首页> 美国卫生研究院文献>Journal of Clinical Laboratory Analysis >First production of fluorescent anti‐ribonucleoproteins conjugate for diagnostic of rabies in Brazil
【2h】

First production of fluorescent anti‐ribonucleoproteins conjugate for diagnostic of rabies in Brazil

机译:在巴西首次生产用于诊断狂犬病的荧光抗核糖核蛋白偶联物

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The laboratory tests recommended by the World Health Organization for detection of rabies virus and evaluation of specific antibodies are performed with fluorescent antibodies against the virus, the ribonucleoproteins (RNPs), or by monoclonal antibodies. In this study, we purified the rabies virus RNPs for the production of a conjugate presenting sensibility and specificity compatible with commercial reagents. The method employed for the purification of RNPs was ultracentrifugation in cesium chloride gradient, the obtained product being used for immunizing rabbits, from which the hyperimmune sera were collected. The serum used for conjugate production was the one presenting the highest titer (1/2,560) when tested by indirect immunofluorescence. The antibodies were purified by anion exchange chromatography (QAE‐Sephadex A‐50),conjugated to fluorescein isothiocyanateand separated by gel filtration (Sephadex G‐50). The resulting conjugate presented titers of 1/400 and 1/500 when assayed by direct immunofluorescence (DIF) and simplified fluorescence inhibition microtest, respectively. Sensibility and specificity tests were performed by DIF in 100 central nervous system samples of different animal species, presenting 100% matches when compared with the commercial reagent used as standard, independent of the conservation state of the samples. The quality reached by our conjugate will enable the standardization of this reagent for use by the laboratories performing diagnosis of rabies in Brazil, contributing to the intensification of the epidemiological vigilance and research on this disease. J. Clin. Lab. Anal. 23:7–13, 2009. © 2009 Wiley‐Liss, Inc.
机译:世界卫生组织推荐的用于检测狂犬病病毒和评估特定抗体的实验室测试是使用针对该病毒的荧光抗体,核糖核蛋白(RNP)或单克隆抗体进行的。在这项研究中,我们纯化了狂犬病毒RNPs,以生产与商业试剂兼容的敏感性和特异性偶联物。纯化RNP的方法是在氯化铯梯度中超速离心,所得产物用于免疫兔,从中收集超免疫血清。当通过间接免疫荧光测试时,用于产生缀合物的血清是具有最高滴度(1 / 2,560)的血清。抗体通过阴离子交换色谱法(QAE-Sephadex A-50)纯化,与异硫氰酸荧光素偶联,并通过凝胶过滤(Sephadex G-50)分离。当通过直接免疫荧光(DIF)和简化的荧光抑制微量试验分别测定时,所得缀合物的滴度分别为1/400和1/500。通过DIF在100种不同动物物种的中枢神经系统样品中进行了敏感性和特异性测试,与用作标准品的商业试剂相比,具有100%的匹配度,而与样品的保存状态无关。通过我们的结合物达到的质量将使该试剂的标准化,供在巴西进行狂犬病诊断的实验室使用,有助于加强对这种疾病的流行病学警惕性和研究。 J.临床实验室肛门2009年23:7–13。©2009 Wiley-Liss,Inc.

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号