A Mata Atlântica é reconhecida como área de prioridade de conservação na América do Sul, devido ao grande número de espécies endêmicas e constantes ameças à sua biodiversidade em decorrência da substituição da vegetação natural. Embora várias informações sobre a diversidade vegetal e animal estejam disponíveis, pouco se sabe sobre a diversidade de microorganismos existentes no solo desse bioma. A diversidade de fungos do solo foi avaliada em três unidades de conservação da Mata Atlântica do estado de São Paulo: Parque Estadual de Carlos Botelho (PECB), Estação Ecológica de Assis (EEA) e Parque Estadual da Ilha do Cardoso (PEIC). Ao todo, foram analisadas 90 amostras de solo, coletadas em épocas de alta e baixa pluviosidade, e sob a copa de três espécies arbóreas: Cabralea canjerana, Guapira opposita e Maytenus robusta. Foram utilizados métodos independentes (PCR-DGGE e pirosequenciamento) e um método dependente do cultivo (lavagem de solo e filtração de partículas) para a análise da diversidade e estrutura das comunidades de fungos do solo. Os resultados obtidos foram analisados conjuntamente com os dados de atributos químicos do solo e frações da matéria orgânica do solo a fim de verificar suas possíveis relações com as comunidades de fungos. Os resultados obtidos sugerem uma grande diversidade de fungos no solo da Mata Atlântica. Através do método de cultivo, um total de 142 espécies de fungos foi identificado nas três áreas, sendo que a estrutura das comunidades de fungos não foi influenciada pelas espécies arbóreas, mas sim pelas áreas e épocas de amostragem. As comunidades de fungos cultiváveis do PECB e do PEIC foram mais similares entre si do que em relação às comunidades de fungos do solo da EEA, assim como os valores dos atributos químicos do solo dessas áreas foram mais semelhantes entre si. Pelo método de PCR-DGGE, as estruturas das comunidades de fungos das três áreas sofreram influência das espécies arbóreas sob a copas das quais as amostras foram coletadas. Somente a estrutura das comunidades de fungos no solo do PEIC não sofreu influência da época de amostragem. Usando pirosequenciamento, foram obtidas 39.152 sequências da região ITS de fungos, as quais foram agrupadas em 1.800 Unidades Taxonômicas Operacionais (UTOs). A diversidade de fungos na EEA e no PEIC variou em função das espécies arbóreas e épocas de coleta. A análise de NMS de cada área amostrada indicou que as comunidades de fungos do solo são muito homogêneas. O filo Ascomycota foi mais frequentemente detectado, tanto usando metodologia dependente quanto independente de cultivo. De maneira geral, as comunidades de fungos cultiváveis apresentaram maior relação com atributos químicos do solo, áreas e épocas de coleta, e as comunidades de fungos acessadas por PCRDGGE mostraram maior relação com as épocas de coleta e espécies arbóreas sob as quais as amostras de solo foram coletadas. A análise dos metadados usando rede neural revelou uma dependência da diversidade de fungos em relação às concentrações de ácidos húmicos, ácidos fúlvicos e humina no solo, além do pH e concentração de matéria orgânica total. / Brazilian Atlantic Forest is recognized as a top priority for conservation in South America because of its large number of innate species and the threats for the biodiversity due to vegetation changes. Although a plethora of data on plant and animal diversity in the Atlantic Forest is available, the diversity of soil microorganisms in this biome is still mostly unknown. Therefore, soil fungi diversity was evaluated in three Atlantic Forest conservation areas of São Paulo state: Estação Ecológica de Assis (EEA), Parque Estadual de Carlos Botelho (PECB) and Parque Estadual da Ilha do Cardoso (PEIC). A total of 90 soil samples were analyzed, collected in two different seasons (high and low precipitation seasons), and under the canopy projection of three tree species: Cabralea canjerana, Guapira opposita and Maytenus robusta. Two independent cultivation methods (PCR-DGGE and pyrosequencing) and one dependent method (soil washing and particles filtration method) were used for the analysis of soil fungi diversity and community structure. The results of these methods were analyzed together with the data on soil chemical attributes and organic matter fractions in the same samples, in order to verify the possible relations with soil fungi communities. The results suggest a great diversity of soil fungi in the Atlantic Forest. Through the cultivation method, a total of 142 fungi species were identified for the three areas. The structure of fungi communities was not affected by the tree species, but were affected by the sampling areas and seasons. Cultivable fungi community in PECB and PEIC were more similar to each other than in EEAs soil fungi community. In addition, the values of the chemical properties of these areas were more similar to each other. The structure of soil fungi community accessed by PCR-DGGE showed that the three areas were influenced by the tree species under the canopy where the soil samples were collected. Only the structure of PEICs fungi communities was not influenced by the season. By means of pyrosequencing, 39,152 sequences were retained from the ITS rDNA region, which were clustered in 1,800 Operational Taxonomic Unities (OTUs). Fungal diversity in EEA and PECB areas was influenced by the tree species and seasons. NMS analysis of each sampled area showed that soil fungi communities are very homogenous. Ascomycota was the most frequent phylum detected by both dependent and independent cultivation methods. Overall, the communities of cultivable fungi were more related to soil chemical attributes, sampling areas and seasons. Fungal communities accessed by PCR-DGGE showed greater relation with the seasons and tree species where the soil samples were collected. Analysis of metadata using neural network revealed fungal diversity dependence of humic acids, fulvic acids and humin concentrations in soil, as well as pH and organic matter concentrations.

