La biogenèse des ribosomes est un processus complexe qui implique la production et l'assemblage de 4 ARN et d'environ 80 protéines. Chez l'Homme, la production des deux sous-unités ribosomiques débute dans le nucléole par la synthèse par l'ARN polymérase I d'un long transcrit contenant les séquences des ARN ribosomiques 5.8S, 18S et 25S, qui s'associe de manière co-transcriptionnelle à des protéines ribosomiques et à des facteurs d'assemblage. Le quatrième ARN ribosomique, l'ARNr 5S est transcrit séparément par l'ARN polymérase III, et s'associe avec les protéines ribosomiques Rpl5 et Rpl11 en dehors du ribosome. Ce sous-complexe, appelé particule 5S, est ensuite intégré au sein de la grande sous-unité. La particule 5S est également impliquée dans le contrôle de la prolifération cellulaire. En effet, en cas de dé-régulation de la biogenèse du ribosome, la particule 5S s'accumule dans le nucléoplasme et interagit directement avec l'ubiquitine-ligase MDM2, provoquant la stabilisation du suppresseur de tumeur p53. L'objectif principal de ma thèse est d'étudier le rôle des facteurs d'assemblage Rpf2 et Rrs1 dans la biogenèse du ribosome. Ces protéines assurent deux fonctions distinctes : elles sont requises pour l'association de la particule 5S avec la sous-unité pré-60S, et stimulent la transcription des ARNr par l'ARN polymérase I. Elles sont donc impliquées dans deux événements fondamentaux qui conditionnent les capacités de prolifération cellulaire. La combinaison d'études structurales par cristallographie aux rayons X, et d'études d'interactions protéine-ARN in vitro et in vivo, m'ont permis de mieux appréhender le rôle du complexe Rpf2/Rrs1 dans l'intégration de la particule 5S et dans la maturation de la grande sous-unité. J'ai également étudié le rôle du complexe Rpf2/Rrs1 dans la régulation de la transcription des ARNr, en caractérisant ses interactions avec la polymérase I. / Ribosome Biogenesis is a complex process that requires the production and the correct assembly of the 4 rRNA with more than 80 proteins. Ribosome biogenesis starts by the transcription of a pre-RNA precursor in the nucleolus. Three of the four ribosomal RNAs, the 5.8S, 18S, and 25S rRNAs, are cotranscribed as a single 35S precursor by polymerase I. This precursor is cotranscriptionally modified, folded, cleaved, and assembled with both ribosomal proteins and non-ribosomal factors to generate the mature ribosomes. The fourth rRNA, the 5S rRNA, is transcribed by RNA polymerase III and is assembled into the 5S particle, containing ribosomal proteins Rpl5 and Rpl11, prior to its incorporation into preribosomes. In mammals, the 5S RNP is also a central regulator of the homeostasis of the tumor suppressor p53 The main objective of my thesis was to understand the precise roles of the two assembly factors Rpf2 and Rrs1 in ribosome biogenesis. These proteins have two distinctive functions : Rpf2 and Rrs1 are required for the 5S particle incorporation into the large subunit, and stimulate the rRNA transciption by polymerase I. Using a combination of structural studies by X-Ray crystallography and biochemical approaches as in vitro and in vivo methods to study proteins-RNA interactions, I was able to uncover the function of the Rpf2/Rrs1 dimer in the maturation of the large subunit through the recruitment of the 5S particle. I also studied the function of Rpf2 and Rrs1 in the rRNA transcription regulation, by characterizing physical connection with polymerase I subunits.

A Mata Atlântica é um importante bioma da costa brasileira, apresenta grande diversidade de plantas e animais, porém, pouco se sabe sobre a diversidade microbiana. Da mesma forma, pouco se sabe sobre o papel funcional desses microrganismos. Vários microrganismos estão envolvidos na ciclagem do nitrogênio na Mata Atlântica, e dentre eles os diazotróficos são de particular interesse, pois contribuem para o aporte direto de nitrogênio nos ecossistemas. O objetivo deste trabalho foi avaliar a diversidade de bactérias diazotróficas que nodulam leguminosas em duas parcelas permanentes do Parque Estadual da Serra do Mar em diferentes altitudes. Nódulos de raízes foram coletados nas quatro estações do ano. As bactérias foram isoladas do interior dos nódulos, resultando em 105 isolados. A análise de diversidade genética destas bactérias foi feita utilizando-se BOX-PCR e sequenciamento parcial do gene 16S rRNA. A capacidade de nodulação dos isolados foi determinada através da formação de nódulos em caupi (Vignia unguiculata). Os resultados indicaram que há uma diferença na distribuição espacial e temporal dos nódulos nas áreas estudadas. A maior quantidade de nódulos foi encontrada na parcela de Picinguaba, em estações com menores índices pluviométricos. Os isolados apresentaram uma grande diversidade fenotípica, sendo separados em 6 grupos com características culturais semelhantes. Os perfis de BOX-PCR formaram 8 grupos genotípicos com mais de 80% de similaridade, agrupando tanto isolados de Picinguaba quanto de Santa Virgínia. Os perfis dos géis do BOX-PCR apresentaram variação no número e mobilidade das bandas. Os dados foram transformados em uma matriz binária de presença e ausência que possibilitou a análise de agrupamento hierárquicos com 8 grupos genotípicos com mais de 80% de similaridade, agrupando tanto isolados de Picinguaba quanto de Santa Virgínia. Através do sequenciamento parcial de fragmentos de gene rRNA 16S verificou-se que a estrutura das comunidades diazotróficas de Picinguaba e Santa Virgínia não apresentaram diferença estatisticamente significativa, indicando que não há seleção de populações bacterianas especificas nas áreas.Dos isolados testados, 88% apresentaram capacidade de nodular caupi, porém alguns não foram eficientes em promover o crescimento das plantas. Nas duas áreas predominou UTOs filogeneticamente associados ao gênero Paenibacillus nos nódulos, sugerindo que essas bactérias são importantes para nodulação de leguminosas na Mata Atlântica. / The Atlantic Rainforest is a major biome of the Brazilian coast, which harbors