A Novel Prototype Biosensor Array Electrode System for Detecting the Bacterial Pathogen Salmonella typhimurium.

Publication history: Accepted - 2 June 2022: Published online - 4 June 2022Salmonellosis caused by Salmonella sp. has long been reported all over the world. Despite the availability of various diagnostic methods, easy and effective detection systems are still required. This report describes a dialysis membrane electrode interface disc with immobilized specific antibodies to capture antigenic Salmonella cells. The interaction of a specific Salmonella antigen with a mouse anti-Salmonella monoclonal antibody complexed to rabbit anti-mouse secondary antibody conjugated with HRP and the substrate o-aminophenol resulted in a response signal output current measured using two electrode systems (cadmium reference electrode and glassy carbon working electrode) and an agilent HP34401A 6.5 digital multimeter without a potentiostat or applied potential input. A maximum response signal output current was recorded for various concentrations of Salmonella viz., 3, 30, 300, 3000, 30,000 and 300,000 cells. The biosensor has a detection limit of three cells, which is very sensitive when compared with other detection sensors. Little non-specific response was observed using Streptococcus, Vibrio, and Pseudomonas sp. The maximum response signal output current for a dialysis membrane electrode interface disc was greater than that for gelatin, collagen, and agarose. The device and technique have a range of biological applications. This novel detection system has great potential for future development and application in surveillance for microbial pathogens.This research work was financially supported by DRDE (DRDE-P1-2003/Task-11)

Temperature Controlled Synthesis of ZnS Nanocrystals by Simple Chemical Precipitation

Nanocrystals of ZnS preparing at 70, 75 and 80 °C have been characterized by X-ray diffraction (XRD), UV-Vis and Fourier transform infrared spectroscopy (FT-IR), atomic force microscopy (AFM) and field emission scanning electron microscopy (FESEM). The investigation suggests that aggregates of small spherical particles with an average size of 8 nm and well defined morphology were obtained at 80 °C. The particle size appears to increase with a decrease in synthesis temperature

An explanatory investigation on the role of communication antecedents in project management

Project management has become a norm in many organizations for project benefit realization commonly aligned to organizational strategic goals. These projects in organizations create additional value to meet organization commitments. Research suggests that communication management is one of the key area in project management. This research therefore embarks empirically to determine the role of project communication impacting project management. The identified antecedents of communication are adapted from Media Synchronicity Theory (MST) to study the impact on communication performance influencing project management. The study uses data gathered by a survey involving respondents from the IT industry analyzed using the Partial Least Squares of the Structural Equation Modeling (PLS-SEM). The empirical evidence demonstrates a significant relationship between communication and project management. The study also contributes to the project management body of knowledge

Symmetry Analyses of Epidemiological Model for Monkeypox Virus with Atangana–Baleanu Fractional Derivative

The monkeypox virus causes a respiratory illness called monkeypox, which belongs to the Poxviridae virus family and the Orthopoxvirus genus. Although initially endemic in Africa, it has recently become a global threat with cases worldwide. Using the Antangana–Baleanu fractional order approach, this study aims to propose a new monkeypox transmission model that represents the interaction between the infected human and rodent populations. An iterative method and the fixed-point theorem are used to prove the existence and uniqueness of the symmetry model’s system of solutions. It shows that the symmetry model has equilibrium points when there are epidemics and no diseases. As well as the local asymptotic stability of the disease-free equilibrium point, conditions for the endemic equilibrium point’s existence have also been demonstrated. For this purpose, the existence of optimal control is first ensured. The aim of the proposed optimal control problem is to minimize both the treatment and prevention costs, and the number of infected individuals. Optimal conditions are acquired Pontryagin’s maximum principle is used. Then, the stability of the symmetry model is discussed at monkeypox-free and endemic equilibrium points with treatment strategies to control the spread of the disease. Numerical simulations clearly show how necessary and successful the proposed combined control strategy is in preventing the disease from becoming epidemic

