Zwei Populus-Pfropfchimären (MA und AI), die aus P. x canadensis ‘Marilandica’ (M), P. maximowizcii x P. trichocarpa ‘Androscoggin’ (A) and P. nigra L. ’Italica’ (I) aufgebaut sind, wurden für Untersuchungen zur Laub- und Blütenblattentwicklung genutzt. In MA bildet M die äußere Lage (L1) und ihr Derivat, die Epidermis, während die inneren Lagen (L2, L3 etc.) von A gebildet werden. Bei AI stammt die L1 von A und L2, L3 etc. werden von I gebildet. Die genotypisch andersartige Epidermis bedingt bei Periklinal-Chimären morphologische Effekte wie zum Beispiel einen Fruchtknoten in einigen MA-Blüten. Morphologische Besonderheiten verschiedener Gewebe sowohl von M und A als auch von MA wurden verglichen, um festzustellen, wie sie durch die Gewebetransplantation verändert oder beeinflusst wurden und, um mögliche Genotyp- Interaktionen oder -Wechselwirkungen in einem Gewebe ausfindig zu machen. Für die Genotypidentifizierung in verschiedenen Organen wurde die RAPD-PCR getestet. Einer von 20 getesteten 10mer Zufallsprimern (GGAGTGGACA) ermöglichte bei der Verwendung von DNA aus Blattmaterial die Erzeugung verschiedener Bandenmuster für M und A. Bei der Verwendung von MA-Blattmaterial zeigte sich eine Kombination der Muster von M und A, sodass ein Chimärennachweis für das MA-Blattmaterial erbracht wurde. Für ein übertragbares System wurde die spezifische PCR getestet. Unter Verwendung spezifischer Primer für die 16s-rDNA zeigten die PCR-Produkte einheitliche Banden und nach anschließender Sequenzierung eine weitgehende Übereinstimmung der phylogenetischen Verwandtschaft von I, M und A. Weiterhin wurden die kernkodierten rDNA Bereiche ITS 1 und ITS 2 zwischen 18S und 25S getestet. Für I, M und A konnten jeweils zwei Banden von unterschiedlicher Größe und Sequenz ermittelt werden, die vermutlich auf funktionierende rDNA aber auch auf Pseudogene (beschnitten) in niedriger Kopienzahl hinweisen. Die ITS-Regionen von I, M und A wurden charakterisiert, um einen Einblick in die Struktur und Phylogenie der Salicacaee-Familie zu erhalten. Aus den Sequenzunterschieden konnten für I und A spezifische Primerpaare abgeleitet werden, die für die Identifizierung von I und A in AI und MA verwendet werden können. Mittels A-Marker konnte nachgewiesen werden, dass Fruchtknoten aus MA-Blüten neben M-Gewebe auch den A-Genotyp enthalten. / Two Populus graft chimeras (MA and AI) produced of P. x canadensis ‘Marilandica’ (M), P. maximowizcii x P. trichocarpa ‘Androscoggin’ (A) and P. nigra L. ’Italica’ (I) were used for investigations of leaf and flower development. In MA the exogenous layer (L1) forms the epidermis and is derived from M while inner layers (L2, L3 etc.) descend from A whereas in AI L1 is formed by A while L2, L3 etc. descend from I. The exogenous epidermis of the periclinal chimeras imposes morphological effects such as an extra female sex in some of the MA flowers. The morphological characteristics of different plant tissues of parents and chimera were compared to determine how they were modified or altered by the tissue transplantation and possibly identify co-existing or interacting genotypes in one tissue. RAPD-PCR was tested for its usefulness to amplify polymorphic fingerprints including donor specific DNA fragments. One random 10mer primer (GGAGTGGACA) out of 20 tested revealed the amplification of patterns including donor specific DNA bands using extracts from leaf tissues of the M and A parents that were combined using extract from leaf tissue of the MA chimera. This indicates that the leaves of the MA chimera are formed by tissues of M and A. However, the inherent disadvantage of RAPD-PCR is the reproducibility of PCR product generation. Therefore the discriminative potential of the ITS region located between the rRNA genes was investigated. The application of specific 16S ribosomal DNA (rDNA) primers for amplification and sequencing of PCR products revealed a closely phylogenetic relationship between I, M and A. Consequently the ITS1 and ITS2 of nuclear rDNA between 18S and 25S were used. The amplified fragments were purified, cloned in E. coli and sequenced. Analyses of multiple clones demonstrated extensive paralogy within and between I, M and A ITS operons. For each parent were at least two rDNA operons as well as multiple paralogous sequences within operons identified. The use of PCR and sequence analyses showed that one of the operons encodes a putative expressed (functional) rDNA whereas the second encodes a pseudogen (truncated) in low copy number. We also characterized the ITS regions of I, M and A to gain insights into structure and phylogeny of the Salicacaee family. Based on sequence divergence primers were designed for A and I and used for the identification of A in MA carpels.