great diversity of flora and fauna, but little is known about its microbial diversity. Furthermore, little is known about the functional role of these abundant microorganisms. Several microorganisms are involved in cycling of the Atlantic Rainforests nitrogen, among them the diazotrophs which are of particular interest because they contribute to the direct input of nitrogen to ecosystems. The aim of this study was to evaluate the diversity of legumes nodulating diazotrophs in two permanent plots of the Serra do Mar State Park at different altitudes. Root nodules were collected throughout the four seasons. The bacteria were isolated from inside of the nodules, resulting in 105 isolates. The analysis of genetic diversity was performed using BOX-PCR and rRNA 16S sequencing. The nodulation capacity of the isolates was determined by the nodule formation in cowpea (Vigna unguiculata). The results indicated that there are spatial and temporal differences distribution in the areas studied. The largest number of nodules was found in the Picinguaba plot during seasons of low rainfall. The isolates showed a wide phenotypic diversity, hence divided into six groups with similar cultural characteristics. The BOX-PCR profiles formed eight genotypic groups with more than 80% similarity, when comparing the isolates from Picinguaba those from Santa Virginia. The BOX-PCR gel profiles showed variation in number and mobility of bands. The data was transformed into a binary matrix of presence and absence that allowed the hierarchical cluster analysis of eight genotypic groups with more than 80% similarity, again comparing both isolates Picinguaba and Santa Virginia. Through partial sequencing of 16S rRNA gene fragments no statistically significant difference was found between the diazotrophs community structures of Picinguaba the and that of Santa Virginia , indicating no selection for specific bacterial populations in these areas. In both isolates tested, 88% showed cowpea nodulating capacity, but some were not effective in promoting plant growth. In both areas OTUs phylogenetically associated with nodule of genus Paenibacillus predominated, suggesting that these bacteria are important for legume nodulation in the Atlantic Rainforest.

A Mata Atlântica é um importante bioma da costa brasileira, apresenta grande diversidade de plantas e animais, porém, pouco se sabe sobre a diversidade microbiana. Da mesma forma, pouco se sabe sobre o papel funcional desses microrganismos. Vários microrganismos estão envolvidos na ciclagem do nitrogênio na Mata Atlântica, e dentre eles os diazotróficos são de particular interesse, pois contribuem para o aporte direto de nitrogênio nos ecossistemas. O objetivo deste trabalho foi avaliar a diversidade de bactérias diazotróficas que nodulam leguminosas em duas parcelas permanentes do Parque Estadual da Serra do Mar em diferentes altitudes. Nódulos de raízes foram coletados nas quatro estações do ano. As bactérias foram isoladas do interior dos nódulos, resultando em 105 isolados. A análise de diversidade genética destas bactérias foi feita utilizando-se BOX-PCR e sequenciamento parcial do gene 16S rRNA. A capacidade de nodulação dos isolados foi determinada através da formação de nódulos em caupi (Vignia unguiculata). Os resultados indicaram que há uma diferença na distribuição espacial e temporal dos nódulos nas áreas estudadas. A maior quantidade de nódulos foi encontrada na parcela de Picinguaba, em estações com menores índices pluviométricos. Os isolados apresentaram uma grande diversidade fenotípica, sendo separados em 6 grupos com características culturais semelhantes. Os perfis de BOX-PCR formaram 8 grupos genotípicos com mais de 80% de similaridade, agrupando tanto isolados de Picinguaba quanto de Santa Virgínia. Os perfis dos géis do BOX-PCR apresentaram variação no número e mobilidade das bandas. Os dados foram transformados em uma matriz binária de presença e ausência que possibilitou a análise de agrupamento hierárquicos com 8 grupos genotípicos com mais de 80% de similaridade, agrupando tanto isolados de Picinguaba quanto de Santa Virgínia. Através do sequenciamento parcial de fragmentos de gene rRNA 16S verificou-se que a estrutura das comunidades diazotróficas de Picinguaba e Santa Virgínia não apresentaram diferença estatisticamente significativa, indicando que não há seleção de populações bacterianas especificas nas áreas.Dos isolados testados, 88% apresentaram capacidade de nodular caupi, porém alguns não foram eficientes em promover o crescimento das plantas. Nas duas áreas predominou UTOs filogeneticamente associados ao gênero Paenibacillus nos nódulos, sugerindo que essas bactérias são importantes para nodulação de leguminosas na Mata Atlântica. / The Atlantic Rainforest is a major biome of the Brazilian coast, which harbors great diversity of flora and fauna, but little is known about its microbial diversity. Furthermore, little is known about the functional role of these abundant microorganisms. Several microorganisms are involved in cycling of the Atlantic Rainforests nitrogen, among them the diazotrophs which are of particular interest because they contribute to the direct input of nitrogen to ecosystems. The aim of this study was to evaluate the diversity of legumes nodulating diazotrophs in two permanent plots of the Serra do Mar State Park at different altitudes. Root nodules were collected throughout the four seasons. The bacteria were isolated from inside of the nodules, resulting in 105 isolates. The analysis of genetic diversity was performed using BOX-PCR and rRNA 16S sequencing. The nodulation capacity of the isolates was determined by the nodule formation in cowpea (Vigna unguiculata). The results indicated that there are spatial and temporal differences distribution in the areas studied. The largest number of nodules was found in the Picinguaba plot during seasons of low rainfall. The isolates showed a wide phenotypic diversity, hence divided into six groups with similar cultural characteristics. The BOX-PCR profiles formed eight