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Published in: Virology Journal 1/2008

Open Access 01-12-2008 | Methodology

Development and evaluation of one step single tube multiplex RT-PCR for rapid detection and typing of dengue viruses

Authors: Parag Saxena, Paban Kumar Dash, SR Santhosh, Ambuj Shrivastava, Manmohan Parida, PV Lakshmana Rao

Published in: Virology Journal | Issue 1/2008

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Abstract

Background

Dengue is emerging as a major public health concern in many parts of the world. The development of a one-step, single tube, rapid, and multiplex reverse transcription polymerase chain reaction (M-RT-PCR) for simultaneous detection and typing of dengue virus using serotype specific primers during acute phase of illness is reported.

Results

An optimal assay condition with zero background was established having no cross-reaction with closely related members of flavivirus (Japanese encephalitis, West Nile, Yellow fever) and alphavirus (Chikungunya). The feasibility of M-RT-PCR assay for clinical diagnosis was validated with 620 acute phase dengue patient sera samples of recent epidemics in India. The comparative evaluation vis a vis conventional virus isolation revealed higher sensitivity. None of the forty healthy serum samples screened in the present study revealed any amplification, thereby establishing specificity of the reported assay for dengue virus only.

Conclusion

These findings clearly suggested that M-RT-PCR assay reported in the present study is the rapid and cost-effective method for simultaneous detection as well as typing of the dengue virus in acute phase patient serum samples. Thus, the M-RT-PCR assay developed in this study will serve as a very useful tool for rapid diagnosis and typing of dengue infections in endemic areas.
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Metadata
Title
Development and evaluation of one step single tube multiplex RT-PCR for rapid detection and typing of dengue viruses
Authors
Parag Saxena
Paban Kumar Dash
SR Santhosh
Ambuj Shrivastava
Manmohan Parida
PV Lakshmana Rao
Publication date
01-12-2008
Publisher
BioMed Central
Published in
Virology Journal / Issue 1/2008
Electronic ISSN: 1743-422X
DOI
https://doi.org/10.1186/1743-422X-5-20

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