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Non-Instrumented Incubation of a Recombinase Polymerase Amplification Assay for the Rapid and Sensitive Detection of Proviral HIV-1 DNA

Sensitive diagnostic tests for infectious diseases often employ nucleic acid amplification technologies (NAATs). However, most NAAT assays, including many isothermal amplification methods, require power-dependent instrumentation for incubation. For use in low resource settings (LRS), diagnostics tha...

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Autores principales: Lillis, Lorraine, Lehman, Dara, Singhal, Mitra C., Cantera, Jason, Singleton, Jered, Labarre, Paul, Toyama, Anthony, Piepenburg, Olaf, Parker, Mathew, Wood, Robert, Overbaugh, Julie, Boyle, David S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180440/
https://www.ncbi.nlm.nih.gov/pubmed/25264766
http://dx.doi.org/10.1371/journal.pone.0108189
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author Lillis, Lorraine
Lehman, Dara
Singhal, Mitra C.
Cantera, Jason
Singleton, Jered
Labarre, Paul
Toyama, Anthony
Piepenburg, Olaf
Parker, Mathew
Wood, Robert
Overbaugh, Julie
Boyle, David S.
author_facet Lillis, Lorraine
Lehman, Dara
Singhal, Mitra C.
Cantera, Jason
Singleton, Jered
Labarre, Paul
Toyama, Anthony
Piepenburg, Olaf
Parker, Mathew
Wood, Robert
Overbaugh, Julie
Boyle, David S.
author_sort Lillis, Lorraine
collection PubMed
description Sensitive diagnostic tests for infectious diseases often employ nucleic acid amplification technologies (NAATs). However, most NAAT assays, including many isothermal amplification methods, require power-dependent instrumentation for incubation. For use in low resource settings (LRS), diagnostics that do not require consistent electricity supply would be ideal. Recombinase polymerase amplification (RPA) is an isothermal amplification technology that has been shown to typically work at temperatures ranging from 25–43°C, and does not require a stringent incubation temperature for optimal performance. Here we evaluate the ability to incubate an HIV-1 RPA assay, intended for use as an infant HIV diagnostic in LRS, at ambient temperatures or with a simple non-instrumented heat source. To determine the range of expected ambient temperatures in settings where an HIV-1 infant diagnostic would be of most use, a dataset of the seasonal range of daily temperatures in sub Saharan Africa was analyzed and revealed ambient temperatures as low as 10°C and rarely above 43°C. All 24 of 24 (100%) HIV-1 RPA reactions amplified when incubated for 20 minutes between 31°C and 43°C. The amplification from the HIV-1 RPA assay under investigation at temperatures was less consistent below 30°C. Thus, we developed a chemical heater to incubate HIV-1 RPA assays when ambient temperatures are between 10°C and 30°C. All 12/12 (100%) reactions amplified with chemical heat incubation from ambient temperatures of 15°C, 20°C, 25°C and 30°C. We also observed that incubation at 30 minutes improved assay performance at lower temperatures where detection was sporadic using 20 minutes incubation. We have demonstrated that incubation of the RPA HIV-1 assay via ambient temperatures or using chemical heaters yields similar results to using electrically powered devices. We propose that this RPA HIV-1 assay may not need dedicated equipment to be a highly sensitive tool to diagnose infant HIV-1 in LRS.
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spelling pubmed-41804402014-10-07 Non-Instrumented Incubation of a Recombinase Polymerase Amplification Assay for the Rapid and Sensitive Detection of Proviral HIV-1 DNA Lillis, Lorraine Lehman, Dara Singhal, Mitra C. Cantera, Jason Singleton, Jered Labarre, Paul Toyama, Anthony Piepenburg, Olaf Parker, Mathew Wood, Robert Overbaugh, Julie Boyle, David S. PLoS One Research Article Sensitive diagnostic tests for infectious diseases often employ nucleic acid amplification technologies (NAATs). However, most NAAT assays, including many isothermal amplification methods, require power-dependent instrumentation for incubation. For use in low resource settings (LRS), diagnostics that do not require consistent electricity supply would be ideal. Recombinase polymerase amplification (RPA) is an isothermal amplification technology that has been shown to typically work at temperatures ranging from 25–43°C, and does not require a stringent incubation temperature for optimal performance. Here we evaluate the ability to incubate an HIV-1 RPA assay, intended for use as an infant HIV diagnostic in LRS, at ambient temperatures or with a simple non-instrumented heat source. To determine the range of expected ambient temperatures in settings where an HIV-1 infant diagnostic would be of most use, a dataset of the seasonal range of daily temperatures in sub Saharan Africa was analyzed and revealed ambient temperatures as low as 10°C and rarely above 43°C. All 24 of 24 (100%) HIV-1 RPA reactions amplified when incubated for 20 minutes between 31°C and 43°C. The amplification from the HIV-1 RPA assay under investigation at temperatures was less consistent below 30°C. Thus, we developed a chemical heater to incubate HIV-1 RPA assays when ambient temperatures are between 10°C and 30°C. All 12/12 (100%) reactions amplified with chemical heat incubation from ambient temperatures of 15°C, 20°C, 25°C and 30°C. We also observed that incubation at 30 minutes improved assay performance at lower temperatures where detection was sporadic using 20 minutes incubation. We have demonstrated that incubation of the RPA HIV-1 assay via ambient temperatures or using chemical heaters yields similar results to using electrically powered devices. We propose that this RPA HIV-1 assay may not need dedicated equipment to be a highly sensitive tool to diagnose infant HIV-1 in LRS. Public Library of Science 2014-09-29 /pmc/articles/PMC4180440/ /pubmed/25264766 http://dx.doi.org/10.1371/journal.pone.0108189 Text en © 2014 Lillis et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lillis, Lorraine
Lehman, Dara
Singhal, Mitra C.
Cantera, Jason
Singleton, Jered
Labarre, Paul
Toyama, Anthony
Piepenburg, Olaf
Parker, Mathew
Wood, Robert
Overbaugh, Julie
Boyle, David S.
Non-Instrumented Incubation of a Recombinase Polymerase Amplification Assay for the Rapid and Sensitive Detection of Proviral HIV-1 DNA
title Non-Instrumented Incubation of a Recombinase Polymerase Amplification Assay for the Rapid and Sensitive Detection of Proviral HIV-1 DNA
title_full Non-Instrumented Incubation of a Recombinase Polymerase Amplification Assay for the Rapid and Sensitive Detection of Proviral HIV-1 DNA
title_fullStr Non-Instrumented Incubation of a Recombinase Polymerase Amplification Assay for the Rapid and Sensitive Detection of Proviral HIV-1 DNA
title_full_unstemmed Non-Instrumented Incubation of a Recombinase Polymerase Amplification Assay for the Rapid and Sensitive Detection of Proviral HIV-1 DNA
title_short Non-Instrumented Incubation of a Recombinase Polymerase Amplification Assay for the Rapid and Sensitive Detection of Proviral HIV-1 DNA
title_sort non-instrumented incubation of a recombinase polymerase amplification assay for the rapid and sensitive detection of proviral hiv-1 dna
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180440/
https://www.ncbi.nlm.nih.gov/pubmed/25264766
http://dx.doi.org/10.1371/journal.pone.0108189
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