A aplicação da digestão anaeróbia aparece como opção para processamento da vinhaça, visto que por meio deste processo é possível aliar a recuperação de energia (hidrogênio e metano) ao enquadramento ambiental deste resíduo sem interferir em suas qualidades como biofertilizante. Nesse sentido, este trabalho avaliou a aplicação da digestão anaeróbia da vinhaça em sistema combinado acidogênico e metanogênico. Inicialmente, avaliou-se a influência de materiais suportes (argila expandida, carvão vegetal, cerâmica porosa e polietileno de baixa densidade) na produção de hidrogênio, em reatores de leito empacotado (APBR) operados em condição mesofílica (25°C) (Etapa 1). De uma forma geral, apenas traços de hidrogênio foram observados nos reatores preenchidos com partículas de carvão vegetal e cerâmica porosa (2 - 7,9 mL-H2.d-1.L-1 reator). Por outro lado, os valores para a produção volumétrica de hidrogênio (PVH) nos reatores com argila expandida e polietileno de baixa densidade foram dez vezes superior (74,3 - 84,2 mL-H2.d-1.L-1 reator), todavia, estatisticamente iguais. O critério de seleção do material suporte ocorreu com base em relatos na literatura que indicaram rebaixamento do leito e entupimento da saída de reatores APBR preenchidos com argila expandida. Portanto, o polietileno de baixa densidade foi escolhido como melhor opção dentre os suportes avaliados. Não obstante, a baixa relação C/N da vinhaça associada à microaeração do sistema (presença de microrganismos anóxicos) afetou severamente os reatores APBR com diferentes materiais suportes, levando-os à falência. Na segunda etapa, adotou-se a operação dos APBR preenchidos com polietileno de baixa densidade, em condição termofílica (55°C) a fim de diminuir o rendimento da biomassa acidogênica e a solubilidade do oxigênio. Adicionalmente, foi avaliada influência da Carga Orgânica Volumétrica aplicada (COVa - 36,4 - 108,6 kg- DQO.m-3.d-1), por meio da variação do Tempo de Detenção Hidráulica (TDH - 8 - 24 h). Produção contínua de hidrogênio foi observada em todos os reatores operados em condição termofílica (Etapa 2). Nessa etapa, estabeleceu-se a condição ótima de operação com COVa de 84,2 kg-DQO.m-3.d-1 e TDH de 10 h, resultando em PVH de valor 575,3 mL-H2.d-1.L-1 reator e rendimento de hidrogênio (Y1H2) de 1,4 mol-H2.mol-1 carboidratos totais. Na Etapa III, essas condições foram impostas na operação do APBR, resultando em aumento de 18,2% e 14,2% nos valores de PVH e Y1H2, respectivamente, em relação aos dados obtidos na Etapa II. Em paralelo, foram operados dois reatores metanogênicos do tipo manta de lodo (UASB), compondo um sistema único (UASB) e um sistema combinado (APBR/UASB). A produção de energia no sistema combinado foi 25,7% superior ao observado no sistema único. A eficiência de remoção da matéria orgânica total e solúvel aumentou de 60,7 ± 0,3% e 72,6% ± 1,2% no sistema único e 74,6 ± 0,3% e 96,1 ± 1,7% no sistema combinado, respectivamente, sob COVa de 25 kg-DQO.m-3.d-1 (calculada para os sistemas metanogênicos). / Anaerobic digestion application appears as an option for sugar cane vinasse processing, since via this process it is possible to combine the energy recovery (hydrogen and methane) to the environmental framework of this residue without interfering in their qualities as biofertilizer. In this sense, this study evaluated the application of anaerobic digestion of vinasse in two-stage system (acidogenic and methanogenic). Initially, it was evaluated the influence of support material (expanded clay, charcoal, porous ceramics, and low-density polyethylene) on hydrogen production in acidogenic packed bed reactors (APBR) operated under mesophilic condition (25°C) (Phase 1). In general, only traces of hydrogen were observed in APBR filled with charcoal and porous ceramics particles (2 - 7.9 mL-H2.d-1.L-1 reactor). On the other hand, in APBR with expanded clay and low-density polyethylene as support, the values for volumetric hydrogen production (VHP) were ten times higher (74.3 - 84.2 mL-H2.d-1.L-1 reactor), however, statistically equal. The selection criteria of support material was based on reports in the literature that indicated bed lowering and clogging in APBR outlet with expanded clay as support. Therefore, the low-density polyethylene was chosen as the best support among those evaluated. Nevertheless, the low C/N ratio of vinasse associated to microaeration condition in the systems (presence of microorganisms anoxic) severely affected the APBR with different support materials, leading them to bankruptcy. In the second phase, it was adopted the operation of APBR filled with low density polyethylene in thermophilic conditions (55°C) in order to reduce the acidogenic biomass yield and oxygen solubility. Moreover, it was evaluated the influence of organic loading rate (OLR - 36.4 to 108.6 kg-COD.m-3.d-1) by hydraulic retention time varying (HRT - 8 - 24 h). Continuous hydrogen production was observed in all reactors operated at 55°C (Phase 2). In this phase, it was established the optimum condition of operation, OLR of 84.2 kg-COD.m-3.d-1 and HRT of 10 h, resulting in values for PVH and hydrogen yield (Y1H2) of 575.3 mL-H2.d-1.L-1 reactor and 1.4 mol-H2.mol-1 total carbohydrates, respectively. In Phase III, these conditions were imposed on the operation of the APBR, resulting in an increase of 18.2% and 14.2% in the values of PVH and Y1H2, respectively, compared to the data obtained in Phase II. In parallel, two methanogenic reactors were operated (Up-flow Anaerobic Sludge Blanket UASB type), which composed a single stage system (UASB) and a two-stage system (APBR/UASB). The energy production in the two-stage system was 25.7% higher compared to the single stage system. The values for total and soluble organic matter removal were 60.7 ± 0.3% and 72.6 ± 1.2% to single stage system and 74.6 ± 0.3% and 96.1 ± 1.7% to two-stage system, respectively, at OLR of 25 kg-COD.m-3.d-1 (calculated for the methanogenic reactors).

