Harrus Shimon, Alleman A Rick, Bark Hylton, Mahan Suman M, Waner Trevor
The Koret School of Veterinary Medicine, Hebrew University of Jerusalem, P.O. Box 12, 76100, Rehovot, Israel.
Vet Microbiol. 2002 May 24;86(4):361-8. doi: 10.1016/s0378-1135(02)00022-6.
The aim of this study was to compare three different enzyme-linked immunosorbant assays (recombinant major antigenic protein 2 (rMAP2)-ELISA, the Immunocomb (Biogal, Israel) and the Snap 3Dx assay (IDEXX Laboratories Inc., USA)) with the indirect immunofluorescent antibody test in detecting anti-Ehrlichia canis immunoglobulin-G (IgG) antibodies. Samples tested were collected from dogs suspected to be naturally infected with E. canis and from experimentally infected dogs. When qualitative results (positive/negative) were compared, there was an overall agreement of 81% (54/67) between the indirect immunofluorescence antibody (IFA) test and the rMAP2-ELISA. An overall agreement of 94% (63/67) was found between the IFA test and the Immunocomb, and an overall agreement of 91% (61/67) was found between the IFA test and the Snap 3Dx assay. In 50 of 67 (74.6%) samples tested, complete agreement in the qualitative results was found in all four tests. Sixteen of 17 samples with disagreement in the qualitative results were found to have IFA titers of 1:320 or less. The sensitivities and specificities of the tests were found to be 0.71 and 0.85 for the rMAP2-ELISA, 0.86 and 0.98 for the Immunocomb, and 0.71 and 1.00 for the Snap 3Dx assay. The tests performed in this study were found to be highly specific in detecting E. canis antibodies. Their sensitivity was found to be low with sera having IFA titers of < or =1:320, while high with sera having titers greater than 1:320. Repeating the serological tests 1-2 weeks after the first antibody assay may overcome the sensitivity problem with titers of < or =1:320.
本研究的目的是比较三种不同的酶联免疫吸附测定法(重组主要抗原蛋白2(rMAP2)-酶联免疫吸附测定、免疫组合法(以色列Biogal公司)和Snap 3Dx检测法(美国IDEXX实验室公司))与间接免疫荧光抗体试验在检测犬埃立希氏体免疫球蛋白-G(IgG)抗体方面的效果。检测样本采集自疑似自然感染犬埃立希氏体的犬以及实验感染犬。当比较定性结果(阳性/阴性)时,间接免疫荧光抗体(IFA)试验与rMAP2-酶联免疫吸附测定之间的总体一致性为81%(54/67)。IFA试验与免疫组合法之间的总体一致性为94%(63/67),IFA试验与Snap 3Dx检测法之间的总体一致性为91%(61/67)。在67个检测样本中的50个(74.6%)中,所有四种检测方法的定性结果完全一致。在定性结果存在差异的17个样本中,有16个样本的IFA滴度为1:320或更低。rMAP2-酶联免疫吸附测定法的敏感性和特异性分别为0.71和0.85,免疫组合法为0.86和0.98,Snap 3Dx检测法为0.71和1.00。本研究中进行的检测方法在检测犬埃立希氏体抗体方面具有高度特异性。对于IFA滴度≤1:320的血清,其敏感性较低,而对于滴度大于1:320的血清,敏感性较高。在首次抗体检测后1至2周重复进行血清学检测可能会克服滴度≤1:320时的敏感性问题。