10 research outputs found
Anticorpos líticos induzidos por infecção pelo Trypanosoma cruzi reconhecem epitopos presentes nas formas tripomastigotas e epimastigotas do parasita
Sera of Chaga's disease patients containing anti-T. cruzi lytic antibodies were submitted to affinity chromatography using Sepharose 4B conjugated with antigen extracted from epimasiigote or trypomasiigote forms of the parasite. Epimastigotes were obtained from culture at the exponential growth phase and the trypomastigotes from blood of infected and immunosuppressed mice. Antigen of both parasite forms was obtained by sonication of the parasites followed by centrifugation. Both antigens were then conjugated to activated Sepharose 4B. Affinity chromatography was performed by passing sera from chagasic patients through an immunoadsorbent column containing either epimasiigote or trypomasiigote antigens. Antibodies bound to the column were eluted with cold 0,2 M glycine buffer pH 2,8. The eluted antibodies were analysed regarding their isotype and lytic activity. The results showed that anti-T. cruzi lytic antibodies present in sera from chagasic patients are mainly located in the IgG isotype and recognize epitopes present in both trypomasiigote and epimastigote forms. A brief report of this work has already been published12.Soro de pacientes com doença de Chagas na fase crônica foram submetidos a cromatografia de afinidade com Sepharose 4B conjugada com um extrato antigênico obtido de formas epimastigotas ou tripomastigotas de T. cruzi: os epimastigotas foram obtidos de cultura na fase exponencial de crescimento e os tripomastigotas de sangue de camundongos infectados e imunossuprimidos. Os antígenos de ambas formas parasitárias foram obtidos por tratamento dos parasitas por ultra-som, seguido de centrifugação. A cromatografia de afinidade foi feita passando-se os soros chagásicos através de uma coluna de imunoadsorvente contendo antígenos de epimastigotas ou tripomastigotas. Os anticorpos foram eluídos da coluna com tampão glicina 0,2 M pH 2,8 a 4°C. Os anticorpos eluidos foram analisados quanto ao seu isotipo e atividade lítica. Os resultados mostraram que os anticorpos anti-T. cruzi com atividade lítica presentes em soros chagásicos estão localizados no isotipo IgG e reconhecem epitopos presentes tanto nos tripomastigotas quanto nos epimastigotas
Per-patch Descriptor Selection using Surface and Scene Properties
Abstract. Local image descriptors are generally designed for describing all possible image patches. Such patches may be subject to complex variations in appearance due to incidental object, scene and recording conditions. Because of this, a single-best descriptor for accurate image representation under all conditions does not exist. Therefore, we propose to automatically select from a pool of descriptors the one that is best suitable based on object surface and scene properties. These properties are measured on the fly from a single image patch through a set of attributes. Attributes are input to a classifier which selects the best descriptor. Our experiments on a large dataset of colored object patches show that the proposed selection method outperforms the best single descriptor and a-priori combinations of the descriptor pool.
Indução de resistência a doenças foliares em tomateiro por indutores biótico (Bacillus subtilis) e abiótico (Acibenzolar-S-Metil) Induction of resistance in tomato by biotic (Bacillus subtilis) and abiotic (Acibenzolar-S-Metil) inducers
O objetivo deste trabalho foi investigar se doenças foliares do tomateiro (Lycopersicon esculentum) podem ser afetadas pela indução de resistência proporcionada pela aplicação de Bacillus subtilis, no solo e nas folhas e aplicação via foliar de acibenzolar-S-metil. A fim de investigar o modo de ação envolvido no controle foi avaliada a atividade de peroxidases nas folhas do tomateiro tratado com os indutores biótico e abiótico. Para se avaliar a severidade das doenças foliares foi avaliado o número de folhas de tomate com algum sintoma de doença e determinado o percentual de folhas doentes em relação ao total de folhas por planta. O aumento significativo da concentração de peroxidases nas plantas tratadas com os indutores, assim como a ausência de controle das doenças no tratamento com pulverização direta de B. subtilis nas folhas, são evidências que sugerem que o mecanismo de controle das doenças em questão está relacionado à resistência induzida.<br>This study was conduced to investigate whether the tomato (Lycopersicon esculentum) leaf diseases may be affected by the induction of resistance provided by the application of Bacillus subtilis, soil and leaf and foliar application of Acibenzolar-S-Methyl. In order to investigate the mode of action involved in the control was measured the peroxidases activity in the leaf of tomato treated with inducers biotic and abiotic. To evaluate the severity of foliar diseases has been estimated the number of leaf of tomatoes with symptoms of disease and determinate the percent of disease leaf in the total of leaf per plant. The significant increase in levels of peroxidase activity in plants exposed to treatment with inducers and lack of control of leaf diseases, in direct spray of B. subtilis in the leaves, are evidence that suggest that the mechanism of control diseases in question is related to induction resistance
The generation and utilization of a cancer-oriented representation of the human transcriptome by using expressed sequence tags.
Whereas genome sequencing defines the genetic potential of an organism, transcript sequencing defines the utilization of this potential and links the genome with most areas of biology. To exploit the information within the human genome in the fight against cancer, we have deposited some two million expressed sequence tags (ESTs) from human tumors and their corresponding normal tissues in the public databases. The data currently define approximately 23,500 genes, of which only approximately 1,250 are still represented only by ESTs. Examination of the EST coverage of known cancer-related (CR) genes reveals that &lt;1% do not have corresponding ESTs, indicating that the representation of genes associated with commonly studied tumors is high. The careful recording of the origin of all ESTs we have produced has enabled detailed definition of where the genes they represent are expressed in the human body. More than 100,000 ESTs are available for seven tissues, indicating a surprising variability of gene usage that has led to the discovery of a significant number of genes with restricted expression, and that may thus be therapeutically useful. The ESTs also reveal novel nonsynonymous germline variants (although the one-pass nature of the data necessitates careful validation) and many alternatively spliced transcripts. Although widely exploited by the scientific community, vindicating our totally open source policy, the EST data generated still provide extensive information that remains to be systematically explored, and that may further facilitate progress toward both the understanding and treatment of human cancers