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Validation of an improved Anaplasma antibody competitive ELISA for detection of Anaplasma ovis antibody in domestic sheep

机译:验证改进的<斜斜体>肛耳>抗体竞争力的竞争力,用于检测家庭绵羊中的<斜体>肛门素>抗体抗体

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摘要

An accurate and simple-to-perform new version of a competitive ELISA (cELISA) kit that became commercially available in 2015 for testing of cattle for antibody to Anaplasma marginale was validated for detection of Anaplasma ovis antibody in domestic sheep. True positives and negatives were identified using nested PCR (nPCR) as the gold standard. Negative bovine control sera supplied with the kit were used to calculate % inhibition (%I), designated bovine control ELISA (BcELISA), and this was compared to %I calculated from negative ovine sera derived from hand-raised, pathogen-free sheep, designated ovine control ELISA (OcELISA). The receiver operating characteristics area under the curve was 1.0 with a p value 0.001 regardless of the source of the control sera. The cutoff values for negative BcELISA and OcELISA were 30%I and 27%I, respectively. Our work confirmed that this Anaplasma antibody cELISA kit version 2 can be used with the serum controls supplied in the kit to test for A. ovis antibody in domestic sheep. Furthermore, this work confirmed the historically high infection prevalence (93%) at the U.S. Sheep Experiment Station (Dubois, Idaho), in spite of efforts to reduce the possibility for iatrogenic transmission there, suggesting high levels of tick-borne transmission.]]>
机译:<![CDATA [>准确且简单地执行的新版本的竞争力的ELISA(CELISA)套件,以2015年商业上可获得的用于对<斜体> ANAPLASMA MARGINALE 的抗体进行测试用于检测家畜中<斜斜体>肛门胰腺癌的抗体。使用嵌套的PCR(NPCR)作为黄金标准鉴定真正的阳性和负面。用试剂盒供应的负牛对照血清用于计算%抑制(%I),指定牛对照ELISA(Bcelisa),并将其与来自来自手工饲养的无病原体的羊膜的阴性胚轴血清计算的%I进行比较。指定的羊烯控制ELISA(ocelisa)。曲线下的接收器操作特性面积为1.0,<斜斜体> P 值& 0.001无论控制血清的源。阴性Bcleisa和ocelisa的截止值分别为30%I和& 27%i。我们的工作证实,这种<斜视> Anaplasma 抗体Celisa套件版本2可以与套件中提供的血清控制一起用于测试<斜视> a。卵巢国内绵羊的抗体。此外,这项工作确认了美国绵羊实验站(Dubois,Idaho)的历史上高感染率(& 93%),尽管有努力降低在那里的认可传播的可能性,表明高水平的蜱传播。 ]]>

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