genotypic groups with more than 80% similarity, when comparing the isolates from Picinguaba those from Santa Virginia. The BOX-PCR gel profiles showed variation in number and mobility of bands. The data was transformed into a binary matrix of presence and absence that allowed the hierarchical cluster analysis of eight genotypic groups with more than 80% similarity, again comparing both isolates Picinguaba and Santa Virginia. Through partial sequencing of 16S rRNA gene fragments no statistically significant difference was found between the diazotrophs community structures of Picinguaba the and that of Santa Virginia , indicating no selection for specific bacterial populations in these areas. In both isolates tested, 88% showed cowpea nodulating capacity, but some were not effective in promoting plant growth. In both areas OTUs phylogenetically associated with nodule of genus Paenibacillus predominated, suggesting that these bacteria are important for legume nodulation in the Atlantic Rainforest.

La caractérisation des réseaux trophiques est nécessaire pour comprendre le fonctionnement des écosystèmes et les mécanismes impliqués dans leur stabilité. Il est parfois difficile de déterminer les régimes alimentaires notamment pour des espèces discrètes et difficiles à observer comme les grands carnivores. Cependant, ces espèces jouent un rôle clé dans les écosystèmes dont elles influencent le fonctionnement et la biodiversité. Ainsi, connaitre le régime alimentaire des grands prédateurs avec précision est essentiel pour établir des stratégies de conservation. Diverses méthodes basées sur le monitoring, l'analyse d'échantillons invasifs ou non ont été utilisées pour étudier les régimes alimentaires. Elles sont généralement biaisées ou peu résolutives. Les méthodes basées sur l'identification des fragments d'ADN dans les fèces ont le potentiel de fournir une meilleure information, notamment dans le cadre d'une approche métabarcoding. Il s'agit de caractériser simultanément l'ensemble des espèces dont l'ADN est présent dans un échantillon environnemental, en utilisant les Nouvelles Techniques de Séquençage. Dans ce cas, les amorces universelles nécessaires pour amplifier toutes les proies potentielles amplifient également l'ADN du prédateur s'il y a proximité taxonomique (par exemple mammifères). Ainsi les produits PCR obtenus à partir des fèces sont essentiellement composés d'ADN du prédateur et ne reflètent pas l'ensemble du régime alimentaire. L'utilisation d'un oligonucléotide de blocage limitant spécifiquement l'amplification de l'ADN du prédateur peut résoudre ce problème. Nous avons développé une méthode de ce type basée sur l'utilisation d'amorces universelles pour les vertébrés (amplifiant la région 12SV5) et d'oligonucléotides de blocage. Bien que non quantitative, cette méthode s'est montrée robuste, adaptée à l'étude de prédateurs à très large spectre de proies, et très résolutive pour identifier les proies au niveau du genre et de l'espèce. Nous l'avons appliquée à l'étude du régime alimentaire du chat léopard (Prionailurus bengalensis) qui s'est avéré très diversifié (mammifères, oiseaux, amphibiens et poissons) dans les deux populations du Pakistan étudiées. Avec la même approche, nous avons démontré la réalité du conflit entre l'homme et le léopard commun (Panthera pardus) dont le régime est presque exclusivement composé d'animaux domestiques. Enfin, nous avons pu proposer des actions de conservations pertinentes après avoir montré que le régime de la très menacée panthère des neiges (Panthera uncia) est principalement composé d'ongulés sauvages. / Information on food webs is central to understand ecosystem functioning. It also provides information of ecosystem stability by evaluating the resource availability and use. Obtaining information on the diet can be critical especially when dealing with elusive carnivores, which are difficult to observe. However, these large carnivores are keystone species that influence the ecosystem through trophic cascades and maintain biodiversity. Thus, precise knowledge of their diet is a prerequisite for designing conservation strategies of these endangered species. Direct and indirect monitoring as well as invasive and non-invasive approaches that have been used to study the diet are either biased or have a low resolution. The DNA-based analysis of feces is an alternative method that may provide better information. It can be implemented through a metabarcoding approach, which is the simultaneous identification of multiple species from a single environmental sample containing degraded DNA by using Next Generation Sequencing. In this case, the use of universal primers for vertebrates amplifying all potential prey also amplifies the predator DNA when it belongs to a close taxon (e.g. mammals). Thus, the PCR products obtained from feces extracts will mainly consist of predator sequences and may not represent the full diet. The use of oligonucleotides specifically blocking the amplification of the predator DNA may overcome this problem. We have developed such a method based on the concomitant use of a universal primer pair (12SV5, amplifying all vertebrates) and blocking oligonucleotides for identifying the prey DNA fragments from predators feces. Even if the method developed is not quantitative, it is robust and adequate for studying predator with a very large dietary range and has a better resolution than traditional methods for identifying prey at the genus or species level. This methodology has been applied to characterize the highly eclectic diet (mammals, birds, amphibians and fishes) of two Northern-Pakistani populations of leopard cat (Prionailurus bengalensis). With the same approach, we demonstrated the importance of the Human-leopard conflict in Pakistan, due to the almost exclusive consumption of domestic animals by the common leopard (Panthera pardus). We could also highlight relevant conservation issues for the highly endangered and cryptic snow leopard (Panthera uncia), based on the fact that it mainly fed on wild ungulates.

