Alessio Glaucia Diniz, de Araújo Fernanda Fortes, Côrtes Denise Fonseca, Sales Júnior Policarpo Ademar, Lima Daniela Cristina, Gomes Matheus de Souza, do Amaral Laurence Rodrigues, Xavier Marcelo Antônio Pascoal, Teixeira-Carvalho Andréa, Martins-Filho Olindo Assis, de Lana Marta
Laboratório de Doença de Chagas, Núcleo de Pesquisas em Ciências Biológicas (NUPEB), Instituto de Ciências Exatas e Biológicas (ICEB), Universidade Federal de Ouro Preto (UFOP), Ouro Preto, Minas Gerais, Brazil.
Grupo Integrado de Pesquisas em Biomarcadores, Centro de Pesquisas René Rachou (CPqRR-FIOCRUZ/ MG), Belo Horizonte, Minas Gerais, Brazil.
PLoS Negl Trop Dis. 2017 Mar 23;11(3):e0005444. doi: 10.1371/journal.pntd.0005444. eCollection 2017 Mar.
Distinct Trypanosoma cruzi genotypes have been considered relevant for patient management and therapeutic response of Chagas disease. However, typing strategies for genotype-specific serodiagnosis of Chagas disease are still unavailable and requires standardization for practical application. In this study, an innovative TcI/TcVI/TcII Chagas Flow ATE-IgG2a technique was developed with applicability for universal and genotype-specific diagnosis of T. cruzi infection. For this purpose, the reactivity of serum samples (percentage of positive fluorescent parasites-PPFP) obtained from mice chronically infected with TcI/Colombiana, TcVI/CL or TcII/Y strain as well as non-infected controls were determined using amastigote-AMA, trypomastigote-TRYPO and epimastigote-EPI in parallel batches of TcI, TcVI and TcII target antigens. Data demonstrated that "α-TcII-TRYPO/1:500, cut-off/PPFP = 20%" presented an excellent performance for universal diagnosis of T. cruzi infection (AUC = 1.0, Se and Sp = 100%). The combined set of attributes "α-TcI-TRYPO/1:4,000, cut-off/PPFP = 50%", "α-TcII-AMA/1:1,000, cut-off/PPFP = 40%" and "α-TcVI-EPI/1:1,000, cut-off/PPFP = 45%" showed good performance to segregate infections with TcI/Colombiana, TcVI/CL or TcII/Y strain. Overall, hosts infected with TcI/Colombiana and TcII/Y strains displayed opposite patterns of reactivity with "α-TcI TRYPO" and "α-TcII AMA". Hosts infected with TcVI/CL strain showed a typical interweaved distribution pattern. The method presented a good performance for genotype-specific diagnosis, with global accuracy of 69% when the population/prototype scenario include TcI, TcVI and TcII infections and 94% when comprise only TcI and TcII infections. This study also proposes a receiver operating reactivity panel, providing a feasible tool to classify serum samples from hosts infected with distinct T. cruzi genotypes, supporting the potential of this method for universal and genotype-specific diagnosis of T. cruzi infection.
不同的克氏锥虫基因型被认为与恰加斯病患者的管理和治疗反应相关。然而,用于恰加斯病基因型特异性血清学诊断的分型策略仍然不可用,并且需要标准化以便实际应用。在本研究中,开发了一种创新的TcI/TcVI/TcII恰加斯流式ATE-IgG2a技术,适用于克氏锥虫感染的通用和基因型特异性诊断。为此,使用无鞭毛体-AMA、锥鞭毛体-TRYPO和上鞭毛体-EPI,在平行批次的TcI、TcVI和TcII靶抗原中,测定从慢性感染TcI/哥伦比亚株、TcVI/CL株或TcII/Y株的小鼠以及未感染对照中获得的血清样本的反应性(阳性荧光寄生虫百分比-PPFP)。数据表明,“α-TcII-TRYPO/1:500,临界值/PPFP = 20%”在克氏锥虫感染的通用诊断中表现出色(AUC = 1.0,敏感性和特异性 = 100%)。“α-TcI-TRYPO/1:4,000,临界值/PPFP = 50%”、“α-TcII-AMA/1:1,000,临界值/PPFP = 40%”和“α-TcVI-EPI/1:1,000,临界值/PPFP = 45%”的组合属性集在区分感染TcI/哥伦比亚株、TcVI/CL株或TcII/Y株方面表现良好。总体而言,感染TcI/哥伦比亚株和TcII/Y株的宿主与“α-TcI TRYPO”和“α-TcII AMA”表现出相反的反应模式。感染TcVI/CL株的宿主表现出典型的交织分布模式。当人群/原型情况包括TcI、TcVI和TcII感染时,该方法在基因型特异性诊断中表现良好,总体准确率为69%;当仅包括TcI和TcII感染时,准确率为94%。本研究还提出了一个受体操作反应性面板,提供了一种可行的工具来对感染不同克氏锥虫基因型的宿主的血清样本进行分类,支持了该方法在克氏锥虫感染的通用和基因型特异性诊断中的潜力。