Schallig H D F H, Schoone G J, Beijer E G M, Kroon C C M, Hommers M, Ozbel Y, Ozensoy S, da Silva E S, Cardoso L M, da Silva E D
Koninklijk Institut voor de Tropen, Biomedical Research, Meibergdreef 39, 1105 AZ Amsterdam, The Netherlands.
Vet Parasitol. 2002 Oct 16;109(1-2):1-8. doi: 10.1016/s0304-4017(02)00268-6.
A fast agglutination screening test (FAST) for the detection of anti-Leishmania antibodies in serum samples from dogs with visceral leishmaniosis was developed. The test is based on the direct agglutination test (DAT), but combines a higher parasite concentration with a smaller test volume. In contrast to the DAT, the FAST makes use of only one serum dilution and the results can be read within 3 h as opposed to 18-20 h for the DAT. The FAST was evaluated using serum samples of confirmed cases of the disease and healthy controls collected in the most important endemic regions of canine visceral leishmaniosis, import cases of canine leishmaniosis in a non-endemic country, from non-endemic healthy controls and from dogs with other diseases. The performance of the FAST was compared with standard DAT. In the present study, the FAST had a sensitivity of 93.6% and a specificity of 89.0%. The DAT had a sensitivity of 88.6% and a specificity of 96.7%. Furthermore, using a large panel of serum samples of previously examined DAT positive or negative dogs it was shown that degree of agreement between the two tests was high (95.7%; kappa value = 0.91). The FAST offers the advantages of the DAT based on freeze-dried antigen with respect to stability of the antigen, sensitivity and specificity. Moreover, the FAST allows the rapid screening of a large number of samples, which makes the test very useful for epidemiological screening of large populations of dogs.
开发了一种快速凝集筛查试验(FAST),用于检测内脏利什曼病犬血清样本中的抗利什曼原虫抗体。该试验基于直接凝集试验(DAT),但将更高的寄生虫浓度与更小的试验体积相结合。与DAT不同,FAST仅使用一种血清稀释度,结果可在3小时内读取,而DAT则需要18 - 20小时。使用从犬内脏利什曼病最重要的流行地区收集的确诊病例血清样本和健康对照、非流行国家的犬利什曼病输入病例、非流行健康对照以及患有其他疾病的犬的血清样本对FAST进行了评估。将FAST的性能与标准DAT进行了比较。在本研究中,FAST的敏感性为93.6%,特异性为89.0%。DAT的敏感性为88.6%,特异性为96.7%。此外,使用大量先前检测为DAT阳性或阴性的犬的血清样本表明,两种试验之间的一致性程度很高(95.7%;kappa值 = 0.91)。FAST基于冻干抗原,在抗原稳定性、敏感性和特异性方面具有DAT的优点。此外,FAST允许快速筛查大量样本,这使得该试验对于大量犬群的流行病学筛查非常有用。