Rating of Perceived Exertion (RPE) relates to how ‘hard’ or ‘easy’ an exercise feels. The Borg 6-20 RPE scale is the most widely used scale to estimate the overall, peripheral and central perception of effort. To date, there are a limited number of studies on the use and efficacy of perceived exertion in persons with spinal cord injury and/or disease. The findings from these studies are also equivocal. Therefore, the aims of this thesis were to assess: i) the relationship between the RPE and physical and physiological markers of exercise intensity during arm cranking exercise in able-bodied and individuals with spinal cord disease, ii) the efficacy of sub-maximal RPE values to predict peak oxygen uptake during arm cranking exercise in able-bodied and paraplegic individuals using different exercise protocols, iii) the scalar property of the RPE during arm cranking exercise in able-bodied and paraplegic individuals. To achieve these goals, the thesis has been broken down to a series of seven studies. In each of these studies, except study 6, a group of able-bodied and a group of paraplegic participants were recruited to asses these hypotheses. Paraplegic individuals had spinal cord injury with neurological levels at or below the sixth thoracic vertebra (T6) or flaccid paralysis as a result of poliomyelitis infection. These individuals were physically active and participated in sports like wheelchair basketball, weightlifting, wheelchair racing and table tennis at both professional and recreational levels. Able-bodied participants were healthy and free from pre-existing injuries and physically active but not arm-trained. There were strong relationships between the RPE and each of the physiological and physical indices of exercise intensity during arm cranking exercise regardless of group or gender. Peak oxygen uptake can be predicted with reasonable accuracy from sub-maximal oxygen uptake values elicited during a sub-maximal perceptually-guided, graded exercise test for paraplegic individuals but not for able-bodied participants. It has also been shown that peak oxygen uptake can be predicted from power output using the equation prescribed by the American College of Sports Medicine (ACSM, 2006). Furthermore, for able-bodied participants using estimation procedures, a passive process in which an individual is asked to rate how ‘hard’ or ‘easy’ an exercise feels, the ramp exercise test provided more accurate prediction of peak oxygen uptake compared to the graded exercise test. For paraplegic persons using estimation procedures, the graded exercise test provided more accurate prediction of peak oxygen uptake compared to the ramp exercise test. Finally, the scalar property of the RPE (i.e., similar proportions of time at a given RPE) was evident during arm cranking exercise regardless of group. In conclusion, the prediction of peak oxygen uptake from sub-maximal exercise tests would provide a safer environment of exercise testing. In addition, using a sub-maximal protocol would make peak oxygen uptake more available for sedentary and clinical population compared to the graded exercise test to volitional exhaustion. Prediction of peak oxygen uptake from power output using the ACSM equation would make the estimation of peak oxygen uptake more available for large groups of people. Similar proportions of time were observed at a given RPE regardless of group or exercise intensity. The early RPE responses will give an indicator for how long a participant is going to exercise. This has important implications for rehabilitation settings. Based on the RPE responses the tester or the observer can increase or decrease the work rate to enable the participant to exercise for the desired duration.

