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No description available.

Microbial desalination cells (MDCs), a recent technological discovery, allow for simultaneous wastewater treatment and desalination of saline water with concurrent electricity production. The premise for MDC performance is based on the principles that bioelectrochemical (BES) systems convert wastewaters into treated effluents accompanied by electricity production and the ionic species migration (i.e. protons) within the system facilitates desalination. One major drawback with microbial desalination cells (MDCs) technology is its unsustainable cathode chamber where expensive catalysts and toxic chemicals are employed for electricity generation. Introducing biological cathodes may enhance the system performance in an environmentally-sustainable manner. This study describes the use of autothrophic microorganism such as algae and Anammox bacteria as sustainable biocatalyst/biocathode in MDCs. Their great potential for high valuable biomass production combined with wastewater treatment presents these systems as a viable option to replace expensive/unsustainable catalysts for oxygen production in MDCs. Since alga is a photosynthetic microorganism, the availability of light as well as the electron-donating anodic process may have significant effects on the biocathode performance. A series of experiments evaluating these effects proved that algae perform better under natural light/dark cycles and that higher COD concentrations do not necessarily improve the power density. Furthermore, three different process configurations of photosynthetic MDCs (using Chlorella vulgaris) were evaluated for their performance and energy generation potentials. Static (fed-batch, SPMDC), continuous flow (CFPMDC) and a photobioreactor MDC (PBMDC, resembling lagoon type PMDCs) were developed to study the impact of process design on wastewater treatment, electricity generation, nutrient removal, and biomass production and the results indicate that PMDCs can be configured with the aim of maximizing the energy recovery through either biomass production or bioelectricity production. In addition, the microbial community analysis of seven different samples from different parts of the anode chamber, disclosed considerable spatial diversity in microbial communities which is a critical factor in sustaining the operation of MDCs. This study provides the first proof of concept that anammox mechanism can be beneficial in enhancing the sustainability of microbial desalination cells to provide simultaneous removal of ammonium from wastewater and contribute in energy generation.

According to USDA-FSIS reports, L. monocytogenes and Salmonella are two important foodborne pathogens that are prevalent throughout catfish environment. Channel catfish (Ictalurus punctatus) is the most important aquaculture species in the United States accounting for more than 60% of its aquaculture production. The objectives of this study were to determine the effect of strain, temperature concentration on the growth, survival and biofilm formation of L. monocytogenes and Salmonella using catfish mucus extract on different food-contact surfaces. Growth and survival of L. monocytogenes and Salmonella was greater at the higher concentration of mucus extract at both 10°C and 22°C. In 15 micrograms/ml catfish mucus extract L. monocytogenes and Salmonella counts increased to 4.5 log CFU/ml after 72 h at 10°C and 5-7 log CFU/ml counts after 32-48 h at 22°C. In 375 micrograms/ml catfish mucus extract L. monocytogenes and Salmonella counts increased to 6-7 log CFU/ml counts after 72 h at 10°C and 8-9 log CFU/ml counts after 32-48 h at 22°C. L. monocytogenes and Salmonella were able to grow and survive for more than 63 days with at least 4-6 log CFU/ml at 10°C and 6-8 log CFU/ml in 375 micrograms/ml and 15 micrograms/ml of catfish mucus extract respectively. No differences (P > 0.05) among L. monocytogenes and Salmonella strains were observed to form biofilms in the presence catfish mucus extract on the stainless steel surface. The biofilm formation by L. monocytogenes and Salmonella in catfish mucus extract was less (P < 0.05) on buna-n rubber when compared to stainless steel, polyethylene and polyurethane surfaces. Therefore, the findings in this study show that catfish mucus promotes L. monocytogenes and Salmonella to grow and subsequently form biofilms on different food-contact surfaces also promotes growth and survival of these pathogens for longer period of time in catfish processing industries.

Listeria monocytogenes is a major concern for the food industry. It is one of the major agents causing listeriosis. The objective of the first part of this study is to evaluate the effect of hydration level on attached listeria monocytogenes on stainless steel/High density polyethylene transferred to food products. Attached cells were prepared on stainless steel/High density polyethylene. Transfer experiments were conducted from inoculated surface material slides to cold smoked salmon fillets. This experiment was repeated 6 times. The results were analyzed with an analysis of variance by SAS. The differences between the different RH% and surface conditions were not statistically significant. There was variability in between packages, brands and over the course of storage after opening, and likely contributed to the variability of transfer observed in this set of experiments. The objective of the second part of the research is to study the effect of hydration level on the detachment of Listeria monocytogenes biofilm growing on stainless steel by using Atomic force microscope. Biofilms were grown on stainless steel in drip flow bioreactor at 32 °C for 72 h. Then biofilms were equilibrated over saturated salt solution at 20 °C for 48 h before the Atomic Force Microscope experiment. The results showed that cohesive energy value of the biofilm increased with biofilm depth. Only square shaped displaced 2.5X2.5 μm region were visualized after serious of raster scanning under high load which means that moisture condition of Listeria monocytogenes biofilm can significantly affect the cohesiveness between of Listeria monocytogenes biofilm.

