RESUMEN
Herbivore selection of plant hosts and plant responses to insect colonization have been subjects of intense investigations. A growing body of evidence suggests that, for successful colonization to occur, (effector/virulence) proteins in insect saliva must modulate plant defense responses to the benefit of the insect. A range of insect saliva proteins that modulate plant defense responses have been identified, but there is no direct evidence that these proteins are delivered into specific plant tissues and enter plant cells. Aphids and other sap-sucking insects of the order Hemiptera use their specialized mouthparts (stylets) to probe plant mesophyll cells until they reach the phloem cells for long-term feeding. Here, we show, by immunogold-labeling of ultrathin sections of aphid feeding sites, that an immuno-suppressive aphid effector localizes in the cytoplasm of mesophyll cells near aphid stylets but not in cells further away from aphid feeding sites. In contrast, another aphid effector protein localizes in the sheaths composed of gelling saliva that surround the aphid stylets. Thus, insects deliver effectors directly into plant tissue. Moreover, different aphid effectors locate extracellularly in the sheath saliva or are introduced into the cytoplasm of plant cells. [Formula: see text] Copyright © 2016 The Author(s). This is an open-access article distributed under the CC BY-NC-ND 4.0 International license .
Asunto(s)
Áfidos/fisiología , Proteínas de Insectos/metabolismo , Plantas/ultraestructura , Animales , Citosol/metabolismo , Citosol/ultraestructura , Herbivoria , Células del Mesófilo/metabolismo , Células del Mesófilo/parasitología , Células del Mesófilo/ultraestructura , Floema/metabolismo , Floema/parasitología , Floema/ultraestructura , Hojas de la Planta/metabolismo , Hojas de la Planta/parasitología , Hojas de la Planta/ultraestructura , Plantas/metabolismo , Plantas/parasitología , Saliva/metabolismoRESUMEN
Few studies have focused on haze as a weather element and its correlation with crime. In this study, we examined haze as a weather variable to investigate its effects on criminal activity. We used both monthly crime data and weather records to build a regression model that contains a sequential statistical approach to reach the correlation coefficients between the variables. Also, we developed a prediction model to predict crime cases considering three weather factors: temperature, humidity, and haze. We applied this model in two different climate provinces in Saudi Arabia, namely, Riyadh and Makkah. Riyadh is a desert area and observes haze approximately 17 days per month on average, while Makkah is a coastal area observing haze an average of 4 days per month. We found a measurable relationship between each of these three variables and criminal activity. We found that a one-degree increase in temperature was associated with an increase in assault of 0.739, when humidity and haze were held constant. For other independent variables measured against the same crime in Riyadh, a one-degree increase in humidity was associated with a 0.164 increase in assault. An increase in the number of times that a haze phenomenon is observed was associated with an increase of 0.359 in assault cases. Haze had the most effect on theft, drug, and assault crimes in Riyadh compared to the other elements. Temperature and humidity have a significant relationship with crime in Makkah, while haze had no significant influence in that region.
Asunto(s)
Clima , Tiempo (Meteorología) , Crimen , Humedad , TemperaturaRESUMEN
Streptomyces are our principal source of antibiotics, which they generate concomitant with a complex developmental transition from vegetative hyphae to spores. c-di-GMP acts as a linchpin in this transition by binding and regulating the key developmental regulators, BldD and WhiG. Here we show that c-di-GMP also binds the glycogen-debranching-enzyme, GlgX, uncovering a direct link between c-di-GMP and glycogen metabolism in bacteria. Further, we show c-di-GMP binding is required for GlgX activity. We describe structures of apo and c-di-GMP-bound GlgX and, strikingly, their comparison shows c-di-GMP induces long-range conformational changes, reorganizing the catalytic pocket to an active state. Glycogen is an important glucose storage compound that enables animals to cope with starvation and stress. Our in vivo studies reveal the important biological role of GlgX in Streptomyces glucose availability control. Overall, we identify a function of c-di-GMP in controlling energy storage metabolism in bacteria, which is widespread in Actinobacteria.
