No description available.

Nitrification, a key step in biological nitrogen removal processes, is the oxidation of ammonia into nitrate performed by ammonia oxidizing bacteria (AOB) and nitrite oxidizing bacteria (NOB) under aerobic condition. Researchers have focused on factors affecting the performance of nitrification for decades, but the inorganic carbon limitation on nitrification had been neglected. However, the increase in nitrogen in wastewater has increased the need to evaluate and improve our understanding of this limitation. In a previous research, the hypothesis that different inorganic carbon concentrations would enrich different AOB populations has been examined. In this study, the focus was on the effect of inorganic carbon concentration on NOB, which has a close relationship with AOB. Two 5L lab–scale continuous–flow stirred tank reactors (CSTR) were operated to evaluate the nitrification performance and microbial ecology of nitrifier populations acclimated under inorganic carbon sufficient (high–IC) and limited (low–IC) conditions for approximately 700 days. During the operation period, both bioreactors were able to maintain satisfactory nitrification efficiency higher than 95% at an influent ammonium concentration of 250 mg–N/L. Nitrate was the major end product and no significant nitrite accumulation was observed. To evaluate the effects of inorganic carbon on NOB community structures, cloning/sequencing and real–time PCR were applied to target and quantify the two common NOB genera, Nitrospira and Nitrobacter, as no molecular probe targeting all known NOB is available presently. The results showed that these two genera were both found in the two reactors. Nitrospira was the dominant NOB population in the high–IC bioreactor, while Nitrobacter was dominant in the low–IC one after one year acclimation. Kinetic analysis revealed that NOB enriched in the two reactors have different kinetic performances. However, IC concentration did not show a significant impact on the nitrite oxidizing kinetics of NOB in the batch tests.

No description available.

Traditionally, bacterial culture has been used for bacterial detection, allowing study of living microorganisms. Molecular methods are rapid and allow simultaneous identification of numerous species and uncultivated phylotypes. The objective of this doctoral thesis was to investigate the role of the oral microbiota, including poorly characterized and uncultivated bacteria, in dental caries and periodontitis, by comprehensive molecular, clinical, and statistical methods. The microbiota of 275 pre-school children (75 with caries and 200 caries-free) was examined by whole genomic DNA probes, 16S rDNA cloning and sequencing, and PCR. Streptococcus mutans, exhibiting a combined association with Streptococcus sobrinus, was significantly associated with Early Childhood Caries (ECC). Plaque from children with Severe Early Childhood Caries (S-ECC) was diverse with 138 identified and 107 unidentified taxa, which possibly included novel phylotypes. Other species/phylotypes associated with childhood caries included Lactobacillus gasseri (p<0.01), Lactobacillus fermentum, Actinomyces israelii, and Actinomyces odontolyticus (all p<0.05, ECC), Veillonella parvula (p<0.01), Veillonella atypica (p<0.05), and Veillonella sp. HOT-780 (p<0.01, S-ECC). Lactobacillus acidophilus and Lactobacillus reuteri, both used as probiotic therapy species, were detected more frequently in caries-free children than those with ECC. Fastidious periodontal species, including Parvimonas micra, Aggregatibacter actinomycetemcomitans, Eubacterium brachy, Filifactor alocis (all p <0.05), and Porphyromonas gingivalis (p<0.01), were also more frequently detected in children with dental caries than in caries-free children. Other variables associated with ECC were race, dental visit, snacking (all p<0.05), and visible dental plaque (p<0.01). The oral microbiota of early periodontitis in young adults (N=141) was analyzed by whole genomic and oligonucleotide DNA probes, and PCR. Species detected more frequently in early periodontitis than periodontal health included Treponema denticola, F. alocis, Porphyromonas endodontalis, Bacteroidetes sp. HOT-274 (oral clone AU126), and A. odontolyticus (p<0.01) by oligonucleotide DNA probes, and P. gingivalis (p<0.001) and T. forsythia (p=0.03) by PCR. Subgingival samples exhibited a higher prevalence of periodontitis-associated species than samples from tongue surface, including A. actinomycetemcomitans, T. denticola, T. forsythia (all p<0.05), and uncultivated TM7, Treponema, and Actinobaculum clones (all p<0.05). P. gingivalis (p<0.01) by PCR was associated with periodontal disease progression. Early periodontitis was associated with older age (p=0.01), male gender (p=0.04), and cigarette smoking (p=0.05). The role of bacterial subgroups in periodontitis was examined by studying the serotypeability of 313 genotyped clinical A. actinomycetemcomitans isolates (189 subjects). A total of 95 strains (30 subjects) remained non-serotypeable, although PCR revealed presence of the serotype- specific genes. The absence of the immunodominant serotype-specific antigen was confirmed by immunoblot assays. No major DNA rearrangement in the studied serotype-specific gene clusters was found. In summary, detection of previously cultured species and uncultivated phylotypes revealed the diversity of the oral microbiota in dental diseases and health already early in life. Bacterial species have insufficiently characterized subgroups that may have attributes to evade the host response. Molecular approaches used in this study enable comprehensive, culture-independent characterization of the oral microbiome that may in the future lead to identification of diagnostic bacterial profiles for dental diseases.

