Post endodontic Aspergillosis in an immunocompetent individual

Non-invasive aspergillosis in immunocompetent individuals subsequent to post endodontic treatment can involve the maxillary antrum. An early and accurate diagnosis will aid in prompt and effective treatment. A 35 year old female patient reported with a painful nasomaxillary swelling. Previous records revealed the failure of the endodontic treatment of maxillary left second premolar which was subsequently extracted. Root piece was accidently left behind which resulted in a painful nasomaxillary swelling. The extraction socket was curetted and tissue was sent for histopathological examination, which revealed abundant septate fungal hyphae with numerous spores characteristic of Aspergillus . The patient showed marked improvement in the symptoms with systemic itraconazole at 3 months follow up and complete resolution occurred within 6 months. Inclusion of aspergilloma infections in the differential diagnosis is advocated when patients present with post-endodontic nasomaxillary swellin

Falstatin, a Cysteine Protease Inhibitor of Plasmodium falciparum, Facilitates Erythrocyte Invasion

Erythrocytic malaria parasites utilize proteases for a number of cellular processes, including hydrolysis of hemoglobin, rupture of erythrocytes by mature schizonts, and subsequent invasion of erythrocytes by free merozoites. However, mechanisms used by malaria parasites to control protease activity have not been established. We report here the identification of an endogenous cysteine protease inhibitor of Plasmodium falciparum, falstatin, based on modest homology with the Trypanosoma cruzi cysteine protease inhibitor chagasin. Falstatin, expressed in Escherichia coli, was a potent reversible inhibitor of the P. falciparum cysteine proteases falcipain-2 and falcipain-3, as well as other parasite- and nonparasite-derived cysteine proteases, but it was a relatively weak inhibitor of the P. falciparum cysteine proteases falcipain-1 and dipeptidyl aminopeptidase 1. Falstatin is present in schizonts, merozoites, and rings, but not in trophozoites, the stage at which the cysteine protease activity of P. falciparum is maximal. Falstatin localizes to the periphery of rings and early schizonts, is diffusely expressed in late schizonts and merozoites, and is released upon the rupture of mature schizonts. Treatment of late schizionts with antibodies that blocked the inhibitory activity of falstatin against native and recombinant falcipain-2 and falcipain-3 dose-dependently decreased the subsequent invasion of erythrocytes by merozoites. These results suggest that P. falciparum requires expression of falstatin to limit proteolysis by certain host or parasite cysteine proteases during erythrocyte invasion. This mechanism of regulation of proteolysis suggests new strategies for the development of antimalarial agents that specifically disrupt erythrocyte invasion

Sheridan School of Architectural Technology Volume 1 [W2017]

Welcome to Sheridan’s School of Architectural Technician/Technology inaugural printed portfolio. This volume is a celebration of the architectural achievements of Sheridan students. Much of the content presented here has been incubated in CADD39788, Architectural Computer Visualisation. Inside you will find an amalgamation of student and faculty work put together into a publication that reflects the rich theatre of creativity and complexity that is architectural education here at Sheridan. Student work within the magazine is from the last year of studies in the Architectural Technology program. Each student has selected their best work to represent some of the skills that they have learned over the years as part of Sheridan. Faculty work is a selection of research, teaching, and professional projects that represents that quality and diversity of educators that serve not only as teachers, but also as mentors to our students. They showcase the talent and skill of some of the individuals that make the Sheridan program a reality.https://source.sheridancollege.ca/fast_books/1001/thumbnail.jp

A study on trypsin, Aspergillus flavus and Bacillus sp. protease inhibitory activity in Cassia tora (L.) syn Senna tora (L.) Roxb. seed extract

<p>Abstract</p> <p>Background</p> <p>Proteases play an important role in virulence of many human, plant and insect pathogens. The proteinaceous protease inhibitors of plant origin have been reported widely from many plant species. The inhibitors may potentially be used for multiple therapeutic applications in viral, bacterial, fungal diseases and physiological disorders. In traditional Indian medicine system, <it>Cassia tora </it>(<it>Senna tora</it>) is reportedly effective in treatment of skin and gastrointestinal disorders. The present study explores the protease inhibitory activity of the above plant seeds against trypsin, <it>Aspergillus flavus </it>and <it>Bacillus </it>sp. proteases.</p> <p>Methods</p> <p>The crushed seeds of <it>Cassia tora </it>were washed thoroughly with acetone and hexane for depigmentation and defatting. The proteins were fractionated by ammonium sulphate (0-30, 30-60, 60-90%) followed by dialysis and size exclusion chromatography (SEC). The inhibitory potential of crude seed extract and most active dialyzed fraction against trypsin and proteases was established by spot test using unprocessed x-ray film and casein digestion methods, respectively. Electrophoretic analysis of most active fraction (30-60%) and SEC elutes were carried employing Sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) and Gelatin SDS-PAGE. Inhibition of fungal spore germination was studied in the presence of dialyzed active inhibitor fraction. Standard deviation (SD) and ANOVA were employed as statistical tools.</p> <p>Results</p> <p>The crude seeds' extract displayed strong antitryptic, bacterial and fungal protease inhibitory activity on x-ray film. The seed protein fraction 30-60% was found most active for trypsin inhibition in caseinolytic assay (P < 0.001). The inhibition of caseinolytic activity of the proteases increased with increasing ratio of seed extract. The residual activity of trypsin, <it>Aspergillus flavus </it>and <it>Bacillus </it>sp. proteases remained only 4, 7 and 3.1%, respectively when proteases were incubated with 3 mg ml^-1seed protein extract for 60 min. The inhibitory activity was evident in gelatin SDS-PAGE where a major band (~17-19 kD) of protease inhibitor (PI) was detected in dialyzed and SEC elute. The conidial germination of <it>Aspergillus flavus </it>was moderately inhibited (30%) by the dialyzed seed extract.</p> <p>Conclusions</p> <p><it>Cassia tora </it>seed extract has strong protease inhibitory activity against trypsin, <it>Aspergillus flavus </it>and <it>Bacillus </it>sp. proteases. The inhibitor in <it>Cassia tora </it>may attenuate microbial proteases and also might be used as phytoprotecting agent.</p

