Morphology and ultrastructure of 25 oscillatorian strains was examined and phylogenetic analysis of 16S rDNA oscillatorian sequences was conducted. Genera Phormidium and Oscillatoria were shown to be polyphyletic. Although morphologically similar strains are found in different branches of the phylogenetic tree, considerable correlation between molecular, ultrastructural and some morphological and ecological traits was detected in several lineages.

Made available in DSpace on 2014-06-12T18:02:57Z (GMT). No. of bitstreams: 2 arquivo3678_1.pdf: 1377857 bytes, checksum: 7d15f520b2b07e3bad5591816c1345df (MD5) license.txt: 1748 bytes, checksum: 8a4605be74aa9ea9d79846c1fba20a33 (MD5) Previous issue date: 2009 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / A água, depois de utilizada para o abastecimento público e nos processos produtivos, retorna com sua composição alterada, constituindo o esgoto. Os esgotos quando lançados aos corpos d água sem tratamento adequado podem causar graves problemas de saúde pública e ambientais como a eutrofização. Reatores biológicos anaeróbios tipo UASB (Reator Anaeróbio de Fluxo Ascendente e Manta de Lodo) são uma alternativa interessante para o tratamento dos esgotos domésticos, combinando baixos custos de implantação e simplicidade operacional. No entanto, o sucesso do processo depende do tipo, adaptação e atividade da população microbiana presente em seu interior. Diante disto, este trabalho vem contribuir para o melhor entendimento do consorcio microbiano em reator tipo UASB para tratamento de esgoto, realizando a identificação dos microrganismos pertencentes aos domínios Bactéria e Archaea por meio da análise das seqüências dos genes rRNA 16S. Neste sentido, foram coletadas amostras de lodo dos cinco níveis do reator UASB localizado na ETE Mangueira, Recife/PE, para posterior extração de DNA. Em seguida foi realizada a clonagem e sequenciamento dos produtos de PCR provenientes dos genes rRNA 16S heterogêneos. A comparação das seqüências com os bancos de dados de rRNA 16S, NCBI e RDP, indicaram a ocorrência de representantes dos filos Actinobacteria (42%), Proteobacteria (13%), Chloroflexi (9%), Firmicutes (6%) e Bacteroidetes (4%) para o domínio Bacteria, e representantes das ordens Methanomicrobiales (43%), Methanobacteriales (17%) e Methanosarcinales (12%) para Archaea, distribuídos distintamente ao longo dos cinco níveis do reator. Do total das seqüências, 26% das de Bacteria e 17% das de Archaea não apresentaram similaridade com seqüências já conhecidas, levando a crer que possivelmente sejam pertencentes a microrganismos ainda não descritos

Philosophiae Doctor - PhD / The El Tatio geyser field (ETGF) is the largest known geothermal field in Chile, forming part of a wide spectrum of extremophilic habitats in the country. The ETGF is NaCl rich, with high concentrations of toxic elements such as Li, As and Cs, which are contributed mainly by volcanic activities in the region. Most previous studies in the area have focused on the geology and geochemistry for mining purposes, as well as on the search for geothermal resources for power generation. Very little is currently known about the composition of the microbial communities of the ETGF, which makes the study reported here of particular novelty.A metagenomic approach, involving the amplification of 16S rRNA gene phylogenetic markers from metagenomic DNA was used to investigate seven different sites within the geyser field. The sample sites were characterized by high temperatures (80-85 °C) and a range of pH values (6.3-8). Various molecular methods, including clone library construction and PCR-DGGE analyses were used to target a wide range of microbial populations within the ETGF sites. Multivariate analysis was also applied to assess differences in the microbial diversity from different sites and to correlate microbial diversity with environmental conditions. Culture-dependent screening of novel nanoarchaeal species was also undertaken.These were coupled with PCR and other detection methods such as fluorescent in situ hybridization (FISH) to trace the presence of nanoarchaeal signals from enriched cultures.The results have shown that the ETGF encompasses a limited microbial diversity represented by only 30 dominant phylotypes, and most likely due to the toxic chemical content of the geyser field. The microbial representatives identified were assigned to OTUs from archaeal,nanoarchaeal and bacterial taxonomic groups. The dominant microbial taxa included members of the Proteobacteria, Firmicutes, Aquificae, Actinobacteria, Euryarchaeota(Halobacteriales, Archaeoglobales), Crenarchaeota (Thermoproteales, Desulfurococcales),together with uncultured representatives of the bacteria, archaea and nanoarchaeota. Notably,representatives of mesophilic, thermophilic and hyperthermophilic taxonomic groups were all detected in ETGF samples. This is attributed to various factors such as temperature gradients and dispersal mechanisms (e.g. natural forces such as rain and volcanic activities). Principal component analysis (PCA) showed significant differences (P < 0.05) in the microbial diversity of the ETGF samples, with principal components (based on the sequenced species from both 16S rRNA clone libraries and PCR-DGGE profiles) explaining up to 62.7% of variance. Furthermore, CCA showed that the differences in phylogenetic diversity were most influenced by temperature and salinity. This was also confirmed by the sequencing results,which showed that hyperthermophilic and haloarchaeal taxa were dominant in the ETGF sites. However, conductivity and pH were also found to contribute to variations in the microbial diversity of the experimental samples, with TDS (total dissolved solids) being a less influential factor. Attempts to generate nanoarchaeal-host co-cultures, and to recover sufficient nanoarchaeal genomic DNA for fosmid and/or large insert cloning for comparative genome analysis, were unsuccessful.This study is the first to employ metagenomic approaches to analyse the microbial diversity of sites in the ETGF, and has expanded our knowledge of microbiota present in this geyser field.