Made available in DSpace on 2017-07-10T14:38:17Z (GMT). No. of bitstreams: 1 Leonardo.pdf: 1018615 bytes, checksum: 9f57d9963ee3262c7c62a9c0e4dc3cfe (MD5) Previous issue date: 2013-03-04 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / Fish represent the largest group and occupy a more basal position in the phylogeny of vertebrates, contain large morphological variety and are present in different habitats, making it an interesting model for the study of genetic variability and evolution. Among these, for species popularly known as minnows, growing numbers of systematic and phylogenetic studies are presented, primarily due to the discovery of synonyms and description of new species. In the present study we analyzed cytogenetically seven species of minnows (abramis A., A. asuncionensis, A. correntinus, Astyanax sp., M. dichroura, R. and T. descalvadensis argenteus) collected downstream of the Iguazu Falls (Lower Basin Paraná River), and this stretch corresponding to the area of environmental preservation of the Iguassu National Park. It is species-specific markers, such as karyotypic macrostructure, pattern of heterochromatin distribution and localization of 5S rDNA genes and 18S rDNA. The results help to distinguish between A. abramis and A. asuncionensis, the first cytogenetic data of A. correntinus suggested correlation with group A. schubarti due to the high similarity of karyotypes. The analysis astyanax sp. confirmed case of a species not yet described taxonomically. The analyzes Moenkhausia, Roeboides Tetragonopterus and showed the first molecular cytogenetic data, revealing variability in the number and location of sites of 5S rDNA and 18S rDNA, confirming the diversity of these genes among different genera of Characidae, and allowing the use of these markers in comparative analyzes with congeneric species / Os peixes representam o grupo mais numeroso e ocupam a posição mais basal na filogenia dos vertebrados, comportam grande variedade morfológica e estão presentes em diversos habitats, tornando-se um grupo interessante para o estudo da variabilidade genética e evolução. Dentre estes, para espécies popularmente conhecidas como lambaris, crescentes números de estudos sistemáticos e filogenéticos são apresentados, principalmente decorrente da descoberta de sinonímias e descrição de novas espécies. No presente estudo foram analisadas citogeneticamente sete espécies de lambaris (A. abramis, A. asuncionensis, A. correntinus, Astyanax sp., M. dichroura, R. descalvadensis e T. argenteus) coletadas à jusante das Cataratas do Iguaçu (Bacia do Baixo rio Paraná), sendo este trecho correspondente a área de preservação ambiental do Parque Nacional do Iguaçu. Verificou-se marcadores espécie-específicos, como macroestrutura cariotípica, padrão de distribuição da heterocromatina e localização dos genes 5S rDNA e 18S rDNA. Os resultados auxiliaram na diferenciação entre A. abramis e A. asuncionensis; os primeiros dados citogenéticos de A. correntinus sugeriram correlação com o grupo A. schubarti devido à alta similaridade cariotípica. A análise de Astyanax sp. confirmou tratar de uma espécie ainda não descrita taxonomicamente. As análises em Moenkhausia, Roeboides e Tetragonopterus evidenciaram os primeiros dados citogenéticos moleculares, revelando variabilidade quanto ao número e localização dos sítios de 5S rDNA e 18S rDNA, confirmando a diversidade destes genes entre os diferentes gêneros de Characidae, e possibilitando a utilização destes marcadores em análises comparativas com espécies congêneres

<p>ABSTRACT</p><p>Nontypable Haemophilus influenzae is a common cause of otitis, sinusitis and conjunctivitis. It is the most common bacterial pathogen associated with chronic obstructive pulmonary disease (COPD). Studies have shown that nonpathogenic Haemophilus haemolyticus are often mistaken for Haemophilus influenzae due to an absent hemolytic reaction on blood agar. Distinguishing H. haemolyticus from H. influenzae is important to prevent unnecessary antibiotic use, and to understand the role of H. influenzae in clinical infections. In this study, PCR-primers for amplifying 16S rDNA sequences were used to set up a method for distinguishing H. haemolyticus from H. influenzae. The aim was to use the method for analyzing apparent H. influenzae strains, to investigate if some strains were in fact H. haemolyticus. However, because of problems with unspecific primerannealing,no conclusions could be drawn regarding misclassification of H. haemolyticus.</p><p>Moraxella catarrhalis is the second most common bacterial pathogen associated with COPD. It also causes otitis and sinusitis. An important virulence factor of M. catarrhalis is the outer membrane protein Moraxella catarrhalis IgD-binding protein (MID). One part of the protein; MID764-913 , has been shown to function as an adhesin, and this part has been fragmented to further investigate its adhesive properties. The aim of this second, independent study, was to express some of these proteinfragments by cloning in E. coli. The time spent on this project was too short, and no proteins could be expressed duing this period.</p>

