271 resultados para PR-proteins


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In the present study, we have analyzed by sodium docecyl sulphate - polyacrilamide gel electrophoresis (SDS-PAGE), immunoblotting and Concanavalin A blotting (Con A blotting) proteins of membrane fractions and soluble fractions obtained from Giardia duodenalis trophozoites of two axenic strains isolated in Brazil from a symptomatic (BTU-11) and an asymptomatic patient (BTU-10), as compared to the reference strain Portland 1. Both Brazilian strains showed a complex and homogeneous electrophoretic pattern of proteins, but some differences could be observed. Several glycoproteins were detected, particularly the proteins of 81, 72, 59 kDa and the protein of 62 kDa in the membrane proteins and cytosol, respectively. Many antigenic components were revealed by anti-Giardia rabbit IgG antibodies in the immunoblotting analysis. Among these components, the membrane protein of 32 kDa and the cytosol protein of 30 kDa could be related to giardin, as previously demonstrated.

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This study evaluated the usefulness of the anti-HBc, hepatitis C virus antibodies (anti-HCV), human T cell lymphotropic virus I and II antibodies (anti-HTLV I/II), serologic tests for syphilis, and surface antigen of hepatitis B virus (HBsAg) as surrogate markers for the risk for HIV infection in 80,284 serum samples from blood donors from the Blood Bank of "Hospital Universitário Regional Norte do Paraná", Londrina, Paraná State, Brazil, analyzed from July 1994 to April 2001. Among 39 blood donors with positive serology for HIV, 12 (30.8%) were anti-HBc positive, 10 (25.6%) for anti-HCV, 1 (2.6%) for anti-HTLV I/I, 1 (2.6%) was positive for syphilis, and 1 (2.6%) for HBsAg. Among the donors with negative serology for HIV, these markers were detected in 8,407 (10.5%), 441 (0.5%), 189 (0.2%), 464 (0.6%), and 473 (0.6%) samples, respectively. The difference was statistically significant (p < 0.001) for anti-HBc and anti-HCV. Although the predictive positive value for these surrogate markers were low for HIV infection, the results confirmed the anti-HBc and anti-HCV as useful surrogate markers for HIV infection thus reinforcing the maintenance of them in the screening for blood donors contributing to the prevention of the small number of cases in which HIV is still transmitted by transfusion.

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Renal damage is an important cause of death in patients who have survived the early effects of severe crotalid envenomation. Extracellular matrix of renal tissue is altered by Crotalus toxin activities. The aim of this study was to describe how cytoskeletal proteins and basal membrane components undergo substantial alterations under the action of Crotalus vegrandis crude venom and its hemorrhagic fraction (Uracoina-1) in mice. To detect the proteins in question, the immunoperoxidase method with monoclonal and polyclonal antibodies was used. Cell types within renal lesions were characterized by phenotypic identification, by means of immunohistologic analysis of marker proteins using different primary antibodies against mesangial cells, endothelial cells, cytoskeletal proteins (intermediate filament), extracellular matrix and basal membranes. Samples for morphological study by standard procedures (biotin-streptavidin-peroxidase technique) using light microscopy were processed. Positive and negative controls for each antigen tested in the staining assay were included. After crude venom and hemorrhagic fraction inoculation of mice, the disappearance of cytoskeletal vimentin and desmin and collagen proteins in the kidney was observed. In extracellular matrix and basal membranes, collagen type IV from envenomed animals tends to disappear from 24 h to 120 h after venom injection.

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Serological, epidemiological and molecular aspects of hepatitis C virus (HCV) infection were evaluated in 183 subjects from Londrina, Paraná, Brazil, and adjacent areas. Serum samples which tested anti-HCV positive by microparticle enzyme immunoassay (MEIA) obtained from eight patients with chronic hepatitis C, 48 blood donors, and 127 patients infected with the human immunodeficiency virus (HIV) were submitted to another enzyme immunoassay (ELISA) and to the polymerase chain reaction (PCR). About 78.7% of samples were also reactive by ELISA, with the greater proportion (70.8%) of discordant results verified among blood donors. A similar finding was observed for HCV-RNA detection by PCR, with 111/165 (67.3%) positive samples, with higher rates among HIV-positive subjects and patients with chronic hepatitis than among blood donors. Sixty-one PCR-positive samples were submitted to HCV genotyping, with 77.1, 21.3 and 1.6% of the samples identified as types 1, 3 and 2, respectively. Finally, analysis of some risk factors associated with HCV infection showed that intravenous drug use was the most common risk factor among HIV/HCV co-infected patients, while blood transfusion was the most important risk factor in the group without HIV infection. The present study contributed to the knowledge regarding risk factors associated with HCV infection and the distribution of HCV genotypes in the population evaluated.

