Advanced Public Health Laboratory, Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Salvador, Brazil.
Interdisciplinary Research Group in Biotechnology and Epidemiology of Infectious Diseases (GRUPIBE), Gonçalo Moniz Institute, Oswaldo Cruz Foundation (FIOCRUZ-BA), Salvador, Brazil.
Parasit Vectors. 2024 Jul 15;17(1):305. doi: 10.1186/s13071-024-06376-5.
Chagas disease (CD), a neglected parasitic disease caused by Trypanosoma cruzi, poses a significant health threat in Latin America and has emerged globally because of human migration. Trypanosoma cruzi infects humans and over 100 other mammalian species, including dogs, which are important sentinels for assessing the risk of human infection. Nonetheless, the serodiagnosis of T. cruzi in dogs is still impaired by the absence of commercial tests. In this study, we investigated the diagnostic accuracy of four chimeric recombinant T. cruzi IBMP antigens (IBMP-8.1, IBMP-8.2, IBMP-8.3, and IBMP-8.4) for detecting anti-T. cruzi antibodies in dogs, using latent class analysis (LCA).
We examined 663 canine serum samples, employing indirect ELISA with the chimeric antigens. LCA was utilized to establish a latent variable as a gold standard for T. cruzi infection, revealing distinct response patterns for each antigen.
The IBMP (Portuguese acronym for the Molecular Biology Institute of Paraná) antigens achieved area under the ROC curve (AUC) values ranging from 90.9% to 97.3%. The highest sensitivity was attributed to IBMP-8.2 (89.8%), while IBMP-8.1, IBMP-8.3, and IBMP-8.4 achieved 73.5%, 79.6%, and 85.7%, respectively. The highest specificity was observed for IBMP-8.4 (98.6%), followed by IBMP-8.2, IBMP-8.3, and IBMP-8.1 with specificities of 98.3%, 94.4%, and 92.7%, respectively. Predictive values varied according to prevalence, indicating higher effectiveness in endemic settings.
Our findings underscore the remarkable diagnostic performance of IBMP-8.2 and IBMP-8.4 for the serodiagnosis of Trypanosoma cruzi in dogs, representing a promising tool for the diagnosis of CD in dogs. These chimeric recombinant antigens may not only enhance CD surveillance strategies but also hold broader implications for public health, contributing to the global fight against this neglected tropical disease.
恰加斯病(CD)是一种由克氏锥虫引起的被忽视的寄生虫病,在拉丁美洲对人类健康构成重大威胁,并因人类迁移而在全球范围内出现。克氏锥虫感染人类和 100 多种其他哺乳动物,包括狗,狗是评估人类感染风险的重要哨兵。尽管如此,由于缺乏商业检测,狗的克氏锥虫血清学诊断仍然受到影响。在这项研究中,我们使用潜在类别分析(LCA)研究了四种嵌合重组克氏锥虫 IBMP 抗原(IBMP-8.1、IBMP-8.2、IBMP-8.3 和 IBMP-8.4)检测狗体内抗克氏锥虫抗体的诊断准确性。
我们使用嵌合抗原进行间接 ELISA 检测了 663 份犬血清样本。LCA 用于建立克氏锥虫感染的潜在变量作为金标准,揭示了每种抗原的不同反应模式。
IBMP 抗原获得了 90.9%至 97.3%的 ROC 曲线下面积(AUC)值。IBMP-8.2 的灵敏度最高(89.8%),而 IBMP-8.1、IBMP-8.3 和 IBMP-8.4 的灵敏度分别为 73.5%、79.6%和 85.7%。IBMP-8.4 的特异性最高(98.6%),其次是 IBMP-8.2(98.3%)、IBMP-8.3(94.4%)和 IBMP-8.1(92.7%)。预测值根据流行率而变化,表明在流行地区更有效。
我们的研究结果强调了 IBMP-8.2 和 IBMP-8.4 在犬克氏锥虫血清学诊断中的出色诊断性能,为犬克氏锥虫病的诊断提供了一种有前途的工具。这些嵌合重组抗原不仅可以增强克氏锥虫病监测策略,还可以为公共卫生带来更广泛的影响,为全球抗击这种被忽视的热带病做出贡献。