Molecular Identification Of Cultivable Bacteria From Infected Root Canals Associated With Acute Apical Abscess

The objective of this study was to investigate the bacterial composition present in root canals of teeth associated with acute apical abscess by molecular identification (16S rRNA) of cultivable bacteria. Two hundred and twenty strains isolated by culture from 20 root canals were subjected to DNA extraction and amplification of the 16S rRNA gene (PCR), followed by sequencing. The resulting nucleotide sequences were compared to the GenBank database from the National Center of Biotechnology Information through BLAST. Strains not identified by sequencing were submitted to clonal analysis. The association of microbiological findings with clinical features and the association between microbial species were also investigated. Fifty-nine different cultivable bacteria were identified by 16S rRNA gene sequencing, belonging to 6 phyla, with an average number of 6 species per root canal. Molecular approaches allowed identification of 99% of isolates. The most frequently identified bacteria were Prevotella spp., Pseudoramibacter alactolyticus, Parvimonas micra, Dialister invisus, Filifactor alocis, and Peptostreptococcus stomatis. Positive association was found between Prevotella buccae and Pseudoramibacter alactolyticus and between Parvimonas micra and Prevotella nigrescens (both p<0.05). It was concluded that the microbiota of infected root canals associated with acute apical abscess is diverse and heterogeneous, composed mainly of anaerobic Gram-negative bacteria, with the great majority belonging to the phyla Firmicutes and Bacteroidetes.27331832

Digestão de óleo lubrificante encapsulado em forno de microondas com radiação focalizada por adição de amostra ao reagente pré-aquecido.

FOCUSED-MICROWAVE-ASSISTED DIGESTION OF ENCAPSULATED LUBRICATING OILS: GRADUAL SAMPLEADDITION TO PRE-HEATED ACID. The applicability of the recently proposed procedure based on gradual sample addition tomicrowave-assisted pre-heated concentrated acid is limited by the sample viscosity. In this work, lubricating oil samples with high viscositywere encapsulated and manually added to the microwave-assisted pre-heated concentrated digestion mixture. The procedure was appliedfor determination of Al, Ca, Cr, Cu, Fe, Mg, Ni, P, Pb, Si, Sn, Sr, V, W, and Zn in lubricating oil by inductively coupled plasma opticalemission spectrometry (ICP OES). Determined and certified values for Ca, Mg, P, and Zn in lubricating oil were in agreement at a 95% confidence level

Slip flows of Newtonian and viscoelastic fluids in a 4:1 contraction

This work presents a numerical study of the 4:1 planar contraction flow of a viscoelastic fluid described by the simplified Phan-Thien–Tanner model under the influence of slip boundary conditions at the channel walls. The linear Navier slip law was considered with the dimensionless slip coefficient varying in the range ½0; 4500. The simulations were carried out for a small constant Reynolds number of 0.04 and Deborah numbers (De) varying between 0 and 5. Convergence could not be achieved for higher values of the Deborah number, especially for large values of the slip coefficient, due to the large stress gradients near the singularity of the reentrant corner. Increasing the slip coefficient leads to the formation of two vortices, a corner and a lip vortex. The lip vortex grows with increasing slip until it absorbs the corner vortex, creating a single large vortex that continues to increase in size and intensity. In the range De = 3–5 no lip vortex was formed. The flow is characterized in detail for De ¼ 1 as function of the slip coefficient, while for the remaining De only the main features are shown for specific values of the slip coefficient.The authors gratefully acknowledge funding by COMPETE, FEDER and Fundacao para a Ciencia e a Tecnologia (FCT) through projects PEst-C/CTM/LA0025/2013 (Strategic Project - LA 25 - 2013-2014, PTDC/EME-MFE/113988/2009 and PTDC/EME-MFE/114322/2009. AMA would also like to thank FCT for the financial support through the scholarship SFRH/BPD/75436/2010

Setting the optimal sheet thickness distribution for plastics thermoforming by multi-objective optimization

