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首页> 外文期刊>Veterinary Parasitology >Comparative evaluation of the DPP (R) CVL rapid test for canine serodiagnosis in area of visceral leishmaniasis
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Comparative evaluation of the DPP (R) CVL rapid test for canine serodiagnosis in area of visceral leishmaniasis

机译:DPP(R)CVL快速测试对内脏利什曼病地区犬血清学诊断的比较评估

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We investigated the performance of the DPP (R) canine visceral leishmaniasis (CVL) rapid test, a novel immunochromatographic assay launched by BioManguinhos (Brazil), which was recently included in the new Brazilian protocol for screening CVL in serological surveys. The present study compared the DPP (R) with the ELISA and IFA produced by BioManguinhos (Brazil) both with L. major-like antigens and with in-house tests using Leishmania infantum chagasi (in-house ELISA and in-house IFA). We analyzed the sera from clinically symptomatic (n = 47) and asymptomatic (n = 38) infected dogs from an endemic area of CVL, as well as from healthy (n = 18) dogs, in addition to the sera of dogs (n = 81) infected with other pathogens. The DPP (R) and the in-house ELISA showed a sensitivity of 90.6% and 94.1%, respectively, and specificity of 95.1% and 97.5%, respectively, and both presented cross-reactivity only with the sera of dogs with babesiosis, 44% for the DPP (R) and 22% for the in-house ELISA. The clinical groups were detected equally by the two assays. The ELISA BioManguinhos, IFA BioManguinhos, and in house-IFA showed a good sensitivity, 90.6%, 96.5% and 89.4%, respectively, but very low specificity, 77.8%, 69.1% and 65.8%, respectively, due to the high cross-reactivity with the sera from the animals harboring other pathogens. The in-house ELISA provided the highest accuracy (95.8%), followed by the DPP (R) (92.7%), ELISA BioManguinhos (84.3%), IFA BioManguinhos (83.1%), and in-house IFA (78.0%). The simultaneous use of the DPP (R) and ELISA BioManguinhos reached a sensitivity of 99.1% and 82.1% when used sequentially. In conclusion, the DPP (R) performed well as serological test for CVL, and detected both asymptomatic and symptomatic dogs in equal proportions. Although its sensitivity is not ideal yet, discarding the IFA and including the DPP (R) improved the accuracy of the new Brazilian CVL diagnostic protocol, particularly of detecting truly infected dogs. Moreover, considering the higher specificity of DPP (R) (95.1% vs 77.8%), positive predictive value (95.1% vs 81.1%) and positive likelihood value (18.3% vs 4.1%) in comparison with the ELISA BioManguinhos, the use of DPP (R) as a confirmatory test instead of a screening test is suggested. (C) 2014 Elsevier B.V. All rights reserved.
机译:我们调查了DPP(R)犬内脏利什曼病(CVL)快速测试的性能,该快速测试是由BioManguinhos(巴西)启动的一种新型免疫色谱分析方法,该方法最近被纳入了在血清学调查中筛选CVL的新巴西规程中。本研究将DPP(R)与BioManguinhos(巴西)生产的ELISA和IFA进行了比较,将L.major-like抗原与使用Leishmania infantum chagasi进行的内部测试(内部ELISA和内部IFA)进行了比较。我们分析了CVL流行地区的临床症状(n = 47)和无症状(n = 38)感染犬的血清以及健康(n = 18)犬的血清,此外还分析了它们的血清(n = 81)感染了其他病原体。 DPP(R)和内部ELISA分别显示出90.6%和94.1%的灵敏度,以及95.1%和97.5%的特异性,并且都仅与狗贝贝病患者的血清具有交叉反应性,44 DPP(R)为%,内部ELISA为22%。通过两种测定法平等地检测了临床组。 ELISA BioManguinhos,IFA BioManguinhos和内部-IFA分别显示出良好的灵敏度,分别为90.6%,96.5%和89.4%,但是由于交叉反应高度高,特异性非常低,分别为77.8%,69.1%和65.8%。与携带其他病原体的动物的血清发生反应。内部ELISA的准确性最高(95.8%),其次是DPP(R)(92.7%),ELISA BioManguinhos(84.3%),IFA BioManguinhos(83.1%)和内部IFA(78.0%)。当顺序使用DPP(R)和ELISA BioManguinhos时,其灵敏度达到99.1%和82.1%。总之,DPP(R)在CVL的血清学测试中表现良好,并以相同比例检测了无症状和有症状的狗。尽管灵敏度还不理想,但丢弃IFA并包括DPP(R)可以提高新的巴西CVL诊断规程的准确性,尤其是检测真正感染的狗时。此外,与ELISA BioManguinhos相比,考虑到DPP(R)的更高特异性(95.1%vs 77.8%),阳性预测值(95.1%vs 81.1%)和阳性似然值(18.3%vs 4.1%),建议使用DPP(R)作为确认测试而不是筛选测试。 (C)2014 Elsevier B.V.保留所有权利。

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