INTRODUÇÃO: O melanoma primário da cavidade oral é uma neoplasia agressiva, rara e originada a partir da proliferação de melanócitos malignos da mucosa. Ele representa aproximadamente de 0,2 a 8% de todos os melanomas. Estudos recentes apontam algumas vias moleculares tem sido encontradas por estarem envolvidas na patogenia dos melanomas. Dentre essas vias destaca-se a via proliferativa da MAPK (mitogen activated protein kinase), esta cascata de sinalização está envolvida no controle do crescimento celular, proliferação e migração, e tem sido relacionada com um papel importante no desenvolvimento e progressão do melanoma cutâneo. OBJETIVOS: Analisar a expressão proteica e mutação pontual dos componentes da via MAPK e correlacionar com os dados clínicos-histológicos. MATERIAL E MÉTODOS: Através da imunoistoquímica avaliar a expressão proteica dos anticorpos RAS; BRAF; MEK1; MEK2; ERK1 e ERK2 em 35 casos de melanomas orais organizados em matriz (TMA: Tissue Microarray) e através de pirosequenciamento avaliar a mutação pontual dos genes BRAF; NRAS; KRAS em 14 casos de melanomas orais. RESULTADOS: Idade dos pacientes entre 9 e 91 anos, sem predileção por sexo, 75% caucasianos, 71,42% acometeram o palato, 80% com aspecto histológico grau III. A análise da expressão proteica foi: RAS (28,57%); BRAF (82,85%); MEK1 (0%); MEK2 (51,43%); ERK1 (20%)e ERK2 (74,28%). Na análise molecular observamos mutações para BRAF (9/14 casos) e NRAS (2/14 casos). CONCLUSÃO: Todos os aspectos da via MAPK necessita de outras elucidações em melanomas de áreas foto-protegidas e melanomas de mucosa e comparando diferentes populações. Entretanto, os resultados deste presente estudo apontam importante alterações na cascata RAS-RAF-MEK-ERK e estes são indicadores de prognóstico ruim em melanomas primários da mucosa oral, independente da exposição solar / BACKGROUND: Primary melanoma of the oral cavity is an aggressive and rare neoplasm and originated from the proliferation of malignant melanocytes of the mucosa. It represents approximately 0.2 to 8% of all melanomas. Recent studies indicate some molecular pathways have been found to be involved in the pathogenesis of melanomas. Among these means there is a proliferative MAPK pathway (\"mitogen activated protein kinase\"), this signaling pathway is involved in controlling cell growth, proliferation and migration, and it has been associated with a role in the development and progression of melanoma skin. OBJECTIVES: To analyze protein expression and mutation of components of the MAPK pathway and to correlate with the clinical, histological data. MATERIALS AND METHODS: Using immunohistochemistry to evaluate the protein expression of RAS, BRAF, MEK1, MEK2, ERK1 and ERK2 antibodies in 35 cases of oral melanomas organized array (TMA: Tissue Microarray) and using pyrosequencing to assess the mutation of the BRAF, NRAS, KRAS in 14 cases of oral melanomas. RESULTS: Age of patients between 9 and 91 years, regardless of gender, 75% Caucasian, 71.42% in palate, 80% with histologic grade III. Analysis of protein expression was: RAS (28.57%); BRAF (82.85%); MEK1 (0%), MEK2 (51.43%); ERK1 (20%) and ERK2 (74.28%). Molecular analysis we found BRAF mutations (9/14 cases) and NRAS (2/14 cases). CONCLUSION: All aspects of the MAPK pathway requires further elucidation in melanomas of photo-protected areas and mucosal melanomas and comparing different populations. However, the results of this study indicate important changes in the cascade RAS-RAF-MEK-ERK and these are indicators of poor prognosis in primary melanomas of the oral mucosa, regardless of sun exposure

L’objectif principal de ce travail était de réaliser une étude écotoxicologique du complexe lac Ichkeul-lagune de Bizerte. Un recensement des pesticides agricoles les plus utilisés dans le bassin versant agricole a été effectué afin de déterminer les pesticides les plus problématiques. Le recensement effectué auprès des agriculteurs, des revendeurs de produits phytosanitaires et le commissariat régional de développement agricole de Bizerte a permis d’identifier les molécules les plus utilisées au niveau des zones agricoles du bassin versant du complexe lac Ichkeul – lagune de Bizerte: l’iodosulfurone, le mésosulfurone, le 2,4D, le glyphosate et le fénoxaprop comme matières actives des herbicides ; le tébuconazole et l’époxiconazole comme fongicide et la deltaméthrine matières active des insecticides. Ensuite, les concentrations en pesticides, HAP et PCB ont été déterminées. Les résultats ont montré une contamination au niveau de certains sites du complexe. Les stations