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Low-Cost, Real-Time Polymerase Chain Reaction System with Integrated RNA Extraction

Rapid, easy-to-use, and low-cost systems for biological sample testing are important for point-of-care diagnostics and various other health applications. The recent pandemic of Coronavirus Disease 2019 (COVID-19) caused by the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) showed an ur...

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Autores principales: Kadja, Tchamie, Sun, Yvonne, Chodavarapu, Vamsy P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222576/
https://www.ncbi.nlm.nih.gov/pubmed/37430517
http://dx.doi.org/10.3390/s23104604
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author Kadja, Tchamie
Sun, Yvonne
Chodavarapu, Vamsy P.
author_facet Kadja, Tchamie
Sun, Yvonne
Chodavarapu, Vamsy P.
author_sort Kadja, Tchamie
collection PubMed
description Rapid, easy-to-use, and low-cost systems for biological sample testing are important for point-of-care diagnostics and various other health applications. The recent pandemic of Coronavirus Disease 2019 (COVID-19) caused by the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) showed an urgent need to rapidly and accurately identify the genetic material of SARS-CoV-2, an enveloped ribonucleic acid (RNA) virus, in upper respiratory specimens from people. In general, sensitive testing methods require genetic material extraction from the specimen. Unfortunately, current commercially available extraction kits are expensive and involve time-consuming and laborious extraction procedures. To overcome the difficulties associated with common extraction methods, we propose a simple enzymatic assay for the nucleic acid extraction step using heat mediation to improve the polymerase chain reaction (PCR) reaction sensitivity. Our protocol was tested on Human Coronavirus 229E (HCoV-229E) as an example, which comes from the large coronaviridae family of viruses that affect birds, amphibians, and mammals, of which SARS-CoV-2 is a member. The proposed assay was performed using a low-cost, custom-made, real-time PCR system that incorporates thermal cycling and fluorescence detection. It had fully customizable reaction settings to allow versatile biological sample testing for various applications, including point-of-care medical diagnosis, food and water quality testing, and emergency health situations. Our results show that heat-mediated RNA extraction is a viable extraction method when compared to commercial extraction kits. Further, our study showed that extraction has a direct impact on purified laboratory samples of HCoV-229E, but no direct impact on infected human cells. This is clinically relevant, as it allows us to circumvent the extraction step on clinical samples when using PCR.
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spelling pubmed-102225762023-05-28 Low-Cost, Real-Time Polymerase Chain Reaction System with Integrated RNA Extraction Kadja, Tchamie Sun, Yvonne Chodavarapu, Vamsy P. Sensors (Basel) Article Rapid, easy-to-use, and low-cost systems for biological sample testing are important for point-of-care diagnostics and various other health applications. The recent pandemic of Coronavirus Disease 2019 (COVID-19) caused by the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) showed an urgent need to rapidly and accurately identify the genetic material of SARS-CoV-2, an enveloped ribonucleic acid (RNA) virus, in upper respiratory specimens from people. In general, sensitive testing methods require genetic material extraction from the specimen. Unfortunately, current commercially available extraction kits are expensive and involve time-consuming and laborious extraction procedures. To overcome the difficulties associated with common extraction methods, we propose a simple enzymatic assay for the nucleic acid extraction step using heat mediation to improve the polymerase chain reaction (PCR) reaction sensitivity. Our protocol was tested on Human Coronavirus 229E (HCoV-229E) as an example, which comes from the large coronaviridae family of viruses that affect birds, amphibians, and mammals, of which SARS-CoV-2 is a member. The proposed assay was performed using a low-cost, custom-made, real-time PCR system that incorporates thermal cycling and fluorescence detection. It had fully customizable reaction settings to allow versatile biological sample testing for various applications, including point-of-care medical diagnosis, food and water quality testing, and emergency health situations. Our results show that heat-mediated RNA extraction is a viable extraction method when compared to commercial extraction kits. Further, our study showed that extraction has a direct impact on purified laboratory samples of HCoV-229E, but no direct impact on infected human cells. This is clinically relevant, as it allows us to circumvent the extraction step on clinical samples when using PCR. MDPI 2023-05-09 /pmc/articles/PMC10222576/ /pubmed/37430517 http://dx.doi.org/10.3390/s23104604 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kadja, Tchamie
Sun, Yvonne
Chodavarapu, Vamsy P.
Low-Cost, Real-Time Polymerase Chain Reaction System with Integrated RNA Extraction
title Low-Cost, Real-Time Polymerase Chain Reaction System with Integrated RNA Extraction
title_full Low-Cost, Real-Time Polymerase Chain Reaction System with Integrated RNA Extraction
title_fullStr Low-Cost, Real-Time Polymerase Chain Reaction System with Integrated RNA Extraction
title_full_unstemmed Low-Cost, Real-Time Polymerase Chain Reaction System with Integrated RNA Extraction
title_short Low-Cost, Real-Time Polymerase Chain Reaction System with Integrated RNA Extraction
title_sort low-cost, real-time polymerase chain reaction system with integrated rna extraction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222576/
https://www.ncbi.nlm.nih.gov/pubmed/37430517
http://dx.doi.org/10.3390/s23104604
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