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首页> 外文期刊>Acta tropica: Journal of Biomedical Sciences >Evaluation of a synthetic peptide from the Taenia saginata 18 kDa surface/secreted oncospheral adhesion protein for serological diagnosis of bovine cysticercosis
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Evaluation of a synthetic peptide from the Taenia saginata 18 kDa surface/secreted oncospheral adhesion protein for serological diagnosis of bovine cysticercosis

机译:牛带en虫18 kDa表面/分泌的外周粘着蛋白合成肽的血清学诊断牛囊尾rc病的评估

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Bovine cysticercosis is a zoonotic infection widely spread throughout Brazil, creating a burden on hygiene maintenance and the economy. Diagnosis of cysticercosis usually relies on post mortem inspection of carcasses in slaughterhouses. This detection method provides only low sensitivity. Recent advancements have improved the performance of serologic tests, such as ELISA, providing greater sensitivity and specificity. The objective of the current study was to identify and evaluate a synthetic peptide derived from the Taenia saginata 18 kDa oncospheric surface protein for the diagnosis of bovine cysticercosis in ELISA. Test performance of the identified peptide was compared to an ELISA based on a heterologous crude Taenia crassiceps antigen (Tcra), widely used for the sero-diagnosis of bovine cysticercosis. Based on the primary sequence of an in silico structural model of the 18 kDa protein, an epitope region designated EP1 was selected (46-WDTKDMAGYGVKKIEV-61). The peptide derived from this region yielded 91.6% (CI = 80-96%) sensitivity and 90% (Cl = 82-95%) specificity when used in an ELISA, whereas the crude antigen yielded 70% (CI = 56-8%) sensitivity and 82% (CI = 73-89%) specificity. Thus, we conclude that EP1 has higher diagnostic potential for detecting bovine cysticercosis than the crude antigen Tcra. (C) 2016 Elsevier B.V. All rights reserved.
机译:牛囊尾rc病是一种人畜共患的感染,广泛分布于整个巴西,给卫生维护和经济造成负担。囊尾rc病的诊断通常取决于对屠宰场屠体的尸检。该检测方法仅提供低灵敏度。最近的进步提高了血清学检测(例如ELISA)的性能,提供了更高的灵敏度和特异性。本研究的目的是鉴定和评估源自牛带Ta虫(Taenia saginata)18 kDa球形表面蛋白的合成肽,用于通过ELISA诊断牛囊尾rc病。将鉴定出的肽的测试性能与基于异源粗制Ta虫(Taenia crassiceps)抗原(Tcra)的ELISA进行了比较,该抗原广泛用于牛囊尾rc病的血清学诊断。基于18 kDa蛋白计算机结构模型的一级序列,选择了一个名为EP1的表位区域(46-WDTKDMAGYGVKKIEV-61)。当用于ELISA中时,源自该区域的肽产生91.6%(CI = 80-96%)的敏感性和90%(Cl = 82-95%)的特异性,而粗抗原产生70%(CI = 56-8%) )敏感性和82%(CI = 73-89%)特异性。因此,我们得出结论,EP1比粗抗原Tcra具有更高的检测牛囊尾rc病的诊断潜力。 (C)2016 Elsevier B.V.保留所有权利。

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