The phylogenetic placement of the phylum Tardigrada among the Metazoa is somewhat uncertain. In analyses based on morphological characters, tardigrades are usually associated with arthropods but tardigrades have also been associated with a number of aschelminth phyla. We have sequenced the nearly complete 18S rRNA gene from a eutardigrade. Neighbor-Joining and Maximum-Parsimony analyses place tardigrades in a clade that includes arthropods and priapulids, but not other aschelminths.

In South Africa, the diagnosis of Theileria parva in cattle and buffalo has been complicated by the presence of mildly pathogenic and non-pathogenic Theileria spp. This can lead to inaccurate diagnostic results and confuse the epidemiology of theileriosis. The aims of this study were to identify and characterize the 18S rRNA genes of novel Theileria spp. of the African buffalo, as well as to test new gene targets that will allow for the development of more accurate diagnostic tests for the identification of T. parvainfections in cattle and buffalo. Buffalo blood samples originating from different geographical regions in South Africa and from Mozambique were screened for the presence of Theileria spp. by the reverse line blot (RLB) hybridization assay. A total of six Theileria spp., namely T. parva, Theileria sp. (buffalo), Theileria mutans, Theileria velifera and Theileria buffeli, were identified from the buffalo samples. These occurred mainly as mixed infections. Some of the samples hybridized only with the Theileria/Babesia genus specific probe that is used in the RLB assay, and not with any of the species-specific probes used, suggesting the presence of novel genotypes or species. The full-length 18S rRNA genes of parasites from selected samples were characterized by cloning and sequencing. In addition to the identification of 18S rRNA gene sequences that were similar to published Theileria spp. of cattle and buffalo, we identified Theileria sp. (bougasvlei), and novel 18S rRNA gene variants of T. mutans, T. velifera, T. bufJeli. This variation explained why the RLB hybridization assay failed to detect these species in some of the analysed samples. As extensive variation was observed within the T. mutan group, specific RLB oligonucleotide probes were designed from the V 4 hypervariable region of the T. mutans-like 1 and 2/3 18S rRNA gene sequences. Unfortunately these cross-hybridized with T. mutans target DNA and could not be used to screen buffalo samples to determine the occurrence of these genotypes in buffalo in South Africa. This problem could be solved by designing probes from a more variable area of the 18S rRNA gene of the T. mutans groups. Alternatively, a quantitative real-time PCR (qPCR) assay could be used for differentiation of these genotypes as it is more sensitive than the RLB assay. Despite the variation observed in the full-length T parva 18S rRNA gene sequences, the area in the V 4 hypervariable region where the T parva RLB and real-time PCR hybridization probes were developed was relatively conserved between sequences obtained in this study. The existing T parva-specific qPCR assay was able to successfully detect all T parva variants identified in this study and, although amplicons were obtained from Theileria sp. (buffalo) and Theileria sp. (bougasvlei) DNA, these species were not detected by the T parva-specific hybridization probes. The sequences of the other Theileria spp. and the novel genotypes identified in this study under the probes were also different from that of T parva and therefore these species do not compromise the specificity of the T parva 18S qPCR assay. In order to determine the sequence variation and phylogenetic positions of T buffeli spp. of the African buffalo, we cloned and sequenced their 18S rRNA gene and complete internal transcribed spacer (ITS). We identified novel T buffeli-like and T sinensis-like 18S rRNA and ITS genotypes from buffalo originating from two different geographical regions in South Africa. There was extensive sequence variation between these novel South African genotypes and known T buffeli-like and T sinensis-like genotypes. The presence of organisms with T buffeli-like and T. sinensis-like genotypes in the African buffalo is of significant importance, particularly to the cattle industry in South Africa as these animals might act as sources of infections to naIve cattle. Recently, a qPCR assay based on the cox III gene was developed for the diagnosis of Theileria spp. in cattle. This test detects and differentiates six Theileria spp. in cattle. We evaluated the use of this assay for the detection of Theileria spp. in buffalo. The results of the cox III qPCR were compared to those of the RLB and 18S qPCR for the simultaneous detection and differentiation of Theileria spp. of the African buffalo, and for the specific detection of T parva, respectively. The cox III genes from selected samples with non-specific melting peaks were characterized by cloning and sequencing. Extensive sequence variation in the cox III gene was observed between and within species. The T mutans group was the most variable. The qPCR assay could be further improved by designing new primers and probes using all known cox III gene sequences of Theileria spp. Of buffalo and cattle. This study highlights the complexity of the diagnosis of T parva in cattle and buffalo in South Africa. It provides invaluable information towards the development of an improved molecular diagnostic assay for T parva and co-infecting species in cattle and buffalo in South Africa which will assist the veterinary regulatory authorities in the control of Corridor disease in South Africa. / Thesis (PhD)--University of Pretoria, 2011. / Veterinary Tropical Diseases / Unrestricted