situées dans la lagune de Bizerte ont des teneurs en HAP dépassant les limites tolérées. Les concentrations en pesticides dépassent les normes au niveau de quelques sites du lac Ichkeul. Enfin, l’impact de ces polluants sur les communautés microbiennes et la densité de nématodes a été déterminé. La CCA combinant les résultats des analyses chimiques et les données T-RFLP des communautés bactériennes met en évidence que les communautés bactériennes du lac sont influencées parles pesticides alors que celles de la lagune sont influencées par les HAP. La répartition des T-RFs montre la présence de T-RFs spécifiques dans les sites contaminés : le T-RF 114 bp caractérise le site le plus contaminé en pesticide, les microorganismes associés à ce T-RF correspondent probablement à des microorganismes résistants aux pesticides et capables de les dégrader. La composition des communautés bactériennes a été déterminée par pyroséquençage 454 sur les sites les plus représentatifs : le moins contaminé du complexe, le plus contaminé en HAP, le plus contaminé en pesticides et un site présentant une contamination multiple HAP-Pesticides. L’impact de la présence des pesticides sur la densité des nématodes libres marins a été étudié. L'analyse taxinomique des données de pyroséquençage regroupe les séquences dans 44 embranchements différents. En général, Proteobacteria étaient l’embranchement le plus dominant avec une prédominance de Gammaproteobacteria, Alphaproteobacteria et deltaproteobacteria dans les sédiments. Les communautés bactériennes des quatre sites ont 211 OTU commun. Le lac Ichkeul a été caractérisé par 219 OTU spécifique et la lagune de Bizerte 235 OTU. Le Site 2, le plus contaminé en pesticides présente l’abondance la plus élevée en nématodes libres marins. / The main objective of this work was to conduct an ecotoxicological study of the complex Ichkeul Lake-Bizerta lagoon. A survey of the most used agricultural pesticides in the watershed of the complex was conducted to determine the most problematic compounds. The survey of pesticides use with farmers, dealers of pesticides and the Regional Commissioner for Agricultural Development Bizerte has helped to identify the most used pesticides in agricultural areas of the watershed of the complex Ichkeul Lake-Bizerta lagoon: iodosulfuron, the mesosulfurone, 2,4D, glyphosate and fenoxaprop as herbicides active materials, tebuconazol epoxiconazol as fungicide active materials and deltamethrin as insecticides. Then, the concentrations of pesticides, PAHs and PCBs were determined in the sediment of the complex. The results showed a contamination of some complex sites. Stations located in the lagoon of Bizerte have a level of PAH in excess of permissible limits. Pesticide concentrations exceed the standards at some sites from the Ichkeul Lake. Finally, the impact of these pollutants on microbial communities and nematode density was determined. CCA combines the results of chemical analyzes and T-RFLP data of bacterial communities shows that the bacterial communities of the lake are influenced by pesticides while those of the lagoon are influenced by PAHs. The distribution of T-RFs showed the presence of specific T-RFs in contaminated sites: the T-RF 114 bp characterizes the most contaminated site in pesticides, microorganisms associated with the T-RF are probably microorganisms resistant to pesticides and capable of degrading this pollutant. The composition of bacterial communities was determined by 454 pyrosequencing of the most representative sites: the least contaminated of the complex, the most contaminated by PAH, the most contaminated by pesticides and a site with multiple PAH-pesticides contamination. The impact of the presence of pesticides on the density of free living marine nematodes was studied. The taxonomic analysis of the pyrosequencing data grouped the sequences into 44 different phyla. In general, Proteobacteria were the most dominant phyla with predominance of Gammaproteobacteria, Alphaproteobacteria and Deltaproteobacteria within the sediments. Besides Proteobacteria, there are a number of sequences affiliated to the following major phyla detected in all four sites: Chloroflexi, Bacteroidetes, Nitrospirae, Planctomycetes, Actinobacteria, Gemmatimonadetes, Firmicutes, Cyanobacteria, Spirochaetes, Acidobacteria. The bacterial communities of the four sites shared 211 common OTUs. The Lake Ichkeul was characterized by 219 specific OTUs and the Bizerta lagoon by 235 OTUs. Site 2, the most contaminated by pesticides has the highest abundance of free living marine nematodes.