The food-borne pathogen Listeria monocytogenes can attach to the environmental surfaces and develop biofilm which can cause food contamination in the food industries. Sortase A and surface proteins are involved in biofilm and virulence of L. monocytogenes. Curcumin was reported to inhibit sortase A and biofilm in gram positive bacteria. The overall objective of this study was to observe the effect of curcumin (Curcuma longa) on the biofilm formation and surface proteins of L. monocytogenes. The antibiofilm effect of curcumin against the strain LM21 (wild type) and s22-11G (sortase A defective mutant) was studied using the microtiter plate assay. No significant differences between the growth of the wild type and the sortase A defective mutant were observed at sub-inhibitory concentrations of curcumin. However, a greater biofilm reduction was observed in the strain s22-11G. The effect of curcumin from two different manufacturers on the wild type was also compared by the microtiter plate assay. Both curcumin did not exhibit statistically different effect on the growth of the wild type. However, a greater biofilm inhibitory effect was observed in one curcumin. The HPLC results suggested that curcumin with the greater antibiofilm activity contained higher amount of curcumin which was reported to be the most potent curcuminoid compound in curcumin. Three different protein extraction methods were evaluated and the most efficient method was used for 2D-GE. When cells were grown in the presence of curcumin, 5 proteins, 16 proteins and 4 proteins were up-regulated, down-regulated and absent, respectively in L. monocytogenes LM21. The influence of the enzyme sortase A upon surface protein expression was evaluated by comparing proteins expressed by wildtype L. monocytogenes LM21 to that of the sortase A mutant, s22-11G. In strain s22-11G, 2 proteins, 8 proteins and 3 proteins were up-regulated, down-regulated and absent in comparison to wildype LM21. The exact information of these differentially expressed proteins still need to be identified by mass spectrometry.

Invasive fungal infections are a significant clinical challenge especially for hospitalized patients as traditional antifungal therapy often fails to resolve these infections. The ability of Candida to undergo yeast-to-hyphae morphological transition is central to this invasive behavior. Morphogenesis is also important for the formation of biofilms which are highly structured communities of microorganisms attached to one another or substratum and embedded within a protective extracellular matrix material. The refractory nature of cells within a biofilm to current antifungal therapies has created a need for alternative antifungal agents for the management of Candida biofilm-related infections. The novel antifungal occidiofungin is a natural product produced by the soil bacteria Burkholderia contaminans shown to be effective against a broad range of fungi including Candida spp. Prior studies have demonstrated that occidiofungin inhibits yeast-to-hyphae morphogenesis in the dimorphic yeast, C. albicans, likely through its impact on disrupting F-actin organization. To extend these findings, the efficacy of occidiofungin on morphogenesis of C. albicans and C. tropicalis strains under different inducing conditions was evaluated. Further, given the role of biofilm on pathogenicity, the anti-biofilm properties of occidiofungin against Candida species was examined using an in vitro static biofilm model developed on a silicon elastomer disk. The accumulated data indicate that occidiofungin inhibits hyphal transformation regardless of the inducing conditions used and prevents hyphal extension when added to cells post switching. Moreover, morphologically switching cells were more sensitive to occidiofungin than their yeast counterpart. In addition, occidiofungin effectively blocks biofilm formation at all stages of development and reduces dispersed cells from the biofilm for both C. albicans and C. tropicalis. Confocal data revealed alterations in actin organization with occidiofungin treatment for both morphologically switching and biofilm cells. These findings correlate with prior observations for occidiofungin activity on yeast form cells indicating the broad activity of occidiofungin against fungi at various stages of pathogenic growth and supports efforts to pursue occidiofungin as a potential therapeutic against Candida based infections.

Thèse numérisée par la Direction des bibliothèques de l'Université de Montréal.

Borrelia burgdorferi is the etiological agent of Lyme disease. Not much is known about the susceptibility of this organism to chemical disinfection. Current antimicrobial susceptibility test methods, such as those published by the American Society for Testing and Materials (ASTM), usually require assessment of the number of colony forming units (cfu) of growing organisms on plates following exposure to an agent. For fast-growing organisms, plates are ready for counting 1-2 days post plating, while several weeks may be needed for slower growing organisms. Spirochetes, like B. burgdorferi are difficult to grow on solid media and typically require long incubation periods, sometimes up to several weeks, to generate visible colonies. These issues make B. burgdorferi cfu assessment by plate counting difficult and unreliable. Furthermore, Borrelia have a demonstrated capacity for pleomorphic forms, and can exist in spirochete, round body, or biofilm forms, depending on culture conditions. Plate counts, by nature, do not allow for assessment of morphological form changes. Additionally, the susceptibility of B. burgdorferi pleomorphic forms to chemical disinfectants has not been tested. In this study, we used the SYBR GREEN I/Propidium Iodide (SG I/PI) viability assay to rapidly estimate the percent kill of B. burgdorferi pleomorphic forms to chemical disinfection. Planktonic spirochete populations in 30-second treated samples showed viability percent values of: >95% for Hanks balanced salt solution (HBSS), ~60% for distilled deionized H2O (dd H2O), <5% for ACS 200, and 1% for 1% glutaraldehyde (GTA). Solutions containing 70% ethanol (ETH) and 1% hypochlorite (HC) showed no viable spirochetes following treatment. The percent of live round body cells following different treatments were: >99% for HBSS and <25% for dd H2O. ACS 200, 1% GTA, and 70% ETH treatments resulted in <1% live round body forms, whereas HC showed no live round cell forms. The susceptibility of B. burgdorferi biofilms to various treatments was also assayed using a SG I/PI viability stain after 30-minute contact times. The percent of viable organisms (green) in the treated biofilms was estimated by microscopic observations. HBSS controls showed >98% of bacteria in the biofilm were alive, while treated biofilms showed the following percent viabilities: ACS 200 - ~2%, 1% HC - <1%, 5% HC - <1%, 1% GTA - ~10%, 70% ETH - ~ 2%, and dd H2O ~40%. These techniques merged standardized assessment of antimicrobial activity in liquid culture using an ASTM-type kill-time procedure with viability techniques used in antibiotic susceptibility testing to rapidly evaluate the percent kill of B. burgdorferi pleomorphic forms in vitro following disinfectant exposure. These results showed that B. burgdorferi biofilm forms are orders of magnitude more resistant to chemical disinfection than other morphological forms of this organism.