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Updated: May 11, 2025

Measuring Dengue Virus RNA in the Culture Supernatant of Infected Cells by Real-time Quantitative Polymerase Chain Reaction
Published on: November 1, 2018
Conventional RT-PCR for Yellow Fever Virus
Nieli Rodrigues da Costa Faria1, Renata Monteiro-Maia2, Priscila Conrado Guerra Nunes3
1Laboratory of Arboviruses and Hemorrhagic Viruses (LARBOH), Oswaldo Cruz Institute (IOC), Oswaldo Cruz Foundation (FIOCRUZ), Rio de Janeiro, RJ, Brazil.
Abstract:
The yellow fever virus (YFV), prototype of the genus Orthoflavivirus (family Flaviviridae), contains a positive-sense RNA genome that is translated as a single polyprotein which comprises approximately 11,000 nucleotides, encoding 3411 amino acids. In recent years, a number of molecular assays have been reported for YFV RNA detection, with different levels of sensitivity and specificity. Reverse transcription Polymerase Chain Reaction (RT-PCR) assays are the most frequent methods for YFV molecular diagnostics currently. Molecular methods of diagnostics for viral genome detection offer a fast, sensitive, and highly specific alternative to serological assays for early diagnostics during the viremic phase of infection or in fatal cases tissues. This chapter presents some conventional RT-PCR protocols used in molecular diagnostics, among the several available in the literature.
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