Submitted by Liliane Ferreira (ljuvencia30@gmail.com) on 2018-04-02T14:29:46Z No. of bitstreams: 2 Dissertação - Marcus Vinícius Forzani Araújo - 2017.pdf: 1549598 bytes, checksum: 0807ed298bd63e9574018c8c399c3ca5 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) / Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2018-04-02T14:41:18Z (GMT) No. of bitstreams: 2 Dissertação - Marcus Vinícius Forzani Araújo - 2017.pdf: 1549598 bytes, checksum: 0807ed298bd63e9574018c8c399c3ca5 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) / Made available in DSpace on 2018-04-02T14:41:18Z (GMT). No. of bitstreams: 2 Dissertação - Marcus Vinícius Forzani Araújo - 2017.pdf: 1549598 bytes, checksum: 0807ed298bd63e9574018c8c399c3ca5 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2017-10-13 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES / Characterized as extremely important, the soil is a complex environment and it shelters a great diversity of microorganisms. However, little is known about the diversity and ecology of the soil microbiota. Thus, the first part of this dissertation reviews the methodological evolution used to characterize the diversity and abundance of microorganisms found in soil. The second part consists of the application of two methodologies reviewed in the previous chapter, serial dilution and solid medium plating, to estimate free-living nitrogen fixing microorganisms, and fumigation-extraction to estimate soil microbial biomass (BMS). The last part employs the most modern microbial soil characterization technique, the metagenomics of 16S rRNA. Hence, our initial hypothesis was that sugarcane fields’ soils would have better soil microbiological indicators than grasslands’ soils. The results confirmed that the hypothesis was partially correct, and it was possible to find about 140% more free-living diazotrophic colony-forming units (CFUs) and a 17% richer alpha diversity in sugarcane fields’ soils than in grasslands’ soils. The beta diversity between sugarcane plantations and pastures presented clear differences. However, sugarcane fields’ soils obtained about 25% less BMS than grasslands’ soils. In relation to the bacterial phyla, the grasslands have more Actinobacteria, Chloroflexi and Planctomycetes and sugarcane fields have a greater number of TM7 and bacteria that were not identified, being Proteobacteria and Acidobacteria the dominating phyla in both types of soil. Although the results of nitrogen fixers and microbial biomass appear to be conflicting, it is an indication that the diazotrophic community undergoes with a diverse biotic and abiotic influences than the total community of soil microorganisms, and thus respond differently. / Caracterizado como de extrema importância, o solo é um ambiente complexo e que abriga uma grande diversidade de micro-organismos. Entretanto ainda pouco se sabe sobre a diversidade e ecologia da microbiota do solo. Deste modo, a primeira parte desta dissertação revisa a evolução metodológica empregada para caracterizar a diversidade e abundância dos micro-organismos encontrados no solo. A segunda parte consiste na aplicação de duas metodologias revisadas no capítulo anterior, a de diluição seriada e plaqueamento em meio sólido, para estimar micro-organismos fixadores de nitrogênio de vida-livre, e a fumigação-extração, para estimar a biomassa microbiana do solo (BMS). E a última parte emprega a técnica mais moderna de caracterização das comunidades microbianas de solo, a técnica de metagenômica de 16S rRNA. À vista disso, a nossa hipótese inicial era que solos de canavial teriam indicadores microbiológicos de solo melhores do que solos de pastagem. Os resultados comprovaram que a hipótese estava parcialmente correta, sendo possível encontrar cerca de 140% a mais de Unidades Formadoras de Colônias (UFCs) de diazotróficos de vida-livre e uma diversidade alfa 17% mais rica em solos de canaviais do que em solos de pastagens. A diversidade beta entre canaviais e pastagens apresentou diferenças nítidas. Entretanto, os solos de canaviais obtiveram cerca de 25% a menos de biomassa microbiana do solo do que solos de pastagens. Em relação aos filos bacterianos, os pastos possuem mais Actinobacteria, Chloroflexi e Planctomycetes e canaviais possuem maior número de TM7 e bactérias que não foram identificados, sendo Proteobacteria e Acidobacteria os filos dominantes nos dois tipos de solo. Apesar de parecerem conflitantes os resultados de fixadores de nitrogênio e biomassa microbiana, é um indicativo de que a comunidade de diazotróficos sofrem influências bióticas e abióticas diversas do que a comunidade total de micro-organismos do solo, e desta forma, respondem de forma diferente.