Em concentrações subletais, agentes antimicrobianos modulam a expressão gênica bacteriana, sendo que o conjunto de genes que é modulado depende tanto da cepa bacteriana, como da natureza do agente antimicrobiano. Neste trabalho, avaliamos o perfil de expressão gênica de Xylella fastidiosa cepa 9a5c em resposta ao tratamento por até 60 minutos com dose subletal do antibiótico estreptomicina. Esta é uma cepa virulenta, originalmente isolada de laranjeiras com sintomas de clorose variegada dos citros. A hibridização de microarranjos de DNA representando 2608 das 2848 sequências codificadoras (CDS) previamente anotadas no genoma desta cepa, revelou que 136 CDS apresentaram expressão gênica diferencial em resposta à exposição à estreptomicina, sendo que destas 109 foram negativamente moduladas e 27 positivamente moduladas. Realizamos, também, ensaios de PCR quantitativo precedido de transcrição reversa (RTqPCR) de 21 CDS para confirmar a modulação observada na análise global da expressão gênica. O perfil de expressão gênica de X. fastidiosa em resposta à estreptomicina foi analisado de forma integrada com outros perfis de expressão gênica desta bactéria. Entre as CDS positivamente moduladas, destacamos aquelas codificadoras das chaperoninas GroEL e GroES, que estão associadas a resposta de choque térmico, e CDS associadas à tradução, tais como proteínas ribossomais e fatores de tradução. Interessantemente, a exposição à estreptomicina induz a expressão da CDS que codifica poligalacturonase, que é um fator de virulência em algumas cepas de X. fastidiosa. Por outro lado, o tratamento com estreptomicina promoveu a modulação negativa de CDS relacionadas à formação e manutenção de biofilme ao contrário do observado quando estas bactérias foram submetidas ao tratamento com gomesina, um peptídeo antimicrobiano. O conjunto destas observações sugere que a exposição à dose subletal de estreptomicina possa promover um fenótipo de maior virulência, contrariamente ao efeito previamente observado com a gomesina. Neste trabalho, também descrevemos o pirosequenciamento do genoma da cepa J1a12 de Xylella fastidiosa, que exibe fenótipo menos virulento em citros e tabaco em relação à cepa 9a5c. A comparação da sequência genômica destas duas cepas confirma diferenças anteriormente observadas utilizando-se microarranjos de DNA e destaca genes potencialmente importantes para virulência de Xylella fastidiosa. / At sublethal concentrations, antimicrobials compounds modulate bacterial gene expression and the gene set that is modulated depends not only on the bacterial strain but also on the nature of antimicrobial agent. In this study, we evaluated changes in gene expression profile of Xylella fastidiosa strain 9a5c exposed up to 60 min to sublethal concentration of streptomycin. This a virulent strain originally isolated from orange trees with symptoms of citrus variegated chlorosis. Hybridization of DNA microarrays representing 2,608 out of 2848 coding sequences (CDS) previously annotated in strain 9a5c genome revealed 136 CDS differentially expressed upon streptomycin treatment. Of which 109 were down-regulated and 27 up-regulated. Differential expression for a subset of 21 CDS was further evaluated by reverse transcriptionquantitative PCR (RT-qPCR). In addition, we performed an integrated analysis of the gene expression profile of X. fastidiosa in response to streptomycin along with other gene expression profiles available for this bacterium. Among the up-regulated CDS, we highlight those encoding chaperonins GroEL and GroES, which are associated with heat shock response, and those CDS related to translation, such as ribosomal proteins and translation factors. Interestingly, exposure to streptomycin induces the expression of a CDS encoding polygalacturonase, which is a virulence factor for some X. fastidiosa strains. Furthermore, treatment with streptomycin down-regulates some CDS related to biofilm formation oppositely to treatment with gomesin, an antimicrobial peptide. Together, these observations suggest that exposure to sublethal dose of streptomycin might promote a higher virulent phenotype, in contrast to the effect previously observed with gomesin. In the present work, we also describe the pyrosequencing of J1a12 genome, a X. fastidiosa strain that exhibits a less virulent phenotype in citrus and tobacco if compared to strain 9a5c. A comparison of genome sequences of these two strains confirms differences previously observed using DNA microarrays and highlights important genes for virulence of X. fastidiosa.

