31 resultados para per-survivor processing


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Abstract: New Delhi metallo-beta-lactamase-1 (NDM-1) is a bacterial enzyme that renders the bacteria resistant to a variety of beta-lactam antibiotics. A 20-year-old man was hospitalized several times for surgical treatment and complications caused by a right-sided vestibular schwannoma. Although the patient acquired several multidrug-resistant infections, this study focuses on the NDM-1-producing Acinetobacter spp. infection. As it was resistant to all antimicrobials tested, the medical team developed a 20-day regimen of 750mg/day metronidazole, 2,000,000IU/day polymyxin B, and 100mg/day tigecycline. The treatment was effective, and the patient recovered and was discharged from the hospital.

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El camu camu es uno de los frutales nativos con gran potencial económico para la agroindustria y agro exportación. Edessa es una de las plagas del camu camu que provoca sequedad en los brotes, y en los frutos una mancha decolorada con círculos concéntricos bien marcados y un punto central al alimentarse. El objetivo del presente trabajo fue determinar el ciclo biológico bajo condiciones de laboratorio y la fluctuación poblacional de Edessa aff. aulacosterna "Chinche del fruto del camu camu" durante enero a noviembre del 2004 en el cultivo de camu camu, en parcelas en desarrollo y producción ubicadas en áreas de restinga inundables en Pucallpa, Ucayali, Perú. Se colectaron huevos, ninfas y adultos procedentes del distrito de Yarinacocha, Pucallpa, Ucayali, Perú para iniciar la crianza artificial. El tiempo de duración del huevo al I estadio ninfal fue 5,1 días. Se encontró un 94,6% de eclosión de los huevos, variando entre 12 hasta 14 huevos por postura. El tiempo transcurrido desde el huevo hasta II estadío fue de 37,3 días y del III al V estadío ninfal fue de 81,9 días. El porcentaje de mortalidad del primer estadio ninfal a adulto fue de 98,1%. Los adultos colectados se localizaron preferentemente sobre las ramas y el tallo de la planta, mientras que las ninfas se encontraron en los brotes tiernos. Con relación a su fluctuación poblacional, solo se registró posturas a lo largo del año en parcelas en producción. No se encontraron diferencias entre ninfas I a V, y adultos de Edessa aff. aulacosterna, entre plantaciones en producción y desarrollo de camu camu. Solo se encontró diferencias entre la época seca y lluviosa en las ninfas de III a V estadio en las plantas de camu camu en desarrollo. Edessa aff. aulacosterna presentó mayormente una distribución contagiosa. El adecuado conocimiento de la bioecología nos permite mejorar la estrategia de control de esta plaga.

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El picudo, Conotrachelus dubiae O'Brien 1995, es una de las plagas mas importantes del camu camu Myrciaria dubia H.B.K. Mc Vaugh en la Amazonía Peruana. El objetivo del presente estudio fue determinar el ciclo biológico de este insecto bajo condiciones de laboratorio y describir su comportamiento y fluctuación en condiciones de campo en Pucallpa, Ucayali, Perú. El porcentaje de eclosión de larvas fue de 87%, la duración del periodo de incubación de los huevos fue de 5,5±0,9 (4 a 7) días, del estado larval en el fruto 22,2±1,9 (20 a 25) días y en el suelo (fase pre-pupa), 54,4±5,5 (46 a 67) días, del periodo pupal 11,8±0,9 (9 a 13) días y la longevidad del adulto fue de 51,8±18,9 (9 a 75) días. Los adultos se alimentaron de frutos de diferentes diámetros y estados de maduración y de botones florales, ramas tiernas y flores. No se registró la presencia de adultos de C. dubiae en frutos secos, ni en la base del tallo, sino en ritidomas. La mayor actividad de alimentación y de reproducción de los adultos fue entre 18:30 a 22:00 h. Los adultos fueron observados en el cultivo durante todo el año, encontrándose con mayor frecuencia en los meses de enero a marzo en pisos bajos inundables y entre octubre a diciembre en tierra firme no inundable, coincidiendo con la fase de floración y fructificación de la planta.

