These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: [Study on the rapid detection of Dengue viruses by Taqman MGB real-time fluorescent PCR].
    Author: Liu JJ, Yang F, He JF, Chen JM, He YQ, Yang H.
    Journal: Wei Sheng Yan Jiu; 2006 Nov; 35(6):736-8. PubMed ID: 17290754.
    Abstract:
    OBJECTIVE: To develop the Taqman MGB real-time fluorescent PCR assay for rapid detection of Dengue viruses. METHODS: Using Taqman MGB technique, a pair of universal primers and Taqman MGB probe were designed according to a highly reserved sequence of the 3'-noncoding region of dengue viruses type 1-4. Dengue virus strains were used as standard and Japanese encephalitis virus strains were used as control, the real-time PCR assay for specific and sensitive detection of the dengue viruses was established. While 8 serum specimens of ELISA positive were detected by the RT-PCR and fluorescent PCR. RESULTS: The sensitivity of real-time PCR was 0.17pg/microl (cDNA)or 10(-5)TCID50. There was no cross-reaction with Japanese encephalitis virus. Of 8 specimens, 2 were positive by RT-PCR and 5 were positive by real-time PCR. The test could be completed in 4 hours. CONCLUSION: The Taqman MGB real-time PCR assay was fast, sensitive and specific. It could be applied to the quick early diagnosis of dengue viruses.
    [Abstract] [Full Text] [Related] [New Search]