As lagoas salino-alcalinas (salinas) da sub-região Nhecolândia do Pantanal, Mato Grosso do Sul, combinam valores de pH elevados com a presença de altas concentrações de sal, assemelhando-se aos lagos de soda da África Oriental. O entendimento atual dos mecanismos físicos, químicos e biológicos nestes ambientes extremos do Brasil é limitado. Embora os micro-organismos estejam envolvidos nos processos biogeoquímicos em ecossistemas aquáticos, investigações sobre os grupos bacterianos que contribuem para a diversidade e funções específicas nessas salinas inexistem. Assim, a presente dissertação centrou-se na avaliação da comunidade bacteriana de duas salinas (Salina Verde e Salina Preta), localizadas na sub-região da Nhecolândia. Especificamente, investigou-se a diversidade e a estrutura das comunidades bacterianas, os perfis metabólicos das lagoas e genes funcionais que codificam enzimas relacionadas a transformação do nitrogênio, mercúrio, selênio e arsênio. As amostras de água foram coletadas durante a estação seca (setembro de 2012) na Salina Verde (pH 9,5, E.C. 2575 mS cm-1), caracterizada pela presença constante de floração de cianobactérias e na Salina Preta (pH 8,9, E.C. 1500 mS cm-1), sem registro de ocorrência de floração. As amostragens foram realizadas em triplicatas em duas profundidades (superfície e fundo) e duas vezes no dia (10:00 h e 15:00 h) devido à ocorrência natural de saturação de oxigênio observada na Salina Verde. O DNA total de cada amostra ambiental foi extraído e a diversidade bacteriana e funcionalidade foram acessadas por pirosequenciamento do gene de 16S RNAr e sequenciamento metagenômico. A análise de PCR quantitativa do gene de 16S RNAr foi realizada de forma a quantificar a comunidade bacteriana. A abundância bacteriana foi maior na Salina Verde do que na Salina Preta (1010 e 109 cópias mL-1, respectivamente). As sequências parciais do gene de 16S RNAr obtidas no pirosequenciamento mostraram a dominância de táxons do gênero Anabaenopsis sp. na floração da Salina Verde, englobando até 92% do total de sequências. A comunidade bacteriana da Salina Preta apresentou os maiores índices de diversidade e riqueza, sendo dominantes os filos Proteobacteria, Bacteroidetes, Acidobacteria e Verrucomicrobia. Apenas a Salina Preta mostrou diferenças na comunidade bacteriana de acordo com as profundidades amostradas. Na superfície desta lagoa, os filos Actinobacteria e Verrucomicrobia predominaram, enquanto no fundo, prevaleceram os filos Proteobacteria e Chlamydiae. A temperatura foi detectada como o fator abiótico que influenciou a heterogeneidade espacial da Salina Preta. Por sua vez, a alcalinidade e o pH foram os fatores que impulsionaram as diferenças e variações das comunidades bacterianas em ambas as lagoas. Genes bacterianos envolvidos nos ciclos biogeoquímicos do nitrogênio, mercúrio e arsênio foram encontrados nas salinas Verde e Preta, sugerindo uma elevada redundância funcional nas transformações desses elementos. Não foram encontrados genes microbianos envolvidos no ciclo do selênio. Os dados gerados revelaram uma comunidade microbiana taxonômica e funcionalmente complexa que habita as salinas. Os resultados deste estudo fornecem uma avaliação aprofundada baseada em abordagens independentes de cultivo, sendo este um passo importante na compreensão da dinâmica funcional desses ambientes no Pantanal brasileiro. / The saline-alkaline lakes (salinas) of the Nhecolândia sub-region of the Pantanal, Mato Grosso do Sul state, combine high pH values with the presence of high salt concentrations, resembling the soda lakes of East Africa. The current understanding of physical, chemical and biological mechanisms in these extreme environments is limited. Although microorganisms are involved in biogeochemical processes in aquatic ecosystem, researches on the bacterial groups that contribute to diversity and specific functions in these salinas are scarce. This dissertation therefore focused on the evaluation of bacterial community of two salinas (Salina Verde and Salina Preta) located in the Nhecolândia subregion. Specifically, it was investigated the diversity and structure of bacterial communities, the metabolic profile of the lakes and functional genes that encode the nitrogen, mercury and arsenic-transforming enzymes. Water samples were collected during the dry season (September 2012) from Salina Verde (pH 9.5, E.C. 2575 mS cm-1), characterized by constant presence of cyanobacterial bloom, and from Salina Preta (pH 8.9, E.C. 1500 mS cm-1), with no report of bloom occurrence. Triplicate samplings were carried out in two depths (surface and bottom) and twice a day (10 AM and 3 PM) due to naturally occurrence of oxygen saturation, observed at Salina Verde. Total DNA of each environmental sample was extracted and bacterial diversity and functionality were accessed by 16S rRNA gene pyrosequencing and metagenomic sequencing. Analysis of quantitative PCR of the 16S rRNA gene was performed in order to quantify the bacterial community. Bacterial abundance was higher in the Salina Verde than in the Salina Preta (1010 and 109 copies mL-1, respectively). The partial sequences of the 16S rRNA gene obtained in the pyrosequencing revealed the genus Anabaenopsis sp. as the dominant taxa in the Salina Verde bloom, encompassing up to 92% of the total bacteria. Bacterial community of the Salina Preta showed the highest diversity and richness index, with dominant phyla Proteobacteria, Bacteroidetes, Acidobacteria and Verrucomicrobia. Only the Salina Preta showed differences in bacterial community in accordance with the depths sampled. On the surface of this lake, the phyla Actinobacteria and Verrucomicrobia predominated, while in the bottom, Proteobacteria and Chlamydiae prevailed. The temperature was detected as the abiotic factor influencing the spatial heterogeneity at Salina Preta. On the other hand, alkalinity and pH were the factors driving the differences and variation of bacterial community in both lakes. Bacterial genes involved in the biogeochemical cycles of nitrogen, mercury and arsenic were found in Salina Verde and Salina Preta, suggesting a high metabolic redundancy in the transformation these elements. No microbial genes involved in selenium cycle were found. The data showed a taxonomic and functional complex microbial community inhabiting salinas. The results of this study provide a detailed assessment based on culture-independent approaches, which is a stepping stone to understand the functional dynamics of these environments in the Brazilian Pantanal.