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This paper deals with the determination of the content of macronutrients in pulp and beans of three coffee varieties, namely 'Mundo Novo', 'Caturra Amarelo' and 'Bourbon Amarelo'. Samples were collected in plantations located in the three types of soils herein most of S. Paulo, Brazil, coffee is grown, that is, "terra roxa legítima" (Ribeirão Preto), "massapé-salmourão" (Mocóca), and "arenito de Bauru" (Pindorama). The following main conclusions were drawn after statistical analysis of data obtained hereby. There is no statistical difference among the three varieties . Average contents of macronutrients, as per cent of the dry matter, are the following: N P K Ca Mg S bean 1,71 0,10 1,53 0,27 0,15 0,12 pulps 1.78 0,14 3,75 0,41 0,13 0,15 Samples collected in Mocóca ("massapé-salmourão") had lower N and K contents, probably due to lack of availability of these elements in the soil, as suggested by its analysis. Results obtained in this work are in good agreement with data described elsewhere. Out of the total of elements contained in the whole fruit the following proportions are exported as clean coffee: N - 2/3, P and K - 1/2, Ca, Mg and S - 1/3. It is clear therefore that a substantial amount of elements absorbed from the soil remains in the pulp or in the dry hulls which result from processing. From this fact raises the interest of using these residues as fertilizer in the coffee plantations.

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Larvas de Leptus sp. (Acari, Prostigmata, Erythraeidae) foram coletadas das membranas intersegmentares dos tergitos e esternitos abdominais de abelhas (Ápis mellifera L.) em Cerro de Pasco, Peru. Não foram relatados danos por este ectoparasito. Fêmeas de Blattisoeius dentriticus (Berlese, 1918) (Acari, Mesostigmata, Ascidae) foram coletadas de colméias de abelhas, junto com Tyrophagus putrescentiae (Schrank, 1781) (Acari, Astigmata, Acaridae), em Lima, Peru.

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The morphology of the cyst cells in Apis mellifera Linné, 1758, Scaptotrigona postica Latreille, 1804, and Melipona bicolor bicolor Lepeletier, 1836 testis, as well as the average number of spermatic cells are reported. The data indicates a supporting and nourrishing role of the cyst cells to the developing cystocytes. The counts of immature spermatozoa in the cysts show an average of 202.8 ± 21.2 spermatozoa for A. mellifera, 117.4 ± 8.68 for S. postica and 88.8 ± 15.57 for M. bicolor, which predict the occurrence of 8 mitotic cycles in the cystocytes of A. mellifera and 7 in the meliponines, considering that only one spermatozoom originates of each final spermatogonium.

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Quatro grupos de 6 gatos (24 gatos) recém-nascidos e desmamados receberam "per os", respectivamente, suspensões de toxoplasmas de camundongos com 3-4 dias de infecção, de 4 amostras de T. gondii. Cada grupo teve um gato testemunha. Nenhum dos gatos de experiência eliminou oocistos atribuíveis a T. gondii, em períodos de observação de 6 a 20 dias; e suas fezes, conservadas 2-4 dais em bicromato de potássio a 2,5% e ministradas "per os" a camundongos, não induziram toxoplasmose nesses roedores. Com exceção dos que eram portadores de Isospora, os gatos não mostraram formas evolutivas de coccídios no epitélio intestinal. Em todos os grupos a infecção toxoplásmica foi comprovada pela positividade da reação de Sabin & Feldman (1:16 a 1:1024); e pelo isolamento de toxoplasmas pela inoculação de triturados dos seus principais órgãos em camundongos indicadores. De um modo geral, os gatos mais crescidos não mostraram sinais de doença, porém os outros, e principalmente os recém-nascidos adoeceram e vários morreram de toxoplasmose sistêmica: esplenite, hepatite, enterite, penumonia e, mais raramente, miocardite e encefalite. Os toxoplasmas foram encontrados em todos esses órgãos e, tamém, nos rins e supra-renais.

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En el estudio helmintológico de anfibios del género Telmatobius Wiegmann, 1834, y del pez Orestias luteus Valenciennes, 1839, de las zonas de Arequipa, Puno y del Lago Titicaca, se han encontrado nematodes de los géneros Hedruris Nitzsch, 1821 y Falcaustra Lane, 1915. Se redescribe Hedruris orestiae Moniez, 1889 y se describen cuatro especies nuevas: Hedruris moniezi sp. n., Falcaustra condorcanquii sp. n., Falcaustra pumacahuai sp. n. y Falcaustra tiahuanaquensis sp. n.

