Mycotoxins are secondary metabolites produced by many fungal species. Health effects induced by the ingestion of these substances are well documented and some mycotoxins are now regulated for their maximum tolerable levels in foods. However, other routes of exposure to these contaminants are possible. Thus, if irritating or allergenic reactions related to the inhalation of fungal spores or mycelial fragments have been demonstrated, inhalation of mycotoxins is also suspected to be causing certain respiratory disorders or certain pathologies. Indeed, mycotoxins can be found in spores but also on finer particles which are easily aerosolized and therefore likely to be inhaled. However, data on the hazard associated with human exposure to mycotoxins by inhalation are still very fragmented. In this context, our main objective was to characterize the aerosolization of mycotoxins during the colonization of different materials encountered in indoor environments by toxinogenic molds. First we studied growth and production of mycotoxins during the colonization of building materials (wallpaper, painted fiberglass wallpaper, vinyl wallpaper, fir, fiberglass) by three fungal species of interest: Aspergillus versicolor, Penicillium brevicompactum, Stachybotrys chartarum. These species were chosen because of their frequent presence in indoor environments and their diverse mycelial organization. In addition, these three species produce different toxins: sterigmatocystin, mycophenolic acid and macrocyclic trichothecenes for A. versicolor, P. brevicompactum and S. chartarum, respectively. These studies have shown that, during their development on tested materials, three species produce mycotoxins. The most favorable material for fungal development and toxinogenesis is wallpaper. Mycophenolic acid, sterigmatocystin and macrocyclic trichothecenes can thus be produced at levels of 1.8, 112.1 and 27.8 mg/m2, respectively, on this material. These toxins can then be partially aerosolized. We have shown that aerosolization depends on species and their mycelial structure, but also on culture conditions and airflow. This transfer to air is nevertheless observed after aeraulic solicitations which can be easily encountered in indoor environments because theycorrespond to the movement of people in a room (0.3 m/s), speed of air in ceiling diffusers (2 m/s), slamming doors or air drafts when opening windows(6 m/s). P. brevicompactum showed to be the easiest to aerosolize. The major part of the aerosols’ toxic charge is found in particles whose size corresponds to that of spores or mycelial fragments. However, for macrocyclic trichothecenes, toxins were also found in particles smaller than spores, which could easily be inhaled by occupants and penetrate deep into the respiratory tract. In order to better characterize the actual hazard associated with inhalation of these compounds, cytotoxicity studies have been performed using lung cells and comparing with results observed on digestive cells. Pulmonary toxicity is comparable to that observed in digestive cells. Macrocyclic trichothecenes are much more toxic than other tested toxins with IC50 in order of ng/ml. In parallel, we analyzed the VOCs specifically produced during active mycotoxinogenesis in order to identify potential biomarkers of the actual production of mycotoxins that could be used as tools for monitoring of indoor environments. Unfortunately, this approach has not, for the moment, led to the identification of specific targets. In the end, we evaluated the persistence of these contaminants during application of bleach, the most frequently used decontamination process. We have shown that a normal cleaning procedure allows only partial removal of mold.