Os microrganismos representam a forma de vida mais abundante e diversificada do planeta. A atividade agrícola leva a uma redução da biodiversidade do solo e a menor diversidade microbiana pode resultar na diminuição da ciclagem de nutrientes e no crescimento das plantas. Como forma de avaliar alterações na atividade microbiana e na estrutura das comunidades de bactérias do solo, decorrentes do cultivo da cana-de-açúcar, foram conduzidos dois experimentos. O primeiro, no município de Novo Horizonte (SP), com o objetivo de determinar ação da queima da cana-de-açúcar sobre a comunidade de bactérias do solo e o segundo experimento, nos municípios de Pirassununga (SP) e Jaboticabal (SP), com o objetivo de verificar o efeito da adubação nitrogenada sobre a comunidade bacteriana do solo. Amostras de terra foram coletadas nas profundidades 0-10 e 10-20 cm, na linha e entrelinha de plantio. No primeiro experimento foram utilizadas três cultivares de cana-de-açúcar (SP81-3250, SP80-1842 e RB72-454) sob os sistemas de manejo de colheita sem queima (mecanizada) e com queima (manual) prévia a colheita. Nesse experimento foram avaliadas a diversidade metabólica (Biolog) e a estrutura das comunidades bacterianas por meio da PCR-DGGE do gene rRNA 16S. A mudança no manejo de colheita da cana-de-açúcar provocou modificações no metabolismo heterotrófico do solo, alterando a diversidade metabólica. No entanto, não houve mudanças na estrutura das comunidades bacterianas do solo com e sem queima sob a variedade SP801842. Dessa forma, a primeira queima da cana-de-açúcar previamente à colheita alterou a capacidade e a diversidade metabólica microbiana, mas não mudou a estrutura das comunidades de bactérias em relação à área sem queima. No segundo experimento foram avaliadas amostras de terra, de duas áreas experimentais, sob cultivo de cana-de-açúcar (SP813250), com diferentes doses de N (0, 40, 80 e 120 kg de N ha-1) na forma de uréia, aplicadas no sulco de plantio. Para verificar possíveis alterações na comunidade bacteriana desses solos, foram avaliadas a estrutura das comunidades bacterianas por PCR-DGGE e a diversidade de bactérias oxidadoras de amônio (AOB), pelo seqüenciamento de bibliotecas do gene rRNA 16S, utilizando oligonucleotídeos iniciadores específicos. As doses de N alteraram a estrutura das comunidades bacterianas do solo nas duas áreas experimentais, determinadas por PCR-DGGE, entretanto, a adubação nitrogenada não alterou a diversidade de AOB no solo, das duas áreas. A estrutura da comunidade de AOB no solo da USA, sem adubação nitrogenada e com 80 kg de N ha-1 diferiu estatisticamente. Nas duas áreas, as unidades taxonômicas operacionais mais abundantes se relacionam filogeneticamente a Nitrosospira multiformes. / The microorganisms are the most abundant and diverse living creatures on earth. The agricultural practices reduce the soil biodiversity and a lower microbial diversity can result in a nutrient cycling and plant growth reduction. Two sugarcane crops experiments were investigated to evaluate modifications in the microbial activity and soil bacterial communities structure. The first of them was done at municipality of Novo Horizonte, Sao Paulo State (SP), and it has the aim to determine the sugarcane burn effects on soil bacterial community. The second experiment was introduced at municipalities of Pirassununga (SP) and Jaboticabal (SP) with the objective to verify the nitrogen fertilizing effect on soil bacterial community. The soil samples were taken in 0-10 cm and 10-20 cm depth, between and in the planting furrows. We used three sugarcane varieties (SP81-3250, SP80-1842 e RB72-454) in the first experiment under unburned and burned sugarcane pre-harvest. We evaluated metabolic diversity (Biolog) and the bacterial community structure performing PCR-DGGE of 16S rRNA gene in the first experiment. The sugarcane harvest management had modified the soil heterotrophic metabolism by altering its diversity. In spite of that, there is no difference between the burned and unburned soil bacterial communities under the variety SP80-1842. For that reason, the first year pre harvest burn altered the microbial metabolic diversity and capacity but did not change the bacterial community structure when related with unburned area. In the second experiment, soil samples under the SP81-3250 variety were analyzed from two sites. Each site received different levels of urea as nitrogen fertilization (0, 40, 80 e 120 kg de N ha-1) applied at planting furrows. The PCR-DGGE was applied to verify changes in the bacterial communities structure in these soils. The ammonia-oxidizing bacteria (AOB) diversity was evaluated by sequencing of 16S rRNA gene libraries after the amplification with specific primers. The levels of nitrogen fertilization altered the soil bacterial communities structure in both study sites, by PCRDGGE evaluation. However, the nitrogen application did not alter the soil AOB diversity in those two sites. The soil AOB community structure under no nitrogen and 80 kg N ha-1 application was different from the community structure under the other levels of fertilization in one of the two sites. The operational taxonomic unit are phylogenetically related to Nitrosospira multiformes in the two sites.