Asunto(s)
Regulación Bacteriana de la Expresión Génica , Streptomyces , Regulación Alostérica , Animales , Antibacterianos/metabolismo , Proteínas Bacterianas/metabolismo , GMP Cíclico/análogos & derivados , GMP Cíclico/metabolismo , Glucosa/metabolismo , Glucógeno/metabolismo , Sistemas de Mensajero Secundario , Streptomyces/metabolismoRESUMEN
Fungi have evolved an array of spore discharge and dispersal processes. Here, we developed a theoretical model that explains the ejection mechanics of aeciospore liberation in the stem rust pathogen Puccinia graminis. Aeciospores are released from cluster cups formed on its Berberis host, spreading early-season inoculum into neighboring small-grain crops. Our model illustrates that during dew or rainfall, changes in aeciospore turgidity exerts substantial force on neighboring aeciospores in cluster cups whilst gaps between spores become perfused with water. This perfusion coats aeciospores with a lubrication film that facilitates expulsion, with single aeciospores reaching speeds of 0.053 to 0.754 m·s-1. We also used aeciospore source strength estimates to simulate the aeciospore dispersal gradient and incorporated this into a publicly available web interface. This aids farmers and legislators to assess current local risk of dispersal and facilitates development of sophisticated epidemiological models to potentially curtail stem rust epidemics originating on Berberis.
Asunto(s)
Humedad , Puccinia/fisiología , Esporas Fúngicas/fisiologíaRESUMEN
The twin-arginine translocation (Tat) pathway is a prokaryotic protein targeting system dedicated to the transmembrane translocation of folded proteins. Substrate proteins are directed to the Tat translocase by signal peptides bearing a conserved SRRxFLK 'twin-arginine' motif. In Escherichia coli, most of the 27 periplasmically located Tat substrates are cofactor-containing respiratory enzymes, and many of these harbour a molybdenum cofactor at their active site. Molybdenum cofactor-containing proteins are not exclusively located in the periplasm, however, with the major respiratory nitrate reductase (NarG) and the biotin sulfoxide reductase (BisC), for example, being located at the cytoplasmic side of the membrane. Interestingly, both NarG and BisC contain 'N-tail' regions that bear some sequence similarity to twin-arginine signal peptides. In this work, we have examined the relationship between the non-exported N-tails and the Tat system. Using a sensitive genetic screen for Tat transport, variant N-tails were identified that displayed Tat transport activity. For the NarG 36-residue N-tail, six amino acid changes were needed to induce transport activity. However, these changes interfered with binding by the NarJ biosynthetic chaperone and impaired biosynthesis of the native enzyme. For the BisC 36-residue N-tail, only five amino acid substitutions were needed to restore Tat transport activity. These modifications also impaired in vivo BisC activity, but it was not possible to identify a biosynthetic chaperone for this enzyme. These data highlight an intimate genetic and evolutionary link between some non-exported redox enzymes and those transported across membranes by the Tat translocation system.
Asunto(s)
Transporte de Electrón/genética , Proteínas de Escherichia coli/genética , Proteínas de Escherichia coli/metabolismo , Señales de Clasificación de Proteína/genética , Secuencia de Aminoácidos , Escherichia coli/genética , Escherichia coli/metabolismo , Proteínas de Escherichia coli/química , Evolución Molecular , Proteínas de Transporte de Membrana/química , Proteínas de Transporte de Membrana/genética , Proteínas de Transporte de Membrana/metabolismo , Datos de Secuencia Molecular , Mutagénesis , Nitrato-Reductasa/química , Nitrato-Reductasa/genética , Nitrato-Reductasa/metabolismo , Oxidorreductasas/química , Oxidorreductasas/genética , Oxidorreductasas/metabolismo , Transporte de Proteínas , Homología de Secuencia de AminoácidoRESUMEN
Post-translational thio-acylation of a fusion protein between the alpha2A-adrenoceptor and the alpha subunit of the G protein G(o1) is both dynamic and regulated by agonist binding. Incorporation of [3H]palmitate into the fusion protein was reduced substantially in the presence of the agonist adrenaline. This was dependent on the concentration of adrenaline and correlated with occupancy of the ligand binding site. Both the receptor and G-protein elements of the fusion construct incorporated [3H]palmitate but this occurred more rapidly for the G-protein element and regulation of acylation by the agonist occurred only for the G protein. The kinetics of de-palmitoylation of the alpha2A-adrenoceptor-Galpha(o1) fusion were accelerated markedly by agonist. Again, this reflected modulation of the G protein but not of the receptor. Agonist-induced regulation of the kinetics of thio-acylation of the G protein was abolished, however, in a mutant unable to bind guanosine 5'-[gamma-[35S]thio]triphosphate ([35S]GTP[S]) in response to adrenaline. Despite the dynamic nature of the post-translational acylation and its regulation by agonist, the ability of adrenaline to activate the G protein, monitored by stimulation of the binding of [35S]GTP[S] to such fusion constructs, was unaffected by the palmitoylation potential of either the receptor or G-protein element.
