Lagatie Ole, Batsa Debrah Linda, Debrah Alex, Stuyver Lieven J
Janssen Diagnostics, Janssen R&D, Turnhoutseweg 30, 2340, Beerse, Belgium.
Kumasi Centre for Collaborative Research, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
Parasitol Res. 2017 Mar;116(3):1013-1022. doi: 10.1007/s00436-017-5382-5. Epub 2017 Jan 22.
River blindness, caused by infection with the filarial nematode Onchocerca volvulus, is a neglected tropical disease affecting millions of people. There is a clear need for diagnostic tools capable of identifying infected patients, but that can also be used for monitoring disease progression and treatment efficacy. Plasma-derived parasitic microRNAs have been suggested as potential candidates for such diagnostic tools. We have investigated whether these parasitic microRNAs are present in sufficient quantity in plasma of Onchocerca-infected patients to be used as a diagnostic biomarker for detection of O. volvulus infection or treatment monitoring. Plasma samples were collected from different sources (23 nodule-positive individuals and 20 microfilaridermic individuals), microRNAs (miRNAs) were extracted using Qiagen miRNeasy kit, and a set of 17 parasitic miRNAs was evaluated on these miRNA extracts using miRCURY Locked Nucleic Acid (LNA) Universal RT microRNA PCR system. Of the 17 miRNAs evaluated, only 7 miRNAs were found to show detectable signal in a number of samples: bma-miR-236-1, bma-miR-71, ov-miR71-22nt, ov-miR-71-23nt, ov-miR-100d, ov-bantam-a, and ov-miR-87-3p. Subsequent melting curve analysis, however, indicated that the signals observed for ov-miR-71 variants and ov-miR-87-3p are non-specific. The other miRNAs only showed positive signal in one or few samples with Cq values just below the cutoff. Our data indicate that parasitic miRNAs are not present in circulation at a sufficiently high level to be used as biomarker for O. volvulus infection or treatment monitoring using LNA-based RT-qPCR analysis.
河盲症由丝状线虫盘尾丝虫感染引起,是一种被忽视的热带疾病,影响着数百万人。显然需要能够识别感染患者的诊断工具,而且该工具还可用于监测疾病进展和治疗效果。血浆来源的寄生性微小RNA已被认为是此类诊断工具的潜在候选物。我们研究了这些寄生性微小RNA在盘尾丝虫感染患者血浆中的含量是否足以用作检测盘尾丝虫感染或监测治疗的诊断生物标志物。从不同来源采集血浆样本(23名结节阳性个体和20名微丝蚴血症个体),使用Qiagen miRNeasy试剂盒提取微小RNA(miRNA),并使用miRCURY锁定核酸(LNA)通用RT微小RNA PCR系统对这些miRNA提取物评估一组17种寄生性miRNA。在评估的17种miRNA中,仅发现7种miRNA在一些样本中显示出可检测信号:bma-miR-236-1、bma-miR-71、ov-miR71-22nt、ov-miR-71-23nt、ov-miR-100d、ov-bantam-a和ov-miR-87-3p。然而,随后的熔解曲线分析表明,观察到的ov-miR-71变体和ov-miR-87-3p的信号是非特异性的。其他miRNA仅在一个或几个样本中显示阳性信号,其Cq值略低于临界值。我们的数据表明,寄生性miRNA在循环中的水平不够高,无法用作基于LNA的RT-qPCR分析检测盘尾丝虫感染或监测治疗的生物标志物。