Thermoforming is a thermoplastic processing technique commonly used in the rigid packaging industry. The process comprises a heating stage, which aims at allowing the sheet to acquire the required deformability, a deformation stage, in which the sheets conform to the mould surface, and, finally, a cooling stage, which allows the part to be extracted from the mould without distorting. Since there are several processing variables associated with those stages, optimizing the thermoforming process is a complex task. In this work, a multi-objective optimization evolutionary algorithm is proposed to optimize the plastics thermoforming process. For that purpose, the thickness distribution of the final part was optimized considering that it is manufactured from uniform temperature sheets with different thickness distributions, such as constant and spline and concentric profiles. The aims were to minimize the sheet volume, as it implies less material use; assure a minimum value for the part thickness distribution, to avoid hindering its mechanical behavior; and minimize the thickness heterogeneity, i.e., the difference between the thickness of the part and a reference thickness. The Pareto optimal solutions found by the algorithm correspond to different thickness profiles for the three different sheet shapes. In all cases, an improvement of the different profiles along the successive generations of the evolutionary algorithm was obtained, which are related to the objectives considered. Moreover, the initial sheet thickness distribution was found to clearly influence the optimization process. The results obtained for these three different initial sheet shapes indicate that the proposed methodology is valid, providing solutions with physical meaning and with great potential to be applied in more complex cases

Molecular identification of cultivable bacteria from infected root canals associated with acute apical abscess

The objective of this study was to investigate the bacterial composition present in root canals of teeth associated with acute apical abscess by molecular identification (16S rRNA) of cultivable bacteria. Two hundred and twenty strains isolated by culture from 20 root canals were subjected to DNA extraction and amplification of the 16S rRNA gene (PCR), followed by sequencing. The resulting nucleotide sequences were compared to the GenBank database from the National Center of Biotechnology Information through BLAST. Strains not identified by sequencing were submitted to clonal analysis. The association of microbiological findings with clinical features and the association between microbial species were also investigated. Fifty-nine different cultivable bacteria were identified by 16S rRNA gene sequencing, belonging to 6 phyla, with an average number of 6 species per root canal. Molecular approaches allowed identification of 99% of isolates. The most frequently identified bacteria were Prevotella spp., Pseudoramibacter alactolyticus, Parvimonas micra, Dialister invisus, Filifactor alocis, and Peptostreptococcus stomatis. Positive association was found between Prevotella buccae and Pseudoramibacter alactolyticus and between Parvimonas micra and Prevotella nigrescens (both p<0.05). It was concluded that the microbiota of infected root canals associated with acute apical abscess is diverse and heterogeneous, composed mainly of anaerobic Gram-negative bacteria, with the great majority belonging to the phyla Firmicutes and Bacteroidetes273318324CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO - CNPQCOORDENAÇÃO DE APERFEIÇOAMENTO DE PESSOAL DE NÍVEL SUPERIOR - CAPESFUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO - FAPESP302575/2009; 308162/2014-5Sem informação2009/07760-5; 2011/09047-4O objetivo deste estudo foi investigar a composição bacteriana de canais radiculares associados com abscesso apical agudo através de identificação molecular (16S rRNA) de bactérias cultiváveis. Duzentas e vinte cepas, de 20 casos, isoladas por cultura foram submetidas a extração de DNA e amplificação do gene 16S rRNA (PCR), seguido de sequenciamento. As sequências de nucleotídeos obtidas foram comparadas com o banco de dados (GenBank) do National Center of Biotechnology Information através do BLAST. Cepas não identificadas pelo sequenciamento foram submetidas à clonagem. Associação de achados microbiológicos e características clínicas e associação entre espécies bacterianas também foram investigadas. Cinquenta e nove bactérias cultiváveis diferentes foram identificadas pelo sequenciamento do gene 16S rRNA, pertencentes a 6 filos, numa média de 6 espécies por canal. Método molecular permitiu identificação de 99% das cepas isoladas. As bactérias mais frequentes foram Prevotella spp., Pseudoramibacter alactolyticus, Parvimonas micra, Dialister invisus, Filifactor alocis, Peptostreptococcus stomatis. Associação positiva foi encontrada entre Prevotella buccae e Pseudoramibacter alactolyticus, e entre Parvimonas micra e Prevotella nigrescens (p<0,05). Foi concluído que a microbiota de canais radiculares infectados associados com abscesso apical agudo é diversa e heterogênea, composta principalmente por anaeróbios Gram-negativos, pertencentes aos filos Firmicutes e Bacteroidete