1. Development of a quantitative one-step multiplex RT-qPCR assay for the detection of SARS-CoV-2 in a biological matrix
- Author
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Cicileia Correia da Silva, Rosiane de Souza Soares Rodrigues, Moreno S. Rodrigues, Marco Aurélio Krieger, Jackson Alves da Silva Queiroz, Caio Henrique Nemeth Santos, Adriana Cristina Salvador Maia, Luan Felipo Botelho Souza, Edivá Basilio da Silva Filho, Francisco de Assis Araújo Aguiar, Alcione de Oliveira dos Santos, Rita de Cássia Pontello Rampazzo, Celina Aparecida Bertoni Lugtenburg, Deusilene Souza Vieira Dall’acqua, Alice Paula Di Sabatino Guimarães, Fernando Rodrigues Máximo, Aline Linhares Ferreira de Melo Mendonça, Suyane da Costa Oliveira, Gabriella Sgorlon Oliveira, Soraya dos Santos Pereira, and Juan Miguel Villalobos Salcedo
- Subjects
0301 basic medicine ,Male ,viruses ,medicine.disease_cause ,law.invention ,0302 clinical medicine ,law ,Multiplex ,030212 general & internal medicine ,skin and connective tissue diseases ,Child ,Polymerase chain reaction ,Coronavirus ,Aged, 80 and over ,education.field_of_study ,General Medicine ,Middle Aged ,Reference Standards ,Viral Load ,Infectious Diseases ,Real-time polymerase chain reaction ,COVID-19 Nucleic Acid Testing ,Child, Preschool ,Female ,Viral load ,Microbiology (medical) ,Adult ,Adolescent ,030106 microbiology ,Population ,Real-Time Polymerase Chain Reaction ,Sensitivity and Specificity ,Article ,lcsh:Infectious and parasitic diseases ,03 medical and health sciences ,Young Adult ,Multiplex polymerase chain reaction ,medicine ,Humans ,lcsh:RC109-216 ,education ,Aged ,business.industry ,SARS-CoV-2 ,fungi ,COVID-19 ,Infant ,Virology ,respiratory tract diseases ,body regions ,Viral replication ,business ,Multiplex Polymerase Chain Reaction - Abstract
Highlights • SARS-CoV-2 Quantification. • Multiplex one-step reaction. • High-sensitivity and specificity assay., Introduction Coronavirus disease-2019 (COVID-19) is a disease caused by Severe Acute Respiratory Syndrome Virus 2 (SARS-CoV-2) that emerged in China in late 2019. The rapid viral spread has made the disease a public health emergency of worldwide concern. The gold standard for diagnosing SARS-CoV-2 is reverse transcription followed by qualitative real-time polymerase chain reaction (RT-qPCR); however, the role of viral load quantification has not been thoroughly investigated yet. Objective The aim of this study was to develop a high-precision quantitative one-step RT-qPCR reaction using the association of the viral target and the human target in the same reaction. Methods The assay standardization involved the absolute quantification method, with serial dilutions of a plasmid with the N gene in a biological matrix to build a standard curve. Results and Discussion The results demonstrated the possibility of quantifying as few as 2.5 copies/reaction and an analysis of 244 patients with known results selected by cross-section that revealed 100% agreement with a qualitative RT-qPCR assay registered by Anvisa. In this population, it was possible to quantify patients with between 2.59 and 3.5 × 107 copies per reaction and negative patients continued to indicate the same result. Conclusion This assay can be a useful tool for a proper patient management, because the level and duration of viral replication are important factors to assess the risk of transmission and to guide decisions regarding the isolation and release of patients; an accurate diagnosis is critical information, whereas the current COVID-19 pandemic represents the biggest current global health problem.
- Published
- 2021