索引于
  • 打开 J 门
  • Genamics 期刊搜索
  • 学术钥匙
  • 期刊目录
  • 研究圣经
  • 乌尔里希的期刊目录
  • 访问全球在线农业研究 (AGORA)
  • 电子期刊图书馆
  • 参考搜索
  • 哈姆达大学
  • 亚利桑那州EBSCO
  • OCLC-WorldCat
  • SWB 在线目录
  • 虚拟生物学图书馆 (vifabio)
  • 普布隆斯
  • 米亚尔
  • 日内瓦医学教育与研究基金会
  • 欧洲酒吧
  • 谷歌学术
分享此页面
期刊传单
Flyer image

抽象的

A Simple Visual Detection Method of Human Zika Virus Using Reverse Transcription Loop Mediated Isothermal Amplification

Yang Li1,2, Zhenzhou Wan3, Yi Zhou2,4, Xia Jin5, Haifeng Shi1* and Chiyu Zhang 2*

Zika virus (ZIKV) is an emerging mosquito-borne pathogen, and belongs to family Flaviviridae, genus Flavivirus. ZIKV infection was associated with microcephaly and male infertility. The surveillance of ZIKA infection is important for human reproductive health, and the control of the virus spread. Development of a fast and sensitive assay for ZIKV detection is urgently needed for China and other Southeast Asian countries. Here, we developed a one-step, single-tube reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay for ZIKV detection. The assay has a limit of detection (LOD) of 88 copies of Zika RNA per 25 μl reaction, and can be completed within 20 min when the template input is more than the LOD. Furthermore, it exhibits high specificity and good reproducibility. Importantly, the result can be visualized by colorimetric change when HNB or calcein is used. To evaluate the viability of the assay, a comparison between the RT-LAMP assay and a more conversional RT-qPCR was performed using 20 cell culture supernatants and three urine samples. The ZIKV RT-LAMP showed perfect agreement in detection with the RT-qPCR. These results demonstrate that the newly developed ZIKV RT-LAMP is simple, rapid and well suited for ZIKV surveillance, especially in a resource-limited regions.