In the first phase of this study, the diversity of methanogenic bacteria in avian ceca was found to be minimal. Based on 16S rDNA clone libraries, a common phylotype, designated CH101, ranged between 92.86 to 100 % of the total clones whereas less than 1% of the other phylotypes were found. On the basis of the sequence identity, all of the sequences, except sequence CH1270, are related from 98.97 to 99.45% to 16S rDNA Methanobrevibacter woesei GS. Sequence CH1270 is 97.62% homologous to the sequence identified to uncultured archaeon clone ConP1-11F. Clearly, the predominant methanogen found to reside in the chicken ceca was M. woesei. By using a MPN enumeration method, methanogen counts were found to be in the range of 6.38 to 8.23 log10 organisms per gram wet weight. The 16S rDNA copy number per gram wet weight in the samples was between log10 5.50 and 7.19. The second phase of the study was conducted to observe the effects of selected nitrocompounds and two different feedstuffs on in vitro methane production in chicken cecal contents and rumen fluid. Initially, one of the three nitrocompounds was added to incubations containing cecal contents from laying hens supplemented with either alfalfa or layer feed. Both feed materials influenced volatile fatty acids (VFA) production and also fostered methane production in the incubations although methane was lower (P < 0.05) in incubations with added nitrocompound, particularly nitroethane. Secondly, nitroethane was examined in incubations of bovine or ovine rumen fluid or cecal contents containing either alfalfa or layer feed. Unlike cecal contents, layer feed significantly (P < 0.05) supported in vitro methane production in incubations of both rumen fluids. The results show that nitroethane impedes methane production, especially in incubations of chicken cecal contents. The final phase of this study was carried out to determine the methanogenic establishment in the chicken ceca by the cultural method with the quantitative PCR. The results suggested that methanogens colonized in chicken ceca at a few days after birth. Litter and house flies could be potential sources for methanogenic colonization in broiler chicks.

Purple nonsulfur bacteria are a group of extraordinary metabolic diverse bacteria. They can grow photoautotrophically, photoheterotrophically , chemoheterotrophically or chemoautotrophically. Under various conditions, they can enjoy exceptional flexibility within each of these modes of metabolism. Due to the special physical characteristics properties, they had attracted scientist¡¦s attention in resent years. These bacteria are widely distributed in nature such as lakes, water ponds, coastal lagoons or high concentration organic waste lagoons. Lotus Pond, located in northern Kaohsiung City, is a serious eutrophied artificial lake. Because of receiving sufficient light and having been polluted by significant amounts of soluble organic matter, the ecology of the lake is suitable for the growth of purple nonsulfur bacteria. In the study, the lake water and sediments by using a Winograsdsky column, we successfully isolated 16 strains bacteria from the Lotus Pond. We also amplified the 16S-rDNA fragments of these strains by PCR and sequenced these PCR products, then aligned these sequences with the data of GeneBank. We affirmed that the 16 isolated strains belong to purple nonsulfur bacteria. From phylogenetic analysis, these 16 strains belong to the following three groups of bacteria: Rhodopseudomonas palustris, Rubrivivax gelatinosus, and Rhodobacter sphaeroides. Characteristic studies of these strains, we found that all isolated strains are Gram negative bacteria and contain bacteriochlorophyll a. The strains that belong to R. palustris and R. sphaeroides group can use several different types of short chain organic acid as their carbon source and have denitrification ability. However, only the strains belong to R. palustris group are able to use the aromatic compound benzoate. From salt tolerant studies, we found the strains in R. sphaeroides group can grow well in 3% NaCl, and both R. palustris and R. gelatinosus group can only grow in 1% NaCl.