abstract: Since its first report in 1976, many outbreaks linked to Legionella have been reported in the world. These outbreaks are a public health concern because of legionellosis, which is found in two forms, Pontiac fever and Legionnaires disease. Legionnaires disease is a type of pneumonia responsible for the majority of the illness in the reported outbreaks of legionellosis. This study consists of an extensive literature review and experimental work on the aerosolization and UV inactivation of E.coli and Legionella under laboratory conditions. The literature review summarizes Legionella general information, occurrence, environmental conditions for its survival, transmission to human, collection and detection methodologies and Legionella disinfection in air and during water treatment processes. E. coli was used as an surrogate for Legionella in experimentation due to their similar bacterial properties such as size, gram-negative rod-shaped, un-encapsulated and non-spore-forming bacterial cells. The accessibility and non-pathogenicity of E. coli also served as factors for the substitution. Three methods of bacterial aerosolization were examined, these included an electric spray gun, an air spray gun and a hand-held spray bottle. A set of experiments were performed to examine E. coli aerosolization and transport in the aerosolization chamber (an air tight box) placed in a Biological Safety Cabinet. Spiked sample was sprayed through the opening from one side of the aerosolization chamber using the selected aerosolization methods. The air sampler was placed at the other side to collect 100 L air sample from the aerosolization chamber. A Tryptic Soy Agar plate was placed inside the air sampler to collect and subsequently culture E. coli cells from air. Results showed that the air spray gun has the best capability of aerosolizing bacteria cells under all the conditions examined in this study compared to the other two spray methods. In this study, we provide a practical and efficient method of bacterial aerosolization technique for microbial dispersion in air. The suggested method can be used in future research for microbial dispersion and transmission studies. A set of experiments were performed to examine UV inactivation of E. coli and Legionella cells in air. Spiked samples were sprayed through the opening from one side of the aerosolization chamber using the air spray gun. A UV-C germicidal lamp inside the Biological Safety Cabinet was turned on after each spray. The air samples were collected as previously described. The application of UV-C for the inactivation of bacterial cells resulted in removing aerosolized E. coli and Legionella cells in air. A 1 log reduction was achieved with 5 seconds UV exposure time while 10 seconds UV exposure resulted in a 2 log bacterial reduction for both bacteria. This study shows the applicability of UV inactivation of pathogenic bacterial cells in air by short UV exposure time. This method may be applicable for the inactivation of Legionella in air ducts by installing germicidal UV lamps for protecting susceptible populations in certain indoor settings such as nursing homes or other community rooms. / Dissertation/Thesis / Masters Thesis Civil and Environmental Engineering 2015

No description available.

Aquatic environments contain a great diversity of microorganisms, some of which may be aerosolized and transported long distances through the atmosphere. The bacterium Pseudomonas syringae can be found in aquatic environments and in the atmosphere and may express an ice nucleation protein (bacteria expressing the protein are Ice+ and bacteria not expressing the protein are Ice-). Ice+ bacteria may be involved in cloud formation and precipitation processes due to their ability to freeze water at warmer temperatures. Freshwater aerosolization processes are not well understood, particularly the role the Ice+ phenotype may play. Water samples were collected from Claytor Lake, Virginia, USA and screened for Ice+ P. syringae. Results indicated that between 6% and 15% of Pseudomonas colonies assayed were Ice+. Preliminary phylogenetic analysis of cts (citrate synthase) sequences from strains of P. syringae showed a surprising diversity of phylogenetic subgroups present in the lake. A Collison nebulizer was used to aerosolize an Ice+ and an Ice- strain of P. syringae under artificial laboratory conditions. The aerosolization of P. syringae was not influenced by water temperature between 5° and 30°C. In general, the culturability (viability) of P. syringae in aerosols increased with temperature between 5 and 30°C. The Ice+ strain was aerosolized in greater numbers than the Ice- strain at all temperatures studied, suggesting a possible connection between the Ice+ phenotype and aerosol production. A quantitative empirical assessment of aerosolized droplets was generated using a laboratory flume and high-speed video. Droplet diameter and initial velocity upon leaving the water surface were examined at four wind speeds (3.5, 4.0, 4.5, and 5.0 m/s), and the results showed that droplet diameter and velocity had a gamma distribution and droplet mass flux increased exponentially with wind speed. An estimate of the potential amount of bacteria capable of aerosolizing was made for each wind speed. An interdisciplinary unit for advanced high school students has been developed presenting biological aerosolization and ice nucleation. This interdisciplinary work combines modeling and experimental approaches across biology and engineering interfaces, with the goal of increasing our understanding of microbial aerosols from aquatic environments that may impact our planet's water cycle. / Ph. D.

