Development and Optimization of a Multiplex Real-Time RT-PCR to Detect SARS-CoV-2 in Human Samples

PCR and its variants (RT-PCR and qRT-PCR) are valuable and innovative molecular techniques for studying nucleic acids. qPCR has proven to be highly sensitive, efficient, and reproducible, generating reliable results that are easy to analyze. During the COVID-19 pandemic, qPCR became the gold standar...

Full description

Saved in:
Bibliographic Details
Main Authors: Camilo Castellar-Mendoza, María-Angélica Calderón-Peláez, Jaime E. Castellanos, Myriam L. Velandia-Romero, Carolina Coronel-Ruiz, Sigrid Camacho-Ortega, Lilia J. Bernal-Cepeda, Lady López-Ibarra, Jhann A. Arturo, Félix G. Delgado, Hernando Gutierrez-Barbosa, Sonia Bohorquez-Avila, Johanna Madroñero, Zayda L. Corredor-Rozo, Sandra J. Perdomo-Lara, Angela Fonseca-Benitez, Eliana Calvo
Format: Article
Language:English
Published: Wiley 2024-01-01
Series:International Journal of Microbiology
Online Access:http://dx.doi.org/10.1155/2024/4894004
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832553129093103616
author Camilo Castellar-Mendoza
María-Angélica Calderón-Peláez
Jaime E. Castellanos
Myriam L. Velandia-Romero
Carolina Coronel-Ruiz
Sigrid Camacho-Ortega
Lilia J. Bernal-Cepeda
Lady López-Ibarra
Jhann A. Arturo
Félix G. Delgado
Hernando Gutierrez-Barbosa
Sonia Bohorquez-Avila
Johanna Madroñero
Zayda L. Corredor-Rozo
Sandra J. Perdomo-Lara
Angela Fonseca-Benitez
Eliana Calvo
author_facet Camilo Castellar-Mendoza
María-Angélica Calderón-Peláez
Jaime E. Castellanos
Myriam L. Velandia-Romero
Carolina Coronel-Ruiz
Sigrid Camacho-Ortega
Lilia J. Bernal-Cepeda
Lady López-Ibarra
Jhann A. Arturo
Félix G. Delgado
Hernando Gutierrez-Barbosa
Sonia Bohorquez-Avila
Johanna Madroñero
Zayda L. Corredor-Rozo
Sandra J. Perdomo-Lara
Angela Fonseca-Benitez
Eliana Calvo
author_sort Camilo Castellar-Mendoza
collection DOAJ
description PCR and its variants (RT-PCR and qRT-PCR) are valuable and innovative molecular techniques for studying nucleic acids. qPCR has proven to be highly sensitive, efficient, and reproducible, generating reliable results that are easy to analyze. During the COVID-19 pandemic, qPCR became the gold standard technique for detecting the SARS-CoV-2 virus that allowed to confirm the infection event, and those asymptomatic ones, and thus save millions of lives. In-house multiplex qPCR tests were developed worldwide to detect different viral targets and ensure results, follow the infections, and favor the containment of a pandemic. Here, we present the detailed fundamentals of the qPCR technique based on fluorogenic probes and processes to develop and optimize a successful multiplex RT-qPCR test for detecting SARS-CoV-2 that could be used to diagnose COVID-19 accurately.
format Article
id doaj-art-6dc2e3b667fb4cde98c630bf72e71a58
institution Kabale University
issn 1687-9198
language English
publishDate 2024-01-01
publisher Wiley
record_format Article
series International Journal of Microbiology
spelling doaj-art-6dc2e3b667fb4cde98c630bf72e71a582025-02-03T05:55:27ZengWileyInternational Journal of Microbiology1687-91982024-01-01202410.1155/2024/4894004Development and Optimization of a Multiplex Real-Time RT-PCR to Detect SARS-CoV-2 in Human SamplesCamilo Castellar-Mendoza0María-Angélica Calderón-Peláez1Jaime E. Castellanos2Myriam L. Velandia-Romero3Carolina Coronel-Ruiz4Sigrid Camacho-Ortega5Lilia J. Bernal-Cepeda6Lady López-Ibarra7Jhann A. Arturo8Félix G. Delgado9Hernando Gutierrez-Barbosa10Sonia Bohorquez-Avila11Johanna Madroñero12Zayda L. Corredor-Rozo13Sandra J. Perdomo-Lara14Angela Fonseca-Benitez15Eliana Calvo16Virology GroupVirology GroupVirology GroupVirology GroupVirology GroupVirology GroupVirology GroupVirology GroupVirology GroupVirology GroupVirology GroupVirology GroupVirology GroupUniversidad El BosqueUniversidad El BosqueUniversidad El BosqueVirology GroupPCR and its variants (RT-PCR and qRT-PCR) are valuable and innovative molecular techniques for studying nucleic acids. qPCR has proven to be highly sensitive, efficient, and reproducible, generating reliable results that are easy to analyze. During the COVID-19 pandemic, qPCR became the gold standard technique for detecting the SARS-CoV-2 virus that allowed to confirm the infection event, and those asymptomatic ones, and thus save millions of lives. In-house multiplex qPCR tests were developed worldwide to detect different viral targets and ensure results, follow the infections, and favor the containment of a pandemic. Here, we present the detailed fundamentals of the qPCR technique based on fluorogenic probes and processes to develop and optimize a successful multiplex RT-qPCR test for detecting SARS-CoV-2 that could be used to diagnose COVID-19 accurately.http://dx.doi.org/10.1155/2024/4894004
spellingShingle Camilo Castellar-Mendoza
María-Angélica Calderón-Peláez
Jaime E. Castellanos
Myriam L. Velandia-Romero
Carolina Coronel-Ruiz
Sigrid Camacho-Ortega
Lilia J. Bernal-Cepeda
Lady López-Ibarra
Jhann A. Arturo
Félix G. Delgado
Hernando Gutierrez-Barbosa
Sonia Bohorquez-Avila
Johanna Madroñero
Zayda L. Corredor-Rozo
Sandra J. Perdomo-Lara
Angela Fonseca-Benitez
Eliana Calvo
Development and Optimization of a Multiplex Real-Time RT-PCR to Detect SARS-CoV-2 in Human Samples
International Journal of Microbiology
title Development and Optimization of a Multiplex Real-Time RT-PCR to Detect SARS-CoV-2 in Human Samples
title_full Development and Optimization of a Multiplex Real-Time RT-PCR to Detect SARS-CoV-2 in Human Samples
title_fullStr Development and Optimization of a Multiplex Real-Time RT-PCR to Detect SARS-CoV-2 in Human Samples
title_full_unstemmed Development and Optimization of a Multiplex Real-Time RT-PCR to Detect SARS-CoV-2 in Human Samples
title_short Development and Optimization of a Multiplex Real-Time RT-PCR to Detect SARS-CoV-2 in Human Samples
title_sort development and optimization of a multiplex real time rt pcr to detect sars cov 2 in human samples
url http://dx.doi.org/10.1155/2024/4894004
work_keys_str_mv AT camilocastellarmendoza developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT mariaangelicacalderonpelaez developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT jaimeecastellanos developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT myriamlvelandiaromero developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT carolinacoronelruiz developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT sigridcamachoortega developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT liliajbernalcepeda developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT ladylopezibarra developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT jhannaarturo developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT felixgdelgado developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT hernandogutierrezbarbosa developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT soniabohorquezavila developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT johannamadronero developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT zaydalcorredorrozo developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT sandrajperdomolara developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT angelafonsecabenitez developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples
AT elianacalvo developmentandoptimizationofamultiplexrealtimertpcrtodetectsarscov2inhumansamples