Les activités industrielles, la production d’énergie le transport et l’urbanisation ont engendré de sérieux problèmes environnementaux qui ont des effets néfastes non seulement pour les divers écosystèmes, mais aussi pour la santé des Humains. Il existe plusieurs méthodes de réhabilitation des sites contaminés. Les méthodes dites conventionnelles consistent le plus souvent à excaver, transporter et entreposer des sols dans des sites d’enfouissements, alors que d’autres technologies utilisent des traitements physico-chimiques ou l’incinération des polluants. Les inconvénients majeur de ces méthodes en sont le coût élevé, l’émission des gaz à effet de serre et la destruction des habitats. Cependant, plusieurs technologies ont émergé ces dernières décennies. Parmi ces technologies émergentes, la phytoremédiation est une méthode prometteuse et dont l’efficacité devienne de plus en plus reconnue. La phytoremédiation consiste à utiliser des plantes et les microbes qui leurs sont associés pour dégrader, extraire ou stabiliser les polluants du sol aussi bien organiques qu’inorganiques. Parmi les microbes associés aux racines des plantes, on trouve les champignons mycorhiziens arbusculaires (CMA) dont le rôle en phytoremédiation a été montré. Cependant, la diversité et les changements des structures des communautés de ces champignons dans des sites hautement contaminés et en association avec les populations des plantes qui poussent spontanément dans ces sites demeurent méconnues. L’objectif de mon projet de maitrise consiste à étudier la diversité et la structure des communautés des CMA dans les racines et les sols rhizosphériques de trois espèces de plantes Eleocharis elliptica, Populus tremuloides et Persicaria maculosa qui poussent spontanément dans des bassins d’une ancienne raffinerie pétro-chimique. J’ai échantillonné trois individus par espèce de plante dans trois bassins qui ont montré des concentrations différentes des polluants pétroliers. J’ai utilisé l’approche de la PCR conventionnelle, le clonage et le séquençage en ciblant le gène 18S de l’ARN ribosomique autant sur des échantillons de racines et des que sur ceux de sols rhizophériques. J’ai analysé au minimum 48 clones par échantillon. L’analyse de la diversité Beta a montré que la structure des communautés des CMA était significativement différente selon les biotopes (racines et sols rhizosphèriques) et les concentrations de contaminants pétroliers. Mes résultats ont montré que l'identité de la plante et la concentration de contaminants ont fortement influencé la structure des communautés de CMA. J’ai aussi observé qu’en plus de l’effet des facteurs biotiques et abiotiques mentionnés ci-dessus, plusieurs OTUs de CMA sont corrélés soit positivement ou négativement entre eux et aussi avec différents types de polluants d'hydrocarbures pétroliers. Cette étude a permis de comprendre les facteurs qui influencent les changements des structures des communautés des CMA et pourrait nous aider à améliorer l’efficacité de la phytoremédiation avec des plantes indigènes poussant spontanément sur des sites hautement contaminés par des hydrocarbures pétroliers. / Industrial activities, energy production, transportation, and urbanization have led to serious environmental problems that have negative effects not only for the natural ecosystems, but also for the human health. Several methods of rehabilitation of contaminated sites such as conventional methods consisting on excavation, transportation and storage of contaminated soils in landfills (known as Dig and Dump), as well as other technologies that use physical and chemical treatments or incineration of polluted soil pollutants, have been largely utilized. However, these methods are very costly and not environmental-friendly because of greenhouse gas emission and destruction of habitats. Several green technologies have emerged in recent decades. Among these emerging technologies, phytoremediation is a promising method whose effectiveness becomes increasingly recognized worldwide. Phytoremediation uses plant and their associated microbes to degrade, uptake or sequestrate organic and inorganic pollutants. Arbuscular mycorrhizal fungi (AMF) are among microbes that live intimately with plant root where they form a symbiosis known as arbuscular mycorrhiza. The objective of my master project was to study the diversity and changes of community structure of AMF in roots and rhizospheric soils of three native plant species Eleocharis elliptica, Populus tremuloides and Persicaria maculosa growing in petroleum-contaminated sedimentation basins of a former petro-chemical plant. I used conventional PCR, cloning and sequencing approach targeting 18S rRNA gene to investigate AMF community structure. I analyzed at minimum 48 clones for each sample. Beta diversity analyses showed that AMF community structure was significantly different across biotopes (roots and rhizospheric soils) and different concentrations of petroleum hydrocarbon contamination. Our results showed that plant identity and concentrations of petroleum hydrocarbon contaminations strongly influenced the AMF community structure as well as the inter-specific relationship among AMF taxa. Moreover, with consideration of both biotic and abiotic factors, we found that several AMF OTUs showed positive and negative correlations between each other and also with petroleum hydrocarbon pollutants. My study brings us in-valuable information to apply AMF for the phytoremediation in the future.