No description available.

Termites are known to harbor within their gut a diverse assemblage of symbiotic microorganisms. Little work has been done, however, to describe the diversity and function of the bacteria in the economically important eastern subterranean termite, Reticulitermes flavipes. The first object of this study was to characterize the bacterial diversity in the gut of R. flavipes using amplified rDNA restriction analysis (ARDRA) and 16S rRNA gene sequencing. It was determined that ARDRA was an effective technique for characterizing the diversity of the termite gut microbiota. Of the 512 clones analyzed in the ARDRA study, 261 different ARDRA profiles were found. Forty-two 16S rRNA gene sequences were also analyzed, resulting in 33 different ribotypes. Representatives from six major bacterial phyla, Proteobacteria, Spirochaetes, Bacteroidetes, Firmicutes, Actinobacteria, and the newly proposed "Endomicrobia," were discovered. Further analysis indicated that the gut of R. flavipes may harbor as many as 1,318 ribotypes per termite. The second objective was to determine if the gut bacterial diversity could be manipulated by changing the termite's food source. Using ARDRA analysis, I found no evidence that changing the food source affected the termite gut bacterial diversity. In addition, changing the food source did not induce aggression in nestmates fed on different food sources. The third objective was to search for patterns of coevolution between termites and their gut symbiotic bacteria. Using rRNA gene sequences from this study and sequences from public databases (1,450 sequences total), a neighbor-joining tree demonstrated strong evidence for coevolution of termites and their symbiotic bacteria, especially in the phyla Bacteroidetes, Actinobacteria, Spirochaetes, and "Endomicrobia." Many monophyletic clusters were entirely composed of phylotypes specific to Isoptera. / Ph. D.

Eukaryotic ribosome biogenesis, a dynamic and coordinated multistep process which requires more than 150 trans-acting factors, has been intensely studied in the yeast Saccharomyces cerevisiae. This evolutionarily conserved process involves numerous cleavages of pre-rRNA, modification of nucleotides, and concomitant assembly of the ribosomal proteins onto the rRNA. Considerable information is available about the importance of conserved pre-rRNA cleavage events in ribosome biogenesis; however, very little is known about the exact role of modified nucleotides, which cluster within the functionally important regions of the ribosome. One conserved group of modifications is the dimethylation of two adjacent adenosines at the 3´ end of the small subunit rRNA which is ubiquitously carried out by the Dim1/KsgA methyltransferase family. Although dimethylation and KsgA are dispensable for survival in bacteria, the eukaryotic enzyme Dim1 is essential because of its requirement in the early pre-rRNA processing events. Similarly, few other members of the family have also evolved to carryout a second unrelated function in the cell. Almost all of the information about Dim1 was obtained from in vivo experiments in yeast, and has been determined that it is an indispensable part of a RNA-protein complex carrying out the pre-rRNA processing. Sequence analysis clearly shows that eukaryotic and archaeal enzymes have an extra insert in their C-terminal domain which is absent in bacterial enzymes and a better understanding of Dim1's function is only possible by its structural characterization which is the aim of this study. After several attempts, the yeast Dim1p was expressed under mild conditions in E. coli and purified in soluble form. Dim1p was able to methylate bacterial 30S subunits both in vivo and in vitro, indicating its ability to recognize bacterial substrate. Supporting our hypothesis, neither the bacterial nor archaeal orthologs were able to complement the processing function of Dim1p in yeast, tested using the plasmid shuffling technique. Our results suggest that the C-terminal insert of Dim1p, along with some structural features of the N-terminal domain, is important for its function in pre-rRNA processing. Further studies are required to understand the complex interactions between proteins and RNA involved in the ribosome biogenesis.