As cianobactérias caracterizam-se como o grupo de micro-organismos fotoautotrófico mais abundante encontrado nas regiões polares. Representantes deste grupo realizam a fotossíntese oxigênica e também podem fixar o nitrogênio atmosférico. A maioria dos levantamentos da comunidade de cianobactérias na Antártica tem sido realizada apenas por meio de observações microscópicas de amostras ambientais. O isolamento de linhagens e consequentes estudos fisiológicos, bem como, análises independentes de cultivo ainda são escassos. Neste estudo a comunidade de cianobactérias de duas ilhas oceânicas da Antártica foi investigada utilizando abordagens moleculares dependentes e independentes de cultivo. O papel ecológico das cianobactérias como fornecedoras de formas assimiláveis de nitrogênio e o potencial genético para biossíntese de produtos naturais também foi avaliado. Sessenta e oito linhagens de cianobactérias foram isoladas a partir de diferentes substratos coletados. Elas pertencem às ordens Chroococcales, Pseudanabaenales, Oscillatoriales e Nostocales, famílias Xenococcaceae, Dermocarpellaceae, Pseudanabaenaceae, Oscillatoriaceae, Nostocaceae, Microchaetaceae e Rivulariaceae. Análises filogenéticas baseadas nas sequências de RNAr 16S dessas cianobactérias revelou a existência de agrupamentos: formado exclusivamente por sequência de linhagem isolada nesse trabalho; composto por sequências antárticas oriundas desse e de outros trabalhos desenvolvidos em outras regiões antárticas; e por sequências originárias de diversas regiões do mundo. Quarenta e uma linhagens apresentaram fragmento do gene nifH, responsável pela codificação do complexo enzimático da nitrogenase, o qual está envolvido na fixação biológica do nitrogênio (FBN). Formas unicelulares (Chroococcales), homocitadas (Pseudanabaenales e Oscillatoriales) e heterocitadas (Nostocales) apresentaram potencial genético para realização da FBN, e 18 delas foram submetidas aos testes de redução de acetileno (ARA) com alta sensibilidade de detecção. Todas as linhagens testadas exibiram alguma atividade em resposta a diferentes concentrações de oxigênio e/ou a luminosidade em diferentes condições de temperatura. Filogeneticamente, as sequências do gene nifH apresentaram três padrões distintos de agrupamento, o que pode estar relacionado aos eventos evolutivos envolvidos na distribuição e ou manutenção deste gene. A presença de genes e ou regiões intergênicas evidenciaram o elevado potencial genético dessas linhagens para sintetizar produtos naturais com interesse biotecnológico. A abundância no número de cópias do gene nifH relacionado às cianobactérias nas amostras de biofilme reforça a importância desse grupo de microorganismos como fornecedor de formas reduzidas de N para o ambiente antártico. A análise da comunidade de cianobactérias por meio do sequenciamento do RNAr 16S de DNA metagenômico evidenciou predominância de UTOs relacionadas às ordens Nostocales, Oscillatoriales e Pseudanabaenales, famílias Pseudanabaenaceae, Phormidiaceae, Nostocaceae e Rivulariaceae. A árvore filogenética contendo as sequências de cianobactérias cultivadas e não-cultivadas mostrou que somente parte da comunidade presente em biofilmes foi acessada por isolamento, indicando a complementariedade entre as duas abordagens utilizadas na análise da comunidade de cianobactérias / Cyanobacteria are characterized as the most abundant group of photoautotrophic microorganisms found in the polar regions. Members of this group perform oxygenic photosynthesis and many of them can also fix atmospheric nitrogen. Investigations on the cyanobacterial community have been made mainly applying microscopic observations of environmental samples. Cyanobacterial isolation, physiological studies and cultureindependent analyses are scarce. In this study the cyanobacterial community from two oceanic islands in Antarctica was investigated using culture-dependent and independent approaches. Also, the ecological role of this group of microorganisms as nitrogen-fixing organisms and the genetic potential for biosynthesis of natural products were evaluated. Sixty-eight cyanobacterial strains were isolated from different environmental samples. They belong to the orders Chroococcales, Pseudanabaenales, Oscillatoriales and Nostocales, families Xenococcaceae, Dermocarpellaceae, Pseudanabaenaceae, Oscillatoriaceae, Nostocaceae, Microchaetaceae and Rivulariaceae. Phylogenetic analyses based on 16S rRNA sequences of these cyanobacteria revealed the existence of groups: exclusively formed by sequence of strain isolated in this work; intermixed sequences from this and other studies developed in other Antarctic regions; and sequences originated from different regions of the world. Fortyone cultured strains possess the nifH gene fragment encoding the nitrogenase enzyme complex, which is related to the biological nitrogen fixation (BNF). Unicellular (Chroococcales), homocytous (Pseudanabaenales and Oscillatoriales) and heterocytous forms (Nostocales) showed genetic potential for BNF, and 18 of them were subjected to acetylene reduction assay (ARA) coupled with a sensitive laser photoacoustic ethylene detector. All strains tested exhibited some nitrogenase activity in response to different concentrations of oxygen and or irradiance under different temperature conditions. Phylogenetically, the nifH gene sequences showed three distinct