首页> 外文期刊>BMC Veterinary Research >Development and evaluation of real-time loop-mediated isothermal amplification assay for rapid detection of cystic echinococcosis
【24h】

Development and evaluation of real-time loop-mediated isothermal amplification assay for rapid detection of cystic echinococcosis

机译:实时回路介导的等温扩增测定的开发与评价,用于快速检测囊性超声波功能

获取原文
           

摘要

Background Cystic echinococcosis (CE) or hydatidosis, caused by the larval stage of Echinococcus granulosus (EG)-complex, is a neglected parasitic disease of public health importance. The disease is endemic in many African and Mediterranean countries including the Sudan. The objective of the present study was to develop and evaluate a real-time loop-mediated isothermal amplification (LAMP) assay for simple and rapid detection of CE in humans and domestic live stock in Sudan. Methods A set of six LAMP primers, designed from the mitochondrial NADH-1 gene of EG cattle strain of genotype 5 (G5), was used as a target for LAMP assay. The assay was performed at a constant temperature (63?°C), with a real-time follow-up using a LightCycler and fluorochrome dye. Following amplification cycles in a simple water bath, LAMP products were observed for color change by naked eye and were visualized under UV light source using agarose gel electrophoresis. Results The real-time LAMP assay identified a variety of hydatid cysts strains recovered in the Sudan, including Echinococcus canadenses (G6) and Echinococcus ortleppi (G5). Real-time LAMP positive results were detected by the presence of an amplification curve, whereas negative results were indicated by absence of fluorescence detection. Positive LAMP results appeared as a bluish-colored reaction as observed by naked eye, whereas negative LAMP results were observed as purple-colored reaction. The sensitivity studies indicated that the LAMP assay detected as little as a 10?fg of parasite DNA. There was 100?% agreement between results of the LAMP assay and our previously described nested PCR when testing 10-fold serial dilution of DNA extracted from EG-complex hydatid cyst. However, there was no cross-reactivity with other parasites including cysticercus bovis, Fasciola gigantica , and Schistosoma bovis and nucleic acid free samples. Conclusion The developed LAMP assay would be expected to prove highly significant in epidemiological surveys of CE in developing countries or areas of resource-poor settings for both ease of use and cost.
机译:背景囊性超声皮肤病(Ce)或裂化菌,由呼吸膜球菌颗粒(例如) - 核心的幼虫阶段引起,是一种忽略的公共卫生疾病的重要性。该疾病在包括苏丹在内的许多非洲和地中海国家的地方。本研究的目的是开发和评估实时回路介导的等温扩增(灯)测定,以便在苏丹的人类和国内生存库存中简单快速地检测CE。方法使用例如牛基因型5(G5)的线粒体Nadh-1基因设计的一组六个灯引物,用作灯测定的靶标。测定在恒定温度(63Ω℃)下进行,使用光环晶和荧光染料染料进行实时随访。在简单的水浴中扩增循环后,观察到灯泡的灯泡通过肉眼变化,并使用琼脂糖凝胶电泳在UV光源下可视化。结果实时灯测定鉴定出在苏丹中回收的各种纳米囊肿菌株,包括海螺腺癌加元(G6)和echinococccus ortlepppp pp ppi(g5)。通过存在扩增曲线检测实时灯阳性结果,而通过不存在荧光检测表明了负面结果。正灯的结果出现为肉眼观察到的蓝色反应,而负灯结果被观察为紫色反应。敏感性研究表明,灯测定检测到寄生虫的10〜FG。在灯测定结果之间有100次达成协议,并且在测试从例如复合物包发囊肿提取的DNA的10倍串联稀释时,我们先前描述的嵌套PCR。然而,没有与其他寄生虫的交叉反应性,包括囊霉属植物,Fasciola gigantica和血吸虫肉肉菌和核酸游离样品。结论,预计发达的灯泡测定将在发展中国家或资源差的环境中的CE流行病学调查中证明非常重要,以便易于使用和成本。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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