Geislinger Thomas M, Chan Sherwin, Moll Kirsten, Wixforth Achim, Wahlgren Mats, Franke Thomas
Experimental Physics I, University of Augsburg, 86159 Augsburg, Germany.
Malar J. 2014 Sep 20;13:375. doi: 10.1186/1475-2875-13-375.
Understanding of malaria pathogenesis caused by Plasmodium falciparum has been greatly deepened since the introduction of in vitro culture system, but the lack of a method to enrich ring-stage parasites remains a technical challenge. Here, a novel way to enrich red blood cells containing parasites in the early ring stage is described and demonstrated.
A simple, straight polydimethylsiloxane microchannel connected to two syringe pumps for sample injection and two height reservoirs for sample collection is used to enrich red blood cells containing parasites in the early ring stage (8-10 h p.i.). The separation is based on the non-inertial hydrodynamic lift effect, a repulsive cell-wall interaction that enables continuous and label-free separation with deformability as intrinsic marker.
The possibility to enrich red blood cells containing P. falciparum parasites at ring stage with a throughput of ~12,000 cells per hour and an average enrichment factor of 4.3 ± 0.5 is demonstrated.
The method allows for the enrichment of red blood cells early after the invasion by P. falciparum parasites continuously and without any need to label the cells. The approach promises new possibilities to increase the sensitivity of downstream analyses like genomic- or diagnostic tests. The device can be produced as a cheap, disposable chip with mass production technologies and works without expensive peripheral equipment. This makes the approach interesting for the development of new devices for field use in resource poor settings and environments, e.g. with the aim to increase the sensitivity of microscope malaria diagnosis.
自从引入体外培养系统以来,对恶性疟原虫引起的疟疾发病机制的理解有了极大的深化,但缺乏一种富集环状体阶段寄生虫的方法仍然是一项技术挑战。在此,描述并展示了一种富集处于早期环状体阶段的含寄生虫红细胞的新方法。
使用一个简单的直型聚二甲基硅氧烷微通道,该微通道连接到两个用于样品注射的注射泵和两个用于样品收集的高位储液器,以富集处于早期环状体阶段(感染后8 - 10小时)的含寄生虫红细胞。分离基于非惯性流体动力升力效应,这是一种排斥性的细胞壁相互作用,能够以可变形性作为内在标记进行连续且无需标记的分离。
证明了有可能以每小时约12,000个细胞的通量和4.3 ± 0.5的平均富集倍数富集处于环状体阶段的恶性疟原虫寄生虫感染的红细胞。
该方法能够在恶性疟原虫寄生虫入侵后早期连续富集含寄生虫红细胞,且无需对细胞进行任何标记。该方法有望为提高基因组分析或诊断测试等下游分析的灵敏度带来新的可能性。该装置可以采用大规模生产技术制成廉价的一次性芯片,并且无需昂贵的外围设备即可工作。这使得该方法对于在资源匮乏的环境中开发用于现场使用的新设备很有吸引力,例如旨在提高显微镜疟疾诊断的灵敏度。