somente 41 (55.4%) amostras foram confirmadas como sendo Staphylococcus aureus, das quais 25 (61,0%) mostraram-se positivas na pesquisa de toxinas estafilocócicas. A enterotoxina de maior frequência identificada foi a SEA. As estirpes de Staphylococcus aureus toxigênico foram mais isoladas nas mãos do manipulador (16,0%), no leite cru do tanque de recepção (12,0%), no leite pasteurizado para elaboração do queijo (12,0%) e no queijo Minas frescal pronto para consumo (12,0%). [Molecular epidemiology applied to monitoring strains of staphylococcus Aureus in minas frescal cheese production]. Abstract: We studied the molecular epidemiology of Staphylococcus aureus strains potentially toxigenic, isolated from the production process of Minas frescal cheese in a small dairy plant in the state of São Paulo. For this, samples were taken during the period from June 2008 to July 2009. Samples were collected from the surface of the receiving and storage tanks of raw milk, the surface of the balance tank of pasteurized milk, the water supply system, the pipes and equipments, the hands of the handler and from the packaged cheese, totaling 140 samples. The colonies isolated on Baird-Parker Agar confirmed as Gram positive and positive for catalase, coagulase and acetoin production, were submitted to extraction of bacterial DNA using the Invitek - Uniscience® kit. Confirmation of the isolated species and enterotoxins SEA, SEB, SEC, SED and TSST-1 toxin was carried out through the amplification of specific fragments of chromosomal DNA. Among the 74 strains of isolated coagulase-positive staphylococci, only 41 (55.4%) strains were confirmed as Staphylococcus aureus, of which 25 (61.0%) were positive to the presence of staphylococcal toxins. The most frequently identified enterotoxin was SEA. The toxigenic strains of Staphylococcus aureus were more frequently isolated from hands of the handler (16.0%), raw milk receiving tank (12.0%), pasteurized milk for cheese making (12.0%) and fresh white cheese ready for consumption (12.0%)

Plasmodium falciparum Apicomplexan-Specific Glucosamine-6-Phosphate N-Acetyltransferase Is Key for Amino Sugar Metabolism and Asexual Blood Stage Development

UDP-N-acetylglucosamine (UDP-GlcNAc), the main product of the hexosamine biosynthetic pathway, is an important metabolite in protozoan parasites since its sugar moiety is incorporated into glycosylphosphatidylinositol (GPI) glycolipids and N- and O-linked glycans. Apicomplexan parasites have a hexosamine pathway comparable to other eukaryotic organisms, with the exception of the glucosamine-phosphate N-acetyltransferase (GNA1) enzymatic step that has an independent evolutionary origin and significant differences from nonapicomplexan GNA1s. By using conditional genetic engineering, we demonstrate the requirement of GNA1 for the generation of a pool of UDP-GlcNAc and for the development of intraerythrocytic asexual Plasmodium falciparum parasites. Furthermore, we present the 1.95 A resolution structure of the GNA1 ortholog from Cryptosporidium parvum, an apicomplexan parasite which is a leading cause of diarrhea in developing countries, as a surrogate for P. falciparum GNA1. The indepth analysis of the crystal shows the presence of specific residues relevant for GNA1 enzymatic activity that are further investigated by the creation of site-specific mutants. The experiments reveal distinct features in apicomplexan GNA1 enzymes that could be exploitable for the generation of selective inhibitors against these parasites, by targeting the hexosamine pathway. This work underscores the potential of apicomplexan GNA1 as a drug target against malaria. IMPORTANCE Apicomplexan parasites cause a major burden on global health and economy. The absence of treatments, the emergence of resistances against available therapies, and the parasite''s ability to manipulate host cells and evade immune systems highlight the urgent need to characterize new drug targets to treat infections caused by these parasites. We demonstrate that glucosamine-6-phosphate N-acetyltransferase (GNA1), required for the biosynthesis of UDP-N-acetylglucosamine (UDP-GlcNAc), is essential for P. falciparum asexual blood stage development and that the disruption of the gene encoding this enzyme quickly causes the death of the parasite within a life cycle. The high-resolution crystal structure of the GNA1 ortholog from the apicomplexan parasite C. parvum, used here as a surrogate, highlights significant differences from human GNA1. These divergences can be exploited for the design of specific inhibitors against the malaria parasite

NP7 protects from cell death induced by oxidative stress in neuronal and glial midbrain cultures from parkin null mice

AbstractParkin mutations produce Parkinson’s disease (PD) in humans and nigrostriatal dopamine lesions related to increased free radicals in mice. We examined the effects of NP7, a synthetic, marine derived, free radical scavenger which enters the brain, on H2O2 toxicity in cultured neurons and glia from wild-type (WT) and parkin null mice (PK-KO).NP7, 5–10μM, prevented the H2O2 induced apoptosis and necrosis of midbrain neuronal and glial cultures from WT and PK-KO mice. NP7 suppressed microglial activation and the H2O2 induced drop-out of dopamine neurons. Furthermore, NP7 prevented the increased phosphorylation of ERK and AKT induced by H2O2. NP7 may be a promising neuroprotector against oxidative stress in PD