Nanotechnology is a rapidly growing industry of global economic importance, with new technologies exploiting the novel characteristics of materials manufactured at the nanoscale being developed for use within the biomedical, electronic, energy production and environmental sectors. The unusual properties of engineered nanomaterials (ENMs) that make them useful in such applications have led to concerns regarding their potential impact on the environment. The aquatic environment is particularly at risk of exposure to ENPs, yet, there is currently little known about their behaviour in aquatic systems, their capacity to be taken up by aquatic organisms or their potential toxic effects. The studies that were conducted during this work sought to investigate the ecotoxicology of a range of metal and metal oxide nanoparticles using fish as a vertebrate model. In order to gain a better understanding of the uptake and effects of ENMs in fish, rainbow trout (Oncorhynchus mykiss) were exposed to nanoparticulate (34 nm) and bulk (>100 nm) titanium dioxide particles via the water column (500 and 5000 µg L-1), and to titanium dioxide nanoparticles via the diet (0.1 and 1 mg g-1 food) and via intravenous injection (1.3 mg kg-1 body weight). Uptake of titanium dioxide into the tissues of trout after waterborne and dietary exposure was found to be very low, suggesting limited bioavailability of the nanoparticles to the fish, although small amounts of uptake of titanium dioxide across the gill epithelial membrane were observed using coherent anti-stokes Raman scattering. Intravenously injected titanium dioxide accumulated and was retained in the kidneys for up to 21 days, but no adverse effect on kidney function was detected. Silver nanoparticles are already in widespread use in a variety of consumer products such as wound dressings, food containers, sock fabrics and paints, principally for their antimicrobial activity. Despite its growing commercialisation, there is little known about the environmental effects of the use of nanoparticulate silver in these products. In order to investigate these potential effects, rainbow trout were also exposed to 10 nm, 35 nm and bulk (0.6-1.6 µm) silver particles via the water column at concentration of 10 and 100 µg L-1. Uptake of silver in the gills and liver of trout occurred, with smaller nanoparticles showing a greater propensity for association with gill tissue, but with no significant differences in uptake between particles of different sizes in the liver. No increases in lipid peroxidation were detected in gills, liver or blood plasma of trout, however, expression of cyp1a2 was significantly up-regulated in exposures to 10 nm silver particles in the gill, suggesting an increase in oxidative metabolism. In an attempt to develop an effective high through-put in vitro screening assay for ENMs, the suitability of isolated rainbow trout primary hepatocytes was examined as a potential model for in vitro screening of a range of toxicological endpoints in response to nanoparticles and for studying uptake of nanoparticles into cells. The hepatocytes retained a good level of functionality after culturing as evidenced by vitellogenin production in response to the synthetic oestrogen, 17β-oestradiol. The cultured hepatocytes, however, showed limited responses on exposure to titanium dioxide, zinc oxide, cerium oxide and silver nanoparticles for lipid peroxidation and glutathione-s-transferase activity assays. Furthermore, the hepatocytes were unresponsive to the induction of these biological responses in the positive controls, suggesting they are not a good model for investigating the potential toxic effects of ENMs in terms of these endpoints. Uptake of the nanoparticles into the cells, however, was demonstrated by coherent anti-stokes Raman spectroscopy, indicating that this in vitro assay may provide a useful model for studying uptake of ENPs into cells. The studies conducted in this thesis contribute the science base regarding the bioavailability of ENPs in aquatic media as well as highlighting the importance of characterisation of ENPs in understanding their behaviour, uptake and effects in aquatic systems and in fish.

The most apparent symptom of boron deficiency in higher plants is a cessation of growth. Deficiency causes a reduction in ascorbate concentration and the absorption of nutrient ions. Addition of ascorbate temporarily relieves deficiency symptoms. In boron sufficient plants the addition of ascorbate to media causes an increased uptake of nutrients. In an attempt to discover if ascorbate addition to deficient plants causes increased ion uptake, radish plants were grown hydroponically in four different strengths of boron solution. A colorimetric assay for phosphorus was performed both before and after supplementation. Results, however, were inconclusive.

