Department of Mechanical Engineering and Applied Mechanics, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
PLoS One. 2012;7(8):e42222. doi: 10.1371/journal.pone.0042222. Epub 2012 Aug 3.
Vector control is one of the most effective measures to prevent the transmission of malaria, a disease that causes over 600,000 deaths annually. Around 30-40 Anopheles mosquito species are natural vectors of malaria parasites. Some of these species cannot be morphologically distinguished, but have behavioral and ecological differences. Emblematic of this is the Anopheles gambiae species complex. The correct identification of vector species is fundamental to the development of control strategies and epidemiological studies of disease transmission.
METHODOLOGY/PRINCIPAL FINDINGS: An inexpensive, disposable, field-deployable, sample-to-answer, microfluidic chip was designed, constructed, and tested for rapid molecular identification of Anopheles gambiae and Anopheles arabiensis. The chip contains three isothermal amplification reactors. One test reactor operates with specific primers to amplify Anopheles gambiae DNA, another with specific primers for Anopheles arabiensis DNA, and the third serves as a negative control. A mosquito leg was crushed on an isolation membrane. Two discs, laden with mosquito tissue, were punched out of the membrane and inserted into the two test chambers. The isolated, disc-bound DNA served as a template in the amplification processes. The amplification products were detected with intercalating fluorescent dye that was excited with a blue light-emitting diode. The emitted light was observed by eye and recorded with a cell-phone camera. When the target consisted of Anopheles gambiae, the reactor containing primers specific to An. gambiae lit up while the other two reactors remained dark. When the target consisted of Anopheles arabiensis, the reactor containing primers specific to An. arabiensis lit up while the other two reactors remained dark.
CONCLUSIONS/SIGNIFICANCE: The microfluidic chip provides a means to identify mosquito type through molecular analysis. It is suitable for field work, allowing one to track the geographical distribution of mosquito populations and community structure alterations due to environmental changes and malaria intervention measures.
病媒控制是预防疟疾传播的最有效措施之一,疟疾每年导致超过 60 万人死亡。约有 30-40 种按蚊是疟原虫的天然媒介。其中一些种类无法通过形态学区分,但具有行为和生态上的差异。这方面的典型例子是冈比亚按蚊复合体。正确识别媒介物种是制定控制策略和进行疾病传播流行病学研究的基础。
方法/主要发现:本研究设计、构建并测试了一种廉价、一次性、可现场部署、样本到答案、微流控芯片,用于快速分子鉴定冈比亚按蚊和阿拉伯按蚊。该芯片包含三个等温扩增反应池。一个测试反应池使用特定的引物来扩增冈比亚按蚊 DNA,另一个使用特定的引物来扩增阿拉伯按蚊 DNA,第三个作为阴性对照。将蚊腿压在隔离膜上。从膜上冲出两个载有蚊组织的圆盘,并将其插入两个测试腔室中。隔离的、圆盘结合的 DNA 作为扩增过程中的模板。扩增产物用嵌入荧光染料检测,该染料用蓝色发光二极管激发。通过肉眼观察和用手机摄像头记录发射光。当目标是冈比亚按蚊时,含有针对 An.gambiae 的引物的反应池会亮起,而其他两个反应池保持黑暗。当目标是阿拉伯按蚊时,含有针对 An.arabiensis 的引物的反应池会亮起,而其他两个反应池保持黑暗。
结论/意义:微流控芯片提供了一种通过分子分析识别蚊子类型的方法。它适用于野外工作,可以跟踪蚊子种群的地理分布和由于环境变化和疟疾干预措施导致的群落结构变化。