Laboratorio de Biología Molecular de la Enfermedad de Chagas, Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr Héctor Torres", INGEBI-CONICET, Buenos Aires, Argentina.
Barcelona Institute for Global Health (ISGlobal), Hospital Clinic-University of Barcelona, Barcelona, Spain.
PLoS Negl Trop Dis. 2023 Apr 14;17(4):e0011290. doi: 10.1371/journal.pntd.0011290. eCollection 2023 Apr.
Chagas disease or American trypanosomiasis, a neglected tropical disease, is a persistent Public Health problem in Latin America and other, non-endemic, countries. Point-of-care (POC) sensitive methods are still needed to improve and extend early diagnosis in acute infections such as congenital Chagas disease. The objective of this study was to analytically evaluate in the lab the performance of a qualitative POC molecular test (Loop-mediated isothermal amplification (LAMP), Eiken, Japan) for rapid diagnosis of congenital Chagas disease employing FTA cards or Whatman 903 filter paper as solid supports for small-scale volumes of human blood.
METHODOLOGY/PRINCIPAL FINDINGS: We used human blood samples artificially infected with cultured T. cruzi strains to assess the analytical performance of the test in comparison with liquid blood anticoagulated with heparin. The DNA extraction process was evaluated using the ultrarapid purification system PURE manufactured by Eiken Chemical Company (Tokio, Japan) over artificially infected liquid blood or different amounts of dried blood spot (DBS) 3- and 6-mm pieces of FTA and Whatman 903 paper. LAMP was performed on a AccuBlock (LabNet, USA) heater or in the Loopamp LF-160 incubator (Eiken, Japan), and visualization of results was either done at naked eye, using the LF-160 device or P51 Molecular Fluorescence Viewer (minipcr bio, USA). Best conditions tested showed a limit of detection (LoD) with 95% accuracy (19/20 replicates) of 5 and 20 parasites/mL, respectively for heparinized fluid blood or DBS samples. FTA cards showed better specificity than Whatman 903 filter paper.
CONCLUSIONS/SIGNIFICANCE: Procedures to operate LAMP reactions from small volumes of fluid blood or DBS in FTA were standardized for LAMP detection of T. cruzi DNA. Our results encourage prospective studies in neonates born to seropositive women or oral Chagas disease outbreaks to operationally evaluate the method in the field.
恰加斯病或美洲锥虫病是一种被忽视的热带病,它仍是拉丁美洲和其他非流行国家的一个持续存在的公共卫生问题。在急性感染(如先天性恰加斯病)中,仍需要即时检测(POC)敏感方法来改善和扩大早期诊断。本研究的目的是在实验室中分析评估一种定性 POC 分子检测(环介导等温扩增(LAMP),Eiken,日本)在使用 FTA 卡或 Whatman 903 滤纸作为小体积人类血液的固体支持物的情况下,对先天性恰加斯病的快速诊断的性能。
方法/主要发现:我们使用人工感染培养的 T. cruzi 株的人类血液样本来评估该检测与肝素抗凝的液态血液相比的分析性能。使用 Eiken Chemical Company(东京,日本)生产的 ultrarapid 纯化系统 PURE 评估 DNA 提取过程,该系统用于人工感染的液态血液或不同量的干血斑(DBS)3-和 6-mm 大小的 FTA 和 Whatman 903 滤纸。LAMP 在 AccuBlock(LabNet,美国)加热器上或在 Loopamp LF-160 孵育器(Eiken,日本)上进行,结果通过肉眼观察、使用 LF-160 设备或 P51 Molecular Fluorescence Viewer(minipcr bio,美国)进行可视化。最佳测试条件显示,肝素化液态血液或 DBS 样本的检测下限(LoD)分别为 95%准确率(20 个重复中有 19 个)5 和 20 个寄生虫/mL。FTA 卡比 Whatman 903 滤纸具有更好的特异性。
结论/意义:从小体积的液态血液或 FTA 的 DBS 中操作 LAMP 反应的程序已标准化,用于 LAMP 检测 T. cruzi DNA。我们的结果鼓励对血清阳性妇女所生新生儿或口服恰加斯病爆发进行前瞻性研究,以在现场操作评估该方法。