首页> 美国卫生研究院文献>other >A no film slot blot for the detection of developing P. falciparum oocysts in mosquitoes
【2h】

A no film slot blot for the detection of developing P. falciparum oocysts in mosquitoes

机译:没有膜缝隙的污点用于检测蚊子中正在发育的恶性疟原虫卵囊

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Non-microscopy-based assays for sensitive and rapid detection of Plasmodium infection in mosquitoes are needed to allow rapid and high throughput measurement of transmission intensity and malaria control program effectiveness. Here, we report on a modified enhanced chemiluminescence-based slot blot assay for detection of Plasmodium falciparum (Pf) circumsporozite protein (PfCSP) expressed on parasite oocysts developing inside the mosquito midgut. This modified assay has several novel features that include eliminating the need for exposure to autoradiography (AR) film, as well as utilizing a novel high affinity anti-CSP antibody, and optimizing assay procedures resulting in significant reduction in the time required to perform the assay. The chemiluminescent signal for the detection of PfCSP in mosquito samples was captured digitally utilizing the C-Digit blot scanner that, allowed the detection of 0.01 pg of recombinant P. falciparum CSP and as few as 0.02 P. falciparum oocysts in a little over two hours. The earlier ECL-SB detected rCSP and oocysts and took approximately 5 h to perform. Whole mosquito lysates from both high and low prevalence—infected mosquito populations were prepared and evaluated for PfCSP detection on the ECL-SB by both AR film and digital data capture and analysis. There was a 100% agreement between the AR film and the C-Digit scanner methods for PfCSP detection in randomly sampled mosquitoes. This novel “No Film” Slot Blot assay obviates the need for AR film exposure and development and significantly reduces the assay time enabling widespread use in field settings.
机译:需要基于非显微镜的检测方法来灵敏和快速检测蚊子中的疟原虫感染,以快速,高通量地测量传播强度和疟疾控制程序的有效性。在这里,我们报告有关改进的基于化学发光的缝隙印迹测定法,用于检测在蚊子中肠内部发育的寄生虫卵囊上表达的恶性疟原虫(Pf)环子孢子蛋白(PfCSP)。这种改进的测定具有几个新颖的功能,包括消除了对放射自显影(AR)胶片的暴露需求,以及利用新型的高亲和力抗CSP抗体,以及优化了测定程序,从而显着减少了执行测定所需的时间。使用C-Digit印迹扫描仪以数字方式捕获用于检测蚊子样品中PfCSP的化学发光信号,该扫描仪可以在两个多小时的时间内检测到0.01 pg重组恶性疟原虫CSP和少至0.02恶性疟原虫卵囊。早期的ECL-SB检测到了rCSP和卵囊,大约需要5个小时才能执行。制备了高流行和低流行两种蚊子的完整蚊子裂解物,并通过AR胶片和数字数据捕获与分析评估了ECL-SB上的PfCSP检测。在随机采样的蚊子中,AR胶片和C-Digit扫描仪方法之间用于PfCSP检测的一致性达到100%。这种新颖的“无胶卷”狭缝印迹测定法消除了对AR胶卷曝光和显影的需要,并显着减少了测定时间,可在野外环境中广泛使用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号