On the statistics of superlocalized states in self-affine disordered potentials

We investigate the statistics of eigenstates in a weak self-affine disordered potential in one dimension, whose Gaussian fluctuations grow with distance with a positive Hurst exponent $H$. Typical eigenstates are superlocalized on samples much larger than a well-defined crossover length, which diverges in the weak-disorder regime. We present a parallel analytical investigation of the statistics of these superlocalized states in the discrete and the continuum formalisms. For the discrete tight-binding model, the effective localization length decays logarithmically with the sample size, and the logarithm of the transmission is marginally self-averaging. For the continuum Schr\"odinger equation, the superlocalization phenomenon has more drastic effects. The effective localization length decays as a power of the sample length, and the logarithm of the transmission is fully non-self-averaging.Comment: 21 pages, 6 figure

Magnetically Driven Outflows in a Starburst Environment

We here investigate the possibility that the observed collimated outflows in luminous infrared galaxies (LIGs) and some Seyfert galaxies can be produced in a starburst (SB) environment. A nuclear disk can be quickly produced by gas infall during star formation in a rotating, stellar cluster. We find that massive nuclear SBs with core disk masses M_d \sim 10^8 - 10^9 M_{\odot}, and supernova rates \nu_{SN} \simeq 5 \times 10^{-3} - 2 yr^{-1} (which are consistent with the \nu_{SN} values inferred from the observed non-thermal radio power in source candidates) may inject kinetic energies which are high enough to blow out directed flows from the accreting disk surface, within the SB lifetimes. In our models, the acceleration and collimation of the nuclear outflow are provided by magnetic fields anchored into the rotating SB-disk. The emerging outflow carries a kinetic power that is only a small fraction (a few percent) of the supernovae energy rate produced in the SB. Based on conditions determined from observed outflows and disks, we find that moderate disk magnetic fields (\gtrsim 8 \times 10^{-4} G) are able to accelerate the outflows up to the observed terminal velocities (\lesssim few 100 km s^{-1} in the case of the Seyfert galaxies, and \sim 400 - 950 km s^{-1} in the case of the LIGs). The outflow is produced within a wind zone in the disk of radius \lesssim 100 pc in the LIGs, and \lesssim 10 pc in the Seyferts, with wind mass loss to disk accretion rate ratios \dot M_w /\dot M_d \gtrsim 0.1 (where \dot M_d \sim 100 M_{\odot} yr^{-1}). The observation of rotating nuclear disks of gas within few 100 pc scales in source candidates like the LIG Arp 220, and magnetized outflows provide observational support for the picture drawn here.Comment: 31 pages, Latex file, 1 Figure, accepted for publication in the Astrophys. Journa

Healthy dietary pattern and their corresponding gut microbiota profile are linked to a lower risk of type 2 diabetes, independent of the presence of obesity

Background: Prediabetes and old age are both high risk factors for developing Type 2 Diabetes (T2D), while obesity is one of the most important factors triggering the disease. Nutritional interventions are the most effective tool for preventing T2D, as they improve different biochemical and anthropometric outcomes and growth-promoting/inhibiting gut microbiota populations. However, to date there are no specific dietary recommendations to stop the development of T2D in elderly groups, for whom hypocaloric diets and other commonly used weight-loss programs could be considered dangerous. The objective of our study, thus, was to understand the impact of dietary patterns on T2D risk as related to gut microbiota profile in obese and non-obese elderly prediabetic subjects. Methods: A cross-sectional study was performed in 182 subjects 65 years old with prediabetes, divided into obese (OB) or non-obese (NOB) subgroups, and their risk of developing T2D was measured according to FINDRISK score and biochemical parameters. Also, clusters into different dietary patterns in each group by PCA analysis was related with gut microbiota, which was analyzed from stool samples by qPCR. The creation of clusters was used to re-evaluate T2D risk. Results: OB was at higher risk of developing T2D and showed worse metabolic outcomes. Unhealthier and healthier dietary pattern clusters were observed for both OB (OB-6 and OB-5 respectively) and NOB (NOB-2 and NOB-3 respectively) groups. Results obtained from the gut microbiota showed that only Prevotella was higher in NOB, but when comparisons were made between clusters, a clear relation with dietary pattern was observed; showing in healthier dietary clusters a decrease in Prevotella, an increase of Faecalibacterium prausnitzii and an increase in lactic acid bacteria. T2D risk was greater in the obese group between unhealthier dietary clusters. No difference between healthier dietary clusters was observed. Conclusion: A healthy dietary pattern and the growth-promoting beneficial and growth-inhibiting disadvantageous gut microbiota populations linked to it provide protection against the development of T2D in an obese population with advanced age and preDM