Internally Controlled, Generic Real-Time PCR for Quantification and Multiplex Real-Time PCR with Serotype-Specific Probes for Serotyping of Dengue Virus Infections

Dengue has become a global public health problem and a sensitive diagnostic test for early phase detection can be life saving. An internally controlled, generic real-time PCR was developed and validated by testing serial dilutions of a DENV positive control RNA in the presence of a fixed amount of I...

Full description

Bibliographic Details
Main Authors: Sandra Menting, Khoa T. D. Thai, Tran T. T. Nga, Hoang L. Phuong, Paul Klatser, Katja C. Wolthers, Tran Q. Binh, Peter J. de Vries, Marcel Beld
Format: Article
Language:English
Published: Hindawi Limited 2011-01-01
Series:Advances in Virology
Online Access:http://dx.doi.org/10.1155/2011/514681
Description
Summary:Dengue has become a global public health problem and a sensitive diagnostic test for early phase detection can be life saving. An internally controlled, generic real-time PCR was developed and validated by testing serial dilutions of a DENV positive control RNA in the presence of a fixed amount of IC with results showing a good linearity (R2=0.9967) and a LOD of at least 1.95×104 copies/mL. Application of the generic PCR on 136 patient samples revealed a sensitivity of 95.8% and specificity of 100%. A newly developed multiplex real-time PCR with serotype-specific probes allowed the serotyping of DENV for 80 out of 92 (87%) generic real-time PCR positive patients. Combined these real-time PCRs offer a convenient diagnostic tool for the sensitive and specific quantification of DENV in clinical specimens with the possibility for serotyping.
ISSN:1687-8639
1687-8647