Biochemical Properties of a Novel Cysteine Protease of Plasmodium vivax, Vivapain-4

Plasmodium vivax affects hundreds of millions each year and results in severe morbidity and mortality. Plasmodial cysteine proteases (CPs) play crucial roles during the progression of malaria since inhibition of these molecules impairs parasite growth. These CPs might be targeted for new antimalarial drugs. We characterized a novel P. vivax CP, vivapain-4 (VX-4), which appeared to evolve differentially among primate Plasmodium species. VX-4 showed highly unique substrate preference depending on surrounding micro-environmental pH. It effectively hydrolyzed benzyloxycarbonyl-Leu-Arg-4-methyl-coumaryl-7-amide (Z-Leu-Arg-MCA) and Z-Phe-Arg-MCA at acidic pH and Z-Arg-Arg-MCA at neutral pH. Three amino acids (Ala90, Gly157 and Glu180) that delineate the S2 pocket were found to be substituted in VX-4. Alteration of Glu180 abolished hydrolytic activity against Z-Arg-Arg-MCA at neutral pH, indicating Glu180 is intimately involved in the pH-dependent substrate preference. VX-4 hydrolyzed actin at neutral pH and hemoglobin at acidic pH, and participated in plasmepsin 4 activation at neutral/acidic pH. VX-4 was localized in the food vacuoles and cytoplasm of the erythrocytic stage of P. vivax. The differential substrate preferences depending on pH suggested a highly efficient mechanism to enlarge biological implications of VX-4, including hemoglobin degradation, maturation of plasmepsin, and remodeling of the parasite architecture during growth and development of P. vivax

Three-dimensional finite element modelling of coupled free/porous flows: applications to industrial and environmental flows

Conjunctive modelling of free/porous flows provides a powerful and cost-effective tool for designing industrial filters used in the process industry and also for quantifying surface–subsurface flow interactions, which play a significant role in urban flooding mechanisms resulting from sea-level rise and climate changes. A number of well-established schemes are available in the literature for simulation of such regimes; however, three-dimensional (3D) modelling of such flow systems still presents numerical and practical challenges. This paper presents the development of a fully 3D, transient finite element model for the prediction and quantitative analyses of the hydrodynamic behaviour encountered in industrial filtrations and environmental flows represented by coupled flows. The weak-variational formulation in this model is based on the use of C0 continuous equal-order Lagrange polynomial functions for velocity and pressure fields represented by 3D hexahedral finite elements. A mixed UVWP finite element scheme based on the standard Galerkin technique satisfying the Ladyzhenskaya–Babuska–Brezzi stability criterion through incorporation of an artificial compressibility term in the continuity equation has been employed for the solution of coupled partial differential equations. We prove that the discretization generates unified stabilization for both the Navier–Stokes and Darcy equations and preserves the geometrical flexibility of the computational grids. A direct node-linking procedure involving the rearrangement of the global stiffness matrix for the interface elements has been developed by the authors, which is utilized to couple the governing equations in a single model. A variety of numerical tests are conducted, indicating that the model is capable of yielding theoretically expected and accurate results for free, porous and coupled free/porous problems encountered in industrial and environmental engineering problems representing complex filtration (dead-end and cross-flow) and interacting surface–subsurface flows. The model is computationally cost-effective, robust, reliable and easily implementable for practical design of filtration equipments, investigation of land use for water resource availability and assessment of the impacts of climatic variations on environmental catastrophes (i.e. coastal and urban floods). The model developed in this work results from the extension of a multi-disciplinary project (AEROFIL) primarily sponsored by the European aerospace industries for development of a computer simulation package (Aircraft Cartridge Filter Analysis Modelling Program), which was successfully utilized and deployed for designing hydraulic dead-end filters used in Airbus A380