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Performance of an indigenous b-mercaptoethanolmodified antigen in comparison with a commercial reference in direct agglutination test for detection of canine visceral leishmaniasis

机译:本地b-巯基乙醇修饰抗原与商业参考在直接凝集试验中检测犬内脏利什曼病的性能比较

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摘要

We compared the performance of a locally produced b-mercaptoethanol-modified promastigoteantigen (b-ME-Ag) of an indigenous Leishmania infantum strain against that of a trypsinizedLeishmania donovani reference (REF-Ag) in the direct agglutination test (DAT) for detection ofcanine visceral leishmaniasis (CVL). One hundred and fifty-one serum samples collected fromdogs belonging to four groups with different conditions were included. At a DAT titre of 1 : 320,statistically determined as optimal cut-off value for b-ME-Ag, and 1 : 160 for REF-Ag, a sensitivityand a specificity of 100% were estimated for b-ME-Ag in comparison with 96.6% and 100 %,respectively, for REF-Ag. Overall, levels of agglutination titres recorded for the two antigens werehighly concordant (Cohen’s k50.879) in both the CVL and non-CVL groups. Based on currentresults, and ease experienced in processing the antigen and reading the test outcome, werecommend incorporation of b-ME-Ag in DAT for confirmation or exclusion of suspected CVL indogs.
机译:在直接凝集试验(DAT)中,我们将本地生产的婴儿利什曼原虫婴儿菌株的b-巯基乙醇修饰的前鞭毛体抗原(b-ME-Ag)与经过胰蛋白酶消化的利什曼原虫多诺万尼参考(REF-Ag)的性能进行了比较。内脏利什曼病(CVL)。包括从不同条件的四组犬中收集的一百一十五份血清样品。在DAT滴度为1:320时(经统计学确定为b-ME-Ag的最佳临界值,对于REF-Ag为1:160),相比而言,b-ME-Ag的灵敏度和特异性估计为100% REF-Ag分别为96.6%和100%。总体而言,在CVL组和非CVL组中,两种抗原记录的凝集滴度水平高度一致(Cohen's k50.879)。根据目前的结果,并在处理抗原和读取测试结果方面经验丰富,建议将b-ME-Ag掺入DAT中以确认或排除可疑CVL犬。

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