La pollution des eaux est une préoccupation majeure relayée par la Communauté Européenne. Cette problématique s'accentue avec les particules métalliques et l'émergence de produits nanostructurés tels les Nano-objets, leurs Agrégats et leurs Agglomérats (NOAA). Ces NOAA constituent un cas particulier de polluants du fait de leurs propriétés physicochimiques. La surveillance et le contrôle de ces polluants dans les eaux, nécessite le développement d'instruments de mesure aptes à répondre à ce fléau environnemental. Dans ce contexte, la technique de spectroscopie de plasma induit par laser ou Laser-Induced Breakdown Spectroscopy (LIBS) a été retenue à l'INERIS. Elle permet l'identification chimique élémentaire des polluants sous forme particulaire dans la matrice liquide et la détermination de leurs concentrations in-situ et en temps réel. Ce travail de thèse a permis d'optimiser l'analyse des suspensions par LIBS avec deux modes d'échantillonnage. La première partie de l'étude a porté sur le couplage LIBS avec un jet liquide et les limites de détection du titane ont été évaluées à 0.5 mg/L. Dans la deuxième partie, les suspensions ont été aérosolisées avec un nébuliseur et analysées par LIBS. Les résultats obtenus en comparant ces deux modes d'échantillonnage montrent que le jet liquide peut être avantageux pour l'analyse de particules dans les liquides. Cependant le mode aérosol présente un intérêt pratique à condition d'avoir un rendement d'aérosolisation supérieur à 50%. Au final, ce travail de thèse démontre l'applicabilité de la LIBS comme outil potentiel pour l'analyse in situ de particules dans les liquides telle que la surveillance et le contrôle des eaux usées / Water pollution is a major concern, as noted by the European Community. This problem is accentuated with metallic particles and the emergence of nanostructured products such as Nano-Objects, their Aggregates and their Agglomerates (NOAA). These are the special types of pollutants owing their physicochemical properties. The monitoring and control of these pollutants in water require the development of measurement instruments which are capable to anwer this environmental problem. In this context, the technique of Laser-Induced Breakdown Spectroscopy (LIBS) has been developed at INERIS. It not only allows the chemical identification of these particles pollutants present in liquids, but also the determination of their concentrations in situ and in real time. This thesis has optimized the analysis of suspensions by LIBS with two sampling modes. The first mode focused on coupling LIBS with a liquid jet in which the detection limits of titanium dioxide were estimated at 0.5 mg/L. In the second mode, the suspensions were aerosolized with a nebulizer and analyzed by LIBS. The results obtained by comparing these two sampling modes show that the liquid jet may be advantageous for the analysis of suspensions. However, the aerosol mode has a practical interest if it has an aerosolization efficiency of over 50%. Finally, this work demonstrates the applicability of LIBS as a potential tool for in situ particle analysis of suspensions such as monitoring and control of wastewater