Les rejets d'effluents liquides des Centres Nucléaires de Production d'Electricité (CNPE) sont constitués d'un mélange de substances stables et radioactives. L'exposition d'organismes à des substances en mélange peut faire l'objet d'interactions diverses, conduisant à une augmentation ou à une diminution des effets observés. Afin d'identifier de possibles interactions dans le cas de mélanges de substances caractéristiques (en termes de toxicité et de quantité) des rejets de CNPE, l'effet d'un mélange binaire composé de cuivre et d'HTO a été étudié sur le modèle d'algue unicellulaire Chlamydomonas reinhardtii. Dans un premier temps, la toxicité de l'HTO a été analysée. L'HTO s'est révélée être peu toxique envers notre modèle biologique. L'effet le plus sensible et le plus précoce est une augmentation du stress oxydant (dès 40 kBq mL-1 - 0.13 µGy h-1). Lors de l'exposition des cellules algales au mélange HTO/Cu, une interaction a été révélée au niveau du stress oxydant cellulaire, celui-ci étant supérieur à une simple addition de l'effet des deux substances. Cette interaction peut s'expliquer par une augmentation de l'internalisation du cuivre en présence d'HTO, mais aussi potentiellement par des interactions toxiques directes (notamment sur les processus de régulation du stress oxydatif). En conclusion, il a été démontré que l'effet de substances stables et radioactives en mélange peut être supérieur à l'addition. Bien qu'étant uniquement représentative du mélange binaire HTO/Cu, cette étude montre néanmoins de potentielles interactions entre substances stables et radioactives, à considérer lors de l'évaluation des risques écologiques relatifs aux rejets de CNPE. / Liquid releases by Nuclear Power Plants (NPP) are composed of a mixture of radioactive and non-radioactive substances. When organisms are exposed to mixtures of contaminants the resultant toxicity can be enhanced, or reduced, due to interactions. In order to identify potential interactions between substances released by NPP, two substances representative of such effluents (in term of toxicity and of quantity) were selected for studies: Tritiated water (HTO) and copper (Cu). Effects of this binary mixture were studied on the unicellular green algae Chlamydomonas reinhardtii. HTO, when examined along, was not very toxic to C. reinhardtii. The most sensitive and early effect of HTO was an increase in oxidative stress at concentrations of 40 kBq mL-1 (0.13 µGy h-1). Algae exposure to the binary mixture HTO/Cu induced interactive effects on oxidative stress. Reactive Oxygen Species production was higher from exposure to the mixture of contaminants than the addition of the effect from each substance individually. This interaction was explained by an enhanced copper uptake by the alge when in the presence of HTO. The observed supra-additive effect could also be due to direct toxic interactions, especially on the antioxidant system. To conclude, this study showed that the effects of a mixture of radioactive and non-radioactive substances can be greater than what would be predicted based on mere addition of individual effects. Even thought this binary mixture is just a small part of NPP effluents, the study showed that potential interactions should be considered when determining ecological risks too aquatic ecosystems from NPP effluents.

Among multiple interconnected pathways for L-Lysine catabolism in pseudomonads, it has been reported that Pseudomonas aeruginosa PAO1 employs the decarboxylase and the transaminase pathways. However, knowledge of several genes involved in operation and regulation of these pathways was still missing. Transcriptome analyses coupled with promoter activity measurements and growth phenotype analyses led us to identify new members in L-Lys and D-Lys catabolism and regulation, including gcdR-gcdHG for glutarate utilization, dpkA, amaR-amaAB and PA2035 for D-Lys catabolism, lysR-lysXE for putative L-Lys efflux and lysP for putative L-Lys uptake. The amaAB operon is induced by L-Lys, D-Lys and pipecolate supporting the convergence of Lys catabolic pathways to pipecolate. Growth on pipecolate was retarded in the gcdG and gcdH mutants, suggesting the importance of glutarate in pipecolate and 2-aminoadipate utilization. Furthermore, this study indicated links in control of interconnected networks of lysine and arginine catabolism in P. aeruginosa. Effect of D-amino acids and the genes involved in their metabolism are of great interest in both bacteria and mammals. D-Arg utilization in PAO1 requires the coupled dehydrogenases DauB and DauA. In this study, DauB was found to use only L-Arg as its substrate unlike its partner dehydrogenase DauA with wide substrate specificity. However, evidence from this study and previous studies suggest that the coupled enzymes DauB and DauA are unique for D-Arg catabolism. The three D-amino acid dehydrogenases DguA, DadA and DauA were found to have somewhat limited in vivo substrate specificity compared to that found in vitro tested using purified enzymes. Many studies showed that D-amino acids are toxic to bacteria. The ΔdguA, ΔdadA and ΔdauA triple mutant had two-fold lower minimum inhibition concentration of carbenicillin and tetracycline compared to wild-type PAO1. Both in the wild-type PAO1 and the triple mutant, synergy was observed between gentamicin or tetracycline (at concentrations below the MIC) and D-amino acids resulting in growth inhibition or reduction, respectively. However, no special synergistic or antagonistic effects were observed specifically in the ΔdguA, ΔdadA and ΔdauA triple mutant as compared to the wild-type PAO1 when D-amino acids were given in combination with antibiotics.

