4.4 Article

Lyophilized visually readable loop-mediated isothermal reverse transcriptase nucleic acid amplification test for detection Ebola Zaire RNA

期刊

JOURNAL OF VIROLOGICAL METHODS
卷 244, 期 -, 页码 32-38

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jviromet.2017.02.013

关键词

Ebola; Lyophilized; Reverse-transcriptase; Nucleic-acid-amplification

资金

  1. Department of Veterans Affairs
  2. National Institutes of Health [AI100665, EB015365, AI036214, AI007384]
  3. James B. Pendleton Charitable Trust
  4. University of California, San Diego
  5. Center for AIDS Research (CFAR), an NIH [P30 AI036214]
  6. NIAID
  7. NCI
  8. NIMH
  9. NIDA
  10. NICHD
  11. NHLBI
  12. NIA
  13. NIGMS
  14. NIDDK

向作者/读者索取更多资源

Recent viral outbreaks highlight the need for reliable, yet broadly deployable diagnostics for detection of epidemic and emerging pathogens. In this study we designed and optimized methods to visually detect viral nucleic acid by isothermal amplification and SYBR dye intercalation. We designed and tested loop mediated isothermal amplification (LAMP) primers and lyophilized reactions to optimize the detection of Zaire Ebola Virus (ZEBOV) and further evolved the LAMP platform to allow room-temperature storage for deployment in resource limited settings. Our results demonstrated excellent sensitivity and specificity for viral nucleic acid sequences with lower limits of detection of less than 100 copies. Moreover, lyophilized reaction mixtures retained activity for prolonged periods under dry conditions at room temperature. This approach offers a way for detection of emerging viruses in resource limited settings. (C) 2017 Published by Elsevier B.V.

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