Les milieux oligotrophes sont pauvres en éléments nutritifs. En utilisant la technologie de séquençage à haut débit, on a étudié la diversité bactérienne dans trois environnements oligotrophes différents, y compris A. sâbles du désert, B. sâbles dans les tempêtes de l'Asie et C. l’eau et biofilms dans les réseaux de distribution d'eau potable.A. Le désert représente 30% de la surface de la terre. Les conditions de vie dans ces environnements sont un réel défi pour les micro-organismes à cause de nombreux facteurs limitants : peu d’eau et/ou de carbone disponible, une variation importante de température et une forte exposition aux irradiations UV. Le but de cette recherche est donc d’étudier la diversité bactérienne à la surface du sable du désert Taklemaken et du désert de Gobi en utilisant la technologie de séquençage à haut débit. Nos résultats ont révélé une grande diversité bactérienne dans le sol du désert comparable à d'autres types de sols. En outre, nous avons observé une corrélation positive entre la richesse bactérienne et le rapport C/N du sol.B. Les tempêtes de sable d'Asie se produisent presque toujours au printemps, elles sont générées dans les régions arides d'Asie telles que le désert Taklamaken et le désert de Gobi. L'arrivée des tempêtes de sable pourrait largement modifier l'environnement de l'air dans ces régions sous l’effet du vent, surtout dans les villes asiatiques qui sont le plus souvent touchées. Nos travaux visent à étudier la modification de la composition et la diversité des bactéries associées aux particules au moment de tempête de sable en Asie par la technologie de séquençage à haut débit. Nos résultats ont démontré que les compositions des bactéries associées aux particules sont modifiées pendant les tempêtes, en particulier, la proportion des Proteobacteria qui augmentent les jours de tempête. Nous avons signalé neuf genres bactériens détectés en plus pendant les jours de tempêtes, cela nécessite des études plus approfondies.C. Après avoir analysé la population bactérienne dans les tempêtes de sable, et celles des déserts, nous poursuivons notre objectif de recherche à un environnement aquatique. Nous avons suivi le flux d'eau provenant de l'usine d'Orly (DW-A) à l'entrée du réservoir (DW-B), et à la sortie du réservoir (DW-C). Nous avons constaté une forte variation de la communauté bactérienne, dans DW-A et DW-B, les bactéries prédominantes appartiennent aux populations des Betaproteobacteria, puis nous avons observé une conversion vers la population de Alphaproteobacteria dans DW-C. Le DW-C a montré une forte similitude avec un échantillon de biofilm (BF-C), ce qui suggère l'effet important du biofilm sur la modification des communautés bactériennes dans l'eau lors de la distribution. / Oligotrophic ecosystems can be loosely defined as environments that exhibit low ambient nutrient levels. During my thesis, I used 454 DNA pyrosequencing of partial 16S rDNA to explore the bacterial diversity in three different oligotrophic environments, including A. surface desert soil, B. Asian sandstorm dust and C. a section of the city of Paris’s drinking water distribution system.A. Arid regions represent nearly 30% of the Earth’s terrestrial surface. The living conditions at the surface of deserts are a challenge for microorganisms, as there is little available water and/or carbon, a very large range of temperatures and high exposure to UV irradiation from the Sun. In surface sand samples from two large Asian deserts, unexpectedly large bacterial diversity residing was revealed. Sequences belonging to the Firmicutes, Proteobacteria, Bacteroidetes and Actinobacteria phyla were the most abundant. An increase in phylotype numbers with increasing C/N ratio was noted, suggesting a possible role in the bacterial richness of these desert sand environments.B. Desert sandstorms are a meteorological phenomenon which have been postulated affect the Earth's climate and public health. We examined the particle-associated (dust and sand-associated) bacterial populations of atmospheric sand in the absence (as control) and presence of sandstorms in five Asian cities. Greater than 90% of the sequences can be classified as representing bacteria belonging to four phyla: Proteobacteria, Bacteriodetes, Actinobacteria and Firmicutes. Principal component analyses showed that the sandstorm-associated bacterial populations were clustered by sampling year, rather than location. Members belonging to nine bacterial genera (Massilia, Planococcus, Carnobacterium, Planomicrobium, Pontibacter, Pedobacter, Lysobacter, Sanguibacter, Ohtaekwangia) were observed to increase in sand-associated samples from sandstorms, versus the controls. C. We characterized the bacterial communities in three water and three biofilm samples from one part of the Parisian drinking water distribution system. A dramatic change in bacterial population in the water during flow through the distribution system from the water treatment plant to the exit from the reservoir was found. The richness of the bacterial population was reduced from the water treatment plant to the reservoir (from 336 to 165 OTUs for water samples leaving the reservoir and from 947 to 275 for biofilm samples in the network). Several OTUs belonging to pathogenic genera were detected in our samples, mostly in the biofilm samples, thus suggesting that the biofilms may be an important source of bacteria during water distribution to the consumers.