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Salivary gland proteins of the human malaria vector, Anopheles dirus B were determined and analyzed. The amount of salivary gland proteins in mosquitoes aged between 3 - 10 days was approximately 1.08 ± 0.04 µg/female and 0.1 ± 0.05 µg/male. The salivary glands of both sexes displayed the same morphological organization as that of other anopheline mosquitoes. In females, apyrase accumulated in the distal regions, whereas alpha-glucosidase was found in the proximal region of the lateral lobes. This differential distribution of the analyzed enzymes reflects specialization of different regions for sugar and blood feeding. SDS-PAGE analysis revealed that at least seven major proteins were found in the female salivary glands, of which each morphological region contained different major proteins. Similar electrophoretic protein profiles were detected comparing unfed and blood-fed mosquitoes, suggesting that there is no specific protein induced by blood. Two-dimensional polyacrylamide gel analysis showed the most abundant salivary gland protein, with a molecular mass of approximately 35 kilodaltons and an isoelectric point of approximately 4.0. These results provide basic information that would lead to further study on the role of salivary proteins of An. dirus B in disease transmission and hematophagy.

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This report describes a preliminary characterization of proteolytic activity of proteins isolated from lysate of Giardia trophozoites of an axenic Brazilian strain. Fractions obtained by high-performance liquid chromatography (FPLC) were tested in SDS-polyacrylamide gel for the protein profiles, and the proteases activity was analyzed using gelatin impregnated SDS-PAGE. The proteases characterization was based on inhibition assays employing synthetic inhibitors for cysteine (E-64, IAA), serine (PMSF, TPCK, TLCK, and elastatinal), metalo (EDTA) and aspartic (pepstatin) proteases. Among thirty eluted fractions, polypeptide bands were observed in eight of them, however, proteolytic activity was detected in four ones (F23, F24, F25 and F26). Protein profiles of these fractions showed a banding pattern composed by few bands distributed in the migration region of 45 to < 18 kDa. The zymograms revealed proteolytic activity in all the four fractions assayed, mainly distributed in the migration region of 62 to 35 kDa. Among the profiles, the main pronounced zones of proteolysis were distinguished at 62, 55, 53, 50, 46 and 40 kDa. In inhibition assays, the protease activities were significantly inhibited by cysteine (E-64) and serine proteases (TPCK, TLCK and elastatinal) inhibitors. Gels incubated with other cysteine and serine protease inhibitors, IAA and PMSF, respectively, showed a decrease in the intensity of hydrolysis zones. Indeed, in the assays with the inhibitors EDTA for metalloproteases and pepstatin for aspartic proteases, none inhibition was detected against the substrate. These observations are relevants, especially if we consider that to define the real role of the proteases in host-parasite interaction, the purification of these enzymes for detailed studies may be warranted.

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São relatadas observações acumuladas nos períodos pré-epidêmico e epidêmico (1973-1975) do atual surto de meningoencefalite meningocócica na área do Grande Rio, e realizados estudos bacteriológicos baseados em 1.000 casos suspeitos de meningoencefalite e submetidos à punção lombar, no Hospital Estadual São Sebastião. É proposto e discutido esquema simples e eficaz para processamento bacteriológico dos LCR suspeitos, a partir da colheita e pronta semeadura do material. É também discutida a real contribuição da bacterioscopia no diagnóstico presuntivo das meningoencefalites, definindo-se as limitações da técnica. Foi obtido elevado grau de isolamento de microorganismos, variando de 3%, para líquores entre zero e 10 células/mm' e 72%, para líquores acima de 1000 células/mm³. No decorrer do estudo, foram isoladas e caracterizadas 356 amostras bacterianas, assim discriminadas: N. meningitidis, 281; Haemophilus sp., 22; Enterobacteriaceae, 15; D. pneumoniae, 26; bastonetes gram negativos oxidattvos, 3; estreptococo beta hemolitico, 1 e enterococo, 1. As amostras de meningococos eram, em 15% dos casos, do grupo sorológico A, em 2% do grupo B e em 14%, do grupo sorológico C. Os testes de sensibilidade, em disco, aos agentes antimicrobianos principalmente utilizados na quimioprofilaxia e tratamento da doença meningocócica revelaram alto grau de sensibilidade das amostras ensaiadas a todos os agentes testados. A resistência à sulfadiazina sódica, em testes realizados segundo as normas preconizadas pela Food and Drug Administration (F.D.A.), revelaram elevado grau de resistência, particularmente dos meningococos do grupo C.