In the first phase of this study, the diversity of methanogenic bacteria in avian ceca was found to be minimal. Based on 16S rDNA clone libraries, a common phylotype, designated CH101, ranged between 92.86 to 100 % of the total clones whereas less than 1% of the other phylotypes were found. On the basis of the sequence identity, all of the sequences, except sequence CH1270, are related from 98.97 to 99.45% to 16S rDNA Methanobrevibacter woesei GS. Sequence CH1270 is 97.62% homologous to the sequence identified to uncultured archaeon clone ConP1-11F. Clearly, the predominant methanogen found to reside in the chicken ceca was M. woesei. By using a MPN enumeration method, methanogen counts were found to be in the range of 6.38 to 8.23 log10 organisms per gram wet weight. The 16S rDNA copy number per gram wet weight in the samples was between log10 5.50 and 7.19. The second phase of the study was conducted to observe the effects of selected nitrocompounds and two different feedstuffs on in vitro methane production in chicken cecal contents and rumen fluid. Initially, one of the three nitrocompounds was added to incubations containing cecal contents from laying hens supplemented with either alfalfa or layer feed. Both feed materials influenced volatile fatty acids (VFA) production and also fostered methane production in the incubations although methane was lower (P < 0.05) in incubations with added nitrocompound, particularly nitroethane. Secondly, nitroethane was examined in incubations of bovine or ovine rumen fluid or cecal contents containing either alfalfa or layer feed. Unlike cecal contents, layer feed significantly (P < 0.05) supported in vitro methane production in incubations of both rumen fluids. The results show that nitroethane impedes methane production, especially in incubations of chicken cecal contents. The final phase of this study was carried out to determine the methanogenic establishment in the chicken ceca by the cultural method with the quantitative PCR. The results suggested that methanogens colonized in chicken ceca at a few days after birth. Litter and house flies could be potential sources for methanogenic colonization in broiler chicks.

The taxonomic status of the Japanese Wonder Shell, Thatcheria mirabilis is questionable, because it has been classified in the family of Thatcheriidae, Turridae or Conidae (Superfamily: Conoidea). Conoidea is a large and diverse superfamily with more than 10,000 species. Based on shell and radula characters, it is classified into three families, i.e. Conidae, Terebridae and Turridae. However, seven families have been proposed based on foregut structure, shell and radula morphology. In the present study, the molecular phylogeny of Conoidea and the taxonomic status of Thatcheria mirabilis were determined by mitochondria DNA 16S rDNA. The results show that Conoidea includes three clades, presuming Conidae, Terebridae and Turridae. The mean genetic distances within clades were 0.12, 0.10 and 0.10, respectively. And, the distances between clades were 0.14~0.17. Phylogenetic trees reveal that Terebridae and Turridae were within the same group or sister group, Terebridae was closer to Turridae than to Conidae. Although Thatcheria mirabilis and Bathytoma luhdorfi have turrid-form shells, their phylogenetic relationship was close to Conus which was in Conidae`s clade. Some other species, i.e. Oenopota sagamiana¡BPhymorhynchus buccinoides and Raphitoma linearis were also in Conidae`s clade which had been placed in Turridae. In general, the results are consistent with the cladistic classification by Taylor et al (1993), Rosenberg (1998) and Bouchet & Rocroi (2005), but differenrt from the classification by Powell (1966) and Kohn (1998) based on shell characters. Additionally, the hollow, harpoon-like teeth and venom apparatus in Conoidea might independently evolve in each family.