A novel prototype biosensor array electrode system for detecting the bacterial pathogen Salmonella typhimurium

Salmonellosis caused by Salmonella sp. has long been reported all over the world. Despite the availability of various diagnostic methods, easy and effective detection systems are still required. This report describes a dialysis membrane electrode interface disc with immobilized specific antibodies to capture antigenic Salmonella cells. The interaction of a specific Salmonella antigen with a mouse anti-Salmonella monoclonal antibody complexed to rabbit anti-mouse secondary antibody conjugated with HRP and the substrate o-aminophenol resulted in a response signal output current measured using two electrode systems (cadmium reference electrode and glassy carbon working electrode) and an agilent HP34401A 6.5 digital multimeter without a potentiostat or applied potential input. A maximum response signal output current was recorded for various concentrations of Salmonella viz., 3, 30, 300, 3000, 30,000 and 300,000 cells. The biosensor has a detection limit of three cells, which is very sensitive when compared with other detection sensors. Little non-specific response was observed using Streptococcus, Vibrio, and Pseudomonas sp. The maximum response signal output current for a dialysis membrane electrode interface disc was greater than that for gelatin, collagen, and agarose. The device and technique have a range of biological applications. This novel detection system has great potential for future development and application in surveillance for microbial pathogens

Expression of heterologous oxalate decarboxylase in HEK293 cells confers protection against oxalate induced oxidative stress as a therapeutic approach for calcium oxalate stone disease

Oxalates stimulate alterations in renal epithelial cells and thereby induce calcium oxalate (CaOx) stone formation. Bacillus subtilis YvrK gene encodes for oxalate decarboxylase (OxdC) which degrades oxalate to formate and CO2. The present work is aimed to clone the oxdC gene in a mammalian expression vector pcDNA and transfect into Human Embryonic Kidney 293 (HEK293) cells and evaluate the oxdC expression, cell survival rate and oxalate degrading efficiency. The results indicate cell survival rate of HEK293/pcDNAOXDC cells pre-incubated with oxalate was enhanced by 28%. HEK293/pcDNAOXDC cells expressing OxdC treated with oxalate, significantly restored antioxidant activity, mitochondrial membrane potential and intracellular reactive oxygen species (ROS) generation compared with HEK293/pcDNA. Apoptotic marker caspase 3 downregulation illustrates HEK293/pcDNAOXDC cells were able to survive under oxalate-mediated oxidative stress. The findings suggest HEK293 cells expressing oxdC capable of degrading oxalate protect cells from oxidative damage and thus serve as a therapeutic option for prevention of CaOx stone disease

Expression of heterologous oxalate decarboxylase in HEK293 cells confers protection against oxalate induced oxidative stress as a therapeutic approach for calcium oxalate stone disease

Oxalates stimulate alterations in renal epithelial cells and thereby induce calcium oxalate (CaOx) stone formation. Bacillus subtilis YvrK gene encodes for oxalate decarboxylase (OxdC) which degrades oxalate to formate and CO2. The present work is aimed to clone the oxdC gene in a mammalian expression vector pcDNA and transfect into Human Embryonic Kidney 293 (HEK293) cells and evaluate the oxdC expression, cell survival rate and oxalate degrading efficiency. The results indicate cell survival rate of HEK293/pcDNAOXDC cells pre-incubated with oxalate was enhanced by 28%. HEK293/pcDNAOXDC cells expressing OxdC treated with oxalate, significantly restored antioxidant activity, mitochondrial membrane potential and intracellular reactive oxygen species (ROS) generation compared with HEK293/pcDNA. Apoptotic marker caspase 3 downregulation illustrates HEK293/pcDNAOXDC cells were able to survive under oxalate-mediated oxidative stress. The findings suggest HEK293 cells expressing oxdC capable of degrading oxalate protect cells from oxidative damage and thus serve as a therapeutic option for prevention of CaOx stone disease