Les mycotoxines sont de métabolites secondaires produits par de nombreuses espèces fongiques. Les effets sanitaires induits par l’ingestion de ces substances sont bien documentés et certaines mycotoxines font désormais l’objet de réglementations quant à leurs teneurs maximales tolérables dans les aliments. Cependant, d’autres voies d’exposition à ces contaminants sont possibles. Si l’action irritante ou allergisante liée à l’inhalation de spores fongiques ou de fragments mycéliens a été démontrée, l’inhalation de mycotoxines est aussi suspectée d’induire certains troubles respiratoires ou certaines pathologies. En effet, les mycotoxines peuvent être retrouvées dans les spores mais également sur des particules plus fines facilement aérosolisables et donc susceptible d’être inhalées. Cependant, les données concernant le danger associé à l’exposition humaine aux mycotoxines par inhalation sont encore très parcellaires. Dans ce contexte, nos travaux ont eu comme objectif principal la caractérisation de l’aérosolisation des mycotoxines lors de la colonisation de différents matériaux rencontrés dans les environnements intérieurs par des moisissures toxinogènes. Tout d’abord nous avons étudié la croissance et la production de mycotoxines lors de la colonisation de matériaux de construction (papier peint, toile de verre peinte, papier peint vinyle, sapin) par trois espèces fongiques d’intérêt: Aspergillus versicolor, Penicillium brevicompactum, Stachybotrys chartarum. Ces espèces ont été choisies à cause de leur présence fréquente dans les environnements intérieurs et de leur diversité d’organisation mycélienne. De plus, ces trois espèces produisent des toxines différentes: stérigmatocystine, acide mycophénolique et trichothécènes macrocycliques pour A. versicolor, P. brevicompactum et S. chartarum, respectivement. Ces travaux ont démontré que, pendant leur développement sur les matériaux testés, les trois espèces produisent des mycotoxines. Le matériau le plus favorable au développement fongique et à la toxinogénèse est le papier peint. L'acide mycophénolique, la stérigmatocystine et les trichothécènes macrocycliques peuvent ainsi être produits à des niveaux de 1.8, 112.1 et 27.8 mg/m2, respectivement, sur ce matériau. Ces toxines peuvent ensuite être partiellement aérosolisées. Nous avons montré que l’aérosolisation dépend des espèces et de leur structure mycélienne mais aussi des conditions de culture et du flux d’air. Ce transfert dans l'air est observé après des sollicitations aérauliques qui peuvent être rencontrées facilement dans les environnements intérieurs car elles correspondent au mouvement de personne dans une pièce (0.3 m/s), à la vitesse de l'air dans les diffuseurs de plafond (2 m/s), à des coutants d’air ou des claquements de porte (6 m/s). P. brevicompactum est l’espèce la plus facile à aérosoliser. La majeure partie de la charge toxique des aérosols est retrouvée dans des particules dont la taille correspond à celle de spores ou de fragments de mycélium. Cependant, pour les trichothécènes macrocycliques, des toxines ont également été trouvées sur des particules plus petites que les spores, qui pourraient être facilement inhalées par les habitants et pénétrer profondément dans les voies respiratoires. Afin de mieux caractériser le danger réel associé à l’inhalation de ces composés, des études de cytotoxicité ont été réalisés en utilisant des cellules pulmonaires et en comparant avec les résultats observés sur cellules digestives. La toxicité sur cellules pulmonaires est comparable à celle observée sur cellules digestives. Les trichothécènes macrocycliques sont beaucoup plus toxiques que les autres toxines testées avec des IC50 de l’ordre du ng/ml. Au final, nous avons évalué la persistance de ces contaminants lors de l’application d’eau de javel, procédé de décontamination le plus fréquemment utilisé. Nous avons montré qu’une procédure de nettoyage normale ne permet qu’une élimination partielle des moisissures. / Mycotoxins are secondary metabolites produced by many fungal species. Health effects induced by the ingestion of these substances are well documented and some mycotoxins are now regulated for their maximum tolerable levels in foods. However, other routes of exposure to these contaminants are possible. Thus, if irritating or allergenic reactions related to the inhalation of fungal spores or mycelial fragments have been demonstrated, inhalation of mycotoxins is also suspected to be causing certain respiratory disorders or certain pathologies. Indeed, mycotoxins can be found in spores but also on finer particles which are easily aerosolized and therefore likely to be inhaled. However, data on the hazard associated with human exposure to mycotoxins by inhalation are still very fragmented. In this context, our main objective was to characterize the aerosolization of mycotoxins during the colonization of different materials encountered in indoor environments by toxinogenic molds. First we studied growth and production of mycotoxins during the colonization of building materials (wallpaper, painted fiberglass wallpaper, vinyl wallpaper, fir, fiberglass) by three fungal species of interest: Aspergillus versicolor, Penicillium brevicompactum, Stachybotrys chartarum. These species were chosen because of their frequent presence in indoor environments and their diverse mycelial organization. In addition, these three species produce different toxins: sterigmatocystin, mycophenolic acid and macrocyclic trichothecenes for A. versicolor, P. brevicompactum and S. chartarum, respectively. These studies have shown that, during their development on tested materials, three species produce mycotoxins. The most favorable material for fungal development and toxinogenesis is wallpaper. Mycophenolic acid, sterigmatocystin and macrocyclic trichothecenes can thus be produced at levels of 1.8, 112.1 and 27.8 mg/m2, respectively, on this material. These toxins can then be partially aerosolized. We have shown that aerosolization depends on species and their mycelial structure, but also on culture conditions and airflow. This transfer to air is nevertheless observed after aeraulic solicitations which can be easily encountered in indoor environments because theycorrespond to the movement of people in a room (0.3 m/s), speed of air in ceiling diffusers (2 m/s), slamming doors or air drafts when opening windows(6 m/s). P. brevicompactum showed to be the easiest to aerosolize. The major part of the aerosols’ toxic charge is found in particles whose size corresponds to that of spores or mycelial fragments. However, for macrocyclic trichothecenes, toxins were also found in particles smaller than spores, which could easily be inhaled by occupants and penetrate deep into the respiratory tract. In order to better characterize the actual hazard associated with inhalation of these compounds, cytotoxicity studies have been performed using lung cells and comparing with results observed on digestive cells. Pulmonary toxicity is comparable to that observed in digestive cells. Macrocyclic trichothecenes are much more toxic than other tested toxins with IC50 in order of ng/ml. In parallel, we analyzed the VOCs specifically produced during active mycotoxinogenesis in order to identify potential biomarkers of the actual production of mycotoxins that could be used as tools for monitoring of indoor environments. Unfortunately, this approach has not, for the moment, led to the identification of specific targets. In the end, we evaluated the persistence of these contaminants during application of bleach, the most frequently used decontamination process. We have shown that a normal cleaning procedure allows only partial removal of mold.

