An updated RT-qPCR assay for the simultaneous detection and quantification of chikungunya, dengue and zika viruses

The real-time reverse transcription-polymerase chain reaction (real-time RT-qPCR) has become a leading technique for the detection and quantification of arboviruses, including Chikungunya, Dengue, and Zika viruses. In this study, an updated real-time RT-qPCR assay was designed and evaluated together...

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Autores:
Álvarez Díaz, Diego Alejandro
Valencia Álvarez, Emmanuel
Rivera, Jorge Alonso
Rengifo, Aura Caterine
Usme Ciro, José Aldemar
Peláez Carvajal, Dioselina
Lozano Jimenez, Yenny Y.
Torres Fernández, Orlando
Tipo de recurso:
Article of investigation
Fecha de publicación:
2021
Institución:
Universidad Cooperativa de Colombia
Repositorio:
Repositorio UCC
Idioma:
OAI Identifier:
oai:repository.ucc.edu.co:20.500.12494/46183
Acceso en línea:
https://hdl.handle.net/20.500.12494/46183
Palabra clave:
Arbovirus
Carga viral
RT-qPCR
Chikungunya
Dengue
Zika
Arbovirus
Viral load
RT-qPCR
Chikungunya
Dengue
Zika
Rights
openAccess
License
Atribución
Description
Summary:The real-time reverse transcription-polymerase chain reaction (real-time RT-qPCR) has become a leading technique for the detection and quantification of arboviruses, including Chikungunya, Dengue, and Zika viruses. In this study, an updated real-time RT-qPCR assay was designed and evaluated together with a synthetic positive-control chimeric RNA for the simultaneous detection and quantification of Chikungunya, Dengue, and Zika viruses. Amplification assays were performed to verify the construct integrity and optimal reaction/thermal cycling conditions. The analytical sensitivity of the assay was determined for each virus in single and multiplex reactions, as well as the performance in the detection and viral load quantification of experimental samples. The real-time RT-qPCR assay presented here allowed for the simultaneous detection and quantification of Chikungunya, Dengue, and Zika viruses and could be applied in several studies where the accurate quantification of viral genomes is required.