112 resultados para Macaca-nemestrina
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We report the assessment and validation of an NS1 epitope-blocking enzyme-linked immunosorbent assay (ELISA) for detection of antibodies to West Nile virus (WNV) in macaques. Sera from naturally infected Macaca nemestrina were tested by ELISA and plaque reduction neutralization test (PRNT). Results were correlated with hemagglutination inhibition (HAI) data. Our results demonstrate that the blocking ELISA rapidly and specifically detects WNV infection in M. nemestrina. In addition, the diagnostic value of 7 commercially available immunoassays (PanBio immunoglobulin [Ig] M ELISA, PanBio IgG ELISA, PanBio immunofluorescence assay (IFA), InBios IgG ELISA, InBios IgM ELISA, Focus Diagnostics IgG ELISA, and Focus Diagnostics IgM ELISA) in M. nemestrina was evaluated and compared with that of the epitope-blocking ELISA. The PanBio IgG ELISA was found to effectively diagnose WNV exposure in M. nemestrina. Further, PanBio IFA slides are fast and reliable screening tools for diagnosing flaviviral exposure in M. nemestrina.
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Pig-tailed macaques (Macaca nemestrina) naturally infected with West Nile virus were monitored from 1999 to 2005 to determine virus-specific antibody seroconversion, prevalence, and persistence. Antibodies persisted for up to 36 months, as detected by epitope-blocking enzyme-linked immunosorbent and hemagglutination inhibition assays. Exposure to cocirculating St. Louis encephalitis virus was evaluated by Western blotting and immunofluorescence assays.
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The basal dendritic arbors of 442 supragranular pyramidal cells in visual cortex of the marmoset monkey were compared by fractal analyses. As detailed in a previous study,(1) individual cells were injected with Lucifer Yellow and processed for a DAB reaction product. The basal dendritic arbors were drawn, in the tangential plane, and the fractal dimension (D) determined by the dilation method. The fractal dimensions were compared between cells in ten cortical areas containing cells involved in visual processing, including the primary visual area (Vi), the second visual area (V2), the dorsoanterior area (DA), the dorsomedial area (DM), the dorsolateral. area (DL), the middle temporal area (MT), the posterior parietal area (PP), the fundus of the superior temporal area (FST) and the caudal and rostral subdivisions of inferotemporal cortex (ITc and ITr, respectively). Of 45 pairwise interareal comparisons of the fractal dimension of neurones, 20 were significantly different. Moreover, comparison of data according to previously published visual processing pathways revealed a trend for cells with greater fractal dimensions in higher cortical areas. Comparison of the present results with those in homologous cortical areas in the macaque monkey(2) revealed some similarities between the two species. The similarity in the trends of D values of cells in both species may reflect developmental features which, result in different functional attributes.
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The orbitofrontal cortex (OfC) is a heterogeneous prefrontal sector selectively connected with a wide constellation of other prefrontal, limbic, sensory and premotor areas. Among the limbic cortical connections, the ones with the bippocampus and parabippocampal cortex are particularly salient. Sensory cortices connected with the OfC include areas involved in olfactory, gustatory, somatosensory, auditory and visual processing. Subcortical structures with prominent OfC connections include the amygdala, numerous thalamic nuclei, the striatum, hypothalamus, periaqueductal gray matter, and biochemically specific cell groups in the basal forebrain and brainstem. Architectonic and connectional evidence supports parcellation of the OfC. The rostrally placed isocortical sector is mainly connected with isocortical areas, including sensory areas of the auditory, somatic and visual modalities, whereas the caudal non-isocortical sector is principally connected with non-isocortical areas, and, in the sensory domain, with olfactory and gustatory areas. The connections of the isocortical and non- isocortical orbital sectors with the amygdala, thalamus, striatum, hypotbalamus and periaqueductal gray matter are also specific. The medial sector of the OfC is selectively connected with the bippocampus, posterior parabippocampal cortex, posterior cingulate and retrosplenial areas, and area prostriata, while the lateral orbitofrontal sector is the most heavily connected with sensory areas of the gustatory, somatic and visual modalities, with premotor regions, and with the amygdala.
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Foram obtidas informações silviculturais sobre a macacaúba - Platymiscium trinitatis Benth (Leguminosae Papilionoideae), abordando aspectos da germinação das sementes e do efeito da inoculação com rizóbios na formação de mudas. A semeadura foi efetuada em areia, acompanhada por 45 dias, e as plântulas repicadas para sacos com latossolo amarelo coletado após a queima da vegetação, no horizonte A (0-20 cm), distribuído em recipientes plásticos com capacidade para 2,0 kg de solo. As mudas foram submetidas a tratamentos de adubação com Ν mineral (50 kg/ha) ou a inoculação com estirpes de rizóbios da coleção do INPA/CPCA. O desenvolvimento das mudas foi acompanhado com avaliação mensal do comprimento do caule e diâmetro do colo das plantas. Aos 126 dias estas foram colhidas e avaliadas. As sementes apresentaram elevada viabilidade com 86% de germinação, iniciada aos 4 dias e distribuindo-se por 37 dias. O índice de Velocidade de Emergência foi de 21,9 (n = 200). A repicagem das plantas para sacos pode ser feita em 40 dias. Os rizóbios utilizados como inoculante formaram colônias brancas, com até 4 mm de diâmetro após a incubação, com características morfológicas e culturais bastante variadas. No viveiro as mudas apresentaram crescimento lento e não apresentaram resposta à inoculação, o que foi relacionado aos níveis elevados de matéria orgânica presentes, o que, entretanto, não favoreceu o seu desenvolvimento. O incremento mensal de comprimento do caule e diâmetro do colo das plantas foi de 2,49 cm e 0,45 mm, respectivamente.
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n.s. no.64(1991)
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n.s. no.10(1982)
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n.s. no.98(2001)
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n.s. no.104(2005)
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n.s. no.107(2006)