Departamento de Clínica, Cirurgia e Reprodução Animal, Faculdade de Odontologia de Araçatuba, Curso de Medicina Veterinária, Universidade Estadual Paulista, Rua Clóvis Pestana, 793, Jardim Dona Amélia, 16050-680 - Araçatuba, SP, Brazil.
Vet Parasitol. 2010 Oct 29;173(3-4):330-3. doi: 10.1016/j.vetpar.2010.07.012. Epub 2010 Aug 6.
In this study, an enzyme-linked immunosorbent assay using crude total antigen (CTA-ELISA) and immunochromatography with antigen rK39 were compared in the diagnosis of canine visceral leishmaniasis (CVL). Fifty-two total blood samples from symptomatic dogs obtained from a location endemic for leishmaniasis and 52 blood samples from healthy dogs from a nonendemic region were tested. Polymerase chain reaction (PCR) was used to detect DNA from Leishmania spp. in both groups. Symptomatic dogs with positive PCR were considered infected by Leishmania spp. and the PCR technique was chosen as a gold standard test. The sensitivity determined for CTA-ELISA was 100%, with specificity of 91.2%, while the immunochromatographic assay with the antigen rK39 showed sensitivity of 91.5%, with specificity of 94.7%. A strong correlation was verified between CTA-ELISA and immunochromatography with antigen rK39, with a kappa coefficient of agreement of 0.88. Analysis of the results suggested that both assays presented good sensitivity and specificity for diagnosing CVL; however, immunochromatography with the antigen rK39 may be more advantageous when a fast field test is required.
本研究比较了应用粗制全抗原的酶联免疫吸附试验(CTA-ELISA)和免疫胶体金渗滤法(rK39 抗原)诊断犬内脏利什曼病(CVL)的效果。检测了 52 份来自利什曼病流行地区的有症状犬的全血样本和 52 份来自非流行地区的健康犬的全血样本。采用聚合酶链反应(PCR)检测两组样本中的利什曼原虫 DNA。PCR 阳性的有症状犬被认为感染了利什曼原虫,将 PCR 技术作为金标准检测。CTA-ELISA 的敏感性为 100%,特异性为 91.2%,而 rK39 抗原免疫胶体金检测的敏感性为 91.5%,特异性为 94.7%。CTA-ELISA 和 rK39 抗原免疫胶体金检测之间的相关性较强,一致性 κ 系数为 0.88。结果分析表明,两种检测方法均具有良好的敏感性和特异性,可用于诊断 CVL;然而,当需要快速现场检测时,rK39 抗原免疫胶体金检测可能更具优势。