Usefulness of an in vitro-transcribed RNA control for the detection and quantification of Yellow fever virus through real-time reverse transcription-polymerase chain reaction

ABSTRACT: Introduction: Unvaccinated individuals in endemic areas with proven enzootic transmission of Yellow fever virus are at risk of infection due to a dramatic shift in the epidemiology of the disease over recent years. For this reason, epidemiological surveillance and laboratory confirmation o...

Full description

Autores:
Navas Navas, María Cristina
Laiton Donato, Katherine
Quintero Cortés, Paula
Franco Salazar, Juan P.
Peláez Carvajal, Dioselina
Junglen, Sandra
Parra Henao, Gabriel
Usme Ciro, Jose A.
Tipo de recurso:
Article of investigation
Fecha de publicación:
2024
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/39595
Acceso en línea:
https://hdl.handle.net/10495/39595
https://www.sciencedirect.com/science/article/pii/S2666991923000167
Palabra clave:
Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
Reverse Transcriptase Polymerase Chain Reaction
Transcripción Reversa
Reverse Transcription
Fiebre Amarilla
Yellow Fever
Virus de la Fiebre Amarilla
Yellow fever virus
Diagnóstico
Diagnosis
Epidemiología
Epidemiology
ARN
RNA
https://id.nlm.nih.gov/mesh/D020133
https://id.nlm.nih.gov/mesh/D048348
https://id.nlm.nih.gov/mesh/D015004
https://id.nlm.nih.gov/mesh/D015005
https://id.nlm.nih.gov/mesh/D003933
https://id.nlm.nih.gov/mesh/D004813
https://id.nlm.nih.gov/mesh/D012313
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-nd/4.0/
Description
Summary:ABSTRACT: Introduction: Unvaccinated individuals in endemic areas with proven enzootic transmission of Yellow fever virus are at risk of infection due to a dramatic shift in the epidemiology of the disease over recent years. For this reason, epidemiological surveillance and laboratory confirmation of cases have become mandatory. Objective: To develop and test a control RNA for YFV detection through real-time RT-PCR. Methods: A 437-bp insert containing the T7 promoter and the target sequences for two different in-house protocols was designed in the context of the pUC57 vector and obtained through gene synthesis. After T7-driven in vitro transcription, standard curves were developed for Log10 serial dilutions of the YFV control RNA with 8 replicates. Results: A dynamic range of quantification of 10 orders of magnitude was observed with a limit of detection of 6.3 GCE/µL (95% CI, 2.6 to 139.4 GCE/µL). Conclusion: The plasmid construct is available for YFV molecular test validation on clinical, entomological, and epizootic samples. Keywords: In vitro transcription; Molecular detection; Plasmid DNA; RT-qPCR; Yellow fever virus.