Neste trabalho desenvolvemos métodos analíticos e moleculares para a detecção, isolamento e classificação filogenética de Alicyclobacillus spp. a partir de sucos de laranja e frutos ácidos, pelas técnicas: RT-PCR, nested RT-PCR, RAPD, seqüenciamento do 16S rRNA e análise por métodos eletroforéticos. A sensibilidade na detecção dos A. acidoterrestris foi melhorada por meio de reações de nested RT-PCR, utilizando primers internos (amplicon de 191 bp) que foram desenhados a partir do primeiro amplicom de 294 bp. O limite de detecção foi estudado com as reações RT-PCR e nested RT-PCR, sendo capazes de detectar concentrações de 0,1 UFC mL-1 para culturas puras e 2 UFC mL-1 em sucos de laranja artificialmente inoculados. A inibição de esporos de A. acidoterrestris também foi estudada para monitorar a diminuição da viabilidade com tratamento térmico e Sapindus saponaria (200 mg L-1), utilizando RT-PCR e nested RT-PCR. Com o tratamento térmico de 99 oC por 1 h o grau de inibição dos esporos foi de 96,3%. Enquanto que, com a fração purificada de S. saponaria (200 mg L-1) incubada à 45 oC por 2 dias foi de 93,6%, mas com incubação de 99 oC por 1 h foi de 98,7%, na mesma concentração de saponina. Todas as análises de quantificação de produtos de RT-PCR e nested RT-PCR foram analisadas por meio de eletroforese em gel de agarose e eletroforese capilar em microchip no Bioanalyzer 2100 (Agilent), com os kits DNA 500 e DNA 1000 LabChip®, obtendo-se maior sensibilidade nos microchips. A classificação molecular de dezenove cepas, isoladas a partir de diferentes sucos e frutos ácidos, foram estudadas utilizando RAPD-PCR e eletroforese capilar em microchips. Utilizando cinco primers aleatórios nas reações de RAPD, foi possível estudar os polimorfismos analisados nos microchips. Segundo as análises eletroforéticas, as cepas de suco concentrado e diluído de laranja (1, 2, 6) suco concentrado de limão (lim) e suco de laranja in natura (T2, T3), apresentaram similaridades genéticas com a A. acidoterrestris. O estudo de análise filogenética baseada na comparação de seqüências de DNA da região variável do gene 16S rRNA de Alicyclobacillus acidoterrestris, foi utilizado para identificar e agrupar onze cepas isoladas de superfícies e sucos de frutos ácidos. Na árvore filogenética gerada pelo método neighbor joining e bootstrap 1000x, as cepas analisadas mostraram similaridades de 99% entre todas elas, observando-se uma maior similaridade do controle A. acidoterretris (C2) com a cepa isolada de suco concentrado de limão (lim), e uma boa discriminação entre controles das espécies A. acidocaldarius, A. cicloheptanicus, A. sendaiensis e Sulfobacillus acidophilus. / In this work, we developed analytical and molecular methods for detection, isolation and phylogenetic classification of Alicyclobacillus spp. from orange juice and acid fruits using RT-PCR, nested RT-PCR, RAPD and sequencing of 16S rRNA techniques and electrophoretic methods of analysis. The sensitivity on the detection of A. acidoterrestris in orange juice was improved by nested RT-PCR, using internal primers (amplicon of 191 bp) that were designed after sequencing the first amplicon (294 bp). The detection limit was studied with RT-PCR and nested RT-PCR assay, it was able to detect concentrations of 0.1 UFC mL-1 for media culture and 2 UFC mL-1 in inoculated orange juice. The inhibition in spores from A. acidoterrestris was also studied to monitoring the diminution of viability with heat treatment and Sapindus saponaria (200 mg mL-1), using RT-PCR and nested RT-PCR assays. The inhibition by heat treatment at 99 oC for 1 h was 96.3%. However, incubation with S. saponaria at 45 oC for 2 days inhibited 93,6%, however, with incubation of 99 oC for 1 h was 98,7%, in the same concentration of saponin. The quantification of the RT-PCR and nested RT-PCR amplification product were accomplished by capillary electrophoresis in microchips using the Bioanalyzer 2100 in conjunction with the LabChip (TM) DNA 500 and DNA 1000. The molecular classification of nineteen strains isolated from different juice and acidic fruit, were studied using RAPD-PCR and capillary electrophoresis in microchips. Using five random primers in the RAPD assay, it was possible to study the polymorphisms analyzed in microchips. According to electrophoresis analyses, the strains from concentrated and diluted orange juices (1, 2, 6), lemon concentrated juice (lim) and natural orange juice (T2, T3), showed genetic similarities with the A. acidoterrestris. The study of the phylogenetic analyses based on DNA comparison sequences of the variable region of 16S rRNA gene from Alicyclobacillus acidoterrestris, was utilized for the identification and grouping of eleven strains isolated from surface and juice of acid fruits. In the phylogenetic tree produced by neighbor joining and bootstrap 1000, the strains showed similarities of 99% among all strains, showing a high similarity of A. acidoterrestris with a strain isolated from lemon concentrate juice (lim), and a good discrimination between the species A. acidocaldarius, A. cycloheptanicus, A. sendaiensis and Sulfobacillus acidophilus.