Human α-N-acetylglucosaminidase (Naglu) is a lysosomal enzyme implicated in the rare metabolic storage disorder Mucopolysaccharidosis III type B (MPS IIIB). A deficiency in Naglu results in a buildup of heparan sulfate in lysosomes, which is most detrimental in the central nervous system, causing mental retardation and a shortened lifespan. Enzyme replacement therapy is currently ineffective in treating the neurological symptoms of MPS IIIB due to the inability of Naglu to cross the blood-brain barrier. This laboratory uses a Spodoptera frugiperda insect cell system to express recombinant Naglu conjugated to a synthetic protein transduction domain with the intent to allow Naglu to cross the blood-brain barrier and treat the neurological symptoms. In the present study, we aimed to purify a recombinant Naglu-PTD4 fusion protein in order to assess its capacity to cross cellular membranes. A three-step method involving multi-modal, hydrophobic interaction, and gel filtration chromatography was optimized to achieve pure Naglu-PTD4, in good yield. Cellular uptake by human MPSIIIB fibroblasts of Naglu-PTD4 was not detectable. It is hypothesized that additional amino acids, including a hexahistidine domain, following the PTD4 domain limited the fusion protein’s membrane transduction capacity. Future studies will focus on removing the additional amino acids and adjusting the purification method as necessary. The ultimate goal of this research is to develop a large-scale recombinant Naglu production protocol for enzyme replacement therapy of MPS IIIB. / Graduate

Manganese and iron homeostasis play an important role in oxidative stress protection in a variety of organisms. However, the transport and role of these metals in the periodontal pathogen Porphyromonas gingivalis were not well understood. Analysis of the genome of P. gingivalis W83 revealed the presence of two genes encoding homologs of ferrous iron transport protein, FeoB1 and FeoB2. The goal of this study was to determine the role of these two putative transporters in metal transport, their contributions to resistance to oxygen radicals and intracellular survival as well as the regulation and genetic organization of these two loci. Isogenic mutant strains deficient in FeoB1 and FeoB2, respectively, were generated and used in this study. The transport ability for manganese and iron was assessed and compared in feoB1, feoB2 mutant and wild type strains using 55Fe2+ and 54Mn2+. We demonstrated that feoB2 encodes a major manganese transporter, while FeoB1 functions as a major ferrous iron transporter. The roles of P. gingivalis FeoB1 and FeoB2 in oxidative stress defense and intracellular survival in host cells were determined using an oxidative stress survival assay and an in vitro infection assay, respectively. The feoB2 mutant exhibited reduced survival after exposure to H2O2 and to atmospheric oxygen and inside the host cells compared to the wild-type strain and its revertant, while the feoB1 mutant survived as well as the wild type strain under oxidative stress and possessed better capability to adhere to and survive in the host cells. Our results demonstrate that FeoB2 is required for protection of the bacterium from oxidative stress and for intracellular survival of P. gingivalis in host cells. However, FeoB1 is dispensable for both processes. Quantitative RT-PCR analysis revealed that expression of feoB2 in P. gingivalis is induced by oxidative stress. However, expression of feoB1 increased 2-fold upon exposure to lower growth temperature. Both observed inductions were specific and not detected under other stress conditions. We have also showed in this study that feoB2 is the second gene transcribed in an operon that is composed of a total of five genes and feoB1 is only co-transcribed with one downstream gene encoding a hypothetical protein. Notably, we also identified tandem repeats with potential to form stable stem-loop RNA secondary structure within the feoB2 and feoB1 transcripts.To our knowledge, this study has demonstrated the first connection among metal homeostasis, oxidative stress resistance and response to host cells in the periodontal pathogen, P. gingivalis.

