Programa de Pós-Graduação em Parasitologia, Departamento de Parasitologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Section on Immunobiology, Joslin Diabetes Center, Harvard Medical School, Boston, MA, United States of America.
PLoS One. 2018 Nov 29;13(11):e0208133. doi: 10.1371/journal.pone.0208133. eCollection 2018.
Despite the improvements in diagnostic tools for detection of Trypanosoma cruzi in human blood samples, the isolation of parasite from bloodstream in the chronic phase of Chagas disease is challenging. Thus, there is an increasing interest in the development of strategies that allow an accurate monitoring of the parasite load in bloodstream of Chagas disease patients. Given that, the comparison of a classical diagnostic method such as blood culture and multiplex quantitative real-time PCR (qPCR) was few explored so far. Therefore, this study aimed to compare the detection and quantification of T. cruzi load in the circulating blood of patients with chronic Chagas disease, using blood culture and qPCR techniques.
METHODS⁄PRINCIPAL FINDINGS: The multiplex real-time quantitative PCR assay (qPCR) based on TaqMan technology was evaluated in 135 blood samples from 91 patients with chronic Chagas disease presenting indeterminate (asymptomatic, n = 23) and cardiac (chronic cardiomyopathy, n = 68) forms, in comparison with the classical blood culture (BC) technique. The total positivity of qPCR and BC was 58.5% and 49.6%, respectively. The median parasite load of all positive patients was 1.18 [0.39-4.23] par. eq.⁄mL, ranging from 0.01 to 116.10 par. eq.⁄mL. We did not find significant differences between T. cruzi load with age and distinct clinical manifestations of patients.
CONCLUSIONS/SIGNIFICANCE: Our data suggest that qPCR can be an auxiliary tool for studies that require T. cruzi isolation from the bloodstream of patients with chronic Chagas disease, after the establishment of a parasite load cut-off that guarantees a relative success rate of parasite isolation using BC technique.
尽管在检测人体血液样本中的克氏锥虫的诊断工具方面有所改进,但在恰加斯病的慢性期从血流中分离寄生虫仍然具有挑战性。因此,人们越来越感兴趣开发能够准确监测恰加斯病患者血流中寄生虫负荷的策略。鉴于此,迄今为止,对诸如血液培养和多重实时定量 PCR(qPCR)等经典诊断方法的比较研究很少。因此,本研究旨在比较血液培养和 qPCR 技术检测和定量慢性恰加斯病患者循环血液中克氏锥虫负荷的方法。
方法/主要发现:基于 TaqMan 技术的多重实时定量 PCR 检测方法(qPCR)在 91 例慢性恰加斯病患者的 135 份血液样本中进行了评估,这些患者表现为不确定(无症状,n=23)和心脏(慢性心肌病,n=68)形式,与经典的血液培养(BC)技术进行比较。qPCR 和 BC 的总阳性率分别为 58.5%和 49.6%。所有阳性患者的寄生虫负荷中位数为 1.18[0.39-4.23]par. eq./mL,范围为 0.01-116.10 par. eq./mL。我们没有发现 T. cruzi 负荷与患者年龄和不同临床表现之间存在显著差异。
结论/意义:我们的数据表明,qPCR 可以作为辅助工具,用于在建立寄生虫负荷截止值后,从慢性恰加斯病患者的血流中分离寄生虫的研究,该截止值可保证使用 BC 技术分离寄生虫的相对成功率。