In forensic sciences, the serological methods used to determine which body fluid was collected from the crime scene are merely presumptive or labor intensive since they rely on protein detection or on microscopic identification of cells. Given that certain forensic cases may need the precise identification of a body fluid to determine criminal contact, such is the example of a suspected sexual assault of a minor; certainty in the body fluid of origin may depict a precise picture of the events. The identification of loci that show differences in methylation according to the tissue of origin can aid forensic analysts in determining the origin of a DNA sample. The process of DNA methylation occurs naturally in the genome of living organisms and consists in the presence of a methyl group on the carbon 5 of a cytosine, which is typically followed by a guanine (CpG). Analyzing patterns of DNA methylation in body fluids collected from a crime scene is preferential to the analysis of proteins or mRNA since the same extracted DNA used for STR typing can be used for DNA methylation analysis. We have validated and identified loci able to discriminate blood, saliva, semen and vaginal epithelia. In the current study, we have also established the minimum amount of DNA able to provide reliable results using methodologies such as pyrosequencing and high-resolution melt (HRM) analysis for the different markers identified. Lastly, we performed an alternative bioinformatic analysis of data collected using an array that studied methylation in over 450,000 individual cytosines on the human genome. We were able to sort the locations that showed potentially higher methylation differences between body fluids and investigated over 100 of them using HRM analysis. The results of that study, allowed the identification of three new loci able to distinguish blood and two new loci able to distinguish saliva and vaginal epithelia, respectively. The use of DNA methylation patterns to aid forensic investigations started with a publication in 2010, therefore each small contribution such as this work may, similarly to what occured in the biochemistry field, result in the discovery of a method able to put the technology in the hands of forensic analysts.

<p>Genetic profiling is commonly performed on the autosomes using multiple DNA markers. Although routine forensic DNA analysis is robust and based on reliable technologies, samples with degraded or limited amounts of DNA often fail. In these cases, the analysis of mitochondrial DNA (mtDNA) can be very valuable due to the high copy number per cell. This thesis describes evaluation and modifications of existing technologies that are useful in forensic DNA typing, mainly focusing on mtDNA.</p><p>DNA quantities isolated from common evidence materials such as hairs, fingerprints and accessories were estimated using a real-time quantification assay. Knowledge of quantitative differences between materials can guide forensic scientists to perform the best analysis (Paper I).</p><p>The current mtDNA analysis is based on hypervariable region (HVI/HVII) sequencing, which is the most rigorous and time-consuming forensic DNA analysis. Therefore, we evaluated the possibility to exclude individuals by screening for non-matching samples using the rapid and easy mtDNA Linear Array Assay (Paper II). </p><p>The major disadvantage using mtDNA is the lower discrimination power compared to multiple nuclear DNA markers. In contrast to the nuclear genome, due to the uniparental (maternal) mode of inheritance, no individual has unique mtDNA. We investigated the possibility of increasing the discrimination power by using pyrosequencing technology to analyse parts of the coding region in addition to HVI/HVII (Paper III). Furthermore, the addition of coding mtDNA information was evaluated by comparing several recently published mtDNA coding region assays (Paper IV). </p><p>Mixtures of DNA are common in forensic genetics due to contribution of DNA from several individuals, contamination or heteroplasmy. To resolve mixtures we have developed a pyrosequencing-based assay for the accurate quantification of the mtDNA mixture components (Paper V).</p><p>In conclusion, this thesis describes several assays that are valuable in forensic genetics for DNA quantification, improved mtDNA analysis, and mtDNA mixture interpretation.</p>

<p>Pancreatic endocrine tumors (PETs) may cause typical syndromes of hormone excess, or appear clinically non-functioning without hormonal symptoms. PETs occur sporadically, in association with the multiple endocrine neoplasia type 1 (MEN1) syndrome, or rarely the von Hippel-Lindau syndrome. Molecular genetic investigations may reveal pathways important for tumor development, and be of clinical use.</p><p>The aim of this thesis was to investigate regulation of different genes involved in cell proliferation, and relate findings to signs of malignancy in PETs.</p><p>The MEN1 gene on chromosome 11q13 was mutated in three out of eleven sporadic malignant PETs. Two nonsense mutations, causing truncation of the protein, and one missense mutation were found.</p><p>Relation of allelic loss at 11q13 and 3p25 to malignant behavior was observed in sporadic PETs. Allelic loss at 18q21 was found in a subset of sporadic and MEN1-associated PETs, and mutation analysis of Smad4 excluded a tumor suppressor gene function.</p><p>In PETs with allelic loss on chromosome 3p25, mutation analysis of WNT7A and HDAC11 excluded function as tumor suppressor genes.</p><p>Menin, encoded by the MEN1 gene, was reported to regulate expression of the cyclin-dependent kinase inhibitors CDKN2C/p18, CDKN1B/p27, and CDKN2B/p15 in mouse pancreatic islet tumor models. Here, the mRNA expression of these genes was not related to MEN1 gene mutations in human PETs.</p><p>Cyclin-dependent kinase 4 (CDK4) and the protooncogene c-Myc were found to be overexpressed regardless of MEN1 gene mutational status of the PETs. The CDK4 gene was neither amplified nor mutated. Targeting of CDK4 may present an alternative to traditional chemotherapy of PETs in the future.</p>