Liposomal ciprofloxacin (Lipo-CPFX) is being developed for inhalation, with a goal of sustaining the therapeutic activity, compared to unformulated ciprofloxacin (CPFX). However, the kinetics and mechanism of its sustained local lung retention and pharmacological activity are yet to be fully characterized. This project hypothesized that Lipo-CPFX enables slower and sustained lung epithelial transport and uptake, compared to CPFX, thereby producing prolonged local pharmacological actions. The human bronchial epithelial Calu-3 cells were used as monolayers to characterize the kinetics and mechanism of transport and/or uptake, and to assess the effects of such slow kinetics for Lipo-CPFX on its inhibition against lipopolysaccharide (LPS)-induced proinflammatory IL-8 release. The transport fluxes for Lipo-CPFX across the highly restricted Calu-3 cell monolayers was transepithelial electrical resistance-independent, which suggested predominant transcellular transport. Compared to CPFX, Lipo-CPFX showed 6-18 times slower transport, while the flux was increased with increasing concentration proportionally without saturation. Its unaltered transport by cellular energy depletion, transport inhibition by a reduced temperature (4 oC) and endocytosis/lipid fusion inhibitors, filipin and LysoPC, and increased transport by excess empty liposomes collectively suggested cell energy-independent, lipid bilayer fusion mechanisms for the Lipo-CPFX transport across the Calu-3 cells. Likewise, Lipo-CPFX showed 2-4 fold lower cellular uptake than CPFX, proportional to concentration. Lipo-CPFX exhibited significant inhibitory activities at ≥ 0.01 mg/mL on LPS-induced IL-8 release from the Calu-3 cells, which was equipotent to CPFX. Upon 24 h pre-incubation, Lipo-CPFX caused 36.9 and 47.5 % inhibition at 0.01 and 0.05 mg/mL, respectively, while CPFX failed to do so. However, the effect was negated upon repeated wash of the mucosal cell surface, speculating the importance of cell membrane-associated drug/formulation on the inhibitory activities for Lipo-CPFX. Upon 24 h transport, Lipo-CPFX retained 79.0 % of the 4 µg dose on the mucosal cell surface, which was 1.9-times greater than 40.7 % for CPFX. As a result, when LPS was added at 24 h of the transport, Lipo-CPFX was still capable of causing 60.1 % inhibition, as its sustained local anti-inflammatory activity; CPFX however also exhibited equipotent inhibition, by virtue of comparable cellular drug uptake/transport.

Neisseria gonowhoeae has evolved a repertoire of high-affinity iron acquisition systems to facilitate essential iron uptake in the human host. Acquisition of iron requires both the energy-harnessing cytoplasmic membrane protein, TonB, as well as specific outer membrane TonB-dependent transporters (TdTs). The overall goal of this study was to investigate the extra- and intracellular iron acquisition mechanisms of N. gonorrhoeae and determine the role of the TonB and TdTs in this process.The ability of gonococci to acquire potential exogenous iron sources was determined by plate bioassay. Gonococcal growth was promoted by various catecholate and hydromate siderophores; however, growth was not dependent upon TonB expression.As all previously characterized siderophore-iron uptake is dependent upon this protein, apotential TonB-bypass mechanism is suggested.The role of the Ton system and TdTs in gonococcal survival within human cervicalepithelial cells was also determined for two gonococcal strains, FA1090 and MS 1 1. Wedemonstrate that intracellular survival of both strains was dependent upon host cell ironacquisition, yet the expression of the Ton system was only critical to the survival ofFA1090. One characterized difference between these two strains is possession of thegonococcal genetic island (GGI) which is present in approximately 80% of gonococcalstrains. This study demonstrates that the GGI provides a mechanism to bypassintracellular TonB-dependent iron acquisition.In the strain lacking the genetic island, none of the characterized TdTs provided abenefit to the gonococcus when grown intracellularly. However, expression of oneuncharacterized TdT, TdfF, was necessary for successful intracellular survival. To ourknowledge, this is the first demonstration of a specific requirement for a single irontransporter in the survival of a bacterial pathogen within host epithelial cells.In the GGI-containing strain, TonB function was not critical to survival withincervical epithelial calls. The presence of the GGI was associated with the ability to bypass TonB-dependant uptake. Specifically, this bypass mechanism was mediated bycomponents of the T4S machinery encoded by the GGI, and replication was directlyrelated to iron acquisition. To our knowledge, this study provides the first direct linkbetween bacterial iron acquisition and a type IV secretion system.

In an effort to apply Cumulative Risk Assessment (CRA) as developed by the U.S. EPA, the present study investigates the cumulative risks to Eastern oysters due to multiple stressors such as salinity, temperature and oxygen and carbon dioxide. I also compared the effectiveness of the Hazard Quotient Method (HQ) in CRA. Ambient conditions in the James River, VA were obtained from the Virginia DEQ database and respiratory responses were estimated using values from the literature. The multiple environmental stresses are evaluated using a probabilistic analysis that combines the environmental conditions. It was concluded that salinity was the most influential stressor in the model. Other risks were identified contributing to the vulnerability of the oysters. Crystal Ball simulations yielded that the oxygen uptake of oysters reduced by more than 29%. The HQ method was found to be inappropriate in analyzing cumulative risks for CRA. Oyster populations are dramatically declining in the James River and the Chesapeake Bay. Hence, effective oyster restoration activities are underway to rebuild oyster populations in the James River and throughout the Bay area.