Asunto(s)
Subunidades alfa de la Proteína de Unión al GTP Gi-Go/metabolismo , Palmitatos/metabolismo , Receptores Adrenérgicos alfa 2/metabolismo , Proteínas Recombinantes de Fusión/metabolismo , Acilación , Línea Celular , Relación Dosis-Respuesta a Droga , Epinefrina/farmacología , Subunidades alfa de la Proteína de Unión al GTP Gi-Go/genética , Guanosina Trifosfato/metabolismo , Humanos , Cinética , Ligandos , Mutación/genética , Receptores Adrenérgicos alfa 2/genética , Proteínas Recombinantes de Fusión/genéticaRESUMEN
Starch degradation in barley endosperm provides carbon for early seedling growth, but the control of this process is poorly understood. We investigated whether endosperm cell wall degradation is an important determinant of the rate of starch degradation. We identified iminosugar inhibitors of enzymes that degrade the cell wall component arabinoxylan. The iminosugar 1,4-dideoxy-1, 4-imino-l-arabinitol (LAB) inhibits arabinoxylan arabinofuranohydrolase (AXAH) but does not inhibit the main starch-degrading enzymes α- and ß-amylase and limit dextrinase. AXAH activity in the endosperm appears soon after the onset of germination and resides in dimers putatively containing two isoforms, AXAH1 and AXAH2. Upon grain imbibition, mobilisation of arabinoxylan and starch spreads across the endosperm from the aleurone towards the crease. The front of arabinoxylan degradation precedes that of starch degradation. Incubation of grains with LAB decreases the rate of loss of both arabinoxylan and starch, and retards the spread of both degradation processes across the endosperm. We propose that starch degradation in the endosperm is dependent on cell wall degradation, which permeabilises the walls and thus permits rapid diffusion of amylolytic enzymes. AXAH may be of particular importance in this respect. These results provide new insights into the mobilization of endosperm reserves to support early seedling growth.
Asunto(s)
Pared Celular/metabolismo , Endospermo/metabolismo , Hordeum/metabolismo , Almidón/metabolismo , Arabinosa/farmacología , Pared Celular/efectos de los fármacos , Endospermo/efectos de los fármacos , Glicósido Hidrolasas/antagonistas & inhibidores , Glicósido Hidrolasas/metabolismo , Hordeum/crecimiento & desarrollo , Iminofuranosas/farmacología , Immunoblotting , Proteínas de Plantas/antagonistas & inhibidores , Proteínas de Plantas/metabolismo , Plantones/genética , Plantones/crecimiento & desarrollo , Plantones/metabolismo , Alcoholes del Azúcar/farmacología , Xilanos/metabolismoRESUMEN
This article examines the relationship of drug use with the social and economic characteristics of rural communities in New South Wales (NSW), Australia. Data is derived from the 1996 Australian Census of Population and Housing, and data on drug-related offenses from the NSW police between 1995 and 1999. Arrest rates for breaking and entering, assault, and vandalism showed statistically significant associations across types of rural communities, but drug-related arrests varied considerably less. The widespread, relatively-even distribution of drug arrests in rural NSW suggests that the underlying causes of drug-related violations are unique when compared to other types of crime.