No description available.

No description available.

No description available.

Les pneumopathies acquises sous ventilation mécanique (PAVM) sont responsables d'une mortalité élevée. La nébulisation d'antibiotiques permet d'améliorer l'efficacité de leur traitement. Pour autant, aucune donnée pharmacocinétique portant sur la colistine et la gentamicine ne permet de recommander un schéma posologique particulier.Nous avons comparé les propriétés pharmacocinétiques plasmatique et intra-pulmonaire de la colistine (administrée sous forme de prodrogue, le colistiméthate sodique ou CMS) et de la gentamicine selon le mode d'administration (nébulisation ou perfusion intraveineuse) chez des patients de réanimation présentant une PAVM.Les concentrations intra-pulmonaires de colistine et de gentamicine étaient, respectivement, de 10 à 40 et 50 à 70 fois supérieures, après nébulisation, à celles retrouvées après administration d'une même dose par voie intraveineuse. La nébulisation permettrait également de limiter le risque de toxicité systémique avec une biodisponibilité inférieure à 10%.En assurant de fortes concentrations intra-pulmonaires et un faible passage systémique, la nébulisation de CMS et de gentamicine pourrait être une bonne alternative à leur administration intraveineuse dans le traitement des PAVM. / Ventilator-associated pneumonia (VAP) is associated with high mortality. Nebulization of antibiotics improves outcome of patient with VAP. However, pharmacokinetic data concerning colistin and gentamicin allowing for optimal dosing regimen recommendation are lacking.We compared systemic and pulmonary concentrations of colistin (administered as an inactive prodrug, colistin methanesulfonate or CMS) and gentamicin according to the route of administration (nebulization and intravenous infusion) in critically ill patients with VAP.Intra-pulmonary concentrations of colistin and gentamicin were 10 to 40-fold and 50 to 70-fold much higher after nebulization than after the same dose by intravenous route, respectively. Nebulization has also the theoretical potential advantage to improve patients' safety in relation to the colistin biodisponibility lower than 10%.With high intra-pulmonary concentrations and very low systemic absorption, CMS and gentamicin nebulization may be good alternatives to intravenous infusion for VAP treatment.