Department of Molecular Biosciences, College of Natural Sciences, The University of Texas at Austin, Austin, United States of America.
Freshman Research Initiative, College of Natural Sciences, The University of Texas at Austin, Austin, United States of America.
PLoS Negl Trop Dis. 2018 Aug 30;12(8):e0006671. doi: 10.1371/journal.pntd.0006671. eCollection 2018 Aug.
Manipulation of natural mosquito populations using the endosymbiotic bacteria Wolbachia is being investigated as a novel strategy to reduce the burden of mosquito-borne viruses. To evaluate the efficacy of these interventions, it will be critical to determine Wolbachia infection frequencies in Aedes aegypti mosquito populations. However, current diagnostic tools are not well-suited to fit this need. Morphological methods cannot identify Wolbachia, immunoassays often suffer from low sensitivity and poor throughput, while PCR and spectroscopy require complex instruments and technical expertise, which restrict their use to centralized laboratories. To address this unmet need, we have used loop-mediated isothermal amplification (LAMP) and oligonucleotide strand displacement (OSD) probes to create a one-pot sample-to-answer nucleic acid diagnostic platform for vector and symbiont surveillance. LAMP-OSD assays can directly amplify target nucleic acids from macerated mosquitoes without requiring nucleic acid purification and yield specific single endpoint yes/no fluorescence signals that are observable to eye or by cellphone camera. We demonstrate cellphone-imaged LAMP-OSD tests for two targets, the Aedes aegypti cytochrome oxidase I (coi) gene and the Wolbachia surface protein (wsp) gene, and show a limit of detection of 4 and 40 target DNA copies, respectively. In a blinded test of 90 field-caught mosquitoes, the coi LAMP-OSD assay demonstrated 98% specificity and 97% sensitivity in identifying Ae. aegypti mosquitoes even after 3 weeks of storage without desiccant at 37°C. Similarly, the wsp LAMP-OSD assay readily identified the wAlbB Wolbachia strain in field-collected Aedes albopictus mosquitoes without generating any false positive signals. Modest technology requirements, minimal execution steps, simple binary readout, and robust accuracy make the LAMP-OSD-to-cellphone assay platform well suited for field vector surveillance in austere or resource-limited conditions.
利用共生细菌沃尔巴克氏体(Wolbachia)来操纵自然蚊群,正被作为一种降低蚊媒病毒负担的新策略进行研究。为了评估这些干预措施的效果,确定埃及伊蚊种群中沃尔巴克氏体的感染频率将是至关重要的。然而,目前的诊断工具并不完全适用。形态学方法无法识别沃尔巴克氏体,免疫测定法通常灵敏度低、通量差,而聚合酶链反应(PCR)和光谱法需要复杂的仪器和技术专业知识,这限制了它们在集中实验室中的使用。为了满足这一未满足的需求,我们使用环介导等温扩增(LAMP)和寡核苷酸链置换(OSD)探针,创建了一种用于媒介和共生生物监测的即插即用的样本到答案核酸诊断平台。LAMP-OSD 检测可直接从捣碎的蚊子中扩增目标核酸,而无需核酸纯化,并产生可通过肉眼或手机摄像头观察到的特异性单终点是/否荧光信号。我们展示了针对两个靶标的手机成像 LAMP-OSD 测试,即埃及伊蚊细胞色素氧化酶 I(coi)基因和沃尔巴克氏体表面蛋白(wsp)基因,检测限分别为 4 和 40 个目标 DNA 拷贝。在对 90 只现场捕获的蚊子进行的盲测中,coi LAMP-OSD 检测在 37°C 下没有干燥剂储存 3 周后,对埃及伊蚊的鉴定具有 98%的特异性和 97%的敏感性。同样,wsp LAMP-OSD 检测也能轻易识别野外采集的白纹伊蚊携带的 wAlbB 沃尔巴克氏体菌株,而不会产生任何假阳性信号。该 LAMP-OSD-手机检测平台要求适度的技术,执行步骤最少,简单的二进制读数,以及稳健的准确性,非常适合在资源匮乏或条件简陋的情况下进行野外媒介监测。