The effect of simple and complex on the composition and diversity of microbial communities and on end-product (biogas and VFAs) synthesis was investigated using an anaerobic batch respirometer at 37 °C and pH 7.2. These experiments, simple substrates were chemically pure and contain a single carbon source (glucose or α-cellulose), while complex substrates were chemically “impure” substrates containing a mixture of two or three carbon sources (biodiesel-derived glycerol or wheat straw) with a substrate/inoculum ratio 6g chemical oxygen demand (COD)/ g volatile solids (VS) seed and 100g of pre-treated dairy manure digestate (DMD), respectively. Concentrations of hydrogen, carbon dioxide, acetate, butyrate, propionate, and ethanol synthesized by different communities selected by growth on the different substrates were measured and confirmed the growth of the microbial communities. 16S rDNA illumina sequencing revealed that DMD without substrates was more diverse than the microbiota cultured by fermentation reactions containing D-glucose, glycerol α-cellulose or wheat straw. The data confirmed that substrates play a crucial role in determining the diversity of species in microbial communities. Dominant operational taxonomic units (OTUs) belonging to families Clostridiaceae, Ruminococcaceae, and Enterobacteriaceae, and the genera Clostridium, Ruminococcus, Sporolactobacillus, and Syntrophomonas were potentially responsible for changes in end-product synthesis patterns in communities cultured with simple and complex substrates. / October 2015

Orientador: Rodney Kozlowiski de Azevedo / Resumo: Os parasitos do filo Myxozoa são endoparasitas obrigatórios que infectam peixes, anfíbios, répteis, mamíferos, aves aquáticas em diversas regiões do mundo, com mais de 2180 espécies descritas, estando entre os mais importantes patógenos de peixes, porém, pouco se conhece deste parasito em peixes do Brasil. Neste estudo foram realizadas coletas entre março e setembro de 2016, na qual foram coletados 30 exemplares de curimba (Prochilodus lineatus) e dezessete exemplares de lambari (Astyanax altiaparanae), oriundos do rio Batalha, em dois locais de coleta, um ponto de coleta no município de Reginópolis e outro ponto no município de Agudos, estado de São Paulo. Foram utilizadas análises morfológicas (microscopia de luz, histologia e análise ultraestrutural), técnicas de biologia molecular (PCR e sequenciamento) na descrição de duas espécies de Henneguya Duas espécies foram documentadas neste estudo, uma delas foi encontrada infectando o filamento primário da brânquia de P. lineatus e é descrita neste estudo como Henneguya prochilodus e outra espécie encontrada infectando o filamento secundário da brânquia de A. altiparanae, a qual foi proposto uma descrição expandida da Henneguya chydadea Barassa et al. (2003), previamente descrita utilizando análises morfológicas e histopatologia. Análise filogenética do gene 18S rDNA foi realizada para avaliar a relação filogenética dessas duas espécies de Henneguya com outras espécies de mixosporídeos da América do Sul e de outras regiões do m... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: The Myxozoa parasites are obligate endoparasites that infect fish, amphibians, reptiles, mammals, waterfowl in several regions of the world, with more than 2180 described species, being among the most important fish pathogens, but little is known of this parasite in fish from Brazil. In this study were collected from March to September 2016, where 30 specimens of Curimba (Prochilodus lineatus) and seventeen specimens of lambari (Astyanax altiaparanae) from the Batalha River, in two collection sites, a collection point in the municipality of Reginópolis and another point in the municipality of Agudos, state of São Paulo. Morphological analyzes (light microscopy, histology and ultrastructural analysis), molecular biology techniques (PCR and sequencing) were used to describe two species of Henneguya. Two species were documented in this study, one of which was found infecting the primary filament of the gill of P. lineatus and is described in this study as Henneguya prochilodus and another species found infecting the secondary filament of the gill of A. altiparanae, which has been proposed an expanded description of Henneguya chydadea Barassa et al. (2003), previously described using morphological analysis and histopathology. Phylogenetic analysis of the 18S rDNA gene was performed to evaluate the phylogenetic relationship of these two species of Henneguya with other species of myxosporids from South America and other regions of the world. / Mestre

