Adhesive ability and biofilm metabolic activity of Listeria monocytogenes strains before and after cold stress

Listeria monocytogenes is an important pathogen responsible for major outbreaks associated with food products. Adhesion to surfaces leads to significant modifications in cell physiology. In this work, the ability of L. monocytogenes to produce biofilm and its ability to adhere to abiotic surfaces under cold stress were evaluated. Metabolic activity of biofilm formed by L. monocytogenes before and after cold stress was measured in vitro using the colorimetric method based on the reduction of the tetrazolium salt 2,3-bis(2methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT). The ability to adhere to abiotic surfaces was determined by the ability of the cells to metabolically reduce bromure de 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium (MTT) to a formazan dye. Our results show that L. monocytogenes strains were able to adhere to abiotic materials with different degrees. In fact, cold stressed strains (-20°C) were more adhesive to polyethylene, glass, polyvinyl chloride and stainless style surfaces than non-stressed cells. Our observations show that the hydrophily varied with cold stress period. At freezing temperature, L. monocytogenes was strongly hydrophobic. Genetic studies of adhesive genes of L. monocytogenes will be required to fully understand the importance of this observation.Keywords: Listeria monocytogenes, slime production, cold stress, abiotic-surfaces, biofilm formatio

DNA as a Next-Generation Biomonitoring Tool of Hospital Effluent Contamination

A DNA biosensor based on a modified gold electrode with a Au/cysteine/DNA matrix was developed for ultratrace determination of genotoxicity antibiotics. The modified Au/cysteine/DNA electrode was characterized by cyclic voltammetry and impedance spectroscopy methods. The interaction between immobilized DNA and genotoxicity antibiotics in hospital wastewater was investigated using differential pulse voltammetry (DPV) technology. Using this technique, ciprofloxacin and ofloxacin were detected in real time in the hospital wastewater (HW) of the Tunisian cities of Gabes, Tozeur, Sfax, and Gbeli. In addition, physicochemical parameters such as the chemical oxygen demand (COD), biological oxygen demand (BOD), and total organic carbon (TOC) of HW samples that may affect the nature of the samples were studied. Comet assay (single-cell gel electrophoresis) was performed to measure the capacity of xenobiotics to induce DNA damage. In our conditions, this test indicated that all tested wastewater was able to alter cell integrity and cause DNA molecular damage, and the most genotoxic effect was found in the wastewater of Gabes hospital. Results show that the concentrations of the two antibiotics reached 33 and 40 ng/mL in the hospital wastewater of Gabes and Tozeur, respectively. The DNA biosensor based on the modified gold electrode exhibited superb performance and offers a probable application for the detection of genotoxicity antibiotics in hospital wastewater. The level of genotoxicity is proportional to the concentration of antibiotics detected in hospital wastewater. We will explore the application of this model for continuous monitoring downstream of hospital discharge and wastewater treatment plants for effective control of the presence of genotoxic products

An immunosensor for pathogenic staphylococcus aureus based on antibody modified aminophenyl-Au electrode

International audienceThe objective of this work is to elaborate an immunosensing system which will detect and quantify Staphylococcus aureus bacteria. A gold electrode was modified by electrografting of 4-nitrophenyl diazonium, in situ synthesized in acidic aqueous solution. The immunosensor was fabricated by immobilizing affinity-purified polyclonal anti S. aureus antibodies on the modified gold electrode. Cyclic voltammetry (CV) and Faradaic Electrochemical Impedance Spectroscopy (EIS) were employed to characterize the stepwise assembly of the immunosensor. The performance of the developed immunosensor was evaluated by monitoring the electron-transfer resistance detected using Faradaic EIS. The experimental results indicated a linear relationship between the relative variation of the electron transfer resistance and the logarithmic value of S. aureus concentration, with a slope of 0.40 ± 0.08 per decade of concentration. A low quantification limit of CFU per ml and a linear range up to CFU per mL were obtained. The developed immunosensors showed high selectivity to Escherichia coli and Staphylococcus saprophyticus

An electrochemical immunosensor for detection of staphylococcus aureus bacteria based on immobilization of Aantibodies on self-assembled monolayers-functionalized gold electrode

International audienceThe detection of pathogenic bacteria remains a challenge for the struggle against biological weapons, nosocomial diseases, and for food safety. In this research, our aim was to develop an easy-to-use electrochemical immunosensor for the detection of pathogenic Staphylococcus aureus ATCC25923. The biosensor was elaborated by the immobilization of anti-S. aureus antibodies using a self-assembled monolayer (SAMs) of 3-Mercaptopropionic acid (MPA). These molecular assemblies were spontaneously formed by the immersion of the substrate in an organic solvent containing the SAMs that can covalently bond to the gold surface. The functionalization of the immunosensor was characterized using two electrochemical techniques: cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Here, the analysis was performed in phosphate buffer with ferro/ferricyanide as the redox probe. The EIS technique was used for affinity assays: antibody-cell binding. A linear relationship between the increment in the electron transfer resistance (RCT) and the logarithmic value of S. aureus concentration was observed between 10 and 106 CFU/mL. The limit of detection (LOD) was observed at 10 CFU/mL, and the reproducibility was calculated to 8%. Finally, a good selectivity versus E. coli and S. epidermidis was obtained for our developed immunosensor demonstrating its specificity towards only S. aureus

Detection of pathogenic Staphylococcus aureus bacteria by Electrochemical Impedance.

communication par afficheInternational audienc