grouping patterns that may be related to the evolutionary events involved in the distribution and or maintenance of this gene. The presence of genes and or intergenic regions in these cyanobacterial strains underscores the genetic potential of them to synthesize natural products with biotechnological interest.The abundance of nifH gene copies related to cyanobacteria in biofilm samples highlights the importance of this group of microorganisms as suppliers of N reduced forms for Antarctic environment. The analysis of the cyanobacteria community revealed by 16S rRNA sequencing of metagenomic DNA showed a predominance of OTUs related to orders Nostocales, Oscillatoriales and Pseudanabaenales, families Pseudanabaenaceae, Phormidiaceae, Nostocaceae and Rivulariaceae. The phylogenetic tree containing Antarctic sequences from cultivated and uncultivated cyanobacteria showed that only part of this community in biofilms has been accessed by isolation, indicating the complementarity between the two approaches used in the analysis of cyanobacterial community

Algae are a group of highly diverse photosynthetic organisms found in variety of habitats. As the primary energy base in ecosystems, knowledge of the diversity and presence of certain algal lineages is paramount to our understanding of the trophic state of aquatic habitats. In recent years, the state of Florida has seen an increase of both marine and freshwater algal blooms. Similarly, filamentous algae have begun outcompeting vascular macrophytes throughout many of Florida’s springs as nutrient enrichment from anthropogenic sources increases. Traditionally, the Florida algal spring communities have been assessed using classic morphological methods, which may underrepresent the true biodiversity present. Therefore, the goal of this study was to conduct a more complete diversity assessment implementing next-generation sequencing techniques (NGS) with morphological analyses and culturing methods. While morphological methods identified a wide variety of algal taxa, belonging to 4 phyla (Bacillariophyta, Charophyta, Chlorophyta, and Cyanobacteria), next-generation sequencing techniques provided greater detail of the diatom community. This is particularly important as many diatom taxa are used as indicators of water quality. We noted discrepancies between these two methods, highlighting how NGS techniques may complement the use of morphological analyses when analyzing algal diversity in this system. Culturing methods also revealed the presence of two taxa new to science (Nodosilinea fontisand Brasilonema variegatus), indicating these springs may represent a potential source of novel cyanobacteria. Taken together, this study showcases Florida springs are rich in algal diversity and a combination of methods is required for more complete biodiversity assessments. Future studies implementing such methods will aid in the preservation and conservation of these ecosystems.

Nearly all deep-sea cephalopod life history studies have been completed by examination of specimens collected in the wild. Much of this work is like piecing together a puzzle; knowledge of the life history of many species remains fragmented and hence, taxonomically and phylogenetically confused. Molecular approaches and sequencing technologies are powerful tools for deciphering wild-type cephalopod life history and population dynamics. Use of molecular markers offers additional certainty for identifying specimens damaged during deep-sea collections and can elucidate often cryptic, intra- and interspecific diversity. The research presented in this study assessed broad genetic patterns of biodiversity in deep-sea cephalopods from the Gulf of Mexico and northwestern Atlantic Ocean. This study has two key objectives: [1] to examine intraspecies variation among regionally disjunct subpopulations, comparing collections separated by the Florida Peninsula, and [2] to examine intraspecies variation within deep-sea cephalopods in the Gulf of Mexico. Through Sanger sequencing marker genes COI, 16S rRNA, and 28S rRNA, this study has generated a genetic baseline characterization of deep-sea cephalopods in the Gulf of Mexico, assessed intraspecies genetic variation, and linked morphological identification with DNA barcodes, testing morphological hypotheses of species identification and naming. Results of investigating intraspecies variation within regionally disjunct subpopulations reveal there is no regional distinction between the Gulf of Mexico subpopulations of Vampyroteuthis infernalis, Pyroteuthis margaritifera, and Cranchia scabra, and the Bear Seamount subpopulations in the northwestern Atlantic Ocean. Results of investigating intraspecies variation within the Gulf of Mexico displayed potential for cryptic species, novel sequence records, and large expansions to sequence records for species known to inhabit the Gulf of Mexico. Analysis of intraspecies variation within the Gulf of Mexico facilitated identification of damaged specimens used for this study, but also revealed GenBank database issues of misidentified records, and outdated nomenclature in accession records. Because cephalopods play a central role in most oceanic ecosystems, characteristics like a short average life span and a rapid growth rate mean that cephalopod populations have the potential to serve as an invaluable reflection of ecosystem change.