Submitted by Nathália Faria da Silva (nathaliafsilva.ufv@gmail.com) on 2017-06-13T18:17:32Z No. of bitstreams: 1 resumo.pdf: 17263 bytes, checksum: 8e51a65fe7d8eecb448411acb64cf05b (MD5) / Made available in DSpace on 2017-06-13T18:17:32Z (GMT). No. of bitstreams: 1 resumo.pdf: 17263 bytes, checksum: 8e51a65fe7d8eecb448411acb64cf05b (MD5) Previous issue date: 2003-02-20 / Fundação de Amparo a Pesquisa do Estado de Minas Gerais / A estirpe probiótica Lactobacillus UFV H2b20, previamente classificada como Lactobacillus acidophilus por suas características de fermentação de açúcares, apresentou-se mais semelhante à espécie Lactobacillus delbrueckii, quanto à seqüência de rDNA 16S, o que levou ao questionamento acerca da identidade da linhagem. Para o esclarecimento da real classificação da linhagem, o método de hibridização DNA-DNA foi empregado. A linhagem apresentou 75,2% e 77,4% de reassociação com L. delbrueckii subsp. lactis (ATCC 12315) e L. delbrueckii subsp. delbrueckii (ATCC 9649), respectivamente. Dado que a homologia de 70% ou mais, por esse método, tem sido usada como padrão para agrupamento de bactérias em uma mesma espécie, sugere-se, aqui, que Lactobacillus UFV H2b20 seja, daqui para frente, denominado L. delbrueckii UFV H2b20. Identificada a linhagem, outro objetivo do trabalho era desenvolver um protocolo para detecção in situ de L. delbrueckii. Uma sonda de 26 nucleotídeos (SA) foi construída e testada com outras espécies de Lactobacillus relacionadas geneticamente entre si. Estes estudos demonstraram que a seqüência de assinatura (SA) estava presente em L. delbrueckii UFV H2b20, L. delbrueckii UFV H2b21, L. delbrueckii subsp. delbrueckii e L. delbrueckii subsp. lactis, o que indica ser ela eficaz para ser usada como sonda para rRNA 16S espécie-específica pelo método de FISH. A hipótese de existência de polimorfismos, levantada em trabalhos prévios no rDNA 16S da linhagem, foi confirmada após as análises dos segmentos de DNA clonados e selecionados do banco genômico construído para a linhagem L. delbrueckii UFV H2b20. As seqüências analisadas demonstraram, também, presença de segmentos correspondentes a quatro genes codificadores de rRNA 16S distintos, e seis segmentos distintos para uma mesma região de rRNA 23S, indicando seis operons putativos. Há evidência de, pelo menos, um operon putativo completo seguido de região codificadora de seis tRNAs. Não se detectou região espaçadora longa entre rDNA 16 e 23S. / Lactobacillus UFV H2b20, a probiotic strain, previously identified as Lactobacillus acidophilus due to its sugar fermentation pattern, was found to be more closely related to Lactobacillus delbrueckii regarding its 16S rDNA sequence. It was demonstrated by DNA-DNA hybridization that this strain presented 75.2% and 77.4% of reassociation with L. delbrueckii subsp. lactis ATCC 12315 and L. delbrueckii subsp. delbrueckii ATCC 9649, respectively. These results place Lactobacillus UFV H2b20 within the L. delbrueckii species, for 70% reassociation as measured by the method used has been a standard to cluster bacteria within the same species. A protocol for in situ detection of L. delbrueckii was developed by means of Fluorescent in situ Hybridization, FISH. A probe consisting of 26 nucleotides labeled with rhodamine was designed based on the signature sequence within the rDNA, and was tested against genetically related Lactobacillus species. A species- specific method was obtained capable of discriminating L. delbrueckii strains from other Lactobacillus species. Previous studies raised the hypothesis of polymorphism among the copies of 16S rDNA in L. delbrueckii UFV H2b20. This was confirmed by sequence analysis of rDNA from a gene library of this strain cloned in phage lambda and subcloned in pBluescript. Sequence analyses of cloned fragments demonstrated the presence of at least four distinct genes encoding 16S rRNAs. Distinct fragments containing 23S rRNA related genes indicated six putative rrn operons. One complete putative rrn operon displays a region encoding 6 different tRNAs. Long spacer regions between 16S and 23S rDNA were not detected.