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Neste trabalho, estudou-se as espécies do gênero Anopheles que se atraem por iscas humanas na Região de Buriticupu, Santa Luzia, Estado do Maranhão. Foram encontradas 7 espécies do subgênero Nyssorhyncus A. (N) darlingi, o principal vetor da malária humana na região, foi a espécie mais freqüente (53,1% da amostra total). Seguem na ordem de importância, A. (N) evansae (21.0%), A. (N) triannulatus (17.4%) e A. (N) nuñeztovari (4,8%). As demais espécies, A. (N) argyritarsis, A. (N) oswaldoi e A. (N) rangeli representaram juntas 3,7% da amostra total. As visitas foram mais frequentes no extra (51,7% da amostra total) do que no peridomicílio (45,7%). A. (N) darlingi e A. (N) evansae foram as únicas espécies encontradas no intradomicílio, numa proporção de aproximadamente 2,6% da amostra total. Os anofelinos ocorreram nas estações seca e chuvosa, com maior frequência na última, coincidindo com os elevados índices de caso de malária naquela região.

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Biomphalaria glabrata de Belo Horizonte, Minas Gerais, Brasil, criada no laboratório, apresenta 90% de taxa de infecção com 20 miracídios da cepa LE, autóctone. O período pré-patente normal varia de 5 a 7 semanas enquanto 5 a 10% dos moluscos expostos não eliminam cercárias. Os descendentes de exemplares negativos foram novamente submetidos à infecção individual com 20 miracídios. A média de infecção da F14 a F20 foi de 43,6%. Cortes histológicos de moluscos da F12, F14 e F15 mostraram reações teciduais nos exemplares eliminando menos de 10 cercárias. Um período pré-patente prolongado, 17 a 32 semanas, foi observado em 35 (17,9%) dos 195 exemplares infectados. Os índices de cercárias da F12, F13 e F15 baixaram de extremamente compatíveis (classe VI) para muito compatíveis e compatíveis (classes V e III) mostrando a compatibilidade menor dos moluscos selecionados.

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O objetivo desta pesquisa foi relacionar a presença de ovos e/ou larvas de helmintos em elementos dos sanitários com a freqüência dos mesmos nas fezes de seus usuários. Três amostras das fezes de 1050 crianças em idade pré-escolar, examinadas pelo método de sedimentação, foram positivas para 184 ovos ou larvas de helmintos, em 162 crianças. Dos 465 elementos dos sanitários (assento, descarga, trinco, maçanetas e registro de torneira) de 12 pré-escolas municipais de Sorocaba examinados com fita adesiva transparente sobre lâmina de microscopia estavam contaminados, sendo encontrados 18 ovos de Ascaris lumbricoides, 1 de Enterobius vermicularis e 4 larvas de nematóides parcialmente alteradas. Não houve correlação significante entre a contaminação de elementos de sanitários e das fezes de seus usuários.

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O objetivo do trabalho foi avaliar a soroepidemiologia do T. gondii e relato de problemas oculares em pacientes da zona rural que procuraram a unidade de saúde de Jaguapitã, Paraná. Soros de 82 pacientes foram submetidos a reação de Imunofluorescência Indireta, para detectar a presença de anticorpos anti-T. gondii da classe IgG, sendo a soropositividade considerada para diluições 3 1:16. Problemas oculares foram avaliados através da Tela de Amsler. Dos 82 soros avaliados 68 (82,9%) foram sororeagentes a toxoplasmose e 14 (17,1%) não reagentes. Os títulos mais frequentes foram de 64 (23/33,8%) e 256 (16/23,5%), e os maiores títulos foram de 4096 (8/11,8%). O teste da Tela de Amsler revelou 22 (26,8%) pacientes que relataram algum tipo de alteração, sendo que o sexo masculino foi um fator de proteção em relação ao sexo feminino (OR = 0,21 0,04 < OR < 0,86 c2 = 4,98 p = 0,02). No presente estudo os fatores de risco avaliados pelo inquérito sócio cultural e epidemiológico não revelaram diferenças estatísticas significativas. Através do presente trabalho observou-se que o T. gondii encontra-se amplamente distribuído na população estudada.

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Coproparasitological analyses were performed on 191 daycare children and 434 elementary school children from urban and rural areas in Rolândia, Parana State, Brazil. The overall prevalence of enteroparasites was 15.2 % for daycare children and 52.5% for elementary school children. Risk factors are discussed.

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Genetic diversity and differentiation, inferred by typing the polymorphic genes coding for the merozoite surface proteins 1 (Msp-1) and 2 (Msp-2), were compared for 345 isolates belonging to seven Plasmodium falciparum populations from three continents. Both loci yielded similar estimates of genetic diversity for each population, but rather different patterns of between-population differentiation, suggesting that natural selection on these loci, rather than the transmission dynamics of P. falciparum, determines the variation in allele frequencies among populations.