A Rapid SARS-CoV-2 RT-PCR Assay for Low Resource Settings

Quantitative reverse transcription polymerase chain reaction (RT-qPCR) assay is the gold standard recommended to test for acute SARS-CoV-2 infection. However, it generally requires expensive equipment such as RNA isolation instruments and real-time PCR thermal cyclers. As a pandemic, COVID-19 has sp...

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Main Authors: Arunkumar Arumugam, Matthew L. Faron, Peter Yu, Cole Markham, Michelle Wu, Season Wong
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Diagnostics
Subjects:
RNA
Online Access:https://www.mdpi.com/2075-4418/10/10/739
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spelling doaj-2e73a79ce360430297ff859643c795262020-11-25T03:13:18ZengMDPI AGDiagnostics2075-44182020-09-011073973910.3390/diagnostics10100739A Rapid SARS-CoV-2 RT-PCR Assay for Low Resource SettingsArunkumar Arumugam0Matthew L. Faron1Peter Yu2Cole Markham3Michelle Wu4Season Wong5AI Biosciences, Inc., College Station, TX 77845, USAThe Medical College of Wisconsin, Milwaukee, WI 53226, USAAI Biosciences, Inc., College Station, TX 77845, USAAI Biosciences, Inc., College Station, TX 77845, USAAI Biosciences, Inc., College Station, TX 77845, USAAI Biosciences, Inc., College Station, TX 77845, USAQuantitative reverse transcription polymerase chain reaction (RT-qPCR) assay is the gold standard recommended to test for acute SARS-CoV-2 infection. However, it generally requires expensive equipment such as RNA isolation instruments and real-time PCR thermal cyclers. As a pandemic, COVID-19 has spread indiscriminately, and many low resource settings and developing countries do not have the means for fast and accurate COVID-19 detection to control the outbreak. Additionally, long assay times, in part caused by slow sample preparation steps, have created a large backlog when testing patient samples suspected of COVID-19. With many PCR-based molecular assays including an extraction step, this can take a significant amount of time and labor, especially if the extraction is performed manually. Using COVID-19 clinical specimens, we have collected evidence that the RT-qPCR assay can feasibly be performed directly on patient sample material in virus transport medium (VTM) without an RNA extraction step, while still producing sensitive test results. If RNA extraction steps can be omitted without significantly affecting clinical sensitivity, the turn-around time of COVID-19 tests, and the backlog we currently experience can be reduced drastically. Furthermore, our data suggest that rapid RT-PCR can be implemented for sensitive and specific molecular diagnosis of COVID-19 in locations where sophisticated laboratory instruments are not available. Our USD 300 set up achieved rapid RT-PCR using thin-walled PCR tubes and a water bath setup using sous vide immersion heaters, a Raspberry Pi computer, and a single servo motor that can process up to 96 samples at a time. Using COVID-19 positive clinical specimens, we demonstrated that RT-PCR assays can be performed in as little as 12 min using untreated samples, heat-inactivated samples, or extracted RNA templates with our low-cost water bath setup. These findings can help rapid COVID-19 testing to become more accessible and attainable across the globe.https://www.mdpi.com/2075-4418/10/10/739SARS-CoV-2 virusRNArapid RT-PCR assaylow resource settingthermal cycler
collection DOAJ
language English
format Article
sources DOAJ
author Arunkumar Arumugam
Matthew L. Faron
Peter Yu
Cole Markham
Michelle Wu
Season Wong
spellingShingle Arunkumar Arumugam
Matthew L. Faron
Peter Yu
Cole Markham
Michelle Wu
Season Wong
A Rapid SARS-CoV-2 RT-PCR Assay for Low Resource Settings
Diagnostics
SARS-CoV-2 virus
RNA
rapid RT-PCR assay
low resource setting
thermal cycler
author_facet Arunkumar Arumugam
Matthew L. Faron
Peter Yu
Cole Markham
Michelle Wu
Season Wong
author_sort Arunkumar Arumugam
title A Rapid SARS-CoV-2 RT-PCR Assay for Low Resource Settings
title_short A Rapid SARS-CoV-2 RT-PCR Assay for Low Resource Settings
title_full A Rapid SARS-CoV-2 RT-PCR Assay for Low Resource Settings
title_fullStr A Rapid SARS-CoV-2 RT-PCR Assay for Low Resource Settings
title_full_unstemmed A Rapid SARS-CoV-2 RT-PCR Assay for Low Resource Settings
title_sort rapid sars-cov-2 rt-pcr assay for low resource settings
publisher MDPI AG
series Diagnostics
issn 2075-4418
publishDate 2020-09-01
description Quantitative reverse transcription polymerase chain reaction (RT-qPCR) assay is the gold standard recommended to test for acute SARS-CoV-2 infection. However, it generally requires expensive equipment such as RNA isolation instruments and real-time PCR thermal cyclers. As a pandemic, COVID-19 has spread indiscriminately, and many low resource settings and developing countries do not have the means for fast and accurate COVID-19 detection to control the outbreak. Additionally, long assay times, in part caused by slow sample preparation steps, have created a large backlog when testing patient samples suspected of COVID-19. With many PCR-based molecular assays including an extraction step, this can take a significant amount of time and labor, especially if the extraction is performed manually. Using COVID-19 clinical specimens, we have collected evidence that the RT-qPCR assay can feasibly be performed directly on patient sample material in virus transport medium (VTM) without an RNA extraction step, while still producing sensitive test results. If RNA extraction steps can be omitted without significantly affecting clinical sensitivity, the turn-around time of COVID-19 tests, and the backlog we currently experience can be reduced drastically. Furthermore, our data suggest that rapid RT-PCR can be implemented for sensitive and specific molecular diagnosis of COVID-19 in locations where sophisticated laboratory instruments are not available. Our USD 300 set up achieved rapid RT-PCR using thin-walled PCR tubes and a water bath setup using sous vide immersion heaters, a Raspberry Pi computer, and a single servo motor that can process up to 96 samples at a time. Using COVID-19 positive clinical specimens, we demonstrated that RT-PCR assays can be performed in as little as 12 min using untreated samples, heat-inactivated samples, or extracted RNA templates with our low-cost water bath setup. These findings can help rapid COVID-19 testing to become more accessible and attainable across the globe.
topic SARS-CoV-2 virus
RNA
rapid RT-PCR assay
low resource setting
thermal cycler
url https://www.mdpi.com/2075-4418/10/10/739
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