Dans les écosystèmes marins, les protistes jouent un rôle important en tant que producteurs primaires, prédateurs ou encore symbiontes. De par leur position clef, l'étude de leur diversité est fondamentale afin d'améliorer notre compréhension du fonctionnement des écosystèmes marins. Pour ce faire, des approches moléculaires couplées à la microscopie ont été utilisées afin d'examiner en profondeur la diversité des communautés microbiennes dans deux écosystèmes contrastes (Manche Orientale et Méditerranée). La première étude conduite en Manche Orientale a permis d'établir une vue d'ensemble de la diversité des protistes eucaryotes sur une période de 4 ans (de mars 2011 à Juillet 2015) et d'examiner l'influence des variables environnementales sur leur distribution temporelle. L'approche novatrice utilisée consistait à séquencer simultanément l'ARNr et l'ADNr. Ce double ciblage a permis de calculer le rapport ARNr : ADNr et de démontrer qu'il pouvait être un paramètre utile et significatif pour évaluer l'activité cellulaire globale de la communauté microbienne. Nous avons également montré la faisabilité d'utiliser ce ration ARNr : ADNr comme indicateur des transitions écologiques d'espèces microbiennes emblématiques (e.g. bloom de Phaeocystis globosa). Ainsi, le calcul individuel de ce rapport pour chaque OTU devrait permettre d'apporter une information supplémentaire indispensable pour une meilleure compréhension du fonctionnement de l'écosystème et de l'influence des paramètres biotiques et abiotiques sur la structuration des communautés microbiennes, en particulier dans un contexte de changement global. La seconde étude a également été menée en Manche Orientale sur les données de séquençage obtenues pendant la période 2011-2013. Elle avait pour objectif de mettre en évidence les relations existantes entre les parasites eucaryotes et les autres taxons ainsi que les paramètres environnementaux. Cette érude a montré la diversité insoupçonnée des symbiontes/décomposeurs en Manche Orientale, et leur importance pour la structuration des communautés et la succession saisonnière. En particulier, des analyses en réseaux de corrélations ont montré la prédominance des relations inter-taxa, plutôt qu'entre OTUs et paramètres abiotiques, et la position centrale des symbiontes/décomposeurs dans ces relations. Cette étude a permis de souligner la complexité et l'importance des interactions microbiennes dans la structuration des communautés toute en apportant des informations cruciales permettant de mieux comprendre les mécanismes sous-jacent qui régissent cette structuration. La dernière étude a été menée dans la Méditerranée Occidentale, au niveu de quatre stations situées dans le Golfe du Lion, soumises à l'influence du fleuve Rhône, sur une période de 2 ans (2012-2014). Elle avait pour objectif de réaliser la liste la plus exhaustive possible de la diversité des protistes eucaryotes et d'évaluer leur variabilité spatiale en relation avec les variables environnementales. Cette étude a confirmé l'effet prépondérant du Rhône sur la structuration des communautés, particulièrement dans la partie Est du Golf du Lion. Globalement, ces travaux de thèse ont permis de renforcer, par le biais d'approches combinées de microscopie et de biologie moléculaire, nos connaissances sur le fonctionnement, la diversité taxonomique et la succession des espèces microbiennes, en relation avec les paramètres environnementaux, de deux écosystèmes marins contrastés. / In marine ecosystems, protists play an important role as primary producers, predators or symbionts. Therefore studying their diversity and metabolic activity is fundamental for understanding the functioning of marine ecosystems. In order to achieve this goal, molecular approaches were coupled with microscopy analysis for an in depth examination of microbial communities diversity in two contrasting ecosystems (Eastern English Channel EEC and Mediterranean). The first study, conducted in the EEC, allowed to establish a precise overview of eukaryotic protists diversity over 4 years (from March 2011 to July 2015) and to examine the influence of environmental variables on their temporal distribution. The innovative approach used during this study was to sequence simultaneously rRNA and rDNA. This double targeting allowed calculating the rRNA : rDNA ratio and demonstrate that it could be an useful and significant parameter for measuring the relative cellular activity of the microbial community. We also showed the feasibility of using this rRNA : rDNA ratio as an indicator of ecological transitions of iconic microbial species (e.g. bloom of Phaeocystis globosa). Thus, calculation of this ratio for each individual OTU provided additional information that are essential for a better understanding of the functioning of the ecosystem and the influence of biotic parameters on the structuring of microbial communities, in particular in the context of global change. The second study was also conducted in the EEC on sequencing data obtained during the period 2011-2013. It aimed to highlight the relationships between eukaryotic parasites and other taxa as well as environmental parameters. This study revealed un unsuspected diversity of symbionts / decomposers in the EEC, and their importance for structuring microbial community and influence seasonal succession. More specifically, correlation network analysis showed the predominance of inter-taxa relations, over those between OTUs and abiotic parameters, and the central position of symbionts / decomposers in these relationships. This study highlighted the complexity and importance of microbial inteactions in the structuring of microbial communities while providing crucial information to better understand underlying lechanisms. The last study was conducted in the Western Mediterranean , at four stations located in the Golfe du Lion, subject to the influence of the Rhône River, over a period of two years. This study aimed to provide the most exhaustive list of eukaryotic protist diversity and to evaluate its spatial variability in relation with environmental variables. This study further underlined the effect of the Rh^ne on the structuring of microbial communities, particularly in the eastern part of the Golfe du Lion. Overall, thesis workhas reinforced, through combined aproaches of microscopy and molecular biology, our knowledge of the functioning, taxonomic diversity and succession of microbial species, in relation to environmental parameters, of two contrasted marine ecosystems.