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Merozoite surface protein-1 (MSP-1, also referred to as P195, PMMSA or MSA 1) is one of the most studied of all malaria proteins. The proteins. The protein is found in all malaria species investigated and structural studies on the gene indicate that parts of the molecule are well-conserved. Studies on Plasmodium falciparum have shown that the protein is in a processed form on the merozoite surface, a result of proteolytic cleavage of the large percursor molecule. Recent studies have identified some of these cleavage sites. During invasion of the new red cell most of the MSP1 molecule is shed from the parasite surface except for a small C-terminal fragment which can be detected in ring stages. Analysis of the structure of this fragment suggests that it contains two growth factor-like domains that may have a functional role.

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An ELISA test for the serological diagnosisof amoebic liver abscess (ALA) was standardized and evaluated in sera from three groups of patients: (1) three patients with diagnosis confirmed by isolation of the parasite,(2) thirty seven patients with diagnosis established by clinical findings and ultrasound studies and (3) seven patients whose diagnosis were established by clinical findings and a positive double immunodifusion test. Ninety one serum samples from healthy subjects and 22 from patients with other liver or parasitic diseases were also included in the study. the optimum concentration of Entamoeba histolytica antigen was 1.25 µg/ml and optimum dilutions of serum and anti-human IgG-alkaline phosphatase conjugate were 1:400 and 1:4000 respectively. The cut-off point of the ELISA test in this study was an absorbance value of 0.34. The test parameters were: sensitivity = 95.7 per cent, specificty = 100 per cent, positive predictive value = 100 per cent and negative predictive value = 98.2 per cent.The ELISA test was found to be of great use as a diagnostic tool for the establishment of amoebic etiology in patients with clinical supposition of ALA. The test could also be used for seroepidemiological surveys of the prevalence of invasive amoebiasis in a given population, since it allows the processing of a greater number of samples at a lower cost tahn other serological tests.

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Five species of monogeneans collected from marine fishes of the Pacific coast of Chile and Perú were studied. Three of them are new species: Interniloculus chilensis n. sp. (Capsalidae), Neoheterobothrium insalaris n. sp. (Diclidophoridae) and Loxura peruensis n. sp. (Axinidae) parasitic on Sebastes capensis (Scorpaenidae), Paralichthys sp. (Bothiidae) and Belone scapularis (Belonidae), respectively. Two new combinations are proposed, Intracotyle neghmei (Microcotylidae) for Neobivagina neghmei Villalba, 1987 and Hargicotlyle conceptionensis (Diclidophoridae) for Choricotyle conceptionensis Villalba, 1987.

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Bacillus thuringiensis produces d-endotoxins that require proteolytic processing to become active. The activation of the B. thuringiensis subsp. medellin 28 kDa (Cyt1Ab1) cytolytic toxin by trypsin, chymotrypsin and gut extract from Culex quinquefasciatus larvae was analyzed. The Cyt1Ab1 toxin of B. thuringiensis subsp. medellin was processed by all proteases tested to fragments between 23 and 25 kDa, while processing of the Cyt1Aa1 toxin produce fragments between 22.5 and 24.5 kDa. The Cyt1Ab1 toxin was preferentially processed at the alkaline pH of 12. The in vitro proteolytic processing of the Cyt1Ab1 toxin by C. quinquefasciatus larvae midgut extract showed a 25 kDa fragment; a similar result was observed when the activation was performed in the in vivo experiments. The solubilized Cyt1Ab1 toxin and the protease resistant cores generated by in vitro processing showed hemolytic activity but not mosquitocidal activity. Amino terminal sequence of the C. quinquefasciatus gut extract resistant fragment indicated that the cutting site was located between Lys31 and Asp32, with a sequence DDPNEKNNHNS; while for the trypsin-resistant fragment the cutting site was determined between Leu29 and Arg30, and for the chymotrypsin-resistant fragment between Arg30 and Lys31.