Em eucariotos, o processamento de pré-rRNA depende de vários fatores como endonucleases, exonucleases, RNA helicases, enzimas modificadoras de rRNA e componentes de snoRNPs. Com o objetivo de caracterizar novas proteínas envolvidas no processamento de pré-rRNA, foi identificada a proteína Nop53p interagindo com a proteína nucleolar Nop17p a partir de uma varredura da biblioteca de cDNAs de Saccharomyces cerevisiae. A cepa condicional contendo a seqüência da ORF NOP53 sob controle do promotor de galactose não cresce em meio contendo glicose, indicando que Nop53p seja uma proteína essencial para a viabilidade celular. Os resultados deste trabalho demonstram que Nop53p está envolvida nas etapas iniciais de clivagem do pré-rRNA, assim como nas clivagens responsáveis pela formação dos rRNAs maduros 5.8S e 25S. Análise mais detalhada do processamento de pré-RNA por Northern blot e \"pulse-chase labeling\", revelou também que Nop53p afeta principalmente o processamento do rRNA intermediário 27S, que origina os rRNAs maduros 5.8S e 25S. Nop53p participa do processamento desses rRNAs afetando a poliadenilação dos precursores dos rRNAs 5.8S e 25S. Experimentos de co-imunoprecipitação de RNA com a proteína de fusão ProtA-Nop53p confirmaram o envolvimento de Nop53p no processamento do 27S rRNA, indicando que essa proteína possa ligar RNA diretamente. A capacidade de Nop53p de ligar RNA foi confirmada através de testes in vitro, enquanto que ensaios de co-imunoprecipitação de cromatina revelaram que Nop53p liga-se ao rRNA 5.8S durante a transcrição. Nop53p regula a função do exossomo através da sua interação direta com a subunidade exclusivamente nuclear deste complexo, Rrp6p. / In eukaryotes, the rRNA processing depends on several factors, such as, endonucleases, exonucleases, RNA helicases, rRNA modifying enzymes and components of the snoRNPs. With the purpose of characterizing new proteins involved in pre-rRNA processing, Nop53p was identified interacting with the nucleolar protein Nop17p in a two hybrid assay. The conditional yeast strain containing the sequence of the ORF NOP53 under the control of the galactose promoter cannot grow in medium containing glucose, indicating that the protein is essential for cell viability. The results of this work demonstrate that Nop53p is involved in the initial steps of pre-rRNA processing and in the cleavages responsible for the formation of the mature rRNAs 5.8S and 25S. A more detailed analysis of the pre-rRNA processing, by Northern blot and pulse-chase labeling, revealed that Nop53p affects the processing of the 27S precursor, that originates the rRNAs 5.8S and 25S. Nop53p participates in the processing of these RNAs by affecting the polyadenylation of the precursors of the rRNAs 5.8S and 25S. RNA co-imunoprecipitation assays with the fusion protein A-Nop53p confirmed the involvement of Nop53p in the processing of the 27S pre-rRNA, indicating that the protein may interact directly with the RNA. The capacity of Nop53p to bind RNA was confirmed by in vitro assays, while chromatin imunoprecipitation assays demonstrated that Nop53p binds the 5.8S rRNA co- transcriptionally. Nop53p regulates the function of the exosome by interacting directly with the exclusively nuclear subunit of the complex, Rrp6p.