Departament of Microbiology, School of Medicine, University of Buenos Aires, Buenos Aires, Argentina.
Institute of Research on Microbiology and Medical Parasitology (IMPaM, UBA-CONICET), University of Buenos Aires, Buenos Aires, Argentina.
PLoS Negl Trop Dis. 2020 Nov 30;14(11):e0008890. doi: 10.1371/journal.pntd.0008890. eCollection 2020 Nov.
Extracellular RNAs (ex-RNAs) are secreted by cells through different means that may involve association with proteins, lipoproteins or extracellular vesicles (EV). In the context of parasitism, ex-RNAs represent new and exciting communication intermediaries with promising potential as novel biomarkers. In the last years, it was shown that helminth parasites secrete ex-RNAs, however, most work mainly focused on RNA secretion mediated by EV. Ex-RNA study is of special interest in those helminth infections that still lack biomarkers for early and/or follow-up diagnosis, such as echinococcosis, a neglected zoonotic disease caused by cestodes of the genus Echinococcus. In this work, we have characterised the ex-RNA profile secreted by in vitro grown metacestodes of Echinococcus multilocularis, the casuative agent of alveolar echinococcosis. We have used high throughput RNA-sequencing together with RT-qPCR to characterise the ex-RNA profile secreted towards the extra- and intra-parasite milieus in EV-enriched and EV-depleted fractions. We show that a polarized secretion of small RNAs takes place, with microRNAs mainly secreted to the extra-parasite milieu and rRNA- and tRNA-derived sequences mostly secreted to the intra-parasite milieu. In addition, we show by nanoparticle tracking analyses that viable metacestodes secrete EV mainly into the metacestode inner vesicular fluid (MVF); however, the number of nanoparticles in culture medium and MVF increases > 10-fold when metacestodes show signs of tegument impairment. Interestingly, we confirm the presence of host miRNAs in the intra-parasite milieu, implying their internalization and transport through the tegument towards the MVF. Finally, our assessment of the detection of Echinococcus miRNAs in patient samples by RT-qPCR yielded negative results suggesting the tested miRNAs may not be good biomarkers for this disease. A comprehensive study of the secretion mechanisms throughout the life cycle of these parasites will help to understand parasite interaction with the host and also, improve current diagnostic tools.
细胞通过不同的方式分泌细胞外 RNA(ex-RNA),这些方式可能涉及与蛋白质、脂蛋白或细胞外囊泡(EV)的结合。在寄生虫的背景下,ex-RNA 代表了新的令人兴奋的交流中介体,具有作为新型生物标志物的潜在前景。在过去的几年中,已经表明寄生虫会分泌 ex-RNA,但大多数工作主要集中在 EV 介导的 RNA 分泌上。ex-RNA 研究对于那些仍然缺乏早期和/或后续诊断生物标志物的寄生虫感染特别感兴趣,例如包虫病,这是一种由细粒棘球绦虫属的绦虫引起的被忽视的人畜共患疾病。在这项工作中,我们对体外培养的多房棘球蚴(导致泡型包虫病的病原体)的外泌体分泌的 ex-RNA 谱进行了表征。我们使用高通量 RNA 测序和 RT-qPCR 来描述 EV 富集和 EV 耗尽部分中向寄生虫内外环境分泌的 ex-RNA 谱。我们表明,小 RNA 发生了极化分泌,其中 miRNA 主要分泌到寄生虫外环境,rRNA 和 tRNA 衍生序列主要分泌到寄生虫内环境。此外,我们通过纳米颗粒跟踪分析表明,有活力的棘球蚴主要将 EV 分泌到棘球蚴内部囊泡液(MVF)中;然而,当棘球蚴出现外被损伤迹象时,培养物中的纳米颗粒数量和 MVF 增加了 10 倍以上。有趣的是,我们在寄生虫内环境中证实了宿主 miRNA 的存在,这意味着它们通过外被向内转运到 MVF。最后,我们通过 RT-qPCR 对患者样本中包虫 miRNA 的检测评估结果为阴性,这表明所测试的 miRNA 可能不是该疾病的良好生物标志物。对这些寄生虫整个生命周期中分泌机制的全面研究将有助于了解寄生虫与宿主的相互作用,并改进当前的诊断工具。